| Literature DB >> 19631532 |
Haihong Jin1, Giovanni Cianchetta, Arokiasamy Devasagayaraj, Kunjian Gu, Brett Marinelli, Lakshman Samala, Sheldon Scott, Terry Stouch, Ashok Tunoori, Ying Wang, Yi Zang, Chengmin Zhang, S David Kimball, Alan J Main, Zhi-Ming Ding, Weimei Sun, Qi Yang, Xiang-Qing Yu, David R Powell, Alan Wilson, Qingyun Liu, Zhi-Cai Shi.
Abstract
Tryptophan hydroxylase (TPH) is a key enzyme in the synthesis of serotonin. As a neurotransmitter, serotonin plays important physiological roles both peripherally and centrally. Here we describe the discovery of substituted triazines as a novel class of tryptophan hydroxylase inhibitors. This class of TPH inhibitors can selectively reduce serotonin levels in murine intestine after oral administration without affecting levels in the brain. These TPH inhibitors may provide novel treatments for gastrointestinal disorders associated with dysregulation of the serotonergic system, such as chemotherapy-induced emesis and irritable bowel syndrome.Entities:
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Year: 2009 PMID: 19631532 DOI: 10.1016/j.bmcl.2009.07.005
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823