has_role organic heterocyclic compound anticoagulant acenocoumarol 0 353.08994 353.33 Nitrovarfarian cas:152-72-7 Nitrowarfarin acenocoumarolum Nicoumalone VABCILAOYCMVPS-UHFFFAOYSA-N Nitrophenylacetylethyl-4-hydroxycoumarine ChemIDplus:152-72-7 KEGG DRUG:152-72-7 Acenocoumarin Acenokumarin lincs.smallmolecule:LSM-5112 3-(alpha-p-Nitrophenyl-beta-acetylethyl)-4-hydroxycoumarin SNOMEDCT:387457003 KEGG DRUG:D07064 Acenocumarolo InChI=1S/C19H15NO6/c1-11(21)10-15(12-6-8-13(9-7-12)20(24)25)17-18(22)14-4-2-3-5-16(14)26-19(17)23/h2-9,15,22H,10H2,1H3 4-Hydroxy-3-(1-(4-nitrophenyl)-3-oxobutyl)-2H-1-benzopyran-2-one 4-hydroxy-3-[1-(4-nitrophenyl)-3-oxobutyl]-2H-chromen-2-one acenocoumarol drugbank:DB01418 Nicumalon NIST Chemistry WebBook:152-72-7 CHEBI:53766 ChEMBL:17275317 kegg.drug:D07064 3-(alpha-Acetonyl-4-nitrobenzyl)-4-hydroxycoumarin 3-(alpha-Acetonyl-p-nitrobenzyl)-4-hydroxycoumarin Beilstein:1269370 3-(alpha-(p-Nitrophenol)-beta-acetylethyl)-4-hydroxycoumarin 3-(alpha-(4'-Nitrophenyl)-beta-acetylethyl)-4-hydroxycoumarin 4-Hydroxy-3-[1-(4-nitrophenyl)-3-oxobutyl]-2H-chromen-2-one 4-hydroxy-3-[1-(4-nitrophenyl)-3-oxobutyl]-2H-chromen-2-one A hydroxycoumarin that is warfarin in which the hydrogen at position 4 of the phenyl substituent is replaced by a nitro group. MESH:D000074 C19H15NO6 acenocumarol CHEBI:494206 patent:US2648682 DrugBank:152-72-7 chebi_ontology reaxys:1269370 NCIt:C75152 pubmed:17275317 CC(=O)CC(c1ccc([N+](=O)[O-])cc1)c1c(O)c2ccccc2oc1=O SNOMEDCT:79356008