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(1R,2R,5R,8R,9R,12R,13R,16S)-8-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-9,13-dimethyl-18,19-dioxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-3-ene-2,16-diol

PubChem CID: 10789469

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Compound Synonyms DTXSID801208308, 348611-57-4, (3I(2),5I+/-,6I(2),22E)-5,9-Epidioxyergosta-7,22-diene-3,6-diol
Topological Polar Surface Area 58.9
Hydrogen Bond Donor Count 2.0
Heavy Atom Count 32.0
Isotope Atom Count 0.0
Molecular Complexity 818.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 10.0
Iupac Name (1R,2R,5R,8R,9R,12R,13R,16S)-8-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-9,13-dimethyl-18,19-dioxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-3-ene-2,16-diol
Prediction Hob 0.0
Xlogp 5.2
Molecular Formula C28H44O4
Prediction Swissadme 0.0
Inchi Key XCRHWCBOUDKLGM-IUMXJWHTSA-N
Fcsp3 0.8571428571428571
Logs -5.092
Rotatable Bond Count 4.0
Logd 4.542
Compound Name (1R,2R,5R,8R,9R,12R,13R,16S)-8-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-9,13-dimethyl-18,19-dioxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-3-ene-2,16-diol
Prediction Hob Swissadme 0.0
Exact Mass 444.324
Formal Charge 0.0
Monoisotopic Mass 444.324
Hydrogen Bond Acceptor Count 4.0
Molecular Weight 444.6
Covalent Unit Count 1.0
Total Atom Stereocenter Count 10.0
Total Bond Stereocenter Count 1.0
Esol -5.596267200000001
Inchi InChI=1S/C28H44O4/c1-17(2)18(3)7-8-19(4)21-9-10-22-23-15-24(30)28-16-20(29)11-12-26(28,6)27(23,31-32-28)14-13-25(21,22)5/h7-8,15,17-22,24,29-30H,9-14,16H2,1-6H3/b8-7+/t18-,19+,20-,21+,22-,24+,25+,26+,27+,28-/m0/s1
Smiles C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@@]34C2=C[C@H]([C@@]5([C@@]3(CC[C@@H](C5)O)C)OO4)O)C
Nring 5.0
Defined Bond Stereocenter Count 1.0

  • 1. Outgoing r'ship FOUND_IN to/from Erythrina Suberosa (Plant) Rel Props:Source_db:cmaup_ingredients
  • 2. Outgoing r'ship FOUND_IN to/from Rhodiola Rosea (Plant) Rel Props:Source_db:cmaup_ingredients