z-logo
Premium
Design, synthesis, and characterization of some new benzimidazole derivatives and biological evaluation
Author(s) -
Bektaş Hakan,
Sökmen Bahar B.,
Aydın Sinem,
Menteşe Emre,
Bektaş Adile,
Dilekçi Gamze
Publication year - 2020
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.3943
Subject(s) - benzimidazole , chemistry , antimicrobial , enterobacter aerogenes , proton nmr , oxadiazole , antioxidant , carbon 13 nmr , 1,2,4 triazole , organic chemistry , combinatorial chemistry , stereochemistry , nuclear chemistry , biochemistry , escherichia coli , gene
A new series of benzimidazole derivatives ( 1‐15 ) containing 1,2,4‐triazole, 1,3,4‐thiadiazole, 1,3,4‐oxadiazole, and thiazolidinon rings have been synthesized. All new synthesized benzimidazole compounds were confirmed by 1 H NMR, 13 C NMR spectra, and LC‐MS, and they were examined for their antioxidant and antimicrobial activities. Compounds 7 and 1 showed the highest and the lowest antioxidant activities, respectively. The lowest minimum inhibition concentration value found in compound 5 against Enterobacter aerogenes .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom