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(1R,2S,2'S,4aR,4bR,6aR,7R,8S,10aR,10bR,12aS)-7-(hydroxymethyl)-2'-[(2S)-1-hydroxypropan-2-yl]-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-1,8-diol

PubChem CID: 21729342

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Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 90.2
Hydrogen Bond Donor Count 4.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC2(CC1)CCC1C(CCC3C4CCCCC4CCC13)C2
Np Classifier Class Oleanane triterpenoids
Deep Smiles OC[C@@H][C@@H]CC[C@]CO6))CC[C@@][C@@H][C@H]6O))CC[C@H][C@@]6C)CC[C@@H][C@]6C)CC[C@@H][C@@]6C)CO)))O)))))))))))))C))))))))C
Heavy Atom Count 35.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CCC2C(C1)CCC1C3CCC4(CCCOC4)CC3CCC21
Classyfire Subclass Triterpenoids
Isotope Atom Count 0.0
Molecular Complexity 804.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 12.0
Iupac Name (1R,2S,2'S,4aR,4bR,6aR,7R,8S,10aR,10bR,12aS)-7-(hydroxymethyl)-2'-[(2S)-1-hydroxypropan-2-yl]-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-1,8-diol
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 5.6
Gsk 4 400 Rule False
Molecular Formula C30H52O5
Scaffold Graph Node Bond Level C1CCC2C(C1)CCC1C3CCC4(CCCOC4)CC3CCC21
Inchi Key JPGKBRDEEANKGY-SWMRXHLFSA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 3.0
Synonyms hosenkol a, hosenkol-a
Esol Class Poorly soluble
Functional Groups CO, COC
Compound Name (1R,2S,2'S,4aR,4bR,6aR,7R,8S,10aR,10bR,12aS)-7-(hydroxymethyl)-2'-[(2S)-1-hydroxypropan-2-yl]-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-1,8-diol
Exact Mass 492.381
Formal Charge 0.0
Monoisotopic Mass 492.381
Hydrogen Bond Acceptor Count 5.0
Molecular Weight 492.7
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 12.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C30H52O5/c1-19(16-31)21-8-13-30(18-35-21)15-14-28(4)20(25(30)34)6-7-23-26(2)11-10-24(33)27(3,17-32)22(26)9-12-29(23,28)5/h19-25,31-34H,6-18H2,1-5H3/t19-,20+,21-,22+,23+,24-,25+,26-,27-,28+,29+,30+/m0/s1
Smiles C[C@@H](CO)[C@@H]1CC[C@@]2(CC[C@@]3([C@@H]([C@H]2O)CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H]([C@@]5(C)CO)O)C)C)C)CO1
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Triterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Impatiens Balsamina (Plant) Rel Props:Reference:ISBN:9788172360818