Synthetic Approaches Toward Imidazo‐Fused Heterocycles: A Comprehensive Review DOI
Pragati Kushwaha,

Rashi,

Ayush Bhardwaj

и другие.

Journal of Heterocyclic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Сен. 24, 2024

ABSTRACT Imidazole moiety when fused with other heterocyclic system form numerous compounds different types of pharmacological and biological activities. In this review, we discussed a comprehensive analysis the synthetic methodologies reaction mechanisms for imidazo‐fused molecules. These molecules represent crucial class due to their significant applications versatile chemical reactivity. This article meticulously examined various routes construction heterocycles, ranging from traditional methods modern approaches such as microwave‐assisted reactions, NPs‐catalyzed light‐mediated synthesis, electrochemical transition metal‐free synthesis routes. By consolidating current knowledge highlighting future directions, review aims serve treasure research community in fields organic chemistry, medicinal material science.

Язык: Английский

New Imidazo[2,1‐b]thiazole Linked Hydrazide–Hydrazones as Potent α‐Glucosidase Inhibitors: Synthesis, Biological Evaluation, and Docking Insights DOI

Nergis Durmaz,

Faika Başoğlu, Efe Doğukan Dincel

и другие.

ChemistrySelect, Год журнала: 2025, Номер 10(15)

Опубликована: Апрель 1, 2025

Abstract Inhibition of the α‐glucosidase enzyme slows glucose absorption, thereby aiding in regulation blood sugar levels. This approach offers a promising way to manage type 2 diabetes with fewer side effects than traditional treatments. Based on this rationale, we designed, synthesised, and characterised novel series hydrazide–hydrazone‐linked imidazo[2,1‐ b ]thiazole derivatives. Inhibiting down helping regulate this, synthesized, characterized new In addition, their efficacy as inhibitors was evaluated, several synthesized compounds exhibited impressive vitro inhibitory activity, compound 4j (IC 50 : 0.0284 ± 0.0006 mM) being most potent among them. To determine key interactions between shed light its mechanism action, docking studies were conducted. As result, found that derivative containing 2,6‐dichlorophenyl moiety highest affinity for could inhibit it by binding either active or allosteric site.

Язык: Английский

Процитировано

0

Synthetic Approaches Toward Imidazo‐Fused Heterocycles: A Comprehensive Review DOI
Pragati Kushwaha,

Rashi,

Ayush Bhardwaj

и другие.

Journal of Heterocyclic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Сен. 24, 2024

ABSTRACT Imidazole moiety when fused with other heterocyclic system form numerous compounds different types of pharmacological and biological activities. In this review, we discussed a comprehensive analysis the synthetic methodologies reaction mechanisms for imidazo‐fused molecules. These molecules represent crucial class due to their significant applications versatile chemical reactivity. This article meticulously examined various routes construction heterocycles, ranging from traditional methods modern approaches such as microwave‐assisted reactions, NPs‐catalyzed light‐mediated synthesis, electrochemical transition metal‐free synthesis routes. By consolidating current knowledge highlighting future directions, review aims serve treasure research community in fields organic chemistry, medicinal material science.

Язык: Английский

Процитировано

1