Structure-activity relationship studies on 3,5-dinitrophenyl tetrazoles as antitubercular agents

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F71009396%3A_____%2F17%3AN0000025" target="_blank" >RIV/71009396:_____/17:N0000025 - isvavai.cz</a>

Alternative codes found

RIV/00216208:11160/17:10364537 RIV/00179906:_____/17:10364537

Result on the web

<a href="https://www.sciencedirect.com/science/article/abs/pii/S0223523417301411?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/abs/pii/S0223523417301411?via%3Dihub</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.ejmech.2017.02.058" target="_blank" >10.1016/j.ejmech.2017.02.058</a>

Result language

angličtina

Original language name

Structure-activity relationship studies on 3,5-dinitrophenyl tetrazoles as antitubercular agents

Original language description

In this study, we described the structure-activity relationships of substituted 3,5-dinitrophenyl tetrazoles as potent antitubercular agents. These simple and readily accessible compounds possessed high in vitro antimycobacterial activities against Mycobacterium tuberculosis, including clinically isolated multidrug (MDR) and extensively drug-resistant (XDR) strains, with submicromolar minimum inhibitory concentrations (MICs). The most promising compounds showed low in vitro cytotoxicity and negligible antibacterial and antifungal activities, highlighting their highly selective antimycobacterial effects. 2-Substituted 5-(3,5- dinitrophenyl)-2H-tetrazole regioisomers, which are the dominant products of 5(3,5- dinitrophenyl)-1H-tetrazole alkylation, showed better properties with respect to antimycobacterial activity and cytotoxicity than their 1-substituted counterparts. The 2-substituent of 5-(3,5dinitrophenyl)-2H-tetrazole can be easily modified and can thus be used for the structure optimization of these promising antitubercular agents. The introduction of a tetrazole-5-thioalkyl moiety at position 2 of the tetrazole further increased the antimycobacterial activity. These compounds showed outstanding in vitro activity against M. tuberculosis (MIC values as low as 0.03 mM) and high activity against non-tuberculous mycobacterial strains. (C) 2017 Elsevier Masson SAS. All rights reserved.

Czech name

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Czech description

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Type

J_imp - Article in a specialist periodical, which is included in the Web of Science database

CEP classification

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OECD FORD branch

30104 - Pharmacology and pharmacy

Project

—

Continuities

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Publication year

2017

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

European Journal of Medicinal Chemistry

ISSN

0223-5234

e-ISSN

—

Volume of the periodical

130

Issue of the periodical within the volume

April

Country of publishing house

FR - FRANCE

Number of pages

14

Pages from-to

419-432

UT code for WoS article

000397180900032

EID of the result in the Scopus database

2-s2.0-85014464603