Synthetic α-glucosidase inhibitors as promising anti-diabetic agents: Recent developments and future challenges

A Mushtaq, U Azam, S Mehreen, MM Naseer - European journal of …, 2023 - Elsevier
Diabetes mellitus is one of the biggest challenges for the scientific community in the 21st
century. It is a well-recognized multifactorial health problem contributes significantly to high …

Research progress on the synthesis and pharmacology of 1, 3, 4-oxadiazole and 1, 2, 4-oxadiazole derivatives: a mini review

JJ Wang, W Sun, WD Jia, M Bian… - Journal of Enzyme …, 2022 - Taylor & Francis
Oxadiazole is a five-membered heterocyclic compound containing two nitrogen atoms and
one oxygen atom. The 1, 3, 4-oxadiazole and 1, 2, 4-oxadiazole have favourable physical …

1, 3, 4-Oxadiazole and 1, 3, 4-thiadiazole nortopsentin derivatives against pancreatic ductal adenocarcinoma: Synthesis, cytotoxic activity, and inhibition of CDK1

D Carbone, C Pecoraro, G Panzeca, G Xu… - Marine Drugs, 2023 - mdpi.com
A new series of nortopsentin analogs, in which the central imidazole ring of the natural lead
was replaced by a 1, 3, 4-oxadiazole or 1, 3, 4-thiadiazole moiety, was efficiently …

Synthetic transformation of 4-fluorobenzoic acid to 4-fluorobenzohydrazide Schiff bases and 1, 3, 4-oxadiazole analogs having DPPH radical scavenging potential

M Khan, Z Fazal, A Alam, M Ibrahim… - Letters in Drug …, 2023 - ingentaconnect.com
Aims: Synthesis of 4-fluorobenzohydrazide Schiff bases and 1, 3, 4-oxadiazole analogs has
a DPPH radical scavenging potential. Background: Synthetic antioxidants are widely used …

Synthesis of novel oxadiazole derivatives: DFT calculations, molecular docking studies, and in vitro, in vivo evaluation of antidiabetic activity using Drosophila …

G Anjanayya, R Gani, A Kudva, S Joshi… - Journal of the Iranian …, 2024 - Springer
Current antidiabetic medications have a plethora of harmful side effects, and most of the
drugs do not contain 1, 3, 4-oxadiazole moiety. Therefore, research into the development of …

Design, synthesis and SAR of novel 7-azaindole derivatives as potential Erk5 kinase inhibitor with anticancer activity

Q Zhang, X Gao, X Duan, H Liang, M Gao… - Bioorganic & Medicinal …, 2023 - Elsevier
The extracellular signal-regulated kinase 5 (Erk5) signaling plays a crucial role in cancer,
and regulating its activity may have potential in cancer chemotherapy. In this study, a series …

α-Glucosidase and α-amylase inhibitory potentials of quinoline–1, 3, 4-oxadiazole conjugates bearing 1, 2, 3-triazole with antioxidant activity, kinetic studies, and …

N Cele, P Awolade, P Seboletswe, K Olofinsan… - Pharmaceuticals, 2022 - mdpi.com
Diabetes mellitus (DM) is a multifaceted metabolic disorder that remains a major threat to
global health security. Sadly, the clinical relevance of available drugs is burdened with an …

[HTML][HTML] In vitro evaluation of novel mefenamic acid derivatives as potential α-glucosidase and urease inhibitors: Design, synthesis, in silico and cytotoxic studies

S Daud, W Rehman, M Niaz, A Sardar… - Journal of Saudi …, 2023 - Elsevier
This study aim to synthesize new 1, 3, 4-oxadiazole derivatives incorporating mefenamic
acid as promising α-glucosidase and urease inhibitors, potentially leading to the treatment of …

Synthesis, activity and in silico studies of novel bisindolylmethanes from xylochemical 5-hydroxymethylfurfural as antidiabetic agents

GD Kotkar, MJ Clement, AS Tilve, RN Shirsat… - Journal of Molecular …, 2022 - Elsevier
Abstract A novel series of 3, 3′-bisindolylmethanes was successfully synthesized from a
xylochemical 5-hydroxymethylfurfural, by condensing with indoles 3a-l employing a green …

Synthesis, In Silico Docking Study, and Biological Evaluation of S-Alkylated 1, 3, 4-Oxadiazole Hybrids

VB Das, B Poojary, V Kamat, A Sharma… - Russian Journal of …, 2024 - Springer
Abstract A library of 3-(5-[(substituted benzyl) sulfanyl]-1, 3, 4-oxadiazol-2-yl)-N-substituted
pyridine-2-amines and 2-[(5-{2-[(substituted phenyl) amino] pyridin-3-yl}-2, 3-dihydro-1, 3, 4 …