Synthetic heterocyclic candidates as promising α-glucosidase inhibitors: An overview

M Dhameja, P Gupta - European journal of medicinal chemistry, 2019 - Elsevier
Abstract α-Glucosidase enzyme inhibition is an effective therapeutic decorum in the
treatment of type 2 diabetes mellitus. Since 1990, three α-glucosidase inhibitors are known …

Antibacterial and antioxidant activities for natural and synthetic dual-active compounds

G Martelli, D Giacomini - European Journal of Medicinal Chemistry, 2018 - Elsevier
Antimicrobial resistance is widely recognized as a grave threat to global health in the 21st
century, since the past decades have seen a dramatic increase in human-pathogenic …

Isatin containing heterocycles for different biological activities: Analysis of structure activity relationship

R Nath, S Pathania, G Grover, MJ Akhtar - Journal of Molecular Structure, 2020 - Elsevier
Isatin has been widely used in drug discovery. The ring is part of many naturally occurring
compounds and is used to design compounds with diverse biological activities. These isatin …

Synthesis, solvent polarity (polar and nonpolar), structural and electronic properties with diverse solvents and biological studies of (E)-3-((3-chloro-4-fluorophenyl) …

VSJ Reeda, VB Jothy, M Asif, M Nasibullah… - Journal of Molecular …, 2023 - Elsevier
Isatin compounds' intriguing biological potential has captivated chemists' interest. A
synthetic (E)-3-((3-chloro-4-fluorophenyl) imino) indolin-2-one (3CF4I) containing isatin …

[HTML][HTML] Spirocyclic derivatives as antioxidants: A review

K Acosta-Quiroga, C Rojas-Pena, LS Nerio… - RSC …, 2021 - pubs.rsc.org
In recent years, spiro compounds have attracted significant interest in medicinal chemistry
due to their numerous biological activities attributed primarily to their versatility and structural …

Isatin, an endogenous nonpeptide biofactor: A review of its molecular targets, mechanisms of actions, and their biomedical implications

A Medvedev, O Buneeva, O Gnedenko, P Ershov… - Biofactors, 2018 - Wiley Online Library
Abstract Isatin (indole‐2, 3‐dione) is an oxidized indole. It is widely distributed in
mammalian tissues and body fluids, where isatin concentrations vary significantly from< 0.1 …

[HTML][HTML] Indole derivatives as potential anticancer agents: A review

H Sachdeva, J Mathur, A Guleria - Journal of the Chilean Chemical …, 2020 - SciELO Chile
Heterocyclic moiety serve as perfect framework on which pharmacophores can be effectively
attached to produce novel drugs. Among various heterocyclic compounds, nitrogen-based …

Synthesis, in silico, in vitro and in vivo evaluations of isatin aroylhydrazones as highly potent anticonvulsant agents

S Emami, M Valipour, FK Komishani… - Bioorganic …, 2021 - Elsevier
In this study, a series of new isatin aroylhydrazones (5a-e and 6a-e) was synthesized and
evaluated for their anticonvulsant activities. The (Z)-configuration of compounds was …

A blueprint for high affinity SARS-CoV-2 Mpro inhibitors from activity-based compound library screening guided by analysis of protein dynamics

J Gossen, S Albani, A Hanke, BP Joseph… - ACS pharmacology & …, 2021 - ACS Publications
The SARS-CoV-2 coronavirus outbreak continues to spread at a rapid rate worldwide. The
main protease (Mpro) is an attractive target for anti-COVID-19 agents. Unexpected …

Design, synthesis, in vitro antimicrobial evaluation and molecular docking studies of indol-2-one tagged with morpholinosulfonyl moiety as DNA gyrase inhibitors

MA Salem, A Ragab, A El-Khalafawy, AH Makhlouf… - Bioorganic …, 2020 - Elsevier
A series of Schiff bases 3, 5, 7 and hydrazones 9 were achieved via reaction of 5-
(morpholinosulfonyl) indol-2, 3-dione (1) with appropriate amines and/or hydrazide …