Crucial components of mycobacterium type II fatty acid biosynthesis (Fas-II) and their inhibitors

X Duan, X Xiang, J Xie - FEMS Microbiology Letters, 2014 - academic.oup.com
Abundant mycolic acids are the hallmark of the mycobacterial cell wall. The biosynthesis of
mycolic acids fulfilled by type I (Fas-I) and type II (Fas-II) synthase systems necessitates long …

Aerobic oxidative amidation of aromatic and cinnamic aldehydes with secondary amines by CuI/2-pyridonate catalytic system

M Zhu, K Fujita, R Yamaguchi - The Journal of Organic Chemistry, 2012 - ACS Publications
A simple and convenient CuI/2-pyridonate catalytic system for the oxidative amidation of
aldehydes with secondary amines has been developed. With this system, a variety of useful …

Multiple receptor conformers based molecular docking study of fluorine enhanced ethionamide with mycobacterium enoyl ACP reductase (InhA)

AM Khan, J Shawon, MA Halim - Journal of Molecular Graphics and …, 2017 - Elsevier
A major limitation in current molecular docking method is that of failure to account for
receptor flexibility. Herein we report multiple receptor conformers based molecular docking …

[HTML][HTML] Improving the binding affinity and interaction of 5-Pentyl-2-Phenoxyphenol against Mycobacterium Enoyl ACP reductase by computational approach

J Shawon, AM Khan, I Shahriar, MA Halim - Informatics in Medicine …, 2021 - Elsevier
Tuberculosis (TB) is one of the leading causes of death worldwide. The development of new
anti-tubercular drugs is required as resistant strains of M. tuberculosis to various first-line …

Piperazine derivatives: Synthesis, inhibition of the Mycobacterium tuberculosis enoyl-acyl carrier protein reductase and SAR studies

M Rotta, K Pissinate, AD Villela, DF Back… - European Journal of …, 2015 - Elsevier
The Mycobacterium tuberculosis NADH-dependent enoyl-acyl carrier protein reductase (Mt
InhA) catalyzes hydride transfer to long-chain enoyl thioester substrates. Mt InhA is a …

Cytotoxic activities of some novel benzhydrylpiperazine derivatives

EE Gurdal, M Yarim, I Durmaz, R Cetin-Atalay - Drug research, 2013 - thieme-connect.com
This study presents the synthesis of nineteen 1-(substitutedbenzoyl)-4-benzhydrylpiperazine
and 1-[(substitutedphenyl) sulfonyl]-4-benzhydrylpiperazine derivatives. In vitro cytotoxic …

Synthesis and cytotoxicity studies of novel benzhydrylpiperazine carboxamide and thioamide derivatives

EE Gurdal, I Durmaz, R Cetin-Atalay… - Journal of Enzyme …, 2014 - Taylor & Francis
Synthesis and cytotoxic activities of 32 benzhydrylpiperazine derivatives with carboxamide
and thioamide moieties were reported. In vitro cytotoxic activities of compounds were …

Synthesis of amides through an oxidative amidation of tetrazoles with aldehydes under transition-metal-free conditions

J Du, K Luo, X Zhang - RSC advances, 2014 - pubs.rsc.org
Synthesis of amides through an oxidative amidation of tetrazoles with aldehydes under
transition-metal-free conditions - RSC Advances (RSC Publishing) DOI:10.1039/C4RA07658C …

An efficient and mild oxidative amidation of aldehydes using B (C 6 F 5) 3 as a catalyst and biological evaluation of the products as potential antimicrobial agents

S DeviáGuggilapu, A RamnatháChari… - New Journal of …, 2017 - pubs.rsc.org
A mild and efficient protocol for oxidative amidation of diverse aldehydes with amines was
developed using 3 mol% tris (pentafluorophenyl) borane and tert-butyl hydroperoxide to …

New N‐benzhydrylpiperazine/1,3,4‐oxadiazoles conjugates inhibit the proliferation, migration, and induce apoptosis in HeLa cancer cells via oxidative stress …

R Khanam, R Kumar, II Hejazi… - Journal of Cellular …, 2019 - Wiley Online Library
Abstract N‐benzhydrylpiperazine and 1, 3, 4‐oxadiazoles are pharmacologically active
scaffolds which exhibits significant inhibitory growth effects against various cancer cells …