BMS-986020   Click here for help

GtoPdb Ligand ID: 9498

Synonyms: am-152 | AM152 | AP-3152 free acid
Compound class: Synthetic organic
Comment: BMS-986020 is an investigational lysophosphatidic acid 1 (LPA1) receptor antagonist [2]. It is claimed as Compound 1-1 in patent WO2010141768 [1], and this document contains extensive in vitro characterisation data and records in vivo anti-fibrotic efficacy in various animal models of fibrosis.
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2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 5
Hydrogen bond donors 2
Rotatable bonds 9
Topological polar surface area 101.66
Molecular weight 482.18
XLogP 6.82
No. Lipinski's rules broken 1
SMILES / InChI / InChIKey
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Canonical SMILES O=C(OC(c1ccccc1)C)Nc1c(C)noc1c1ccc(cc1)c1ccc(cc1)C1(CC1)C(=O)O
Isomeric SMILES O=C(O[C@@H](c1ccccc1)C)Nc1c(C)noc1c1ccc(cc1)c1ccc(cc1)C1(CC1)C(=O)O
InChI InChI=1S/C29H26N2O5/c1-18-25(30-28(34)35-19(2)20-6-4-3-5-7-20)26(36-31-18)23-10-8-21(9-11-23)22-12-14-24(15-13-22)29(16-17-29)27(32)33/h3-15,19H,16-17H2,1-2H3,(H,30,34)(H,32,33)/t19-/m1/s1
InChI Key GQBRZBHEPUQRPL-LJQANCHMSA-N
No information available.
Summary of Clinical Use Click here for help
BMS-986020 has completed Phase 2 clinical trial for treating idiopathic pulmonary fibrosis. Results from NCT01766817) were reported in late 2017 [3]. The study was terminated early because of hepatotoxicity issues. BMS-986020 retains its FDA Orphan Drug designation that was granted in 2011 for the treatment of idiopathic pulmonary fibrosis (link to FDA Orphan Drug Designation record here).
Mechanism Of Action and Pharmacodynamic Effects Click here for help
Activation of the LPA1 receptor by LPA has been implicated in a number of disease processes, including tissue fibrosis. LPA1 receptor antagonists have displayed efficacy in a wide range of preclinical fibrosis models, including lung, skin, eye, liver and kidney.
Clinical Trials
Clinical Trial ID Title Type Source Comment References
NCT01766817 Safety and Efficacy of a Lysophosphatidic Acid Receptor Antagonist in Idiopathic Pulmonary Fibrosis Phase 2 Interventional Bristol-Myers Squibb