| Literature DB >> 29259743 |
Christian A Kuttruff1, Marco Ferrara2, Tom Bretschneider1, Stefan Hoerer1, Sandra Handschuh1, Bernd Nosse1, Helmut Romig1, Paul Nicklin1, Gerald J Roth1.
Abstract
In an effort to find new therapeutic interventions addressing the unmet medical need of patients with idiopathic pulmonary fibrosis, we initiated a program to identify new autotaxin (ATX) inhibitors. Starting from a recently published compound (PF-8380), we identified several highly potent ATX inhibitors with improved pharmacokinetic and safety profiles. Further optimization efforts resulted in the identification of a single-digit nanomolar lead compound (BI-2545) that shows substantial lowering of LPA in vivo and is therefore considered a valuable tool for further studies.Entities:
Year: 2017 PMID: 29259743 PMCID: PMC5733304 DOI: 10.1021/acsmedchemlett.7b00312
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345