Synthesis of N'-(Quinazolin-4-yl)isonicotinohydrazides and their biological screening, docking and ADME studies

A wide range of 4-chloro-3,4-dihydroquinazolines hybrid isoniazid derivatives were synthesised efficiently via reaction of 4-chloro-3,4-dihydroquinazolines with isoniazid in the presence of catalytic amount of N,N-diisopropylethylamine (DIPEA) under refluxing methanol. All the title molecules were characterized by 13C NMR, 1H NMR, Mass and IR spectroscopy. All the compounds were tested for anti-malarial, anti-microbial and anti-tuberculosis activities. They were further tested for the cytotoxic feature. In-silico molecular docking study and ADME properties were also studied for the title molecules. Keywords: Molecular hybridization, Anti-malarial, Anti-microbial, Anti-tuberculosis, MTT assay, Docking, ADME.

Medienart:

E-Artikel

Erscheinungsjahr:

2020

Erschienen:

2020

Enthalten in:

Zur Gesamtaufnahme - volume:13

Enthalten in:

Arabian Journal of Chemistry - 13(2020), 1, Seite 1986-2000

Sprache:

Englisch

Beteiligte Personen:

Kinjal D. Patel [VerfasserIn]
Rajesh H. Vekariya [VerfasserIn]
Neelam P. Prajapati [VerfasserIn]
Dhaval B. Patel [VerfasserIn]
Hitesh D. Patel [VerfasserIn]
Tauhid Shaikh [VerfasserIn]
Dhanji P. Rajani [VerfasserIn]
Smita Rajani [VerfasserIn]
Naumita S. Shah [VerfasserIn]
Devendrasinh Jhala [VerfasserIn]

Links:

doi.org [kostenfrei]
doaj.org [kostenfrei]
www.sciencedirect.com [kostenfrei]
Journal toc [kostenfrei]

Themen:

Chemistry

doi:

10.1016/j.arabjc.2018.02.017

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

DOAJ031958559