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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 …
products and synthetic molecules. The unique structural feature of imidazole ring with …
Recent advances of chroman-4-one derivatives: synthetic approaches and bioactivities
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 …
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 …
property. This special structure endows azole-based derivatives easily bind with the …
An overview of azoles targeting sterol 14α-demethylase for antileishmanial therapy
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 …
spectrum of activity against yeasts and filamentous fungi, act in the ergosterol biosynthetic …
Imidazoles as potential antifungal agents: A review
Imidazoles are one of the most promising and vigorously pursued areas of contemporary
antifungal chemotherapy depicting broad spectrum and potent activity. They have relatively …
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
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 …
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
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 …
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
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 …
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 …
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 …
with improved efficiency and to overcome drug resistance, a library of 3960 compounds was …