The development of novel analogues for the pancreatic lipase (PL) inhibitors and
antioxidant candidates remains a significant research objective, as these studies are …

Pancreatic lipase (PL) inhibitors have received considerable attention by several
researchers because of its ability to hydrolyse the triglycerides in the small intestine. This …

Pancreatic lipase (PL), a key target for the prevention and treatment of obesity, plays crucial
roles in the hydrolysis and absorption of in dietary fat. In this study, a series of pyrazolones …

The novel benzothiazole sulfonate hybrid derivatives containing azomethine group were
synthesized and characterized using 1H‐NMR, 13C‐NMR, and HR‐MS analysis. The …

One of the primary purposes of this study is to synthesize new aryl sulfonate-naphthalene
hybrid structures possessing divergent electron-withdrawing and electron-releasing …

A series of novel diaryl substituted pyrazolyl 2, 4-thiazolidinediones were synthesized via
reaction of appropriate pyrazolecarboxaldehydes with 2, 4-thiazolidinedione (TZD) and …

A series of novel indole-thiazolidinedione hybrid analogues (7a to 7 u) were synthesised,
characterised and evaluated for their potential Pancreatic Lipase (PL) inhibition. Amongst …

The synthesis of 1, 3-benzoselenazoles was achieved by the reaction of corresponding bis
[3-amino-N-(p-tolyl) benzamide-2-yl] diselenide, bis [3-amino-N-(4-methoxyphenyl) …

Dihydropyrazole (1–22) derivatives were synthesized from already synthesized chalcones.
The structures of all of the synthesized compounds were confirmed by elemental analysis …

In this study, a two pyrazole derivatives; 2-(5-methyl-1H-pyrazole-3-carbonyl)-N-
phenylhydrazine-1-carboxamide (Pyz-1) and 4-amino-5-(5-methyl-1H-pyrazol-3-yl)-4H-1, 2 …