| Literature DB >> 29259741 |
Abir Bhattacharjee1, Antara Sinha1, Kiira Ratia2, Liang Yin2, Loruhama Delgado-Rivera2, Pavel A Petukhov2, Gregory R J Thatcher2, Duncan J Wardrop1.
Abstract
Hydrogen sulfide is produced from l-cysteine by the action of both cystathionine γ-lyase (CSE) and cystathionine β-synthase (CBS) and increasingly has been found to play a profound regulatory role in a range of physiological processes. Mounting evidence suggests that upregulation of hydrogen sulfide biosynthesis occurs in several disease states, including rheumatoid arthritis, hypertension, ischemic injury, and sleep-disordered breathing. In addition to being critical tools in our understanding of hydrogen sulfide biology, inhibitors of CSE hold therapeutic potential for the treatment of diseases in which increased levels of this gasotransmitter play a role. We describe the discovery and development of a novel series of potent CSE inhibitors that show increased activity over the benchmark inhibitor and, importantly, display high selectivity for CSE versus CBS.Entities:
Year: 2017 PMID: 29259741 PMCID: PMC5733271 DOI: 10.1021/acsmedchemlett.7b00313
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345