Can You Really Do Chemisty Experiments About 2-(2-(4-Chlorophenyl)acetyl)benzoic acid

Interested yet? Read on for other articles about 53242-76-5, you can contact me at any time and look forward to more communication. SDS of cas: 53242-76-5.

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 53242-76-5, Name is 2-(2-(4-Chlorophenyl)acetyl)benzoic acid, SMILES is O=C(O)C1=CC=CC=C1C(CC2=CC=C(Cl)C=C2)=O, in an article , author is Regiec, A., once mentioned of 53242-76-5, SDS of cas: 53242-76-5.

Synthesis and biological activity of 4-amino-1-methyl-5-imidazolecarboxylic acid derivatives

The main goal of our study was the synthesis and biological evaluation of 4-amino- and 4-[(4-chlorobenzoyl)amino]-1-methylimidazole N-substituted 5-carboxamides. Biological in vitro tests indicated their remarkable influence on some cellular immune and inflammatory responses compared with ibuprofen and leflunomide as reference drugs. The toxicity of the tested compounds on murine bone marrow cells was also determined. The anti-inflammatory activity of 4-[(4-chlorobenzoyl)amino]-5-[N-(4-chlorophenyl)]-1-methyl-5-imidazolecarboxamide (7a) was confirmed in vivo in the carrageenan-induced oedema test. Comparison of the biological activity of 7a with that of the isosteric isothiazole derivative MR-2/94 suggests that replacement of the isothiazole core ring system with an imidazole one resulted in a considerable lowering of toxicity while maintaining anti-inflammatory and immunotropic properties.

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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com