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Z Naturforsch C J Biosci ; 66(3-4): 93-103, 2011.
Article in English | MEDLINE | ID: mdl-21630582

ABSTRACT

Benzothiophene carboxamide derivatives of aminobenzophenone, aminopyridine, aminobenzimidazole, and aniline derivatives (compounds 1-9) were synthesized and compounds 3, 6, 7, 8, and 9 tested in vivo for their hypolipidemic activity. Compounds 1-8 were prepared adopting the fusion process at 130-150 degrees C between benzothiophene-2-carbonyl chloride and aminobenzophenones, aminopyridine, and anilines, respectively, and were obtained in high yield, while compound 9 was obtained from the reaction of benzothiophene acyl chloride with aminobenzimidazole in DMF at 160 degrees C. At a dose of 15 mg/kg body weight compounds 6, 7, and 9 significantly reduced plasma triglyceride levels in Triton WR-1339-induced hyperlipidemic rats in comparison to control rats. Furthermore, they significantly increased high-density lipoprotein levels. It is therefore reasonable to assume that compounds 6, 7, and 9 may have a promising potential in the treatment of hyperlipidemia and atherosclerosis.


Subject(s)
Hypertriglyceridemia/drug therapy , Hypolipidemic Agents/chemical synthesis , Hypolipidemic Agents/pharmacology , Thiophenes/chemical synthesis , Thiophenes/pharmacology , Animals , Hypolipidemic Agents/therapeutic use , Magnetic Resonance Spectroscopy , Male , Rats , Rats, Wistar , Spectrometry, Mass, Electrospray Ionization , Spectrophotometry, Infrared , Thiophenes/therapeutic use
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