Search Results - "EUN JOO ROH" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Design, Synthesis, In Vitro, and In Silico Studies of New N5-Substituted-pyrazolo[3,4-d]pyrimidinone Derivatives as Anticancer CDK2 Inhibitors

Design, Synthesis, In Vitro, and In Silico Studies of New N5-Substituted-pyrazolo[3,4-d]pyrimidinone Derivatives as Anticancer CDK2 Inhibitors

by Zaki, Waheed A., El-Sayed, Selwan M., Alswah, Mohamed, El-Morsy, Ahmed, Bayoumi, Ashraf H., Mayhoub, Abrahman S., Moustafa, Walaa H., Awaji, Aeshah A., Roh, Eun Joo, Hassan, Ahmed H.E., Mahmoud, Kazem
Published in Pharmaceuticals (Basel, Switzerland) (11.11.2023)

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Highly Potent, Selective, and Competitive Indole-Based MAO-B Inhibitors Protect PC12 Cells against 6-Hydroxydopamine- and Rotenone-Induced Oxidative Stress

Highly Potent, Selective, and Competitive Indole-Based MAO-B Inhibitors Protect PC12 Cells against 6-Hydroxydopamine- and Rotenone-Induced Oxidative Stress

by Elsherbeny, Mohamed H, Kim, Jushin, Gouda, Noha A, Gotina, Lizaveta, Cho, Jungsook, Pae, Ae Nim, Lee, Kyeong, Park, Ki Duk, Elkamhawy, Ahmed, Roh, Eun Joo
Published in Antioxidants (19.10.2021)

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Correction: Elsherbeny et al. 2-(3-Bromophenyl)-8-fluoroquinazoline-4-carboxylic Acid as a Novel and Selective Aurora A Kinase Inhibitory Lead with Apoptosis Properties: Design, Synthesis, In Vitro and In Silico Biological Evaluation. Life 2022, 12 , 876

Correction: Elsherbeny et al. 2-(3-Bromophenyl)-8-fluoroquinazoline-4-carboxylic Acid as a Novel and Selective Aurora A Kinase Inhibitory Lead with Apoptosis Properties: Design, Synthesis, In Vitro and In Silico Biological Evaluation. Life 2022, 12 , 876

by Elsherbeny, Mohamed H, Ammar, Usama M, Abdellattif, Magda H, Abourehab, Mohammed A S, Abdeen, Ahmed, Ibrahim, Samah F, Abdelrahaman, Doaa, Mady, Wessam, Roh, Eun Joo, Elkamhawy, Ahmed
Published in Life (Basel, Switzerland) (22.03.2024)

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Development of New Meridianin/Leucettine-Derived Hybrid Small Molecules as Nanomolar Multi-Kinase Inhibitors with Antitumor Activity

Development of New Meridianin/Leucettine-Derived Hybrid Small Molecules as Nanomolar Multi-Kinase Inhibitors with Antitumor Activity

by Elsherbeny, Mohamed H., Elkamhawy, Ahmed, Nada, Hossam, Abdellattif, Magda H., Lee, Kyeong, Roh, Eun Joo
Published in Biomedicines (01.09.2021)

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Novel Rhodanine Derivative, 5-[4-(4-Fluorophenoxy) phenyl]methylene-3-{4-[3-(4-methylpiperazin-1-yl) propoxy]phenyl}-2-thioxo-4-thiazolidinone dihydrochloride, Induces Apoptosis via Mitochondria Dysfunction and Endoplasmic Reticulum Stress in Human Colon Cancer Cells

Novel Rhodanine Derivative, 5-[4-(4-Fluorophenoxy) phenyl]methylene-3-{4-[3-(4-methylpiperazin-1-yl) propoxy]phenyl}-2-thioxo-4-thiazolidinone dihydrochloride, Induces Apoptosis via Mitochondria Dysfunction and Endoplasmic Reticulum Stress in Human Colon Cancer Cells

by Jung, Hye-Uk, Lee, Jeong-Hun, Chung, Kyung-Sook, Hong, Joo Young, Choi, Jung-Hye, Kim, Soo-Dong, Roh, Eun Joo, Shin, Kye Jung, Lee, Kyung-Tae
Published in Molecules (Basel, Switzerland) (06.11.2018)

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Integrating computational methods guided the discovery of phytochemicals as potential Pin1 inhibitors for cancer: pharmacophore modeling, molecular docking, MM-GBSA calculations and molecular dynamics studies

Integrating computational methods guided the discovery of phytochemicals as potential Pin1 inhibitors for cancer: pharmacophore modeling, molecular docking, MM-GBSA calculations and molecular dynamics studies

by Alzain, Abdulrahim A, Elbadwi, Fatima A, Shoaib, Tagyedeen H, Sherif, Asmaa E, Osman, Wadah, Ashour, Ahmed, Mohamed, Gamal A, Ibrahim, Sabrin R M, Roh, Eun Joo, Hassan, Ahmed H E
Published in Frontiers in chemistry (2024)

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Exploring the sedative properties of natural molecules from hop cones ( Humulus lupulus ) as promising natural anxiolytics through GABA receptors and the human serotonin transporter

Exploring the sedative properties of natural molecules from hop cones ( Humulus lupulus ) as promising natural anxiolytics through GABA receptors and the human serotonin transporter

by Belal, Amany, Elballal, Mohammed S, Al-Karmalawy, Ahmed A, Hassan, Ahmed H E, Roh, Eun Joo, Ghoneim, Mohammed M, Ali, Mohamed A M, Obaidullah, Ahmad J, Alotaibi, Jawaher M, Shaaban, Salwa, Elanany, Mohamed A
Published in Frontiers in chemistry (10.07.2024)

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2-(3-Bromophenyl)-8-fluoroquinazoline-4-carboxylic Acid as a Novel and Selective Aurora A Kinase Inhibitory Lead with Apoptosis Properties: Design, Synthesis, In Vitro and In Silico Biological Evaluation

2-(3-Bromophenyl)-8-fluoroquinazoline-4-carboxylic Acid as a Novel and Selective Aurora A Kinase Inhibitory Lead with Apoptosis Properties: Design, Synthesis, In Vitro and In Silico Biological Evaluation

by Elsherbeny, Mohamed H, Ammar, Usama M, Abdellattif, Magda H, Abourehab, Mohammed A S, Abdeen, Ahmed, Ibrahim, Samah F, Abdelrahaman, Doaa, Mady, Wessam, Roh, Eun Joo, Elkamhawy, Ahmed
Published in Life (Basel, Switzerland) (01.06.2022)

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AF8c, a Multi-Kinase Inhibitor Induces Apoptosis by Activating DR5/Nrf2 via ROS in Colorectal Cancer Cells

AF8c, a Multi-Kinase Inhibitor Induces Apoptosis by Activating DR5/Nrf2 via ROS in Colorectal Cancer Cells

by Jeong, Soyeon, Farag, Ahmed K., Yun, Hye Kyeong, Jeong, Yoon A., Kim, Dae Yeong, Jo, Min Jee, Park, Seong Hye, Kim, Bo Ram, Kim, Jung Lim, Kim, Bu Gyeom, Lee, Dae-Hee, Roh, Eun Joo, Oh, Sang Cheul
Published in Cancers (21.06.2022)

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Trifluoperazine and Its Analog Suppressed the Tumorigenicity of Non-Small Cell Lung Cancer Cell; Applicability of Antipsychotic Drugs to Lung Cancer Treatment

Trifluoperazine and Its Analog Suppressed the Tumorigenicity of Non-Small Cell Lung Cancer Cell; Applicability of Antipsychotic Drugs to Lung Cancer Treatment

by Jeong, Joo Yeon, Park, Haangik, Yoo, Hong, Kim, Eun-Jin, Jeon, Borami, Lee, Jong Deog, Kang, Dawon, Lee, Changjoon Justin, Paek, Sun Ha, Roh, Eun Joo, Yi, Gwan-Su, Kang, Sang Soo
Published in Biomedicines (30.04.2022)

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Small molecules that protect against β-amyloid-induced cytotoxicity by inhibiting aggregation of β-amyloid

Small molecules that protect against β-amyloid-induced cytotoxicity by inhibiting aggregation of β-amyloid

by Lee, Yun Suk, Kim, Hye Yun, Kim, YoungSoo, Seo, Jae Hong, Roh, Eun Joo, Han, Hogyu, Shin, Kye Jung
Published in Bioorganic & medicinal chemistry (15.08.2012)

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Synthesis and biological evaluation of novel 3-(quinolin-4-ylamino)benzenesulfonamides as carbonic anhydrase isoforms I and II inhibitors

Synthesis and biological evaluation of novel 3-(quinolin-4-ylamino)benzenesulfonamides as carbonic anhydrase isoforms I and II inhibitors

by Al-Sanea, Mohammad M., Elkamhawy, Ahmed, Paik, Sora, Bua, Silvia, Ha Lee, So, Abdelgawad, Mohamed A., Roh, Eun Joo, Eldehna, Wagdy M., Supuran, Claudiu T.
Published in Journal of enzyme inhibition and medicinal chemistry (01.01.2019)

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Scandium(III) triflate immobilised in ionic liquids: a novel and recyclable catalytic system for Friedel-Crafts alkylation of aromatic compounds with alkenes

Scandium(III) triflate immobilised in ionic liquids: a novel and recyclable catalytic system for Friedel-Crafts alkylation of aromatic compounds with alkenes

by Song, CE, Shim, WH, Roh, EJ, Choi, JH
Published in Chemical communications (Cambridge, England) (01.01.2000)

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Synthesis and biological evaluation of novel 3,4-diaryl lactam derivatives as triple reuptake inhibitors

Synthesis and biological evaluation of novel 3,4-diaryl lactam derivatives as triple reuptake inhibitors

by Park, Jung-eun, Song, Chiman, Choi, Keehyun, Sim, Taebo, Moon, Bongjin, Roh, Eun Joo
Published in Bioorganic & medicinal chemistry letters (15.10.2013)

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Structure–activity relationships of 1,4-dihydropyridines that act as enhancers of the vanilloid receptor 1 (TRPV1)

Structure–activity relationships of 1,4-dihydropyridines that act as enhancers of the vanilloid receptor 1 (TRPV1)

by Roh, Eun Joo, Keller, Jason M., Olah, Zoltan, Iadarola, Michael J., Jacobson, Kenneth A.
Published in Bioorganic & medicinal chemistry (15.10.2008)

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Discovery of potent and selective rhodanine type IKKβ inhibitors by hit-to-lead strategy

Discovery of potent and selective rhodanine type IKKβ inhibitors by hit-to-lead strategy

by Song, Hyeseung, Lee, Yun Suk, Roh, Eun Joo, Seo, Jae Hong, Oh, Kwang-Seok, Lee, Byung Ho, Han, Hogyu, Shin, Kye Jung
Published in Bioorganic & medicinal chemistry letters (01.09.2012)

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Synthesis and biological evaluation of 4-piperidinecarboxylate and 4-piperidinecyanide derivatives for T-type calcium channel blockers

Synthesis and biological evaluation of 4-piperidinecarboxylate and 4-piperidinecyanide derivatives for T-type calcium channel blockers

by Woo, Hyun Min, Lee, Yun Suk, Roh, Eun Joo, Seo, Seon Hee, Song, Chi Man, Chung, Hye Jin, Pae, Ae Nim, Shin, Kye Jung
Published in Bioorganic & medicinal chemistry letters (01.10.2011)

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Discovery of piperidinyl aminopyrimidine derivatives as IKK-2 inhibitors

Discovery of piperidinyl aminopyrimidine derivatives as IKK-2 inhibitors

by Kim, Sora, Jung, Jin Kyo, Lee, Hyo Seon, Kim, Youngjae, Kim, Jiyoon, Choi, Kihang, Baek, Du-Jong, Moon, Bongjin, Oh, Kwang-Seok, Lee, Byung Ho, Shin, Kye Jung, Pae, Ae Nim, Nam, Ghilsoo, Roh, Eun Joo, Cho, Yong Seo, Choo, Hyunah
Published in Bioorganic & medicinal chemistry letters (15.05.2011)

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Cr(salen) catalysed asymmetric ring opening reactions of epoxides in room temperature ionic liquids

Cr(salen) catalysed asymmetric ring opening reactions of epoxides in room temperature ionic liquids

by Song, CE, Oh, CR, Roh, EJ, Choo, DJ
Published in Chemical communications (Cambridge, England) (01.01.2000)

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Synthesis and evaluation of α,α′-disubstituted phenylacetate derivatives for T-type calcium channel blockers

Synthesis and evaluation of α,α′-disubstituted phenylacetate derivatives for T-type calcium channel blockers

by Lee, Hyung Kook, Lee, Yun Suk, Roh, Eun Joo, Rhim, Hyewhon, Lee, Jae Yeol, Shin, Kye Jung
Published in Bioorganic & medicinal chemistry (01.08.2008)

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