Design, synthesis and in vitro evaluation of novel derivatives as serotonin N-acetyltransferase inhibitors

被引:14
作者
Beaurain, N
Mésangeau, C
Chavatte, P
Ferry, G
Audinot, V
Boutin, JA
Delagrange, P
Bennejean, C
Yous, S
机构
[1] Univ Lille 2, Fac Sci Pharmaceut & Biol, Chim Therapeut Lab, F-59006 Lille, France
[2] Inst Rech Int Servier, F-78290 Croissy Sur Seine, France
[3] Inst Rech Int Servier, F-92415 Courbevoie, France
关键词
arylalkylamine N-acetyltransferase; melatonin; inhibition;
D O I
10.1080/1475636021000005721
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Serotonin N-acetyltransferase (arylalkylamine N -acetyltransferase, AANAT) is an enzyme that catalyses the first rate limiting step in the biosynthesis of melatonin (5-methoxy- N -acetyltryptamine). Different physiopathological disorders in human may be due to abnormal secretion of melatonin leading to an inappropriate exposure of melatonin receptors to melatonin. For that reason, we have designed, synthesized and evaluated as inhibitors of human serotonin N -acetyltransferase, a series of compounds that were able to react with coenzyme A to give a bisubstrate analog inhibitor. Compound 12d was found to be a potent AANAT inhibitor (IC50 =0.18 muM).
引用
收藏
页码:409 / 414
页数:6
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