Premium
Synthesis, biological evaluation, and molecular docking studies of novel pyrazole, pyrazoline‐clubbed pyridine as potential antimicrobial agents
Author(s) -
Desai Nisheeth C.,
Vaja Darshita V.,
Monapara Jahnvi D.,
Manga Vijjulatha,
Vani Tamalapakula
Publication year - 2021
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.4208
Subject(s) - chemistry , pyrazole , antimicrobial , adme , pyridine , docking (animal) , combinatorial chemistry , pyrazoline , molecule , stereochemistry , antifungal , proton nmr , carbon 13 nmr , in silico , organic chemistry , in vitro , biochemistry , nursing , dermatology , gene , medicine
We have prepared 15 hybrid pyrazole, pyrazoline‐clubbed pyridine–containing compounds (5a‐o) and tested for their antibacterial and antifungal activities for the development of potential antimicrobial agents. The structures of this novel series were characterized by various spectral techniques like IR, 1 H NMR, 13 C NMR, LC–MS, and elemental analysis. The synthesized compounds 5d, 5e, 5i, 5k, 5m, and 5o exhibited significant antimicrobial activity in the comparison of standard drugs. Molecular docking studies that have been carried out to emphasize the binding orientations of these molecules were in good compliance with crystal structure interactions. The predicted drug‐likeness (ADME) properties were found to be in the acceptable range.