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Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease
Authors:Suvarna H. Pagire  Haushabhau S. Pagire  Kun-Young Park  Eun Jung Bae  Kwang-eun Kim  Minhee Kim  Jihyeon Yoon  Saravanan Parameswaran  Jun-Ho Choi  Sungmi Park  Jae-Han Jeon  Jin Sook Song  Myung Ae Bae  In-Kyu Lee  Hail Kim  Jae Myoung Suh  Jin Hee Ahn
Abstract:Serotonin (5-hydroxytryptophan) is a hormone that regulates emotions in the central nervous system. However, serotonin in the peripheral system is associated with obesity and fatty liver disease. Because serotonin cannot cross the blood-brain barrier (BBB), we focused on identifying new tryptophan hydroxylase type I (TPH1) inhibitors that act only in peripheral tissues for treating obesity and fatty liver disease without affecting the central nervous system. Structural optimization inspired by para-chlorophenylalanine (pCPA) resulted in the identification of a series of oxyphenylalanine and heterocyclic phenylalanine derivatives as TPH1 inhibitors. Among these compounds, compound 18i with an IC50 value of 37 nM was the most active in vitro. Additionally, compound 18i showed good liver microsomal stability and did not significantly inhibit CYP and Herg. Furthermore, this TPH1 inhibitor was able to actively interact with the peripheral system without penetrating the BBB. Compound 18i and its prodrug reduced body weight gain in mammals and decreased in vivo fat accumulation.
Keywords:tryptophan hydroxylase inhibitor   obesity   fatty liver   treatment
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