Novel trifluoroacetophenone derivatives as malonyl-CoA decarboxylase inhibitors

…, M Haramura, JF Cheng, T Arrhenius…

Index: Wallace, David M.; Haramura, Masayuki; Cheng, Jie-Fei; Arrhenius, Thomas; Nadzan, Alex M. Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 4 p. 1127 - 1130

Full Text: HTML

Citation Number: 10

Abstract

A series of trifluoroacetophenone derivatives were prepared and evaluated as malonyl-CoA decarboxylase (MCD) inhibitors. Some of the 'reverse amide'analogs were found to be potent inhibitors of MCD enzyme activity. The trifluoroacetyl group may interact with the MCD active site as the hydrate in a similar fashion to the hexafluoroisopropanol analogs reported previously. Adding electron-withdrawing groups to the phenyl ring stabilizes the hydrated ...

Related Articles:

Cross-linked dendrimer hosts containing reporter groups for amine guests

[Journal of the American Chemical Society, , vol. 125, # 12 p. 3424 - 3425]

Novel trifluoroacetophenone derivatives as malonyl-CoA decarboxylase inhibitors

[Bioorganic and Medicinal Chemistry Letters, , vol. 17, # 4 p. 1127 - 1130]

The reduction of aryl trifluoromethyl ketones by sodium borohydride. The hydride transfer process

[Canadian Journal of Chemistry, , vol. 58, p. 2491 - 2496]

More Articles...