| Metabolic stability in rat liver microsomes - BioAssay Summary Based on a high-throughput screen, cyclopentanecarboxanilides were identified as a new chemotype of non-covalent inhibitors of type I fatty acid synthase (FAS). Starting from initial hits we aimed at generating a tool compound suitable for the in vivo validation of FAS as a therapeutic target. Optimisation yielded BI 99179 which is characterised by high potency, remarkably high selectivity and significant exposure (both peripheral and central) upon oral administration in rats. ..more |
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BioActive Compound: 1 Description: Title: Discovery of BI 99179, a potent and selective inhibitor of type I fatty acid synthase with central exposure. Abstract: Based on a high-throughput screen, cyclopentanecarboxanilides were identified as a new chemotype of non-covalent inhibitors of type I fatty acid synthase (FAS). Starting from initial hits we aimed at generating a tool compound suitable for the in vivo validation of FAS as a therapeutic target. Optimisation yielded BI 99179 which is characterised by high potency, remarkably high selectivity and significant exposure (both peripheral and central) upon oral administration in rats. (PMID: 21873051) Comment Putative Target: ChEMBL Target ID: 102178 Target Type: SUBCELLULAR Pref Name: Liver microsomes Organism: Rattus norvegicus Tax ID: 10116 Confidence: Target assigned is subcellular fraction Relationship Type: Subcellular target assigned Categorized Comment ChEMBL Assay Type: ADMET ChEMBL Assay Data Source: Scientific Literature Result Definitions
Data Table (Concise)
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