Isatin-hydrazide conjugates as potent α-amylase and α-glucosidase inhibitors: Synthesis, structure and in vitro evaluations-Reference-Cited by-同舟云学术

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Isatin-hydrazide conjugates as potent α-amylase and α-glucosidase inhibitors: Synthesis, structure and in vitro evaluations

Published:2021-11 Issue: Volume:116 Page:105385
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Abbasi Inzamam,Nadeem Humaira,Saeed Adil,Kharl Hafiz Aamir Ali,Tahir Muhammad Nawaz,Naseer Muhammad Moazzam

Funder

TWAS

The World Academy of Sciences

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference63 articles.

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2. Structure-activity relationship (SAR) study and design strategies of nitrogen-containing heterocyclic moieties for their anticancer activities;Akhtar;Eur. J. Med. Chem.,2017

3. A comprehensive review on biological activities of oxazole derivatives;Kakkar;BMC Chem.,2019

4. The chemistry and biological activity of heterocycle-fused quinolinone derivatives: A review;Shiro;Eur. J. Med. Chem.,2015

5. Biological activities of isatin and its derivatives;Pandeya;Acta. Pharm.,2005

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3. Synthesis, In Vitro α-Amylase Inhibition Activity and Molecular Docking of some Coumarin Derivatives;Chemistry Africa;2024-07-09

4. Facile synthesis, Spectral investigation, in vitro and in silico studies of Thiophenecarboxamide-α,β-unsaturated ketone hybrids;Journal of Molecular Structure;2024-07

5. The Efficient Synthesis, Molecular Docking and Biological Evaluation of Novel Isatine linked Spiroheterocycle through Multi-Component Reaction;Indian Journal of Chemistry;2024-04-16

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