Application and synthesis of thiazole ring in clinically approved drugs

The development of heterocyclic derivatives has progressed considerably over the past few decades, and many new agents of synthetic and natural origin have been produced. Among heterocyclic compounds, thiazole is a unique five-membered heterocyclic motif characterized by nitrogen and sulfur atoms, w...

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Published inEuropean journal of medicinal chemistry Vol. 250; p. 115172
Main Authors Niu, Zhen-Xi, Wang, Ya-Tao, Zhang, Sheng-Nan, Li, Yan, Chen, Xiao-Bing, Wang, Sai-Qi, Liu, Hong-Min
Format Journal Article
LanguageEnglish
Published France Elsevier Masson SAS 15.03.2023
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Abstract The development of heterocyclic derivatives has progressed considerably over the past few decades, and many new agents of synthetic and natural origin have been produced. Among heterocyclic compounds, thiazole is a unique five-membered heterocyclic motif characterized by nitrogen and sulfur atoms, which is widely used as an important core skeleton in a variety of pharmaceutically important compounds due to their diverse biological activities, such as antibacterial, antivirus, and antifungal. To the best of our knowledge, more than 90 thiazole-containing derivatives have been currently under clinical investigation, and some thiazole analogs have been approved to treat various diseases. As the potentially privileged scaffolds, thiazole derivatives can be further extensively explored to search for new drugs characterized by improved therapeutic efficacy and similar biological targets. This review aims to outline the applications and synthetic routes of some representative thiazole-containing drugs approved in the clinic, which may guide medicinal researchers to rationally design more effective thiazole-containing drug candidates. [Display omitted] •Thiazole ring is widely used in many drugs to treat various diseases.•Recent advances in thiazole-containing drugs have been summarized.•The clinical applications and synthetic routes of 33 thiazole-containing drugs are highlighted.•Summary and prospect are briefly discussed to guide future design of thiazole-containing drugs.
AbstractList The development of heterocyclic derivatives has progressed considerably over the past few decades, and many new agents of synthetic and natural origin have been produced. Among heterocyclic compounds, thiazole is a unique five-membered heterocyclic motif characterized by nitrogen and sulfur atoms, which is widely used as an important core skeleton in a variety of pharmaceutically important compounds due to their diverse biological activities, such as antibacterial, antivirus, and antifungal. To the best of our knowledge, more than 90 thiazole-containing derivatives have been currently under clinical investigation, and some thiazole analogs have been approved to treat various diseases. As the potentially privileged scaffolds, thiazole derivatives can be further extensively explored to search for new drugs characterized by improved therapeutic efficacy and similar biological targets. This review aims to outline the applications and synthetic routes of some representative thiazole-containing drugs approved in the clinic, which may guide medicinal researchers to rationally design more effective thiazole-containing drug candidates.
The development of heterocyclic derivatives has progressed considerably over the past few decades, and many new agents of synthetic and natural origin have been produced. Among heterocyclic compounds, thiazole is a unique five-membered heterocyclic motif characterized by nitrogen and sulfur atoms, which is widely used as an important core skeleton in a variety of pharmaceutically important compounds due to their diverse biological activities, such as antibacterial, antivirus, and antifungal. To the best of our knowledge, more than 90 thiazole-containing derivatives have been currently under clinical investigation, and some thiazole analogs have been approved to treat various diseases. As the potentially privileged scaffolds, thiazole derivatives can be further extensively explored to search for new drugs characterized by improved therapeutic efficacy and similar biological targets. This review aims to outline the applications and synthetic routes of some representative thiazole-containing drugs approved in the clinic, which may guide medicinal researchers to rationally design more effective thiazole-containing drug candidates.The development of heterocyclic derivatives has progressed considerably over the past few decades, and many new agents of synthetic and natural origin have been produced. Among heterocyclic compounds, thiazole is a unique five-membered heterocyclic motif characterized by nitrogen and sulfur atoms, which is widely used as an important core skeleton in a variety of pharmaceutically important compounds due to their diverse biological activities, such as antibacterial, antivirus, and antifungal. To the best of our knowledge, more than 90 thiazole-containing derivatives have been currently under clinical investigation, and some thiazole analogs have been approved to treat various diseases. As the potentially privileged scaffolds, thiazole derivatives can be further extensively explored to search for new drugs characterized by improved therapeutic efficacy and similar biological targets. This review aims to outline the applications and synthetic routes of some representative thiazole-containing drugs approved in the clinic, which may guide medicinal researchers to rationally design more effective thiazole-containing drug candidates.
The development of heterocyclic derivatives has progressed considerably over the past few decades, and many new agents of synthetic and natural origin have been produced. Among heterocyclic compounds, thiazole is a unique five-membered heterocyclic motif characterized by nitrogen and sulfur atoms, which is widely used as an important core skeleton in a variety of pharmaceutically important compounds due to their diverse biological activities, such as antibacterial, antivirus, and antifungal. To the best of our knowledge, more than 90 thiazole-containing derivatives have been currently under clinical investigation, and some thiazole analogs have been approved to treat various diseases. As the potentially privileged scaffolds, thiazole derivatives can be further extensively explored to search for new drugs characterized by improved therapeutic efficacy and similar biological targets. This review aims to outline the applications and synthetic routes of some representative thiazole-containing drugs approved in the clinic, which may guide medicinal researchers to rationally design more effective thiazole-containing drug candidates. [Display omitted] •Thiazole ring is widely used in many drugs to treat various diseases.•Recent advances in thiazole-containing drugs have been summarized.•The clinical applications and synthetic routes of 33 thiazole-containing drugs are highlighted.•Summary and prospect are briefly discussed to guide future design of thiazole-containing drugs.
ArticleNumber 115172
Author Wang, Ya-Tao
Wang, Sai-Qi
Liu, Hong-Min
Li, Yan
Chen, Xiao-Bing
Niu, Zhen-Xi
Zhang, Sheng-Nan
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  organization: Department of Pharmacy, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, 450018, China
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  fullname: Wang, Ya-Tao
  organization: First People's Hospital of Shangqiu, Henan Province, Shangqiu, 476100, China
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  givenname: Sheng-Nan
  surname: Zhang
  fullname: Zhang, Sheng-Nan
  organization: Department of Pharmacy, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, 450018, China
– sequence: 4
  givenname: Yan
  surname: Li
  fullname: Li, Yan
  organization: Department of Pharmacy, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, 450018, China
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  givenname: Xiao-Bing
  surname: Chen
  fullname: Chen, Xiao-Bing
  email: zlyychenxb0807@zzu.edu.cn
  organization: The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Henan Engineering Research Center of Precision Therapy of Gastrointestinal Cancer, Zhengzhou Key Laboratory for Precision Therapy of Gastrointestinal Cancer, Zhengzhou, 450008, China
– sequence: 6
  givenname: Sai-Qi
  surname: Wang
  fullname: Wang, Sai-Qi
  email: zlyywangsq3925@zzu.edu.cn
  organization: The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Henan Engineering Research Center of Precision Therapy of Gastrointestinal Cancer, Zhengzhou Key Laboratory for Precision Therapy of Gastrointestinal Cancer, Zhengzhou, 450008, China
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  givenname: Hong-Min
  orcidid: 0000-0001-6771-9421
  surname: Liu
  fullname: Liu, Hong-Min
  email: liuhm@zzu.edu.cn
  organization: School of Pharmaceutical Sciences & Key Laboratory of Advanced Drug Preparation Technologies, Ministry of Education, Zhengzhou University, Zhengzhou, 450001, China
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Cites_doi 10.1158/1538-7445.AM2018-4004
10.1158/1535-7163.MCT-08-0999
10.1128/AAC.05760-11
10.1128/AAC.01454-17
10.1016/S0021-5198(19)40053-X
10.1080/17512433.2019.1649137
10.1007/BF03256641
10.1016/j.ejphar.2017.02.046
10.1097/00008469-199702000-00010
10.1016/j.bmcl.2013.05.007
10.3390/molecules26113166
10.1007/BF01645372
10.1016/S0006-2952(99)00026-X
10.1371/journal.pone.0012041
10.1016/j.ejmech.2014.12.031
10.1136/bjo.73.7.574
10.1016/S1473-3099(07)70109-3
10.3390/molecules27133994
10.1074/jbc.M109.029470
10.1016/j.clinthera.2006.08.004
10.1002/jbt.22029
10.1016/j.bmc.2008.12.037
10.1093/jac/10.5.391
10.1016/j.lfs.2004.10.031
10.4103/0250-474X.45393
10.1124/jpet.110.174847
10.1158/1535-7163.MCT-11-0989
10.1158/1535-7163.MCT-13-0865
10.1093/jac/30.6.871
10.1021/jm00092a006
10.1016/j.ejmech.2015.04.015
10.1128/AAC.01217-06
10.1111/j.1538-7836.2008.03064.x
10.1159/000127837
10.7164/antibiotics.40.1468
10.1021/jm049486a
10.2174/1573406412666160920091146
10.1021/op900031h
10.1128/AAC.18.2.257
10.1021/acscentsci.0c01186
10.1111/bcp.13517
10.4103/0253-7613.111922
10.1039/b005804l
10.1159/000007106
10.1111/1346-8138.14607
10.1155/2018/4196961
10.1097/00006454-199803000-00022
10.1242/dmm.033860
10.1016/j.bmcl.2008.07.088
10.1128/AAC.01569-16
10.7164/antibiotics.33.783
10.1046/j.1365-2125.1997.00644.x
10.2174/1568026616666160506130731
10.1371/journal.pone.0101118
10.1128/AAC.00742-16
10.2165/00003495-198427060-00001
10.1002/jps.2600670944
10.1016/j.cbi.2016.07.024
10.1021/cc000002f
10.4049/jimmunol.152.5.2447
10.2165/00003495-200464220-00009
10.1124/jpet.106.115840
10.1007/s11095-015-1787-y
10.1128/MMBR.69.4.585-607.2005
10.1152/ajprenal.00454.2007
10.3892/ol.2017.6400
10.1016/S0002-9610(02)01125-X
10.1007/BF01273182
10.1002/ijc.29040
10.4155/fmc-2018-0196
10.1097/00006454-198710000-00034
10.5483/BMBRep.2016.49.4.220
10.7164/antibiotics.43.1047
10.1016/j.ijfoodmicro.2011.12.032
10.1002/bdrb.21165
10.1021/jm9607010
10.2174/1573406412666160201121310
10.1111/nmo.13813
10.1016/j.lfs.2007.01.035
10.1021/jm00362a014
10.1016/j.bmcl.2007.05.036
10.1007/s40265-015-0525-4
10.1002/(SICI)1521-4184(199910)332:10<343::AID-ARDP343>3.0.CO;2-0
10.1007/s00044-011-9685-2
10.1016/0223-5234(87)90169-3
10.1002/jlcr.2580330812
10.1007/s11307-022-01735-z
10.1016/j.lfs.2020.118119
10.1016/S0968-0896(03)00126-3
10.1021/jm00386a009
10.1128/AAC.35.10.2078
10.1007/s00044-008-9089-0
10.1128/AAC.01242-06
10.1186/s41936-020-00196-6
10.1016/0732-8893(95)00080-T
10.1111/j.1600-0609.2008.01198.x
10.1021/ml1000257
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Keywords Heterocycles
Thiazole ring
Chemical synthesis
Clinical application
Privileged scaffold
Language English
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References T. Takaya, H. Takasugi, T. Masugi, H. Yamanaka, K. Kawabata, 7-Acylamino-3-vinylcephalosporanic Acid Derivatives and Processes for the Preparation Thereof, US4409214A..
Schneider, Mierau (bib107) 1987; 30
H. Jianjin, L. Xiaojun, S. Bo, Y. Yan, Process for Producing 2-hydroxybenzamide Derivs, CN103709191A..
Richards, Heel, Brogden, Speight, Avery (bib35) 1984; 27
Jacqueline, Caillon, Le Mabecque, Miegeville, Hamel, Bugnon, Ge, Potel (bib63) 2007; 51
Woodfield, Van Rij, Pettigrew, van der Linden, Solomon, Bolt (bib26) 2003; 185
Greger, Eastman, Zhang, Bleam, Hughes, Smitheman, Dickerson, Laquerre, Liu, Gilmer (bib92) 2012; 11
Vengurlekar, Prachand, Jain, Gupta (bib14) 2014; 5
Wellington, Curran (bib60) 2004; 64
Andrabi, Ali, Tabassum, Parveen, Parvez (bib105) 2019; 12
Khames, Gad, Abd El-Raouf (bib142) 2017; 805
Kvernmo, Härtter, Burger (bib101) 2006; 28
Mezei, Mesterházy, Bakó, Porcs-Makkay, Simig, Volk (bib137) 2009; 13
Karade, Acharya, Sathe, Kaushik (bib11) 2008; 17
Y. Kumar, M. Prasad, A. Prasad, S.K. Singh, N.P. Kumar, Preparation of Crystalline Cefdinir Potassium Dihydrate, WO2003050124A1..
Standridge, Swigor (bib56) 1993; 33
Rajagopalan, Pan, Schaefer, Nicholas, Lim, Misialek, Stevens, Hooi, Aleskovski, Ruhrmund (bib76) 2017; 61
Fukushima‐Shintani, Suzuki, Iwatsuki, Abe, Sugasawa, Hirayama, Kawasaki, Nakahata (bib128) 2009; 82
Gurupadayya, Gopal, Padmashali, Manohara (bib6) 2008; 70
Jang, Choi, Kim, Kim, Kang, Park, Ryu, Lee, Kim, Rhee (bib23) 2014; 9
Yoshii, Iikura, Hirayama, Toda, Kawabata (bib117) 2016; 33
Fikry, Hasan, Mohamed (bib136) 2018; 32
Jubie, Gowramma, Nitin, Jawahar, Kalirajan, Gomathy, Sankar, Elango (bib17) 2009; 1
Reiner, Weiss, Brombacher, Lanz, Montavon, Furlenmeier, Angehrn, Probst (bib36) 1980; 32
Ito, Sato, Ota, Takemura, Nishikawa, Toba, Kohira, Miyagawa, Ishibashi, Matsumoto (bib65) 2018; 62
M. Soukup, Process for the Manufacture of Enantiomerically Pure Antifungal Azoles as Ravuconazole and Isavuconazole, US8207352B2..
Ayati, Emami, Asadipour, Shafiee, Foroumadi (bib18) 2015; 97
Benedetti, Norbedo (bib83) 2001
Sánchez-Lozada, Tapia, Bautista-García, Soto, Ávila-Casado, Vega-Campos, Nakagawa, Zhao, Franco, Johnson (bib139) 2008; 294
Van, Nguyen, Smooker, Coloe (bib24) 2012; 154
Rossignol, La Frazia, Chiappa, Ciucci, Santoro (bib85) 2009; 284
W.E. Klunk, C.A.M. Jr, Amyloid Imaging as a Surrofate Marker for Efficacy of Anti-amyloid Therapies, US8147798B2..
Nagata, Yoshino, Haginoya, Yoshikawa, Nagamochi, Kobayashi, Komoriya, Yokomizo, Muto, Yamaguchi, Osanai, Suzuki, Kanno (bib125) 2009; 17
Pattan, Dighe, Nirmal, Merekar, Laware, Shinde, Musmade (bib12) 2009; 2
Raboisson, de Kock, Rosenquist, Nilsson, Salvador-Oden, Lin, Roue, Ivanov, Wahling, Wickstrom, Hamelink, Edlund, Vrang, Vendeville, Van de Vreken, McGowan, Tahri, Hu, Boutton, Lenz, Delouvroy, Pille, Surleraux, Wigerinck, Samuelsson, Simmen (bib77) 2008; 18
Z Laczkowski, Biernasiuk, Baranowska-Laczkowska, Misiura, Malm, Plech, Paneth (bib9) 2016; 12
Hakimizadeh, Hassanshahi, Kaeidi, Nematollahi, Taghipour, Rahmani, Fatemi (bib30) 2020; 258
Foye (bib31) 2008
Okura, Ito, Ishiguro, Tamai, Deguchi (bib102) 2007; 80
Hantzsch, Weber (bib2) 1887; 20
Scheffers, Pinho (bib32) 2005; 69
Ishikawa, Matsunaga, Tawada, Kuroda, Nakayama, Ishibashi, Tomimoto, Ikeda, Tagawa, Iizawa (bib64) 2003; 11
Raboisson, de Kock, Rosenquist, Nilsson, Salvador-Oden, Lin, Roue, Ivanov, Wähling, Wickström (bib74) 2008; 18
Kim (bib126) 2016; 76
Matsunaga, Tanaka, Yoshinaga, Ueki, Hori, Eta, Kawabata, Yoshii, Yoshida, Matsumura (bib115) 2011; 336
M. Numata, I. Mimamida, M. Yamaoka, M. Shiraishi, Toshio Miyawaki, Cephalosporin Derivatives, US4421912.
Carvey, Pieri, Ling (bib104) 1997; 104
Lazer, Miao, Cywin, Sorcek, Wong, Meng, Potocki, Hoermann, Snow, Tschantz (bib134) 1997; 40
R.B. Sykes, W.L. Parker, C.M. Cimarusti, W.H. Koster, W.A. Slusarchyk, 2-Oxo-1-azetidinesulfonic Acid Salts, US4775670A..
M. Nagasawa, M. Murata, H. Nishioka, T. Kurimoto, S. Ueki, O. Kitagawa, Preparation of Aminothiazole Derivatives as Ameliorating Agents for Digestive Tract Movements, WO9636619A1..
M. Takayama, N. Kurose, Pharmaceutical Composition Containing Optically Active Compound Having Thrombopoietin Receptor Agonist Activity and Intermediate Thereof, WO2009017098A1..
Petrou, Fesatidou, Geronikaki (bib3) 2021; 26
Labro, El Benna, Charlier, Abdelghaffar, Hakim (bib57) 1994; 152
Koufaki, Kiziridi, Nikoloudaki, Alexis (bib16) 2007; 17
Falci, Pasqualotto (bib69) 2013; 6
Hamashima, Kubota, Minami, Ishikura, Konoike, Yoshioka, Yoshida, Nakashimizu, Motokawa (bib53) 1987; 40
R. Heymes, A. Lutz, 3-Acetoxymethyl-7-(hydroxyiminoacetamido)-cephalosporanic Acid Derivatives, US4283396A.
Mishra, Kumari, Tiwari (bib21) 2015; 92
Collo, Cavalleri, Bono, Mora, Fedele, Invernizzi, Gennarelli, Piovani, Kunath, Millan (bib103) 2018; 2018
Scholz, Hofmann, Noack, Edwards, Stoeckel (bib25) 1998; 44
Simmons, Gelfand, Grogan, Craft (bib27) 1995; 22
Lombardo, Lee, Chen, Norris, Barrish, Behnia, Castaneda, Cornelius, Das, Doweyko (bib89) 2004; 47
R.P. Pioch
Kashyap, Garg, Sharma, Kumar, Dudhe, Gupta (bib20) 2012; 21
Sur, Adamczuk, Scott, Kost, Sampat, Buckley, Farrar, Newton, Suhy, Bennacef (bib108) 2022; 24
Yamawaki, Futagami, Sakasegawa, Murakami, Agawa, Ikeda, Noda, Kirita, Gudis, Higuchi (bib116) 2020; 32
Iwahi, Tsuchiya (bib41) 1980; 18
Gobin, Huin, Lamoureux, Ory, Charrier, Lanel, Battaglia, Redini, Lezot, Blanchard (bib99) 2015; 136
Muhammad, S Masaret, M Amin, Abdallah, Farghaly (bib8) 2017; 13
Takano, Hase-Aoki, Horiuchi, Zhao, Kasahara, Kondo, Becker (bib138) 2005; 76
U. Yasutsugu, M.J. D, G. Jerzy, H.T. W, C. Chung-Pin, Process for Preparation of Water Soluble Azole Compounds, WO0152852A1..
Y. Nishitani, Cephalosporin Having Catechol Group, WO2010050468A1..
Weichold, Bryant, Pati, Barabitskaya, Gallo, Reitz (bib80) 1999; 2
Posobiec, Vidal, Hughes‐Earle, Laffan, Hart (bib95) 2015; 104
M.V. Thippannachar, D.D. Gulabrao, V.S. Popat, A Process for Preparation of Mirabegron and Alpha Cryatalline Form Thereof, WO2015044965A1..
Hunt (bib87) 2009; 8
Gudnason, Gudbrandsson, Barsanti, Kristinsson (bib34) 1998; 17
Gobeaux, Ambart, Couderc, Renard, De Charnace, Lokiec (bib33) 1989; 73
Gümüş, Yakan, Koca (bib19) 2019; 11
thiazolylmethylthloalkyl-
Sun, Ye, Liang, Liu, Li, Lu, Huang, Zhao, Tan, Lai (bib79) 2021; 6
Lin, Evans, Warrick, Pioch (bib111) 1986; 239
Li, Ghoshal, Arora, Erstad, Sojoodi, Lanuti, Hoshida, Baumert, Tanabe, Fuchs (bib112) 2018; 78
Drewe, Gutmann, Fricker, Török, Beglinger, Huwyler (bib81) 1999; 57
Parish, Scheinfeld (bib62) 2008; 9
Ergenç, Çapan, Günay, Özkirimli, Güngör, Özbey, Kendi (bib15) 1999; 332
K. Fujimoto, E. Nakayama, H. Nakao, Process for Preparing 3-alkoxymethylcephalosporin Derivatives, US4482710..
Guay, Koskoletos (bib38) 1985; 4
Z. Matej, G. Stanislav, A. Borut, Z. Rok, K. Ivanka, Novel Process for Synthesis of Pramipexole and its Pharmaceutically Acceptable Salts, WO2008097203A1..
Donnelley, Zhu, Thompson (bib67) 2016; 9
B. Erb, I.S. Gallou, F.K. Kleinbeck, Synthesis of 2-carboxamide Cycloamino Urea Derivatives, US20130331579A1..
Kearns, Reed, Jacobs, Ardite, Yogev, Blumer (bib52) 1991; 35
Takasu, Ukai, Sato, Matsui, Nagase, Maruyama, Sasamata, Miyata, Uchida, Yamaguchi (bib132) 2007; 321
Nomoto, Zamora, Schuck, Boyd, Chang, Aluri, Siu, Lai, Yasuda, Ferry (bib130) 2018; 84
Kobayashi, Uchida, Kawakami (bib37) 1992; 30
M. Gharpure, S. Deshmukh, R. Mahale, Process for the Manufacture of Cefpodoxime Proxetil, US10541473..
Hara, Sato, Miyagishi, Aisaka, Hibino (bib122) 1978; 67
Bishayee, Karmakar, Mandal, Kundu, Chatterjee (bib5) 1997
McLeod, Nahata, Barson (bib29) 1985; 19
Furet, Guagnano, Fairhurst, Imbach-Weese, Bruce, Knapp, Fritsch, Blasco, Blanz, Aichholz (bib97) 2013; 23
Hargrave, Hess, Oliver (bib7) 1983; 26
H. Axel, G. Joel, Antitumor Combination of B-Raf, MEK, and EGFR inhibitors, WO2014066606A2..
Iturriaga, Paredes, Arias, Torres (bib135) 2017; 14
Zhou, Hong, Zhang, Chen, Han, Shen, Zhu, Gao (bib120) 2014; 9
Jung, Kang, Lee, Noh, Kim, Han, Baek, Kim, Bae (bib94) 2016; 49
Steinmann, Dittmer, Houbraken, Buer, Rath (bib68) 2016; 60
Watanabe, Tsubouchi, Okubo (bib72) 2018; 45
Fritsch, Huang, Chatenay-Rivauday, Schnell, Reddy, Liu, Kauffmann, Guthy, Erdmann, De Pover (bib98) 2014; 13
Sánchez-Lozada, Tapia, Soto, Ávila-Casado, Franco, Wessale, Zhao, Johnson (bib140) 2008; 108
X. He, L. Du, J. Zhu, Y. Wang, Method for Preparation of Febuxostat, WO2011082623A1..
Patt, Hamilton, Taylor, Ryan, Taylor, Connolly, Doherty, Klutchko, Sircar (bib10) 1992; 35
K. Sugasawa, S. Watanuki, Y. Koga, H. Nagata, K. Obitsu, R. Wakayama, F. Hirayama, K.-i. Suzuki, Preparation of 2-acylaminothiazole Derivatives or Salts Thereof as C-Mpl Receptor Ligands, WO2003062233A1..
Andreani, Rambaldi, Mascellani, Rugarli (bib13) 1987; 22
T Chhabria, Patel, Modi, S Brahmkshatriya, Thiazole (bib22) 2016; 16
W. Yong, W. Jian, D. Zexin, Y. Guiju, C. Xuejiao, J. Xiaojun, Method for Preparing Nitazoxanide, CN103159697A..
A.E. Storey, C.L. Jones, D.R.C. Bouvet, N. Lasbistes, S.M. Fairway, L. Williams, A.M. Gibson, R.J. Nairne, F. Karimi, B. Langstrom, Fluorination Process of Anilide Derivatives and Benzothiazole Fluorinate Derivatives as
Werner, Heizmann, Höflsauer (bib48) 1991; 19
J. Lajeunesse, J.D. DiMarco, M. Galella, R. Chidambaram, Process for Preparing 2-Aminothiazole-5-Aromatic Carboxamides as Kinase Inhibitors, US8242270B2..
Neu (bib45) 1987; 6
G.D. Vite, R.M. Borzilleri, S.-h. Kim, J.A. Johnson, Epothilone Derivatives, WO9902514A2..
Xu, Cai (bib129) 2019; 12
Cafini, Yuste, Giménez, Sevillano, Aguilar, Alou, Ramos-Sevillano, Torrico, González, García (bib59) 2010; 5
Xu, Liu, Murray, Callebaut, Lee, Hong, Strickley, Tsai, Stray, Wang (bib84) 2010; 1
Y. Kumar, N. Tewari, R. Aryan, B. Rai, H. Nizar, Process for the Preparation of Cefpodoxime Acid, US20050020561A1..
Imaging Agents, WO2007020400A1..
Alazzouni, Abdel Aziz, Elnabtity, Salem (bib113) 2020; 81
alkylamidines and Ralated Compounds, US4375547..
Tsuchihashi, Nakashima, Kinami, Nagatomo (bib121) 1990; 52
S. Tsushima, M. Sendai, M. Shiraishi, Novel 3-Acyloxymethyl-Cephem Co
Standridge (10.1016/j.ejmech.2023.115172_bib56) 1993; 33
T Chhabria (10.1016/j.ejmech.2023.115172_bib22) 2016; 16
Guay (10.1016/j.ejmech.2023.115172_bib38) 1985; 4
Patt (10.1016/j.ejmech.2023.115172_bib10) 1992; 35
10.1016/j.ejmech.2023.115172_bib71
10.1016/j.ejmech.2023.115172_bib73
Alazzouni (10.1016/j.ejmech.2023.115172_bib113) 2020; 81
Fikry (10.1016/j.ejmech.2023.115172_bib136) 2018; 32
Petrou (10.1016/j.ejmech.2023.115172_bib3) 2021; 26
Lombardo (10.1016/j.ejmech.2023.115172_bib89) 2004; 47
Rossignol (10.1016/j.ejmech.2023.115172_bib85) 2009; 284
Gümüş (10.1016/j.ejmech.2023.115172_bib19) 2019; 11
Yamawaki (10.1016/j.ejmech.2023.115172_bib116) 2020; 32
Eagling (10.1016/j.ejmech.2023.115172_bib78) 1997; 44
Takasu (10.1016/j.ejmech.2023.115172_bib132) 2007; 321
Mishra (10.1016/j.ejmech.2023.115172_bib21) 2015; 92
Scheffers (10.1016/j.ejmech.2023.115172_bib32) 2005; 69
Matsunaga (10.1016/j.ejmech.2023.115172_bib115) 2011; 336
Fukushima‐Shintani (10.1016/j.ejmech.2023.115172_bib128) 2009; 82
Fritsch (10.1016/j.ejmech.2023.115172_bib98) 2014; 13
Koufaki (10.1016/j.ejmech.2023.115172_bib16) 2007; 17
Seifert (10.1016/j.ejmech.2023.115172_bib70) 2007; 51
Yahav (10.1016/j.ejmech.2023.115172_bib54) 2007; 7
Gobeaux (10.1016/j.ejmech.2023.115172_bib33) 1989; 73
Xu (10.1016/j.ejmech.2023.115172_bib84) 2010; 1
Richards (10.1016/j.ejmech.2023.115172_bib35) 1984; 27
Watt (10.1016/j.ejmech.2023.115172_bib42) 1982; 10
10.1016/j.ejmech.2023.115172_bib82
Ergenç (10.1016/j.ejmech.2023.115172_bib15) 1999; 332
10.1016/j.ejmech.2023.115172_bib86
Parish (10.1016/j.ejmech.2023.115172_bib62) 2008; 9
Sakagami (10.1016/j.ejmech.2023.115172_bib61) 1990; 43
10.1016/j.ejmech.2023.115172_bib88
Collo (10.1016/j.ejmech.2023.115172_bib103) 2018; 2018
10.1016/j.ejmech.2023.115172_bib127
Carvey (10.1016/j.ejmech.2023.115172_bib104) 1997; 104
Kobayashi (10.1016/j.ejmech.2023.115172_bib37) 1992; 30
Wellington (10.1016/j.ejmech.2023.115172_bib60) 2004; 64
Hara (10.1016/j.ejmech.2023.115172_bib122) 1978; 67
Sánchez-Lozada (10.1016/j.ejmech.2023.115172_bib140) 2008; 108
Schneider (10.1016/j.ejmech.2023.115172_bib107) 1987; 30
Furugohri (10.1016/j.ejmech.2023.115172_bib123) 2008; 6
Woodfield (10.1016/j.ejmech.2023.115172_bib26) 2003; 185
Bishayee (10.1016/j.ejmech.2023.115172_bib5) 1997
Sur (10.1016/j.ejmech.2023.115172_bib108) 2022; 24
Yoshii (10.1016/j.ejmech.2023.115172_bib117) 2016; 33
10.1016/j.ejmech.2023.115172_bib50
10.1016/j.ejmech.2023.115172_bib51
Andrabi (10.1016/j.ejmech.2023.115172_bib105) 2019; 12
Sun (10.1016/j.ejmech.2023.115172_bib79) 2021; 6
Gobin (10.1016/j.ejmech.2023.115172_bib99) 2015; 136
10.1016/j.ejmech.2023.115172_bib58
Furet (10.1016/j.ejmech.2023.115172_bib97) 2013; 23
10.1016/j.ejmech.2023.115172_bib131
Lazer (10.1016/j.ejmech.2023.115172_bib134) 1997; 40
10.1016/j.ejmech.2023.115172_bib133
Kashyap (10.1016/j.ejmech.2023.115172_bib20) 2012; 21
Muhammad (10.1016/j.ejmech.2023.115172_bib8) 2017; 13
Hamashima (10.1016/j.ejmech.2023.115172_bib53) 1987; 40
Arshad (10.1016/j.ejmech.2023.115172_bib4) 2022; 27
Nomoto (10.1016/j.ejmech.2023.115172_bib130) 2018; 84
Donnelley (10.1016/j.ejmech.2023.115172_bib67) 2016; 9
Kearns (10.1016/j.ejmech.2023.115172_bib52) 1991; 35
Pattan (10.1016/j.ejmech.2023.115172_bib12) 2009; 2
Cafini (10.1016/j.ejmech.2023.115172_bib59) 2010; 5
Kvernmo (10.1016/j.ejmech.2023.115172_bib101) 2006; 28
Gudnason (10.1016/j.ejmech.2023.115172_bib34) 1998; 17
Benedetti (10.1016/j.ejmech.2023.115172_bib83) 2001
Falci (10.1016/j.ejmech.2023.115172_bib69) 2013; 6
10.1016/j.ejmech.2023.115172_bib66
Ishikawa (10.1016/j.ejmech.2023.115172_bib64) 2003; 11
Lee (10.1016/j.ejmech.2023.115172_bib93) 2016; 256
Khames (10.1016/j.ejmech.2023.115172_bib142) 2017; 805
10.1016/j.ejmech.2023.115172_bib143
McLeod (10.1016/j.ejmech.2023.115172_bib29) 1985; 19
Jacqueline (10.1016/j.ejmech.2023.115172_bib63) 2007; 51
10.1016/j.ejmech.2023.115172_bib109
Ito (10.1016/j.ejmech.2023.115172_bib65) 2018; 62
Lin (10.1016/j.ejmech.2023.115172_bib111) 1986; 239
10.1016/j.ejmech.2023.115172_bib106
Raboisson (10.1016/j.ejmech.2023.115172_bib77) 2008; 18
Jubie (10.1016/j.ejmech.2023.115172_bib17) 2009; 1
Mezei (10.1016/j.ejmech.2023.115172_bib137) 2009; 13
Gurupadayya (10.1016/j.ejmech.2023.115172_bib6) 2008; 70
Posobiec (10.1016/j.ejmech.2023.115172_bib95) 2015; 104
Ganellin (10.1016/j.ejmech.2023.115172_bib40) 2010
Hargrave (10.1016/j.ejmech.2023.115172_bib7) 1983; 26
10.1016/j.ejmech.2023.115172_bib114
Andreani (10.1016/j.ejmech.2023.115172_bib13) 1987; 22
10.1016/j.ejmech.2023.115172_bib39
Simmons (10.1016/j.ejmech.2023.115172_bib27) 1995; 22
Watanabe (10.1016/j.ejmech.2023.115172_bib72) 2018; 45
10.1016/j.ejmech.2023.115172_bib110
Drewe (10.1016/j.ejmech.2023.115172_bib81) 1999; 57
Karade (10.1016/j.ejmech.2023.115172_bib11) 2008; 17
Iturriaga (10.1016/j.ejmech.2023.115172_bib135) 2017; 14
Menzies (10.1016/j.ejmech.2023.115172_bib91) 2012; 6
10.1016/j.ejmech.2023.115172_bib118
10.1016/j.ejmech.2023.115172_bib119
Franzén (10.1016/j.ejmech.2023.115172_bib1) 2000; 2
Jung (10.1016/j.ejmech.2023.115172_bib94) 2016; 49
Labro (10.1016/j.ejmech.2023.115172_bib57) 1994; 152
Hunt (10.1016/j.ejmech.2023.115172_bib87) 2009; 8
10.1016/j.ejmech.2023.115172_bib43
10.1016/j.ejmech.2023.115172_bib44
Vengurlekar (10.1016/j.ejmech.2023.115172_bib14) 2014; 5
10.1016/j.ejmech.2023.115172_bib47
10.1016/j.ejmech.2023.115172_bib124
Okura (10.1016/j.ejmech.2023.115172_bib102) 2007; 80
10.1016/j.ejmech.2023.115172_bib49
Greger (10.1016/j.ejmech.2023.115172_bib92) 2012; 11
Iwahi (10.1016/j.ejmech.2023.115172_bib41) 1980; 18
Tsuchihashi (10.1016/j.ejmech.2023.115172_bib121) 1990; 52
Xu (10.1016/j.ejmech.2023.115172_bib129) 2019; 12
Jang (10.1016/j.ejmech.2023.115172_bib23) 2014; 9
Hakimizadeh (10.1016/j.ejmech.2023.115172_bib30) 2020; 258
Weichold (10.1016/j.ejmech.2023.115172_bib80) 1999; 2
Li (10.1016/j.ejmech.2023.115172_bib112) 2018; 78
10.1016/j.ejmech.2023.115172_bib90
Foye (10.1016/j.ejmech.2023.115172_bib31) 2008
10.1016/j.ejmech.2023.115172_bib96
Kim (10.1016/j.ejmech.2023.115172_bib126) 2016; 76
Karve (10.1016/j.ejmech.2023.115172_bib141) 2013; 45
Hantzsch (10.1016/j.ejmech.2023.115172_bib2) 1887; 20
Werner (10.1016/j.ejmech.2023.115172_bib48) 1991; 19
Rajagopalan (10.1016/j.ejmech.2023.115172_bib76) 2017; 61
Chapman (10.1016/j.ejmech.2023.115172_bib55) 2003; 2
Z Laczkowski (10.1016/j.ejmech.2023.115172_bib9) 2016; 12
Nagata (10.1016/j.ejmech.2023.115172_bib125) 2009; 17
Sánchez-Lozada (10.1016/j.ejmech.2023.115172_bib139) 2008; 294
Lo (10.1016/j.ejmech.2023.115172_bib75) 2021; 7
Reiner (10.1016/j.ejmech.2023.115172_bib36) 1980; 32
Ayati (10.1016/j.ejmech.2023.115172_bib18) 2015; 97
Takano (10.1016/j.ejmech.2023.115172_bib138) 2005; 76
Zhou (10.1016/j.ejmech.2023.115172_bib120) 2014; 9
Steinmann (10.1016/j.ejmech.2023.115172_bib68) 2016; 60
Scholz (10.1016/j.ejmech.2023.115172_bib25) 1998; 44
Unemo (10.1016/j.ejmech.2023.115172_bib46) 2012; 56
10.1016/j.ejmech.2023.115172_bib28
Raboisson (10.1016/j.ejmech.2023.115172_bib74) 2008; 18
Van (10.1016/j.ejmech.2023.115172_bib24) 2012; 154
Neu (10.1016/j.ejmech.2023.115172_bib45) 1987; 6
10.1016/j.ejmech.2023.115172_bib100
References_xml – volume: 13
  start-page: 1117
  year: 2014
  end-page: 1129
  ident: bib98
  article-title: Characterization of the novel and specific PI3Kα inhibitor NVP-BYL719 and development of the patient stratification strategy for clinical trialsNVP-BYL719 PI3Kα inhibitor and predictive response modeling
  publication-title: Mol. Cancer Therapeut.
– volume: 17
  start-page: 258
  year: 1998
  end-page: 260
  ident: bib34
  article-title: Penetration of ceftriaxone into the middle ear fluid of children
  publication-title: Pediatr. Infect. Dis. J.
– volume: 6
  start-page: 1
  year: 2021
  end-page: 3
  ident: bib79
  article-title: Bardoxolone and bardoxolone methyl, two Nrf2 activators in clinical trials, inhibit SARS-CoV-2 replication and its 3C-like protease
  publication-title: Signal Transduct. Tar.
– volume: 1
  start-page: 209
  year: 2010
  end-page: 213
  ident: bib84
  article-title: Cobicistat (GS-9350): a potent and selective inhibitor of human CYP3A as a novel pharmacoenhancer
  publication-title: ACS Med. Chem. Lett.
– volume: 19
  start-page: 377
  year: 1991
  end-page: 379
  ident: bib48
  article-title: Comparative
  publication-title: Infection
– year: 2010
  ident: bib40
  article-title: Analogue-based Drug Discovery II
– volume: 7
  start-page: 338
  year: 2007
  end-page: 348
  ident: bib54
  article-title: Efficacy and safety of cefepime: a systematic review and meta-analysis
  publication-title: Lancet Infect. Dis.
– reference: R. Heymes, A. Lutz, 3-Acetoxymethyl-7-(hydroxyiminoacetamido)-cephalosporanic Acid Derivatives, US4283396A.
– reference: A.E. Storey, C.L. Jones, D.R.C. Bouvet, N. Lasbistes, S.M. Fairway, L. Williams, A.M. Gibson, R.J. Nairne, F. Karimi, B. Langstrom, Fluorination Process of Anilide Derivatives and Benzothiazole Fluorinate Derivatives as
– volume: 26
  start-page: 1158
  year: 1983
  end-page: 1163
  ident: bib7
  article-title: -(4-Substituted-thiazolyl) oxamic acid derivatives, new series of potent, orally active antiallergy agents
  publication-title: J. Med. Chem.
– volume: 23
  start-page: 3741
  year: 2013
  end-page: 3748
  ident: bib97
  article-title: Discovery of NVP-BYL719 a potent and selective phosphatidylinositol-3 kinase alpha inhibitor selected for clinical evaluation
  publication-title: Bioorg. Med. Chem. Lett.
– reference: H. Jianjin, L. Xiaojun, S. Bo, Y. Yan, Process for Producing 2-hydroxybenzamide Derivs, CN103709191A..
– volume: 9
  start-page: 201
  year: 2008
  end-page: 209
  ident: bib62
  article-title: Ceftaroline fosamil, a cephalosporin derivative for the potential treatment of MRSA infection
  publication-title: Curr. Opin. Invest. Drugs
– volume: 81
  start-page: 1
  year: 2020
  end-page: 13
  ident: bib113
  article-title: Comparative histological and histochemical studies between ranitidine and nizatidine in treatment of peptic ulcer with evaluation of their adverse effects on male sex hormones
  publication-title: J. Basic Appl. Zool.
– volume: 67
  start-page: 1334
  year: 1978
  end-page: 1335
  ident: bib122
  article-title: Synthesis and β-adrenergic blocking action of a new thiazolylthiopropanolamine derivative
  publication-title: J. Pharmacol. Sci.
– volume: 805
  start-page: 118
  year: 2017
  end-page: 124
  ident: bib142
  article-title: Ameliorative effects of sildenafil and/or febuxostat on doxorubicin-induced nephrotoxicity in rats
  publication-title: Eur. J. Pharmacol.
– volume: 64
  start-page: 2597
  year: 2004
  end-page: 2618
  ident: bib60
  publication-title: Cefditoren Pivoxil, Drugs
– volume: 321
  start-page: 642
  year: 2007
  end-page: 647
  ident: bib132
  article-title: Effect of (
  publication-title: J. Pharmacol. Exp. Therapeut.
– volume: 17
  start-page: 4223
  year: 2007
  end-page: 4227
  ident: bib16
  article-title: Design and synthesis of 1, 2-dithiolane derivatives and evaluation of their neuroprotective activity
  publication-title: Bioorg. Med. Chem. Lett.
– start-page: 58
  year: 1997
  end-page: 70
  ident: bib5
  article-title: Vanadium-mediated chemoprotection against chemical hepatocarcinogenesis in rats: haematological and histological characteristics
  publication-title: Eur. J. Cancer Prev.
– volume: 284
  start-page: 29798
  year: 2009
  end-page: 29808
  ident: bib85
  article-title: Thiazolides, a new class of anti-influenza molecules targeting viral hemagglutinin at the post-translational level
  publication-title: J. Biol. Chem.
– volume: 2
  start-page: 196
  year: 2009
  end-page: 201
  ident: bib12
  article-title: Synthesis and biological evaluation of some substituted amino thiazole derivatives
  publication-title: Asian J. Res. Chem.
– volume: 45
  start-page: 1151
  year: 2018
  end-page: 1159
  ident: bib72
  article-title: Efficacy and safety of fosravuconazole L‐lysine ethanolate, a novel oral triazole antifungal agent, for the treatment of onychomycosis: a multicenter, double‐blind, randomized phase III study
  publication-title: J. Dermatol.
– volume: 32
  year: 2018
  ident: bib136
  article-title: Rutin and meloxicam attenuate paw inflammation in mice: affecting sorbitol dehydrogenase activity
  publication-title: J. Biochem. Mol. Toxicol.
– reference: M. Gharpure, S. Deshmukh, R. Mahale, Process for the Manufacture of Cefpodoxime Proxetil, US10541473..
– volume: 92
  start-page: 1
  year: 2015
  end-page: 34
  ident: bib21
  article-title: Thiazole: a promising heterocycle for the development of potent CNS active agents
  publication-title: Eur. J. Med. Chem.
– reference: W.E. Klunk, C.A.M. Jr, Amyloid Imaging as a Surrofate Marker for Efficacy of Anti-amyloid Therapies, US8147798B2..
– reference: S. Tsushima, M. Sendai, M. Shiraishi, Novel 3-Acyloxymethyl-Cephem Compounds Useful as Intermediates for Preparing Cephalosporin Antibiotics, US4245088A..
– volume: 2018
  start-page: 4196961
  year: 2018
  ident: bib103
  article-title: Ropinirole and pramipexole promote structural plasticity in human iPSC-derived dopaminergic neurons via BDNF and mTOR signaling
  publication-title: Neural Plast
– volume: 8
  start-page: 275
  year: 2009
  end-page: 281
  ident: bib87
  article-title: Discovery of ixabepilone
  publication-title: Mol. Cancer Therapeut.
– reference: '-alkylamidines and Ralated Compounds, US4375547..
– volume: 22
  start-page: 155
  year: 1995
  end-page: 157
  ident: bib27
  article-title: Cefotaxime twice daily versus ceftriaxone once daily: a randomized controlled study in patients with serious infections, Diagn
  publication-title: Microorg. Infect. Dis.
– volume: 26
  start-page: 3166
  year: 2021
  ident: bib3
  article-title: Thiazole ring-a biologically active scaffold
  publication-title: Molecules
– volume: 9
  start-page: 79
  year: 2016
  end-page: 86
  ident: bib67
  article-title: Isavuconazole in the treatment of invasive aspergillosis and mucormycosis infections
  publication-title: Infect. Drug Resist.
– volume: 14
  start-page: 2198
  year: 2017
  end-page: 2206
  ident: bib135
  article-title: Meloxicam decreases the migration and invasion of CF41. Mg canine mammary carcinoma cells
  publication-title: Oncol. Lett.
– volume: 69
  start-page: 585
  year: 2005
  end-page: 607
  ident: bib32
  article-title: Bacterial cell wall synthesis: new insights from localization studies
  publication-title: Microbiol. Mol. Biol. Rev.
– volume: 11
  start-page: 2427
  year: 2003
  end-page: 2437
  ident: bib64
  article-title: TAK-599, a novel
  publication-title: Bioorg. Med. Chem.
– reference: L. Al-Razzak, D. Kaul, L.P. Manning, K.C. Marsh, Pharmaceutical Compositions Containing HIV Protease Inhibitors, AU700942B2..
– volume: 32
  year: 2020
  ident: bib116
  article-title: Acotiamide attenuates central urocortin 2‐induced intestinal inflammatory responses, and urocortin 2 treatment reduces TNF‐α productions in LPS‐stimulated macrophage cell lines
  publication-title: Neurogastroent. Motil.
– volume: 2
  start-page: 195
  year: 2000
  end-page: 214
  ident: bib1
  article-title: Recent advances in the preparation of heterocycles on solid support: a review of the literature
  publication-title: J. Comb. Chem.
– volume: 24
  start-page: 862
  year: 2022
  end-page: 873
  ident: bib108
  article-title: Evaluation of
  publication-title: Mol. Imag. Biol.
– volume: 33
  start-page: 292
  year: 2016
  end-page: 300
  ident: bib117
  article-title: Physiologically-based pharmacokinetic and pharmacodynamic modeling for the inhibition of acetylcholinesterase by acotiamide, a novel gastroprokinetic agent for the treatment of functional dyspepsia, in rat stomach
  publication-title: Pharm. Res. (N. Y.)
– volume: 45
  start-page: 244
  year: 2013
  end-page: 247
  ident: bib141
  article-title: Evaluation of effect of allopurinol and febuxostat in behavioral model of depression in mice
  publication-title: Indian J. Pharmacol.
– volume: 61
  year: 2017
  ident: bib76
  article-title: Preclinical characterization and human microdose pharmacokinetics of ITMN-8187, a nonmacrocyclic inhibitor of the hepatitis C virus NS3 protease
  publication-title: Antimicrob. Agents Chemother.
– reference: J. Lajeunesse, J.D. DiMarco, M. Galella, R. Chidambaram, Process for Preparing 2-Aminothiazole-5-Aromatic Carboxamides as Kinase Inhibitors, US8242270B2..
– volume: 76
  start-page: 1835
  year: 2005
  end-page: 1847
  ident: bib138
  article-title: Selectivity of febuxostat, a novel non-purine inhibitor of xanthine oxidase/xanthine dehydrogenase
  publication-title: Life Sci.
– volume: 44
  start-page: 190
  year: 1997
  end-page: 194
  ident: bib78
  article-title: Differential inhibition of cytochrome P450 isoforms by the protease inhibitors, ritonavir, saquinavir and indinavir, Brit
  publication-title: J. Clin. Pharmacol.
– volume: 6
  start-page: 1542
  year: 2008
  end-page: 1549
  ident: bib123
  article-title: DU‐176b, a potent and orally active factor Xa inhibitor:
  publication-title: J. Thromb. Haemostasis
– volume: 6
  start-page: 163
  year: 2013
  end-page: 174
  ident: bib69
  article-title: Profile of isavuconazole and its potential in the treatment of severe invasive fungal infections
  publication-title: Infect. Drug Resist.
– volume: 57
  start-page: 1147
  year: 1999
  end-page: 1152
  ident: bib81
  article-title: HIV protease inhibitor ritonavir: a more potent inhibitor of P-glycoprotein than the cyclosporine analog SDZ PSC 833
  publication-title: Biochem. Pharmacol.
– reference: -thiazolylmethylthloalkyl-
– reference: K. Sugasawa, S. Watanuki, Y. Koga, H. Nagata, K. Obitsu, R. Wakayama, F. Hirayama, K.-i. Suzuki, Preparation of 2-acylaminothiazole Derivatives or Salts Thereof as C-Mpl Receptor Ligands, WO2003062233A1..
– reference: K. Fujimoto, E. Nakayama, H. Nakao, Process for Preparing 3-alkoxymethylcephalosporin Derivatives, US4482710..
– volume: 73
  start-page: 574
  year: 1989
  end-page: 575
  ident: bib33
  article-title: Ceftriaxone diffusion from blood to aqueous humour in man
  publication-title: Br. J. Ophthalmol.
– volume: 256
  start-page: 266
  year: 2016
  end-page: 273
  ident: bib93
  article-title: Anti-inflammatory effects of dabrafenib on polyphosphate-mediated vascular disruption
  publication-title: Chem. Biol. Interact.
– volume: 30
  start-page: 871
  year: 1992
  end-page: 872
  ident: bib37
  article-title: Synergy with aztreonam and arbekacin or tobramycin against Pseudomonas aeruginosa from blood
  publication-title: J. Antimicrob. Chemother.
– reference: M. Soukup, Process for the Manufacture of Enantiomerically Pure Antifungal Azoles as Ravuconazole and Isavuconazole, US8207352B2..
– volume: 18
  start-page: 4853
  year: 2008
  end-page: 4858
  ident: bib74
  article-title: Structure-activity relationship study on a novel series of cyclopentane-containing macrocyclic inhibitors of the hepatitis C virus NS3/4A protease leading to the discovery of TMC435350
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 11
  start-page: 1979
  year: 2019
  end-page: 1998
  ident: bib19
  article-title: Recent advances of thiazole hybrids in biological applications
  publication-title: Future Med. Chem.
– volume: 17
  start-page: 1193
  year: 2009
  end-page: 1206
  ident: bib125
  article-title: Discovery of
  publication-title: Bioorg. Med. Chem.
– volume: 44
  start-page: 142
  year: 1998
  end-page: 147
  ident: bib25
  article-title: Prospective comparison of ceftriaxone and cefotaxime for the short-term treatment of bacterial meningitis in children
  publication-title: Chemotherapy
– year: 2008
  ident: bib31
  article-title: Foye's Principles of Medicinal Chemistry
– volume: 17
  start-page: 19
  year: 2008
  end-page: 29
  ident: bib11
  article-title: Design, synthesis, and antimalarial evaluation of thiazole-derived amino acids
  publication-title: Med. Chem. Res.
– reference: B. Erb, I.S. Gallou, F.K. Kleinbeck, Synthesis of 2-carboxamide Cycloamino Urea Derivatives, US20130331579A1..
– reference: Imaging Agents, WO2007020400A1..
– volume: 18
  start-page: 4853
  year: 2008
  end-page: 4858
  ident: bib77
  article-title: Structure-activity relationship study on a novel series of cyclopentane-containing macrocyclic inhibitors of the hepatitis C virus NS3/4A protease leading to the discovery of TMC435350
  publication-title: Bioorg. Med. Chem. Lett.
– reference: M. Nagasawa, M. Murata, H. Nishioka, T. Kurimoto, S. Ueki, O. Kitagawa, Preparation of Aminothiazole Derivatives as Ameliorating Agents for Digestive Tract Movements, WO9636619A1..
– volume: 7
  start-page: 792
  year: 2021
  end-page: 802
  ident: bib75
  article-title: Simeprevir potently suppresses SARS-CoV-2 replication and synergizes with remdesivir
  publication-title: ACS Cent. Sci.
– volume: 20
  start-page: 3118
  year: 1887
  end-page: 3132
  ident: bib2
  article-title: Ueber verbindungen des thiazols (pyridins der thiophenreihe)
  publication-title: Eur. J. Inorg. Chem.
– volume: 80
  start-page: 1564
  year: 2007
  end-page: 1571
  ident: bib102
  article-title: Blood-brain barrier transport of pramipexole, a dopamine D2 agonist
  publication-title: Life Sci.
– volume: 70
  start-page: 572
  year: 2008
  end-page: 577
  ident: bib6
  article-title: Synthesis and pharmacological evaluation of azetidin-2-ones and thiazolidin-4-ones encompassing benzothiazole
  publication-title: Indian J. Pharmaceut. Sci.
– volume: 13
  start-page: 226
  year: 2017
  end-page: 238
  ident: bib8
  article-title: Anti-inflammatory, analgesic and anti-ulcerogenic activities of novel bis-thiadiazoles, bis-thiazoles and bis-formazanes
  publication-title: Med. Chem.
– volume: 51
  start-page: 1818
  year: 2007
  end-page: 1821
  ident: bib70
  article-title: activities of isavuconazole and other antifungal agents against Candida bloodstream isolates
  publication-title: Antimicrob. Agents Chemother.
– volume: 104
  start-page: 209
  year: 1997
  end-page: 228
  ident: bib104
  article-title: Attenuation of levodopa-induced toxicity in mesencephalic cultures by pramipexole
  publication-title: J. Neural. Transm.
– volume: 12
  start-page: 859
  year: 2019
  end-page: 865
  ident: bib129
  article-title: Avatrombopag for the treatment of thrombocytopenia in patients with chronic liver disease
  publication-title: Expet Rev. Clin. Pharmacol.
– volume: 336
  start-page: 791
  year: 2011
  end-page: 800
  ident: bib115
  article-title: Acotiamide hydrochloride (Z-338), a new selective acetylcholinesterase inhibitor, enhances gastric motility without prolonging QT interval in dogs: comparison with cisapride, itopride, and mosapride
  publication-title: J. Pharmacol. Exp. Therapeut.
– volume: 9
  year: 2014
  ident: bib120
  article-title: Mechanisms of improved aortic stiffness by arotinolol in spontaneously hypertensive rats
  publication-title: PLoS One
– volume: 5
  start-page: 3526
  year: 2014
  end-page: 3530
  ident: bib14
  article-title: Synthesis and evaluation of some thiazole derivatives as an antifungal agent
  publication-title: Int. J. Pharm. & Life Sci.
– volume: 22
  start-page: 19
  year: 1987
  end-page: 22
  ident: bib13
  article-title: Synthesis and diuretic activity of imidazo [2, 1-b] thiazole acetohydrazones
  publication-title: Eur. J. Med. Chem.
– reference: U. Yasutsugu, M.J. D, G. Jerzy, H.T. W, C. Chung-Pin, Process for Preparation of Water Soluble Azole Compounds, WO0152852A1..
– volume: 2
  start-page: 261
  year: 1999
  end-page: 269
  ident: bib80
  article-title: HIV-1 protease inhibitor ritonavir modulates susceptibility to apoptosis of uninfected T cells
  publication-title: J. Hum. Virol.
– volume: 27
  start-page: 469
  year: 1984
  end-page: 527
  ident: bib35
  article-title: Ceftriaxone: a review of its antibacterial activity, pharmacological properties and therapeutic use
  publication-title: Drugs
– volume: 6
  start-page: 958
  year: 1987
  end-page: 962
  ident: bib45
  article-title: activity of a new broad spectrum, β-lactamase-stable oral cephalosporin, cefixime, Pediatr
  publication-title: infect. Dis. J.
– reference: M. Takayama, N. Kurose, Pharmaceutical Composition Containing Optically Active Compound Having Thrombopoietin Receptor Agonist Activity and Intermediate Thereof, WO2009017098A1..
– volume: 185
  start-page: 45
  year: 2003
  end-page: 49
  ident: bib26
  article-title: A comparison of the prophylactic efficacy of ceftriaxone and cefotaxime in abdominal surgery
  publication-title: Am. J. Surg.
– volume: 28
  start-page: 1065
  year: 2006
  end-page: 1078
  ident: bib101
  article-title: A review of the receptor-binding and pharmacokinetic properties of dopamine agonists
  publication-title: Clin. Therapeut.
– volume: 19
  start-page: 900
  year: 1985
  end-page: 906
  ident: bib29
  article-title: Ceftriaxone: a third-generation cephalosporin
  publication-title: Drug Intell. Clin. Pharm.
– volume: 35
  start-page: 2078
  year: 1991
  end-page: 2084
  ident: bib52
  article-title: Single-dose pharmacokinetics of ceftibuten (SCH 39720) in infants and children
  publication-title: Antimicrob. Agents Chemother.
– volume: 12
  start-page: 553
  year: 2016
  end-page: 562
  ident: bib9
  article-title: Synthesis, antibacterial activity, interaction with nucleobase and molecular docking studies of 4-formylbenzoic acid based thiazoles
  publication-title: Med. Chem.
– volume: 21
  start-page: 2123
  year: 2012
  end-page: 2132
  ident: bib20
  article-title: Thiazoles: having diverse biological activities
  publication-title: Med. Chem. Res.
– volume: 108
  start-page: p69
  year: 2008
  end-page: p78
  ident: bib140
  article-title: Effect of febuxostat on the progression of renal disease in 5/6 nephrectomy rats with and without hyperuricemia
  publication-title: Nephron. Physiol.
– volume: 258
  year: 2020
  ident: bib30
  article-title: Ceftriaxone improves hepatorenal damages in mice subjected to D-galactose-induced aging
  publication-title: Life Sci.
– volume: 35
  start-page: 2562
  year: 1992
  end-page: 2572
  ident: bib10
  article-title: Structure-activity relationships of a series of 2-amino-4-thiazole-containing renin inhibitors
  publication-title: J. Med. Chem.
– volume: 11
  start-page: 909
  year: 2012
  end-page: 920
  ident: bib92
  article-title: Combinations of BRAF, MEK, and PI3K/mTOR inhibitors overcome acquired resistance to the BRAF inhibitor GSK2118436 dabrafenib, mediated by NRAS or MEK mutations
  publication-title: Mol. Cancer Therapeut.
– volume: 154
  start-page: 98
  year: 2012
  end-page: 106
  ident: bib24
  article-title: The antibiotic resistance characteristics of non-typhoidal Salmonella enterica isolated from food-producing animals, retail meat and humans in South East Asia
  publication-title: Int. J. Food Microbiol.
– reference: T. Ohta, S. Komoriya, T. Yoshino, K. Uoto, Y. Nakamoto, H. Naito, A. Mochizuki, T. Nagata, H. Kanno, N. Haginoya, K. Yoshikawa, M. Nagamochi, S. Kobayashi, M. Ono, Preparation of Heterocyclyl Moiety-Containing Diamine Derivatives as Factor Xa Inhibitors, WO2004058715A1..
– volume: 40
  start-page: 980
  year: 1997
  end-page: 989
  ident: bib134
  article-title: Effect of structural modification of enol-carboxamide-type nonsteroidal antiinflammatory drugs on COX-2/COX-1 selectivity
  publication-title: J. Med. Chem.
– volume: 12
  year: 2019
  ident: bib105
  article-title: Pramipexole prevents ischemic cell death via mitochondrial pathways in ischemic stroke
  publication-title: Dis. Model. Mech.
– volume: 43
  start-page: 1047
  year: 1990
  end-page: 1050
  ident: bib61
  article-title: Synthesis and oral activity of ME1207, a new orally active cephalosporin
  publication-title: J. Antibiot.
– volume: 84
  start-page: 952
  year: 2018
  end-page: 960
  ident: bib130
  article-title: Pharmacokinetic/pharmacodynamic drug-drug interactions of avatrombopag when coadministered with dual or selective CYP2C9 and CYP3A interacting drugs
  publication-title: Br. J. Clin. Pharmacol.
– reference: R.P. Pioch,
– volume: 97
  start-page: 699
  year: 2015
  end-page: 718
  ident: bib18
  article-title: Recent applications of 1, 3-thiazole core structure in the identification of new lead compounds and drug discovery
  publication-title: Eur. J. Med. Chem.
– reference: M. Numata, I. Mimamida, M. Yamaoka, M. Shiraishi, Toshio Miyawaki, Cephalosporin Derivatives, US4421912.
– volume: 60
  start-page: 6890
  year: 2016
  end-page: 6891
  ident: bib68
  article-title: activity of isavuconazole against Rasamsonia species
  publication-title: Antimicrob. Agents Chemother.
– volume: 30
  start-page: 494
  year: 1987
  end-page: 498
  ident: bib107
  article-title: Dopamine autoreceptor agonists: resolution and pharmacological activity of 2, 6-diaminotetrahydrobenzothiazole and an aminothiazole analog of apomorphine
  publication-title: J. Med. Chem.
– volume: 78
  start-page: 4004
  year: 2018
  ident: bib112
  article-title: The H2 receptor antagonist nizatidine inhibits carcinogenesis in two rodent models of hepatocellular carcinoma
  publication-title: Cancer Res.
– volume: 51
  start-page: 3397
  year: 2007
  end-page: 3400
  ident: bib63
  article-title: efficacy of ceftaroline (PPI-0903), a new broad-spectrum cephalosporin, compared with linezolid and vancomycin against methicillin-resistant and vancomycin-intermediate Staphylococcus aureus in a rabbit endocarditis model
  publication-title: Antimicrob. Agents Chemother.
– volume: 13
  start-page: 567
  year: 2009
  end-page: 572
  ident: bib137
  article-title: Manufacture of high-purity meloxicam via its novel potassium salt monohydrate
  publication-title: Org. Process Res. Dev.
– reference: G.D. Vite, R.M. Borzilleri, S.-h. Kim, J.A. Johnson, Epothilone Derivatives, WO9902514A2..
– volume: 104
  start-page: 244
  year: 2015
  end-page: 252
  ident: bib95
  article-title: Early vaginal opening in juvenile female rats given BRAF‐inhibitor dabrafenib is not associated with early physiologic sexual maturation
  publication-title: Birth Defects Res. B Dev. Reprod. Toxicol.
– volume: 18
  start-page: 257
  year: 1980
  end-page: 263
  ident: bib41
  article-title: Comparative activities of cefotiam and cefazolin against urinary tract infections with proteus mirabilis in mice
  publication-title: Antimicrob. Agents Chemother.
– volume: 294
  start-page: F710
  year: 2008
  end-page: F718
  ident: bib139
  article-title: Effects of febuxostat on metabolic and renal alterations in rats with fructose-induced metabolic syndrome
  publication-title: Am. J. Physiol. Renal
– start-page: 203
  year: 2001
  end-page: 204
  ident: bib83
  article-title: Epoxyalcohol route to hydroxyethylene dipeptide isosteres: a new synthesis of the diaminoalcohol core of HIV-protease inhibitor ABT-538 (Ritonavir)
  publication-title: Chem. Commun.
– volume: 47
  start-page: 6658
  year: 2004
  end-page: 6661
  ident: bib89
  article-title: Discovery of
  publication-title: J. Med. Chem.
– volume: 5
  year: 2010
  ident: bib59
  article-title: Enhanced
  publication-title: PLoS One
– reference: R.B. Sykes, W.L. Parker, C.M. Cimarusti, W.H. Koster, W.A. Slusarchyk, 2-Oxo-1-azetidinesulfonic Acid Salts, US4775670A..
– volume: 10
  start-page: 391
  year: 1982
  end-page: 395
  ident: bib42
  article-title: activity of cefotiam against bacteria of clinical interest
  publication-title: J. Antimicrob. Chemother.
– volume: 76
  start-page: 155
  year: 2016
  end-page: 158
  ident: bib126
  article-title: Lusutrombopag: first global approval
  publication-title: Drugs
– volume: 49
  start-page: 214
  year: 2016
  end-page: 219
  ident: bib94
  article-title: Anti-septic effects of dabrafenib on HMGB1-mediated inflammatory responses
  publication-title: BMB Rep
– volume: 239
  start-page: 406
  year: 1986
  end-page: 410
  ident: bib111
  article-title: Actions of nizatidine, a selective histamine H2-receptor antagonist, on gastric acid secretion in dogs, rats and frogs
  publication-title: J. Pharmacol. Exp. Therapeut.
– volume: 32
  start-page: 783
  year: 1980
  end-page: 786
  ident: bib36
  article-title: Ro-13-9904/001, a novel potent and long-acting parenteral cephalosporin
  publication-title: J. Antibiot.
– volume: 56
  start-page: 1273
  year: 2012
  end-page: 1280
  ident: bib46
  article-title: High-level cefixime-and ceftriaxone-resistant Neisseria gonorrhoeae in France: novel penA mosaic allele in a successful international clone causes treatment failure
  publication-title: Antimicrob. Agents Chemother.
– volume: 332
  start-page: 343
  year: 1999
  end-page: 347
  ident: bib15
  article-title: Synthesis and hypnotic activity of new 4‐thiazolidinone and 2‐thioxo‐4,5‐imidazolidinedione derivatives
  publication-title: Arch. Pharm.
– volume: 152
  start-page: 2447
  year: 1994
  end-page: 2455
  ident: bib57
  article-title: Cefdinir (CI-983), a new oral amino-2-thiazolyl cephalosporin, inhibits human neutrophil myeloperoxidase in the extracellular medium but not the phagolysosome
  publication-title: J. Immunol.
– volume: 52
  start-page: 195
  year: 1990
  end-page: 200
  ident: bib121
  article-title: Characteristics of 125I-lodocyanopindolol binding to β-adrenergic and serotonin-1B receptors of rat brain: selectivity of β-adrenergic agents
  publication-title: Jpn. J. Pharmacol.
– volume: 16
  start-page: 2841
  year: 2016
  end-page: 2862
  ident: bib22
  article-title: A review on chemistry, synthesis and therapeutic importance of its derivatives
  publication-title: Curr. Top. Med. Chem.
– reference: T. Takaya, H. Takasugi, T. Masugi, H. Yamanaka, K. Kawabata, 7-Acylamino-3-vinylcephalosporanic Acid Derivatives and Processes for the Preparation Thereof, US4409214A..
– volume: 82
  start-page: 247
  year: 2009
  end-page: 254
  ident: bib128
  article-title: AKR‐501 (YM477) a novel orally‐active thrombopoietin receptor agonist
  publication-title: Eur. J. Haematol.
– reference: H. Axel, G. Joel, Antitumor Combination of B-Raf, MEK, and EGFR inhibitors, WO2014066606A2..
– volume: 27
  start-page: 3994
  year: 2022
  ident: bib4
  article-title: Thiazole: a versatile standalone moiety contributing to the development of various drugs and biologically active agents
  publication-title: Molecules
– reference: X. He, L. Du, J. Zhu, Y. Wang, Method for Preparation of Febuxostat, WO2011082623A1..
– volume: 4
  start-page: 516
  year: 1985
  end-page: 526
  ident: bib38
  article-title: Aztreonam, a new monobactam antimicrobial
  publication-title: Clin. Pharm.
– reference: Y. Kumar, N. Tewari, R. Aryan, B. Rai, H. Nizar, Process for the Preparation of Cefpodoxime Acid, US20050020561A1..
– volume: 40
  start-page: 1468
  year: 1987
  end-page: 1470
  ident: bib53
  article-title: Synthesis and biological properties of 7β-[(
  publication-title: J. Antibiot.
– reference: M.V. Thippannachar, D.D. Gulabrao, V.S. Popat, A Process for Preparation of Mirabegron and Alpha Cryatalline Form Thereof, WO2015044965A1..
– reference: W. Yong, W. Jian, D. Zexin, Y. Guiju, C. Xuejiao, J. Xiaojun, Method for Preparing Nitazoxanide, CN103159697A..
– volume: 6
  start-page: 391
  year: 2012
  end-page: 405
  ident: bib91
  article-title: Dabrafenib and its potential for the treatment of metastatic melanoma
  publication-title: Drug Des. Dev. Ther.
– reference: Z. Matej, G. Stanislav, A. Borut, Z. Rok, K. Ivanka, Novel Process for Synthesis of Pramipexole and its Pharmaceutically Acceptable Salts, WO2008097203A1..
– volume: 33
  start-page: 759
  year: 1993
  end-page: 765
  ident: bib56
  article-title: Synthesis of 7-[α-( 2-amino-[2-14C]thiazol-4-yl)-α-(Z)-methoxyiminoacetamido]-3-(1-methylpyrrolldinlo)methyl-3-cephem-4-carboxylate hydrochloride ([14C] cefepime hydrochloride)
  publication-title: J. Label. Compd. Radiopharm.
– volume: 136
  start-page: 784
  year: 2015
  end-page: 796
  ident: bib99
  article-title: BYL719, a new α‐specific PI3K inhibitor: single administration and in combination with conventional chemotherapy for the treatment of osteosarcoma
  publication-title: Int. J. Cancer
– reference: Y. Nishitani, Cephalosporin Having Catechol Group, WO2010050468A1..
– volume: 62
  year: 2018
  ident: bib65
  article-title: antibacterial properties of cefiderocol, a novel siderophore cephalosporin, against Gram-negative bacteria
  publication-title: Antimicrob. Agents Chemother.
– volume: 1
  start-page: 32
  year: 2009
  end-page: 38
  ident: bib17
  article-title: Synthesis and biological evaluation of some 3-(methoxy phenyl)-2-aryl-thiazolidin-4-one derivatives
  publication-title: Indian J. Pharmaceut. Sci.
– reference: Y. Kumar, M. Prasad, A. Prasad, S.K. Singh, N.P. Kumar, Preparation of Crystalline Cefdinir Potassium Dihydrate, WO2003050124A1..
– volume: 2
  start-page: 75
  year: 2003
  end-page: 107
  ident: bib55
  article-title: Cefepime: a review of its use in the management of hospitalized patients with pneumonia
  publication-title: Am. J. Respir. Med.
– volume: 9
  year: 2014
  ident: bib23
  article-title: efficacy of the combination of ciprofloxacin and cefotaxime against vibrio vulnificus sepsis
  publication-title: PLoS One
– ident: 10.1016/j.ejmech.2023.115172_bib131
– volume: 78
  start-page: 4004
  year: 2018
  ident: 10.1016/j.ejmech.2023.115172_bib112
  article-title: The H2 receptor antagonist nizatidine inhibits carcinogenesis in two rodent models of hepatocellular carcinoma
  publication-title: Cancer Res.
  doi: 10.1158/1538-7445.AM2018-4004
– volume: 8
  start-page: 275
  year: 2009
  ident: 10.1016/j.ejmech.2023.115172_bib87
  article-title: Discovery of ixabepilone
  publication-title: Mol. Cancer Therapeut.
  doi: 10.1158/1535-7163.MCT-08-0999
– volume: 6
  start-page: 391
  year: 2012
  ident: 10.1016/j.ejmech.2023.115172_bib91
  article-title: Dabrafenib and its potential for the treatment of metastatic melanoma
  publication-title: Drug Des. Dev. Ther.
– volume: 56
  start-page: 1273
  year: 2012
  ident: 10.1016/j.ejmech.2023.115172_bib46
  article-title: High-level cefixime-and ceftriaxone-resistant Neisseria gonorrhoeae in France: novel penA mosaic allele in a successful international clone causes treatment failure
  publication-title: Antimicrob. Agents Chemother.
  doi: 10.1128/AAC.05760-11
– ident: 10.1016/j.ejmech.2023.115172_bib86
– volume: 62
  year: 2018
  ident: 10.1016/j.ejmech.2023.115172_bib65
  article-title: In vitro antibacterial properties of cefiderocol, a novel siderophore cephalosporin, against Gram-negative bacteria
  publication-title: Antimicrob. Agents Chemother.
  doi: 10.1128/AAC.01454-17
– ident: 10.1016/j.ejmech.2023.115172_bib119
– volume: 52
  start-page: 195
  year: 1990
  ident: 10.1016/j.ejmech.2023.115172_bib121
  article-title: Characteristics of 125I-lodocyanopindolol binding to β-adrenergic and serotonin-1B receptors of rat brain: selectivity of β-adrenergic agents
  publication-title: Jpn. J. Pharmacol.
  doi: 10.1016/S0021-5198(19)40053-X
– volume: 12
  start-page: 859
  year: 2019
  ident: 10.1016/j.ejmech.2023.115172_bib129
  article-title: Avatrombopag for the treatment of thrombocytopenia in patients with chronic liver disease
  publication-title: Expet Rev. Clin. Pharmacol.
  doi: 10.1080/17512433.2019.1649137
– volume: 4
  start-page: 516
  year: 1985
  ident: 10.1016/j.ejmech.2023.115172_bib38
  article-title: Aztreonam, a new monobactam antimicrobial
  publication-title: Clin. Pharm.
– volume: 2
  start-page: 75
  year: 2003
  ident: 10.1016/j.ejmech.2023.115172_bib55
  article-title: Cefepime: a review of its use in the management of hospitalized patients with pneumonia
  publication-title: Am. J. Respir. Med.
  doi: 10.1007/BF03256641
– volume: 805
  start-page: 118
  year: 2017
  ident: 10.1016/j.ejmech.2023.115172_bib142
  article-title: Ameliorative effects of sildenafil and/or febuxostat on doxorubicin-induced nephrotoxicity in rats
  publication-title: Eur. J. Pharmacol.
  doi: 10.1016/j.ejphar.2017.02.046
– ident: 10.1016/j.ejmech.2023.115172_bib51
– start-page: 58
  year: 1997
  ident: 10.1016/j.ejmech.2023.115172_bib5
  article-title: Vanadium-mediated chemoprotection against chemical hepatocarcinogenesis in rats: haematological and histological characteristics
  publication-title: Eur. J. Cancer Prev.
  doi: 10.1097/00008469-199702000-00010
– year: 2010
  ident: 10.1016/j.ejmech.2023.115172_bib40
– ident: 10.1016/j.ejmech.2023.115172_bib28
– volume: 23
  start-page: 3741
  year: 2013
  ident: 10.1016/j.ejmech.2023.115172_bib97
  article-title: Discovery of NVP-BYL719 a potent and selective phosphatidylinositol-3 kinase alpha inhibitor selected for clinical evaluation
  publication-title: Bioorg. Med. Chem. Lett.
  doi: 10.1016/j.bmcl.2013.05.007
– volume: 26
  start-page: 3166
  year: 2021
  ident: 10.1016/j.ejmech.2023.115172_bib3
  article-title: Thiazole ring-a biologically active scaffold
  publication-title: Molecules
  doi: 10.3390/molecules26113166
– volume: 19
  start-page: 377
  year: 1991
  ident: 10.1016/j.ejmech.2023.115172_bib48
  article-title: Comparative in vitro activity of cefpodoxime against anaerobes other than Bacteroides fragilis
  publication-title: Infection
  doi: 10.1007/BF01645372
– volume: 57
  start-page: 1147
  year: 1999
  ident: 10.1016/j.ejmech.2023.115172_bib81
  article-title: HIV protease inhibitor ritonavir: a more potent inhibitor of P-glycoprotein than the cyclosporine analog SDZ PSC 833
  publication-title: Biochem. Pharmacol.
  doi: 10.1016/S0006-2952(99)00026-X
– volume: 5
  year: 2010
  ident: 10.1016/j.ejmech.2023.115172_bib59
  article-title: Enhanced in vivo activity of cefditoren in pre-immunized mice against penicillin-resistant S. pneumoniae (serotypes 6B, 19F and 23F) in a sepsis model
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0012041
– volume: 92
  start-page: 1
  year: 2015
  ident: 10.1016/j.ejmech.2023.115172_bib21
  article-title: Thiazole: a promising heterocycle for the development of potent CNS active agents
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2014.12.031
– volume: 73
  start-page: 574
  year: 1989
  ident: 10.1016/j.ejmech.2023.115172_bib33
  article-title: Ceftriaxone diffusion from blood to aqueous humour in man
  publication-title: Br. J. Ophthalmol.
  doi: 10.1136/bjo.73.7.574
– volume: 7
  start-page: 338
  year: 2007
  ident: 10.1016/j.ejmech.2023.115172_bib54
  article-title: Efficacy and safety of cefepime: a systematic review and meta-analysis
  publication-title: Lancet Infect. Dis.
  doi: 10.1016/S1473-3099(07)70109-3
– ident: 10.1016/j.ejmech.2023.115172_bib39
– ident: 10.1016/j.ejmech.2023.115172_bib143
– ident: 10.1016/j.ejmech.2023.115172_bib66
– volume: 9
  start-page: 79
  year: 2016
  ident: 10.1016/j.ejmech.2023.115172_bib67
  article-title: Isavuconazole in the treatment of invasive aspergillosis and mucormycosis infections
  publication-title: Infect. Drug Resist.
– volume: 27
  start-page: 3994
  year: 2022
  ident: 10.1016/j.ejmech.2023.115172_bib4
  article-title: Thiazole: a versatile standalone moiety contributing to the development of various drugs and biologically active agents
  publication-title: Molecules
  doi: 10.3390/molecules27133994
– volume: 2
  start-page: 196
  year: 2009
  ident: 10.1016/j.ejmech.2023.115172_bib12
  article-title: Synthesis and biological evaluation of some substituted amino thiazole derivatives
  publication-title: Asian J. Res. Chem.
– volume: 284
  start-page: 29798
  year: 2009
  ident: 10.1016/j.ejmech.2023.115172_bib85
  article-title: Thiazolides, a new class of anti-influenza molecules targeting viral hemagglutinin at the post-translational level
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M109.029470
– volume: 28
  start-page: 1065
  year: 2006
  ident: 10.1016/j.ejmech.2023.115172_bib101
  article-title: A review of the receptor-binding and pharmacokinetic properties of dopamine agonists
  publication-title: Clin. Therapeut.
  doi: 10.1016/j.clinthera.2006.08.004
– volume: 32
  year: 2018
  ident: 10.1016/j.ejmech.2023.115172_bib136
  article-title: Rutin and meloxicam attenuate paw inflammation in mice: affecting sorbitol dehydrogenase activity
  publication-title: J. Biochem. Mol. Toxicol.
  doi: 10.1002/jbt.22029
– volume: 17
  start-page: 1193
  year: 2009
  ident: 10.1016/j.ejmech.2023.115172_bib125
  article-title: Discovery of N-[(1R,2S,5S)-2-{[(5-chloroindol-2-yl)carbonyl]amino}-5-(dimethylcarbamoyl)cycloh exyl]-5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxamide hydrochloride: a novel, potent and orally active direct inhibitor of factor Xa
  publication-title: Bioorg. Med. Chem.
  doi: 10.1016/j.bmc.2008.12.037
– volume: 10
  start-page: 391
  year: 1982
  ident: 10.1016/j.ejmech.2023.115172_bib42
  article-title: Vitro activity of cefotiam against bacteria of clinical interest
  publication-title: J. Antimicrob. Chemother.
  doi: 10.1093/jac/10.5.391
– volume: 76
  start-page: 1835
  year: 2005
  ident: 10.1016/j.ejmech.2023.115172_bib138
  article-title: Selectivity of febuxostat, a novel non-purine inhibitor of xanthine oxidase/xanthine dehydrogenase
  publication-title: Life Sci.
  doi: 10.1016/j.lfs.2004.10.031
– volume: 70
  start-page: 572
  year: 2008
  ident: 10.1016/j.ejmech.2023.115172_bib6
  article-title: Synthesis and pharmacological evaluation of azetidin-2-ones and thiazolidin-4-ones encompassing benzothiazole
  publication-title: Indian J. Pharmaceut. Sci.
  doi: 10.4103/0250-474X.45393
– ident: 10.1016/j.ejmech.2023.115172_bib100
– volume: 336
  start-page: 791
  year: 2011
  ident: 10.1016/j.ejmech.2023.115172_bib115
  article-title: Acotiamide hydrochloride (Z-338), a new selective acetylcholinesterase inhibitor, enhances gastric motility without prolonging QT interval in dogs: comparison with cisapride, itopride, and mosapride
  publication-title: J. Pharmacol. Exp. Therapeut.
  doi: 10.1124/jpet.110.174847
– volume: 11
  start-page: 909
  year: 2012
  ident: 10.1016/j.ejmech.2023.115172_bib92
  article-title: Combinations of BRAF, MEK, and PI3K/mTOR inhibitors overcome acquired resistance to the BRAF inhibitor GSK2118436 dabrafenib, mediated by NRAS or MEK mutations
  publication-title: Mol. Cancer Therapeut.
  doi: 10.1158/1535-7163.MCT-11-0989
– volume: 6
  start-page: 1
  year: 2021
  ident: 10.1016/j.ejmech.2023.115172_bib79
  article-title: Bardoxolone and bardoxolone methyl, two Nrf2 activators in clinical trials, inhibit SARS-CoV-2 replication and its 3C-like protease
  publication-title: Signal Transduct. Tar.
– volume: 13
  start-page: 1117
  year: 2014
  ident: 10.1016/j.ejmech.2023.115172_bib98
  article-title: Characterization of the novel and specific PI3Kα inhibitor NVP-BYL719 and development of the patient stratification strategy for clinical trialsNVP-BYL719 PI3Kα inhibitor and predictive response modeling
  publication-title: Mol. Cancer Therapeut.
  doi: 10.1158/1535-7163.MCT-13-0865
– volume: 1
  start-page: 32
  year: 2009
  ident: 10.1016/j.ejmech.2023.115172_bib17
  article-title: Synthesis and biological evaluation of some 3-(methoxy phenyl)-2-aryl-thiazolidin-4-one derivatives
  publication-title: Indian J. Pharmaceut. Sci.
– volume: 30
  start-page: 871
  year: 1992
  ident: 10.1016/j.ejmech.2023.115172_bib37
  article-title: Synergy with aztreonam and arbekacin or tobramycin against Pseudomonas aeruginosa from blood
  publication-title: J. Antimicrob. Chemother.
  doi: 10.1093/jac/30.6.871
– volume: 35
  start-page: 2562
  year: 1992
  ident: 10.1016/j.ejmech.2023.115172_bib10
  article-title: Structure-activity relationships of a series of 2-amino-4-thiazole-containing renin inhibitors
  publication-title: J. Med. Chem.
  doi: 10.1021/jm00092a006
– volume: 97
  start-page: 699
  year: 2015
  ident: 10.1016/j.ejmech.2023.115172_bib18
  article-title: Recent applications of 1, 3-thiazole core structure in the identification of new lead compounds and drug discovery
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2015.04.015
– volume: 51
  start-page: 1818
  year: 2007
  ident: 10.1016/j.ejmech.2023.115172_bib70
  article-title: In vitro activities of isavuconazole and other antifungal agents against Candida bloodstream isolates
  publication-title: Antimicrob. Agents Chemother.
  doi: 10.1128/AAC.01217-06
– volume: 6
  start-page: 1542
  year: 2008
  ident: 10.1016/j.ejmech.2023.115172_bib123
  article-title: DU‐176b, a potent and orally active factor Xa inhibitor: in vitro and in vivo pharmacological profiles
  publication-title: J. Thromb. Haemostasis
  doi: 10.1111/j.1538-7836.2008.03064.x
– volume: 108
  start-page: p69
  year: 2008
  ident: 10.1016/j.ejmech.2023.115172_bib140
  article-title: Effect of febuxostat on the progression of renal disease in 5/6 nephrectomy rats with and without hyperuricemia
  publication-title: Nephron. Physiol.
  doi: 10.1159/000127837
– volume: 40
  start-page: 1468
  year: 1987
  ident: 10.1016/j.ejmech.2023.115172_bib53
  article-title: Synthesis and biological properties of 7β-[(Z)-2-(2-amino-4-thiazoyl)-4-carboxy-2-butenoylamino]-3-cephem-4-carboxilic acid (7432-S), a new oral cephem antibiotic
  publication-title: J. Antibiot.
  doi: 10.7164/antibiotics.40.1468
– ident: 10.1016/j.ejmech.2023.115172_bib47
– volume: 9
  year: 2014
  ident: 10.1016/j.ejmech.2023.115172_bib120
  article-title: Mechanisms of improved aortic stiffness by arotinolol in spontaneously hypertensive rats
  publication-title: PLoS One
– volume: 47
  start-page: 6658
  year: 2004
  ident: 10.1016/j.ejmech.2023.115172_bib89
  article-title: Discovery of N-(2-chloro-6-methyl-phenyl)-2-(6-(4-(2-hydroxyethyl)-piperazin-1-yl)-2-methylpyrimidin-4-ylamino) thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays
  publication-title: J. Med. Chem.
  doi: 10.1021/jm049486a
– volume: 13
  start-page: 226
  year: 2017
  ident: 10.1016/j.ejmech.2023.115172_bib8
  article-title: Anti-inflammatory, analgesic and anti-ulcerogenic activities of novel bis-thiadiazoles, bis-thiazoles and bis-formazanes
  publication-title: Med. Chem.
  doi: 10.2174/1573406412666160920091146
– volume: 13
  start-page: 567
  year: 2009
  ident: 10.1016/j.ejmech.2023.115172_bib137
  article-title: Manufacture of high-purity meloxicam via its novel potassium salt monohydrate
  publication-title: Org. Process Res. Dev.
  doi: 10.1021/op900031h
– ident: 10.1016/j.ejmech.2023.115172_bib114
– volume: 18
  start-page: 257
  year: 1980
  ident: 10.1016/j.ejmech.2023.115172_bib41
  article-title: Comparative activities of cefotiam and cefazolin against urinary tract infections with proteus mirabilis in mice
  publication-title: Antimicrob. Agents Chemother.
  doi: 10.1128/AAC.18.2.257
– ident: 10.1016/j.ejmech.2023.115172_bib58
– volume: 7
  start-page: 792
  year: 2021
  ident: 10.1016/j.ejmech.2023.115172_bib75
  article-title: Simeprevir potently suppresses SARS-CoV-2 replication and synergizes with remdesivir
  publication-title: ACS Cent. Sci.
  doi: 10.1021/acscentsci.0c01186
– volume: 84
  start-page: 952
  year: 2018
  ident: 10.1016/j.ejmech.2023.115172_bib130
  article-title: Pharmacokinetic/pharmacodynamic drug-drug interactions of avatrombopag when coadministered with dual or selective CYP2C9 and CYP3A interacting drugs
  publication-title: Br. J. Clin. Pharmacol.
  doi: 10.1111/bcp.13517
– volume: 45
  start-page: 244
  year: 2013
  ident: 10.1016/j.ejmech.2023.115172_bib141
  article-title: Evaluation of effect of allopurinol and febuxostat in behavioral model of depression in mice
  publication-title: Indian J. Pharmacol.
  doi: 10.4103/0253-7613.111922
– volume: 5
  start-page: 3526
  year: 2014
  ident: 10.1016/j.ejmech.2023.115172_bib14
  article-title: Synthesis and evaluation of some thiazole derivatives as an antifungal agent
  publication-title: Int. J. Pharm. & Life Sci.
– start-page: 203
  year: 2001
  ident: 10.1016/j.ejmech.2023.115172_bib83
  article-title: Epoxyalcohol route to hydroxyethylene dipeptide isosteres: a new synthesis of the diaminoalcohol core of HIV-protease inhibitor ABT-538 (Ritonavir)
  publication-title: Chem. Commun.
  doi: 10.1039/b005804l
– volume: 44
  start-page: 142
  year: 1998
  ident: 10.1016/j.ejmech.2023.115172_bib25
  article-title: Prospective comparison of ceftriaxone and cefotaxime for the short-term treatment of bacterial meningitis in children
  publication-title: Chemotherapy
  doi: 10.1159/000007106
– volume: 45
  start-page: 1151
  year: 2018
  ident: 10.1016/j.ejmech.2023.115172_bib72
  article-title: Efficacy and safety of fosravuconazole L‐lysine ethanolate, a novel oral triazole antifungal agent, for the treatment of onychomycosis: a multicenter, double‐blind, randomized phase III study
  publication-title: J. Dermatol.
  doi: 10.1111/1346-8138.14607
– ident: 10.1016/j.ejmech.2023.115172_bib96
– volume: 2018
  start-page: 4196961
  year: 2018
  ident: 10.1016/j.ejmech.2023.115172_bib103
  article-title: Ropinirole and pramipexole promote structural plasticity in human iPSC-derived dopaminergic neurons via BDNF and mTOR signaling
  publication-title: Neural Plast
  doi: 10.1155/2018/4196961
– ident: 10.1016/j.ejmech.2023.115172_bib106
– ident: 10.1016/j.ejmech.2023.115172_bib50
– volume: 17
  start-page: 258
  year: 1998
  ident: 10.1016/j.ejmech.2023.115172_bib34
  article-title: Penetration of ceftriaxone into the middle ear fluid of children
  publication-title: Pediatr. Infect. Dis. J.
  doi: 10.1097/00006454-199803000-00022
– ident: 10.1016/j.ejmech.2023.115172_bib44
– ident: 10.1016/j.ejmech.2023.115172_bib73
– volume: 12
  year: 2019
  ident: 10.1016/j.ejmech.2023.115172_bib105
  article-title: Pramipexole prevents ischemic cell death via mitochondrial pathways in ischemic stroke
  publication-title: Dis. Model. Mech.
  doi: 10.1242/dmm.033860
– volume: 18
  start-page: 4853
  year: 2008
  ident: 10.1016/j.ejmech.2023.115172_bib74
  article-title: Structure-activity relationship study on a novel series of cyclopentane-containing macrocyclic inhibitors of the hepatitis C virus NS3/4A protease leading to the discovery of TMC435350
  publication-title: Bioorg. Med. Chem. Lett.
  doi: 10.1016/j.bmcl.2008.07.088
– volume: 61
  year: 2017
  ident: 10.1016/j.ejmech.2023.115172_bib76
  article-title: Preclinical characterization and human microdose pharmacokinetics of ITMN-8187, a nonmacrocyclic inhibitor of the hepatitis C virus NS3 protease
  publication-title: Antimicrob. Agents Chemother.
  doi: 10.1128/AAC.01569-16
– volume: 32
  start-page: 783
  year: 1980
  ident: 10.1016/j.ejmech.2023.115172_bib36
  article-title: Ro-13-9904/001, a novel potent and long-acting parenteral cephalosporin
  publication-title: J. Antibiot.
  doi: 10.7164/antibiotics.33.783
– volume: 44
  start-page: 190
  year: 1997
  ident: 10.1016/j.ejmech.2023.115172_bib78
  article-title: Differential inhibition of cytochrome P450 isoforms by the protease inhibitors, ritonavir, saquinavir and indinavir, Brit
  publication-title: J. Clin. Pharmacol.
  doi: 10.1046/j.1365-2125.1997.00644.x
– volume: 16
  start-page: 2841
  year: 2016
  ident: 10.1016/j.ejmech.2023.115172_bib22
  article-title: A review on chemistry, synthesis and therapeutic importance of its derivatives
  publication-title: Curr. Top. Med. Chem.
  doi: 10.2174/1568026616666160506130731
– volume: 9
  year: 2014
  ident: 10.1016/j.ejmech.2023.115172_bib23
  article-title: In vivo efficacy of the combination of ciprofloxacin and cefotaxime against vibrio vulnificus sepsis
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0101118
– volume: 60
  start-page: 6890
  year: 2016
  ident: 10.1016/j.ejmech.2023.115172_bib68
  article-title: In vitro activity of isavuconazole against Rasamsonia species
  publication-title: Antimicrob. Agents Chemother.
  doi: 10.1128/AAC.00742-16
– volume: 27
  start-page: 469
  year: 1984
  ident: 10.1016/j.ejmech.2023.115172_bib35
  article-title: Ceftriaxone: a review of its antibacterial activity, pharmacological properties and therapeutic use
  publication-title: Drugs
  doi: 10.2165/00003495-198427060-00001
– ident: 10.1016/j.ejmech.2023.115172_bib82
– volume: 67
  start-page: 1334
  year: 1978
  ident: 10.1016/j.ejmech.2023.115172_bib122
  article-title: Synthesis and β-adrenergic blocking action of a new thiazolylthiopropanolamine derivative
  publication-title: J. Pharmacol. Sci.
  doi: 10.1002/jps.2600670944
– volume: 256
  start-page: 266
  year: 2016
  ident: 10.1016/j.ejmech.2023.115172_bib93
  article-title: Anti-inflammatory effects of dabrafenib on polyphosphate-mediated vascular disruption
  publication-title: Chem. Biol. Interact.
  doi: 10.1016/j.cbi.2016.07.024
– volume: 2
  start-page: 195
  year: 2000
  ident: 10.1016/j.ejmech.2023.115172_bib1
  article-title: Recent advances in the preparation of heterocycles on solid support: a review of the literature
  publication-title: J. Comb. Chem.
  doi: 10.1021/cc000002f
– ident: 10.1016/j.ejmech.2023.115172_bib49
– ident: 10.1016/j.ejmech.2023.115172_bib109
– volume: 152
  start-page: 2447
  year: 1994
  ident: 10.1016/j.ejmech.2023.115172_bib57
  article-title: Cefdinir (CI-983), a new oral amino-2-thiazolyl cephalosporin, inhibits human neutrophil myeloperoxidase in the extracellular medium but not the phagolysosome
  publication-title: J. Immunol.
  doi: 10.4049/jimmunol.152.5.2447
– volume: 2
  start-page: 261
  year: 1999
  ident: 10.1016/j.ejmech.2023.115172_bib80
  article-title: HIV-1 protease inhibitor ritonavir modulates susceptibility to apoptosis of uninfected T cells
  publication-title: J. Hum. Virol.
– volume: 64
  start-page: 2597
  year: 2004
  ident: 10.1016/j.ejmech.2023.115172_bib60
  publication-title: Cefditoren Pivoxil, Drugs
  doi: 10.2165/00003495-200464220-00009
– volume: 321
  start-page: 642
  year: 2007
  ident: 10.1016/j.ejmech.2023.115172_bib132
  article-title: Effect of (R)-2-(2-aminothiazol-4-yl)-4′-{2-[(2-hydroxy-2-phenylethyl) amino] ethyl} acetanilide (YM178), a novel selective β3-adrenoceptor agonist, on bladder function
  publication-title: J. Pharmacol. Exp. Therapeut.
  doi: 10.1124/jpet.106.115840
– volume: 33
  start-page: 292
  year: 2016
  ident: 10.1016/j.ejmech.2023.115172_bib117
  article-title: Physiologically-based pharmacokinetic and pharmacodynamic modeling for the inhibition of acetylcholinesterase by acotiamide, a novel gastroprokinetic agent for the treatment of functional dyspepsia, in rat stomach
  publication-title: Pharm. Res. (N. Y.)
  doi: 10.1007/s11095-015-1787-y
– volume: 69
  start-page: 585
  year: 2005
  ident: 10.1016/j.ejmech.2023.115172_bib32
  article-title: Bacterial cell wall synthesis: new insights from localization studies
  publication-title: Microbiol. Mol. Biol. Rev.
  doi: 10.1128/MMBR.69.4.585-607.2005
– volume: 294
  start-page: F710
  year: 2008
  ident: 10.1016/j.ejmech.2023.115172_bib139
  article-title: Effects of febuxostat on metabolic and renal alterations in rats with fructose-induced metabolic syndrome
  publication-title: Am. J. Physiol. Renal
  doi: 10.1152/ajprenal.00454.2007
– volume: 14
  start-page: 2198
  year: 2017
  ident: 10.1016/j.ejmech.2023.115172_bib135
  article-title: Meloxicam decreases the migration and invasion of CF41. Mg canine mammary carcinoma cells
  publication-title: Oncol. Lett.
  doi: 10.3892/ol.2017.6400
– volume: 185
  start-page: 45
  year: 2003
  ident: 10.1016/j.ejmech.2023.115172_bib26
  article-title: A comparison of the prophylactic efficacy of ceftriaxone and cefotaxime in abdominal surgery
  publication-title: Am. J. Surg.
  doi: 10.1016/S0002-9610(02)01125-X
– volume: 104
  start-page: 209
  year: 1997
  ident: 10.1016/j.ejmech.2023.115172_bib104
  article-title: Attenuation of levodopa-induced toxicity in mesencephalic cultures by pramipexole
  publication-title: J. Neural. Transm.
  doi: 10.1007/BF01273182
– volume: 6
  start-page: 163
  year: 2013
  ident: 10.1016/j.ejmech.2023.115172_bib69
  article-title: Profile of isavuconazole and its potential in the treatment of severe invasive fungal infections
  publication-title: Infect. Drug Resist.
– ident: 10.1016/j.ejmech.2023.115172_bib90
– volume: 9
  start-page: 201
  year: 2008
  ident: 10.1016/j.ejmech.2023.115172_bib62
  article-title: Ceftaroline fosamil, a cephalosporin derivative for the potential treatment of MRSA infection
  publication-title: Curr. Opin. Invest. Drugs
– volume: 20
  start-page: 3118
  year: 1887
  ident: 10.1016/j.ejmech.2023.115172_bib2
  article-title: Ueber verbindungen des thiazols (pyridins der thiophenreihe)
  publication-title: Eur. J. Inorg. Chem.
– volume: 19
  start-page: 900
  year: 1985
  ident: 10.1016/j.ejmech.2023.115172_bib29
  article-title: Ceftriaxone: a third-generation cephalosporin
  publication-title: Drug Intell. Clin. Pharm.
– volume: 136
  start-page: 784
  year: 2015
  ident: 10.1016/j.ejmech.2023.115172_bib99
  article-title: BYL719, a new α‐specific PI3K inhibitor: single administration and in combination with conventional chemotherapy for the treatment of osteosarcoma
  publication-title: Int. J. Cancer
  doi: 10.1002/ijc.29040
– volume: 11
  start-page: 1979
  year: 2019
  ident: 10.1016/j.ejmech.2023.115172_bib19
  article-title: Recent advances of thiazole hybrids in biological applications
  publication-title: Future Med. Chem.
  doi: 10.4155/fmc-2018-0196
– volume: 6
  start-page: 958
  year: 1987
  ident: 10.1016/j.ejmech.2023.115172_bib45
  article-title: Vitro activity of a new broad spectrum, β-lactamase-stable oral cephalosporin, cefixime, Pediatr
  publication-title: infect. Dis. J.
  doi: 10.1097/00006454-198710000-00034
– volume: 49
  start-page: 214
  year: 2016
  ident: 10.1016/j.ejmech.2023.115172_bib94
  article-title: Anti-septic effects of dabrafenib on HMGB1-mediated inflammatory responses
  publication-title: BMB Rep
  doi: 10.5483/BMBRep.2016.49.4.220
– volume: 43
  start-page: 1047
  year: 1990
  ident: 10.1016/j.ejmech.2023.115172_bib61
  article-title: Synthesis and oral activity of ME1207, a new orally active cephalosporin
  publication-title: J. Antibiot.
  doi: 10.7164/antibiotics.43.1047
– volume: 154
  start-page: 98
  year: 2012
  ident: 10.1016/j.ejmech.2023.115172_bib24
  article-title: The antibiotic resistance characteristics of non-typhoidal Salmonella enterica isolated from food-producing animals, retail meat and humans in South East Asia
  publication-title: Int. J. Food Microbiol.
  doi: 10.1016/j.ijfoodmicro.2011.12.032
– volume: 104
  start-page: 244
  year: 2015
  ident: 10.1016/j.ejmech.2023.115172_bib95
  article-title: Early vaginal opening in juvenile female rats given BRAF‐inhibitor dabrafenib is not associated with early physiologic sexual maturation
  publication-title: Birth Defects Res. B Dev. Reprod. Toxicol.
  doi: 10.1002/bdrb.21165
– volume: 40
  start-page: 980
  year: 1997
  ident: 10.1016/j.ejmech.2023.115172_bib134
  article-title: Effect of structural modification of enol-carboxamide-type nonsteroidal antiinflammatory drugs on COX-2/COX-1 selectivity
  publication-title: J. Med. Chem.
  doi: 10.1021/jm9607010
– volume: 12
  start-page: 553
  year: 2016
  ident: 10.1016/j.ejmech.2023.115172_bib9
  article-title: Synthesis, antibacterial activity, interaction with nucleobase and molecular docking studies of 4-formylbenzoic acid based thiazoles
  publication-title: Med. Chem.
  doi: 10.2174/1573406412666160201121310
– ident: 10.1016/j.ejmech.2023.115172_bib133
– ident: 10.1016/j.ejmech.2023.115172_bib71
– ident: 10.1016/j.ejmech.2023.115172_bib127
– volume: 32
  year: 2020
  ident: 10.1016/j.ejmech.2023.115172_bib116
  article-title: Acotiamide attenuates central urocortin 2‐induced intestinal inflammatory responses, and urocortin 2 treatment reduces TNF‐α productions in LPS‐stimulated macrophage cell lines
  publication-title: Neurogastroent. Motil.
  doi: 10.1111/nmo.13813
– volume: 80
  start-page: 1564
  year: 2007
  ident: 10.1016/j.ejmech.2023.115172_bib102
  article-title: Blood-brain barrier transport of pramipexole, a dopamine D2 agonist
  publication-title: Life Sci.
  doi: 10.1016/j.lfs.2007.01.035
– volume: 26
  start-page: 1158
  year: 1983
  ident: 10.1016/j.ejmech.2023.115172_bib7
  article-title: N-(4-Substituted-thiazolyl) oxamic acid derivatives, new series of potent, orally active antiallergy agents
  publication-title: J. Med. Chem.
  doi: 10.1021/jm00362a014
– volume: 17
  start-page: 4223
  year: 2007
  ident: 10.1016/j.ejmech.2023.115172_bib16
  article-title: Design and synthesis of 1, 2-dithiolane derivatives and evaluation of their neuroprotective activity
  publication-title: Bioorg. Med. Chem. Lett.
  doi: 10.1016/j.bmcl.2007.05.036
– volume: 76
  start-page: 155
  year: 2016
  ident: 10.1016/j.ejmech.2023.115172_bib126
  article-title: Lusutrombopag: first global approval
  publication-title: Drugs
  doi: 10.1007/s40265-015-0525-4
– ident: 10.1016/j.ejmech.2023.115172_bib88
– volume: 239
  start-page: 406
  year: 1986
  ident: 10.1016/j.ejmech.2023.115172_bib111
  article-title: Actions of nizatidine, a selective histamine H2-receptor antagonist, on gastric acid secretion in dogs, rats and frogs
  publication-title: J. Pharmacol. Exp. Therapeut.
– volume: 332
  start-page: 343
  year: 1999
  ident: 10.1016/j.ejmech.2023.115172_bib15
  article-title: Synthesis and hypnotic activity of new 4‐thiazolidinone and 2‐thioxo‐4,5‐imidazolidinedione derivatives
  publication-title: Arch. Pharm.
  doi: 10.1002/(SICI)1521-4184(199910)332:10<343::AID-ARDP343>3.0.CO;2-0
– volume: 21
  start-page: 2123
  year: 2012
  ident: 10.1016/j.ejmech.2023.115172_bib20
  article-title: Thiazoles: having diverse biological activities
  publication-title: Med. Chem. Res.
  doi: 10.1007/s00044-011-9685-2
– volume: 22
  start-page: 19
  year: 1987
  ident: 10.1016/j.ejmech.2023.115172_bib13
  article-title: Synthesis and diuretic activity of imidazo [2, 1-b] thiazole acetohydrazones
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/0223-5234(87)90169-3
– volume: 33
  start-page: 759
  year: 1993
  ident: 10.1016/j.ejmech.2023.115172_bib56
  article-title: Synthesis of 7-[α-( 2-amino-[2-14C]thiazol-4-yl)-α-(Z)-methoxyiminoacetamido]-3-(1-methylpyrrolldinlo)methyl-3-cephem-4-carboxylate hydrochloride ([14C] cefepime hydrochloride)
  publication-title: J. Label. Compd. Radiopharm.
  doi: 10.1002/jlcr.2580330812
– volume: 24
  start-page: 862
  year: 2022
  ident: 10.1016/j.ejmech.2023.115172_bib108
  article-title: Evaluation of 18F-flutemetamol amyloid PET image analysis parameters on the effect of verubecestat on brain amlyoid load in Alzheimer's disease
  publication-title: Mol. Imag. Biol.
  doi: 10.1007/s11307-022-01735-z
– volume: 258
  year: 2020
  ident: 10.1016/j.ejmech.2023.115172_bib30
  article-title: Ceftriaxone improves hepatorenal damages in mice subjected to D-galactose-induced aging
  publication-title: Life Sci.
  doi: 10.1016/j.lfs.2020.118119
– volume: 11
  start-page: 2427
  year: 2003
  ident: 10.1016/j.ejmech.2023.115172_bib64
  article-title: TAK-599, a novel N-phosphono type prodrug of anti-MRSA cephalosporin T-91825: synthesis, physicochemical and pharmacological properties
  publication-title: Bioorg. Med. Chem.
  doi: 10.1016/S0968-0896(03)00126-3
– ident: 10.1016/j.ejmech.2023.115172_bib124
– ident: 10.1016/j.ejmech.2023.115172_bib43
– volume: 30
  start-page: 494
  year: 1987
  ident: 10.1016/j.ejmech.2023.115172_bib107
  article-title: Dopamine autoreceptor agonists: resolution and pharmacological activity of 2, 6-diaminotetrahydrobenzothiazole and an aminothiazole analog of apomorphine
  publication-title: J. Med. Chem.
  doi: 10.1021/jm00386a009
– volume: 35
  start-page: 2078
  year: 1991
  ident: 10.1016/j.ejmech.2023.115172_bib52
  article-title: Single-dose pharmacokinetics of ceftibuten (SCH 39720) in infants and children
  publication-title: Antimicrob. Agents Chemother.
  doi: 10.1128/AAC.35.10.2078
– volume: 17
  start-page: 19
  year: 2008
  ident: 10.1016/j.ejmech.2023.115172_bib11
  article-title: Design, synthesis, and antimalarial evaluation of thiazole-derived amino acids
  publication-title: Med. Chem. Res.
  doi: 10.1007/s00044-008-9089-0
– volume: 51
  start-page: 3397
  year: 2007
  ident: 10.1016/j.ejmech.2023.115172_bib63
  article-title: In vivo efficacy of ceftaroline (PPI-0903), a new broad-spectrum cephalosporin, compared with linezolid and vancomycin against methicillin-resistant and vancomycin-intermediate Staphylococcus aureus in a rabbit endocarditis model
  publication-title: Antimicrob. Agents Chemother.
  doi: 10.1128/AAC.01242-06
– volume: 81
  start-page: 1
  year: 2020
  ident: 10.1016/j.ejmech.2023.115172_bib113
  article-title: Comparative histological and histochemical studies between ranitidine and nizatidine in treatment of peptic ulcer with evaluation of their adverse effects on male sex hormones
  publication-title: J. Basic Appl. Zool.
  doi: 10.1186/s41936-020-00196-6
– year: 2008
  ident: 10.1016/j.ejmech.2023.115172_bib31
– volume: 18
  start-page: 4853
  year: 2008
  ident: 10.1016/j.ejmech.2023.115172_bib77
  article-title: Structure-activity relationship study on a novel series of cyclopentane-containing macrocyclic inhibitors of the hepatitis C virus NS3/4A protease leading to the discovery of TMC435350
  publication-title: Bioorg. Med. Chem. Lett.
  doi: 10.1016/j.bmcl.2008.07.088
– volume: 22
  start-page: 155
  year: 1995
  ident: 10.1016/j.ejmech.2023.115172_bib27
  article-title: Cefotaxime twice daily versus ceftriaxone once daily: a randomized controlled study in patients with serious infections, Diagn
  publication-title: Microorg. Infect. Dis.
  doi: 10.1016/0732-8893(95)00080-T
– ident: 10.1016/j.ejmech.2023.115172_bib118
– ident: 10.1016/j.ejmech.2023.115172_bib110
– volume: 82
  start-page: 247
  year: 2009
  ident: 10.1016/j.ejmech.2023.115172_bib128
  article-title: AKR‐501 (YM477) a novel orally‐active thrombopoietin receptor agonist
  publication-title: Eur. J. Haematol.
  doi: 10.1111/j.1600-0609.2008.01198.x
– volume: 1
  start-page: 209
  year: 2010
  ident: 10.1016/j.ejmech.2023.115172_bib84
  article-title: Cobicistat (GS-9350): a potent and selective inhibitor of human CYP3A as a novel pharmacoenhancer
  publication-title: ACS Med. Chem. Lett.
  doi: 10.1021/ml1000257
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Snippet The development of heterocyclic derivatives has progressed considerably over the past few decades, and many new agents of synthetic and natural origin have...
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SubjectTerms Anti-Bacterial Agents - pharmacology
Anti-Bacterial Agents - therapeutic use
Antifungal Agents - therapeutic use
Chemical synthesis
Clinical application
Heterocycles
Heterocyclic Compounds
Privileged scaffold
Thiazole ring
Thiazoles
Title Application and synthesis of thiazole ring in clinically approved drugs
URI https://dx.doi.org/10.1016/j.ejmech.2023.115172
https://www.ncbi.nlm.nih.gov/pubmed/36758304
https://www.proquest.com/docview/2775612798
Volume 250
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