Recent studies of nitrogen and sulfur containing heterocyclic analogues as novel antidiabetic agents: a review

S Gharge, SG Alegaon - Chemistry & Biodiversity, 2024 - Wiley Online Library
The prevalence of diabetes mellitus is on the rise, which demands the identification of novel
antidiabetic drugs. There is a need for safer and more effective alternatives because the …

Novel thiazolidin-4-one benzenesulfonamide hybrids as PPARγ agonists: Design, synthesis and in vivo anti-diabetic evaluation

IH Ali, RM Hassan, AM El Kerdawy… - European Journal of …, 2024 - Elsevier
In the current study, two series of novel thiazolidin-4-one benzenesulfonamide arylidene
hybrids 9a-l and 10a-f were designed, synthesized and tested in vitro for their PPARɣ …

Synthesis, characterization, crystallographic, binding, in silico and antidiabetic studies of novel 2, 4-thiazolidinedione-phenothiazine molecular hybrids

MA Doddagaddavalli, VKA Kalalbandi… - Journal of Molecular …, 2023 - Elsevier
thiazolidinedione-phenothiazine molecular hybrids, 9a–9t were synthesized, characterized
and screened for antidiabetic activities viz., α-amylase inhibition and glucose uptake assay …

Expression of PPAR-γ TF by newly synthesized thiazolidine-2, 4-diones to manage glycemic control: Insights from in silico, in vitro and experimental pharmacology in …

S Gharge, SG Alegaon, SD Ranade, RS Kavalapure… - Bioorganic …, 2024 - Elsevier
In pursuit of novel antidiabetic agents to combat type II diabetes mellitus, our study focused
on identifying pharmacophoric features responsible for PPAR-γ expression, a key regulator …

Giardia lamblia G6PD::6PGL Fused Protein Inhibitors Decrease Trophozoite Viability: A New Alternative against Giardiasis

L Morales-Luna, B Hernández-Ochoa… - International Journal of …, 2022 - mdpi.com
Treatments to combat giardiasis have been reported to have several drawbacks, partly due
to the drug resistance and toxicity of current antiparasitic agents. These constraints have …

Synthesis and biological evaluation of O4′-benzyl-hispidol derivatives and analogs as dual monoamine oxidase-B inhibitors and anti-neuroinflammatory agents

AHE Hassan, Y Choi, R Kim, HJ Kim… - Bioorganic & Medicinal …, 2024 - Elsevier
Abstract Design, synthesis, and biological evaluation of two series of O 4′-benzyl-hispidol
derivatives and the analogous corresponding O 3′-benzyl derivatives aiming to develop …

Computational studies, synthesis, in-vitro binding and transcription analysis of novel imidazolidine-2, 4‑dione and 2-thioxo thiazolidine-4-one based glitazones for …

AP Kumar, P Prabitha, S Mandal, BRP Kumar… - Journal of Molecular …, 2023 - Elsevier
Herein, we describe the structure-based designing and synthesis of novel glitazones with
imidazolidine 2, 4‑dione and 2-thioxo thiazolidine-4-one ring structures as the fundamental …

Rational design of thiazolidine-4-one-gallic acid hybrid derivatives as selective partial PPARγ modulators: an in-silico approach for type 2 diabetes treatment

Aryan, B Babu, S Divakar, B Gowramma… - Journal of …, 2025 - Taylor & Francis
Type 2 diabetes mellitus is a bipolar metabolic disorder characterized by abnormalities in
insulin production from β-cells and insulin resistance. Thiazolidinediones are potent anti …

Design and Synthesis of Barbiturates and Hydantoins with Multitarget Antidiabetic Effect☆

S Juárez-Cruz, S Estrada-Soto… - Journal of the Mexican …, 2024 - jmcs.org.mx
En este trabajo se preparó una serie de diez 4-ariloxi-5-bencilidenobarbituratos e
hidantoínas como bioisósteros de la 1, 3-tiazolidina-2, 4-diona. Se realizó un análisis de …

Derivatives Incorporating Acridine, Pyrrole, and Thiazolidine Rings as Promising Antitumor Agents

M Garberová, I Potočňák, M Tvrdoňová, M Majirská… - Molecules, 2023 - mdpi.com
Derivatives combining acridine, pyrrole, and thiazolidine rings have emerged as promising
candidates in the field of antitumor drug discovery. This paper aims to highlight the …