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(6S,9S)-vomifoliol

PubChem CID: 10537120

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Compound Synonyms Corchoionol C, (6S,9S)-vomifoliol, 189351-15-3, (4S)-4-hydroxy-4-[(E,3S)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one, CHEBI:49158, (4S)-4-hydroxy-4-[(1E,3S)-3-hydroxybut-1-en-1-yl]-3,5,5-trimethylcyclohex-2-en-1-one, 2-Cyclohexen-1-one, 4-hydroxy-4-[(1E,3S)-3-hydroxy-1-buten-1-yl]-3,5,5-trimethyl-, (4S)-, (4S)-4-hydroxy-4-((1E,3S)-3-hydroxybut-1-en-1-yl)-3,5,5-trimethylcyclohex-2-en-1-one, (4S)-4-hydroxy-4-((E,3S)-3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohex-2-en-1-one, CHEMBL4562613, HY-N3621, AKOS040761525, DA-62458, FS-10525, CS-0023951, Q27121504
Topological Polar Surface Area 57.5
Hydrogen Bond Donor Count 2.0
Heavy Atom Count 16.0
Isotope Atom Count 0.0
Molecular Complexity 352.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 2.0
Iupac Name (4S)-4-hydroxy-4-[(E,3S)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one
Prediction Hob 1.0
Xlogp 0.5
Molecular Formula C13H20O3
Prediction Swissadme 1.0
Inchi Key KPQMCAKZRXOZLB-ZOLRFCATSA-N
Fcsp3 0.6153846153846154
Logs -2.0
Rotatable Bond Count 2.0
Logd 1.305
Compound Name (6S,9S)-vomifoliol
Prediction Hob Swissadme 1.0
Exact Mass 224.141
Formal Charge 0.0
Monoisotopic Mass 224.141
Hydrogen Bond Acceptor Count 3.0
Molecular Weight 224.3
Covalent Unit Count 1.0
Total Atom Stereocenter Count 2.0
Total Bond Stereocenter Count 1.0
Esol -1.44516
Inchi InChI=1S/C13H20O3/c1-9-7-11(15)8-12(3,4)13(9,16)6-5-10(2)14/h5-7,10,14,16H,8H2,1-4H3/b6-5+/t10-,13+/m0/s1
Smiles CC1=CC(=O)CC([C@]1(/C=C/[C@H](C)O)O)(C)C
Nring 1.0
Defined Bond Stereocenter Count 1.0