Drugs Information:
Vorapaxar
Basic Information
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ID | DDInter1945 | |
Drug Type | small molecule | |
Molecular Formula | C29H33FN2O4 | |
Molecular Weight | 492.582 | |
CAS Number | 618385-01-6 | |
Description | Vorapaxar is a tricyclic himbacine-derived selective inhibitor of protease activated receptor (PAR-1) indicated for reducing the incidence of thrombotic cardiovascular events in patients with a history of myocardial infarction (MI) or with peripheral arterial disease (PAD). By inhibiting PAR-1, a thrombin receptor expressed on platelets, vorapaxar prevents thrombin-related platelet aggregation. | |
ATC Classification | B01AC26 | |
IUPAC Name | ethyl N-[(1R,3aR,4aR,6R,8aR,9S,9aS)-9-[(1E)-2-[5-(3-fluorophenyl)pyridin-2-yl]ethenyl]-1-methyl-3-oxo-dodecahydronaphtho[2,3-c]furan-6-yl]carbamate | |
InChI | ZBGXUVOIWDMMJE-QHNZEKIYSA-N | |
Canonical SMILES | [H][C@@]12C[C@]3([H])C[C@@H](CC[C@@]3([H])[C@H](\C=C\C3=CC=C(C=N3)C3=CC(F)=CC=C3)[C@]1([H])[C@@H](C)OC2=O)NC(=O)OCC | |
Useful Links | DrugBank ChEBI PubChem Substance KEGG Drug ChemSpider BindingDB Wikipedia ChEMBL ZINC |
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Vorapaxar
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