Tetracarboxylic acids on a thiacalixarene scaffold: synthesis and binding of dopamine hydrochlorideElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nj03953k

For the first time thiacalix[4]arene derivatives in 1,3- alternate conformation simultaneously containing amide, carboxyl and hydroxyl groups capable of forming 1 : 1 stoichiometry complexes with dopamine hydrochloride were obtained. The efficiency of dopamine hydrochloride binding was evaluated by...

Full description

Saved in:
Bibliographic Details
Main Authors Mostovaya, O. A, Padnya, P. L, Vavilova, A. A, Shurpik, D. N, Khairutdinov, B. I, Mukhametzyanov, T. A, Khannanov, A. A, Kutyreva, M. P, Stoikov, I. I
Format Journal Article
LanguageEnglish
Published 18.12.2017
Online AccessGet full text

Cover

Abstract For the first time thiacalix[4]arene derivatives in 1,3- alternate conformation simultaneously containing amide, carboxyl and hydroxyl groups capable of forming 1 : 1 stoichiometry complexes with dopamine hydrochloride were obtained. The efficiency of dopamine hydrochloride binding was evaluated by a number of spectral methods. Using the methods of fluorescent, UV-Vis and NMR spectroscopy, the mechanism of interaction of the synthesized macrocycles with dopamine has been studied. It was shown that quenching of dopamine fluorescence by the studied macrocycles is carried out through a static mechanism. Tetracarboxylic acids based on thiacalix[4]arene in 1,3- alternate conformation quench fluorescence of dopamine hydrochloride according to the static mechanism.
AbstractList For the first time thiacalix[4]arene derivatives in 1,3- alternate conformation simultaneously containing amide, carboxyl and hydroxyl groups capable of forming 1 : 1 stoichiometry complexes with dopamine hydrochloride were obtained. The efficiency of dopamine hydrochloride binding was evaluated by a number of spectral methods. Using the methods of fluorescent, UV-Vis and NMR spectroscopy, the mechanism of interaction of the synthesized macrocycles with dopamine has been studied. It was shown that quenching of dopamine fluorescence by the studied macrocycles is carried out through a static mechanism. Tetracarboxylic acids based on thiacalix[4]arene in 1,3- alternate conformation quench fluorescence of dopamine hydrochloride according to the static mechanism.
Author Khairutdinov, B. I
Stoikov, I. I
Vavilova, A. A
Shurpik, D. N
Mukhametzyanov, T. A
Kutyreva, M. P
Padnya, P. L
Mostovaya, O. A
Khannanov, A. A
AuthorAffiliation A.M. Butlerov Chemistry Institute
Kazan Federal University
Kazan Institute of Biochemistry and Biophysics
AuthorAffiliation_xml – name: Kazan Federal University
– name: A.M. Butlerov Chemistry Institute
– name: Kazan Institute of Biochemistry and Biophysics
Author_xml – sequence: 1
  givenname: O. A
  surname: Mostovaya
  fullname: Mostovaya, O. A
– sequence: 2
  givenname: P. L
  surname: Padnya
  fullname: Padnya, P. L
– sequence: 3
  givenname: A. A
  surname: Vavilova
  fullname: Vavilova, A. A
– sequence: 4
  givenname: D. N
  surname: Shurpik
  fullname: Shurpik, D. N
– sequence: 5
  givenname: B. I
  surname: Khairutdinov
  fullname: Khairutdinov, B. I
– sequence: 6
  givenname: T. A
  surname: Mukhametzyanov
  fullname: Mukhametzyanov, T. A
– sequence: 7
  givenname: A. A
  surname: Khannanov
  fullname: Khannanov, A. A
– sequence: 8
  givenname: M. P
  surname: Kutyreva
  fullname: Kutyreva, M. P
– sequence: 9
  givenname: I. I
  surname: Stoikov
  fullname: Stoikov, I. I
BookMark eNqFjzFPwzAUhC1UJFpgYUd6bDCkxCRN1a4QRCeGdo9e7BfyimNHdkDN_-IH1gMSAxJMd9J3utPNxMQ6S0JcyXQu02x1r5Z2H3WRvZ-IqcyKVbJ6KOQkepnnSbrIizMxC2GfplIuCzkVXzsaPCr0tTuMhhWgYh3AWUAYWo7E8AE9WYKgsGmc0WsIox1aChwArYaarWb7Bq4B7XrsOGbbUXunWuM8ayoNqcE7G9vDR98b6sgO6Edg2zjf4cBx7rbcbu4AP5EN1obmsCWCp9fNGn5_uxCnDZpAl996Lq6fy93jS-KDqnrPXSyvfuLZ__zmL171usmONG1xOg
ContentType Journal Article
DOI 10.1039/c7nj03953k
DatabaseTitleList
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1369-9261
EndPage 183
ExternalDocumentID c7nj03953k
GroupedDBID -JG
0-7
1TJ
705
70J
70~
7~J
AAEMU
ABGFH
ACLDK
ADSRN
AEFDR
AFVBQ
AGSTE
AUDPV
BSQNT
C6K
EE0
EF-
GNO
H~N
IDZ
J3I
R7B
R7C
R7D
RCNCU
RPMJG
RRC
RSCEA
SKA
SKF
SKH
SLH
VH6
ID FETCH-rsc_primary_c7nj03953k3
ISSN 1144-0546
IngestDate Mon Jan 28 17:15:13 EST 2019
Sat Jun 01 02:23:50 EDT 2019
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
LinkModel OpenURL
MergedId FETCHMERGED-rsc_primary_c7nj03953k3
Notes 10.1039/c7nj03953k
Electronic supplementary information (ESI) available. See DOI
PageCount 7
ParticipantIDs rsc_primary_c7nj03953k
ProviderPackageCode J3I
ACLDK
RRC
7~J
AEFDR
70~
VH6
GNO
RCNCU
SLH
70J
EE0
RSCEA
AFVBQ
C6K
H~N
0-7
IDZ
RPMJG
1TJ
SKA
-JG
AGSTE
AUDPV
EF-
BSQNT
SKF
SKH
ADSRN
ABGFH
705
R7B
R7D
AAEMU
R7C
PublicationCentury 2000
PublicationDate 20171218
PublicationDateYYYYMMDD 2017-12-18
PublicationDate_xml – month: 12
  year: 2017
  text: 20171218
  day: 18
PublicationDecade 2010
PublicationYear 2017
References_xml – issn: 2017
  issue: 21
  volume-title: In vivo Neuropharmacology and Neurophysiology
  end-page: 428
  publication-title: Neuromethods
– issn: 2006
  end-page: 954
  publication-title: Principles of Fluorescence Spectroscopy
  doi: Lakowicz
– issn: 2005
  end-page: 238
  publication-title: Anion Sensing (Top. Curr. Chem., 255)
– doi: Garabagiu
SSID ssj0011761
Score 4.494202
Snippet For the first time thiacalix[4]arene derivatives in 1,3- alternate conformation simultaneously containing amide, carboxyl and hydroxyl groups capable of...
SourceID rsc
SourceType Enrichment Source
Publisher
StartPage 177
Title Tetracarboxylic acids on a thiacalixarene scaffold: synthesis and binding of dopamine hydrochlorideElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nj03953k
Volume 42
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Nb9NAEF2F9gAXRIGKForm0AMosqntOG56i9pUDaK0UgPqLdq116qr4FRuGjX8GH4FP5A3Xn8kTSoBF8fatS2v5mX27XjnjRC7oe9KvYc_Uhu_VsuRypLOnmeFsQJ7bvmYJjg5-fRr--Rb6_Olf9lo_JrbtXQ3UXb4c2Veyf9YFW2wK2fJ_oNlq4eiAeewL46wMI5_Z2M9yWQoMzW-n7FYtQyTKA__S_DJBD2j5J6TvXTzNpRxzAWivS6LFID1sRAJB81VYvJaQBojLKB_MOu8mkVcSYs350W6VxfKueUSoGa7ecb5glXmI_PU3kWfQwxyKpMR52PZ8EO6eXTWz4MOed49i46GQXqNM9-rUoROWdtjKmc5jT2z6-jquYxS03puN6sg9Xc5TUa4Pvdqc1dfXAEzSe7cj-ziC1MRzsAU6bjWggfGCs8Cjyz0sU2b1-5YHdeotpduu-UuwdP4YKeoC2Omc8fUyVmaKVaOeVF5u-58ItbdoONjcb_e7Q36X6rvVE5gFHnLly4FcL3Op_pu0JasLCeT05bBC_G8WG9Q14BnQzR0-lI8PSzL_L0Svx-AiHIQ0TglSYsgohJEB1RBiAAhKiBE45hKCNEjEKIFCNEchOgDAPSRavgQ4EOAzwEtj_W12DnuDQ5PLIx4eGMEU4Z1t7cp1tJxqt8IUiCKTnsfBH0fHDhWSsZBXlxB6wA8VG2JzdXP2BLbqzuGN1G8_dhdb8WzGm7vxNoku9M74JMT9b4w6h8vRnyq
link.rule.ids 315,786,790,27957,27958
linkProvider Royal Society of Chemistry
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Tetracarboxylic+acids+on+a+thiacalixarene+scaffold%3A+synthesis+and+binding+of+dopamine+hydrochlorideElectronic+supplementary+information+%28ESI%29+available.+See+DOI%3A+10.1039%2Fc7nj03953k&rft.au=Mostovaya%2C+O.+A&rft.au=Padnya%2C+P.+L&rft.au=Vavilova%2C+A.+A&rft.au=Shurpik%2C+D.+N&rft.date=2017-12-18&rft.issn=1144-0546&rft.eissn=1369-9261&rft.volume=42&rft.issue=1&rft.spage=177&rft.epage=183&rft_id=info:doi/10.1039%2Fc7nj03953k&rft.externalDocID=c7nj03953k
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1144-0546&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1144-0546&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1144-0546&client=summon