Archives for Chemistry Experiments of (4-Oxo-5-(palmitoyloxy)-4H-pyran-2-yl)methyl palmitate

Interested yet? Read on for other articles about 79725-98-7, you can contact me at any time and look forward to more communication. Formula: C38H66O6.

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 79725-98-7, Name is (4-Oxo-5-(palmitoyloxy)-4H-pyran-2-yl)methyl palmitate, SMILES is O1C(=CC(=O)C(=C1)C(=O)OCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCC, in an article , author is Bhat, Mashooq Ahmad, once mentioned of 79725-98-7, Formula: C38H66O6.

Synthesis and in vivo anti-ulcer evaluation of some novel piperidine linked dihydropyrimidinone derivatives

Dihydropyrimidinone derivatives containing piperidine moiety were synthesised in a good yield. All the compounds were confirmed by elemental analysis and spectral data. Anti-ulcer activity of novel dihydropyrimidinone-piperidine hybrids (1-18) was evaluated. Among them, four compounds (3, 8, 11 and 15) were found to be most active in 80% ethanol-induced ulcer experimental animal model. All the potent compounds were further evaluated for anti-ulcer activity by different in vivo anti-ulcer models to study the effect of compounds on anti-secretory and cytoprotective activities. All the active compounds inhibited the formation of gastric ulcers and increased the formation of gastric mucin secretion. Compound 15 was found to be the most potent compound of the series as anti-ulcer agent. Additional experimental studies on lead compound 15 will result in a new class of orally active molecule for anti-ulcer activity.

Interested yet? Read on for other articles about 79725-98-7, you can contact me at any time and look forward to more communication. Formula: C38H66O6.

Reference:
Piperidine – Wikipedia,
,Piperidine | C5H11N – PubChem