Summary
IMPPAT Phytochemical identifier: IMPHY007300
Phytochemical name: Pregnenolone
Synonymous chemical names:pregnenolone
External chemical identifiers:CID:8955, ChEMBL:CHEMBL253363, ChEBI:16581, ZINC:ZINC000003861150, FDASRS:73R90F7MQ8, SureChEMBL:SCHEMBL129572, MolPort-002-506-906
Chemical structure information
SMILES:
O[C@H]1CC[C@]2(C(=CC[C@@H]3[C@@H]2CC[C@]2([C@H]3CC[C@@H]2C(=O)C)C)C1)CInChI:
InChI=1S/C21H32O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h4,15-19,23H,5-12H2,1-3H3/t15-,16-,17+,18-,19-,20-,21+/m0/s1InChIKey:
ORNBQBCIOKFOEO-QGVNFLHTSA-NDeepSMILES:
O[C@H]CC[C@]C=CC[C@@H][C@@H]6CC[C@][C@H]6CC[C@@H]5C=O)C))))))C))))))))C6))CFunctional groups:
CC(C)=O, CC=C(C)C, CO
Molecular scaffolds
Scaffold Graph/Node/Bond level:
C1=C2CCCCC2C2CCC3CCCC3C2C1Scaffold Graph/Node level:
C1CCC2C(C1)CCC1C3CCCC3CCC21Scaffold Graph level:
C1CCC2C(C1)CCC1C3CCCC3CCC21
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Steroids and steroid derivatives
ClassyFire Subclass: Pregnane steroids
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Steroids
NP Classifier Class: Pregnane steroids
NP-Likeness score: 2.596
Chemical structure download