Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease
Authors:
- Suvarna H. PagireSPSuvarna H. Pagire
- Haushabhau S. PagireHPHaushabhau S. Pagire
- Kun-Young ParkKPKun-Young Park
- Eun Jung BaeEBEun Jung Bae
- Kwang-Eun KimKKKwang-Eun Kim
- Minhee KimMKMinhee Kim
- Jihyeon YoonJYJihyeon Yoon
- Saravanan ParameswaranSaravanan Parameswaran
- Jun-Ho ChoiJCJun-Ho Choi
- Sungmi ParkSPSungmi Park
- Jae-Han JeonJJJae-Han Jeon
- Jin Sook SongJSJin Sook Song
Open Access
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
Funding Information
- National Research Foundation of Korea (2016M3A9B6902868, 2021R1A2C2008062, 20202020800330)
- Korea Institute of Energy Technology Evaluation and Planning (2016M3A9B6902868, 2021R1A2C2008062, 20202020800330)
- Ministry of Science (2016M3A9B6902868, 2021R1A2C2008062, 20202020800330)
- ICT (2016M3A9B6902868, 2021R1A2C2008062, 20202020800330)
This publication has 22 references indexed in Scilit:
- Serotonin control of sleep-wake behaviorSleep Medicine Reviews, 2011
- Brain serotonin system in the coordination of food intake and body weightPharmacology Biochemistry and Behavior, 2010
- Mechanism of Inhibition of Novel Tryptophan Hydroxylase Inhibitors Revealed by Co-crystal Structures and Kinetic AnalysisCurrent Chemical Genomics, 2010
- AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibilityJournal of Computational Chemistry, 2009
- The Expanded Biology of SerotoninAnnual Review of Medicine, 2009
- Modulation of Peripheral Serotonin Levels by Novel Tryptophan Hydroxylase Inhibitors for the Potential Treatment of Functional Gastrointestinal DisordersJournal of Medicinal Chemistry, 2008
- The role of serotonin in human mood and social interactionPharmacology Biochemistry and Behavior, 2002
- Correlation and prediction of a large blood–brain distribution data set—an LFER studyEuropean Journal of Medicinal Chemistry, 2001
- Development of a new physicochemical model for brain penetration and its application to the design of centrally acting H2 receptor histamine antagonistsJournal of Medicinal Chemistry, 1988
- Relationship of octanol/water partition coefficient and molecular weight to rat brain capillary permeabilityJournal of Medicinal Chemistry, 1980