Comprehensive review in current developments of imidazole‐based medicinal chemistry

L Zhang, XM Peng, GLV Damu… - Medicinal research …, 2014 - Wiley Online Library
Imidazole ring is an important five‐membered aromatic heterocycle widely present in natural
products and synthetic molecules. The unique structural feature of imidazole ring with …

Recent advances of chroman-4-one derivatives: synthetic approaches and bioactivities

S Emami, Z Ghanbarimasir - European Journal of Medicinal Chemistry, 2015 - Elsevier
Chroman-4-one scaffold is a privileged structure in heterocyclic chemistry and drug
discovery. Also, chroman-4-ones are important intermediates and interesting building blocks …

Recent developments in azole compounds as antibacterial and antifungal agents

XM Peng, GX Cai, CH Zhou - Current topics in medicinal …, 2013 - ingentaconnect.com
Azole compounds are an important class of nitrogen heterocycles with electron-rich
property. This special structure endows azole-based derivatives easily bind with the …

An overview of azoles targeting sterol 14α-demethylase for antileishmanial therapy

S Emami, P Tavangar, M Keighobadi - European journal of medicinal …, 2017 - Elsevier
The azole antifungal drugs are an important class of chemotherapeutic agents with broad-
spectrum of activity against yeasts and filamentous fungi, act in the ergosterol biosynthetic …

Imidazoles as potential antifungal agents: A review

N Rani, A Sharma, G Kumar Gupta… - Mini reviews in …, 2013 - ingentaconnect.com
Imidazoles are one of the most promising and vigorously pursued areas of contemporary
antifungal chemotherapy depicting broad spectrum and potent activity. They have relatively …

In vitro antileishmanial activity of novel azoles (3-imidazolylflavanones) against promastigote and amastigote stages of Leishmania major

A Shokri, S Emami, M Fakhar, SH Teshnizi… - Acta tropica, 2017 - Elsevier
Leishmaniasis is a protozoan infectious disease widely distributed all around the world. First
line drugs including antimoniales are insufficient due to resistance in endemic areas and …

Novel triazole alcohol antifungals derived from fluconazole: design, synthesis, and biological activity

SM Hashemi, H Badali, MA Faramarzi, N Samadi… - molecular …, 2015 - Springer
A series of new triazole alcohol antifungals were designed by replacing one of the triazolyl
moiety from fluconazole with a distinct 4-amino-3-mercapto-1, 2, 4-triazole motif, which is …

Synthesis, in vitro antifungal activity and in silico study of 3-(1, 2, 4-triazol-1-yl) flavanones

S Emami, S Shojapour, MA Faramarzi… - European Journal of …, 2013 - Elsevier
Abstract A series of novel 3-(1, 2, 4-triazol-1-yl) flavanones were synthesized based on the N-
phenethylazole pharmacophore of azole antifungals. The results of antifungal assay …

Synthesis of furo[3,2‐g]chromones under microwave irradiation and their antitumor activity evaluation

SM Abu‐Bakr, MD Khidre, MA Omar… - Journal of …, 2020 - Wiley Online Library
Abstract A series of furo [3, 2‐g] chromone derivatives were synthesized via the reaction of
furochromone carbaldehyde 1 with amines 3a‐d and thioglycolic acid to give …

An in silico molecular docking, ADMET and molecular dynamics simulations studies of azolyl-2H-chroman-4-ones as potential inhibitors against pathogenic fungi and …

KVSM Chandrika, PV - Journal of Biomolecular Structure and …, 2024 - Taylor & Francis
Antimicrobial resistance is a major global threat. In an attempt to discover new compounds
with improved efficiency and to overcome drug resistance, a library of 3960 compounds was …