emricasan   Click here for help

GtoPdb Ligand ID: 6508

Synonyms: IDN-6556 | PF-03491390
Compound class: Synthetic organic
Comment: Emricasan is a pan caspase inhibitor. Its development as a treatment for nonalcoholic steatohepatitis (NASH) was unsuccessful.
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2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 9
Hydrogen bond donors 4
Rotatable bonds 15
Topological polar surface area 150.9
Molecular weight 569.18
XLogP 3.1
No. Lipinski's rules broken 1
SMILES / InChI / InChIKey
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Canonical SMILES OC(=O)CC(C(=O)COc1c(F)c(F)cc(c1F)F)NC(=O)C(NC(=O)C(=O)Nc1ccccc1C(C)(C)C)C
Isomeric SMILES OC(=O)C[C@@H](C(=O)COc1c(F)c(F)cc(c1F)F)NC(=O)[C@@H](NC(=O)C(=O)Nc1ccccc1C(C)(C)C)C
InChI InChI=1S/C26H27F4N3O7/c1-12(31-24(38)25(39)32-16-8-6-5-7-13(16)26(2,3)4)23(37)33-17(10-19(35)36)18(34)11-40-22-20(29)14(27)9-15(28)21(22)30/h5-9,12,17H,10-11H2,1-4H3,(H,31,38)(H,32,39)(H,33,37)(H,35,36)/t12-,17-/m0/s1
InChI Key SCVHJVCATBPIHN-SJCJKPOMSA-N
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Summary of Clinical Use Click here for help
Clinical candidate being investigated as a treatment for liver failure, including that ensuing from hepatitis C infection and nonalcoholic steatohepatitis. Click here to view emricasan related clinical trials registered with ClinicalTrials.gov. This drug candidate has been granted orphan designation by the US FDA, for the treatment of liver transplant patients with reestablished fibrosis. Drug treatment is intended to delay the progression to cirrhosis and end-stage liver disease in these patients.
Mechanism Of Action and Pharmacodynamic Effects Click here for help
Emricasan irreversibly inhibits caspase proteases and is designed to reduce the activity of enzymes that mediate inflammation and cell death, or apoptosis. It is postulated that this action has the potential to interrupt the progression of liver disease [1].