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 …

Heterocyclic compounds as dipeptidyl peptidase-IV inhibitors with special emphasis on oxadiazoles as potent anti-diabetic agents

BD Mohammad, MS Baig, N Bhandari, FA Siddiqui… - Molecules, 2022 - mdpi.com
Dipeptidyl peptidase-IV (DPP-IV) inhibitors, often known as gliptins, have been used to treat
type 2 diabetes mellitus (T2DM). They may be combined with other medications as an …

Synthesis, biological evaluation and action mechanism of 7H-[1, 2, 4] triazolo [3, 4-b][1, 3, 4] thiadiazine-phenylhydrazone derivatives as α-glucosidase inhibitors

Q Feng, J Zhang, S Luo, Y Huang, Z Peng… - European Journal of …, 2023 - Elsevier
In our work, several 7H-[1, 2, 4] triazolo [3, 4-b][1, 3, 4] thiadiazine-phenylhydrazone
derivatives as α-glucosidase inhibitors (α-GIs) were synthesized and characterized by 1 H …

Novel hybrids of benzothiazole-1, 3, 4-oxadiazole-4-thiazolidinone: Synthesis, in silico ADME study, molecular docking and in vivo anti-diabetic assessment

R Bhutani, DP Pathak, G Kapoor, A Husain… - Bioorganic chemistry, 2019 - Elsevier
A series of new benzothiazole-1, 3, 4-oxadiazole-4-thiazolidinone hybrid analogs (Tz1-
Tz28) were synthesized in search of potential anti-diabetic agents. Molecular docking study …

Design, synthesis, molecular modelling, ADME prediction and anti-hyperglycemic evaluation of new pyrazole-triazolopyrimidine hybrids as potent α-glucosidase …

V Pogaku, K Gangarapu, S Basavoju, KK Tatapudi… - Bioorganic …, 2019 - Elsevier
The aim of the present study is to design and synthesis of new pyrazole-triazolopyrimidine
hybrids as potent α-glucosidase inhibitors. The target compounds 4a-n were synthesized by …

[HTML][HTML] Synthesis, spectral characterization, antimicrobial evaluation studies and cytotoxic activity of some transition metal complexes with tridentate (N, N, O) donor …

HAK Kyhoiesh, KJ Al-Adilee - Results in Chemistry, 2021 - Elsevier
A new azo dye ligand 2-[2'-(6-methoxybenzothiazolyl) azo]-4-ethoxyphenol (6-MBTAEP)
was prepared by reacting a diazonium chloride salt solution of 2-amino-6-methoxy …

Quantitative structure activity relationship studies of novel hydrazone derivatives as α-amylase inhibitors with index of ideality of correlation

M Duhan, J Sindhu, P Kumar, M Devi… - Journal of …, 2022 - Taylor & Francis
The present manuscript describes the synthesis, α-amylase inhibition, in silico studies and in-
depth quantitative structure–activity relationship (QSAR) of a library of aroyl hydrazones …

Discovery potent of thiazolidinedione derivatives as antioxidant, α-amylase inhibitor, and antidiabetic agent

MY Sameeh, MM Khowdiary, HS Nassar, MM Abdelall… - Biomedicines, 2021 - mdpi.com
This work aimed to synthesize safe antihyperglycemic derivatives bearing thiazolidinedione
fragment based on spectral data. The DFT theory discussed the frontier molecular orbitals …

[HTML][HTML] In Silico and In Vivo Evaluation of Novel 2-Aminobenzothiazole Derivative Compounds as Antidiabetic Agents

JA Alvarado Salazar, M Valdes, A Cruz… - International Journal of …, 2025 - mdpi.com
Currently, there are several drugs used for the treatment of type 2 diabetes (T2D); however,
all of them have adverse effects. Benzothiazoles have a broad spectrum of biological …

2, 5-Disubstituted structures of 1, 3, 4-oxadiazole and 1, 3, 4-thiodiazole for anti-inflammatory potential: DFT approach for the structural aspects

V Veeramani, PSKP Ganesh, S Bharanidharan… - Journal of Molecular …, 2024 - Elsevier
Abstract We suggest a [3+ 2] annulation method that combines aromatic acid with acyl
hydrazide using p-TSA, resulting in the formation of highly substituted 1, 3, 4-oxadiazole …