A series of 2, 3-disubstituted quinazolin-4 (1H)-ones (3a–j) were screened for their
antimicrobial activity via the minimum inhibitory concentration method (MIC). The in vitro anti …

Abstract A new series of 1-((1-(4-substituted benzyl)-1 H-1, 2, 3-triazol-4-yl) methoxy)-2-(2-
substituted quinolin-4-yl) propan-2-ol (9a-x) have been synthesized. The newly synthesized …

In this work, synthesis, antimicrobial activities and molecular docking studies of some new
series of substituted quinazolinone 2a–h and 3a–d were described. Starting form 2 …

In search of novel biologically potent compounds, some new oxazolyl pyrimidines (7a-g)
have been prepared in the current investigation. All new compounds were characterized …

In this investigation, a series of 2-quinolone-benzimidazole hybrids linked by a 1, 2, 3-
triazole moiety were prepared using copper-catalyzed Huisgen 1, 3-dipolar cycloaddition …

New 2-arylquinazoline benzamide derivatives were synthesized and screened against
H37RV strain, compounds displayed specific and potent anti-mycobacterial activity against …

In search of new potent molecules against tuberculosis, 3, 4-dihydro-2 (1H)-quinolinone
based 1, 2, 3-triazoles were synthesized efficiently by means of click chemistry and their …

Abstract Quinazolin-4-ones linked to 1, 2, 3-triazol (10) were identified as inhibitors of the
bisphosphonate BPH-700 transcriptional factor from a high throughput screen. A series of 1 …

In the present investigation, a series of 1, 5-dimethyl-2-phenyl-4-{[(5-aryl-1, 3, 4-oxadiazol-2-
yl) methyl] amino}-1, 2-dihydro-3H-pyrazol-3-one were subjected to molecular properties …

Multidrug resistance tuberculosis (TB) is one of the major problems in the world, accounting
for morbidity and mortality [1, 2]. The literature report and per World Health Organization …