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Eriocasin C

PubChem CID: 50901032

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Compound Synonyms Eriocasin C, CHEBI:70357, ((1R,2S,4aS,4bR,7R,8aR,10S,10aS)-2,10-dihydroxy-1,4a-dimethyl-9-oxo-7-(3-oxoprop-1-en-2-yl)-3,4,4b,5,6,7,8,8a,10,10a-decahydro-2H-phenanthren-1-yl)methyl acetate, [(1R,2S,4aS,4bR,7R,8aR,10S,10aS)-2,10-dihydroxy-1,4a-dimethyl-9-oxo-7-(3-oxoprop-1-en-2-yl)-3,4,4b,5,6,7,8,8a,10,10a-decahydro-2H-phenanthren-1-yl]methyl acetate, CHEMBL1641888, Q27138697
Topological Polar Surface Area 101.0
Hydrogen Bond Donor Count 2.0
Heavy Atom Count 28.0
Isotope Atom Count 0.0
Molecular Complexity 687.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name [(1R,2S,4aS,4bR,7R,8aR,10S,10aS)-2,10-dihydroxy-1,4a-dimethyl-9-oxo-7-(3-oxoprop-1-en-2-yl)-3,4,4b,5,6,7,8,8a,10,10a-decahydro-2H-phenanthren-1-yl]methyl acetate
Prediction Hob 1.0
Xlogp 2.1
Molecular Formula C22H32O6
Prediction Swissadme 1.0
Inchi Key JZFWRUQOQHVXDM-UDTDVKRRSA-N
Fcsp3 0.7727272727272727
Logs -2.325
Rotatable Bond Count 5.0
Logd 0.981
Compound Name Eriocasin C
Prediction Hob Swissadme 1.0
Exact Mass 392.22
Formal Charge 0.0
Monoisotopic Mass 392.22
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 392.5
Covalent Unit Count 1.0
Total Atom Stereocenter Count 8.0
Total Bond Stereocenter Count 0.0
Esol -3.2727504000000005
Inchi InChI=1S/C22H32O6/c1-12(10-23)14-5-6-16-15(9-14)18(26)19(27)20-21(16,3)8-7-17(25)22(20,4)11-28-13(2)24/h10,14-17,19-20,25,27H,1,5-9,11H2,2-4H3/t14-,15-,16-,17+,19-,20+,21+,22-/m1/s1
Smiles CC(=O)OC[C@@]1([C@H](CC[C@@]2([C@@H]1[C@@H](C(=O)[C@H]3[C@H]2CC[C@H](C3)C(=C)C=O)O)C)O)C
Nring 3.0
Defined Bond Stereocenter Count 0.0

  • 1. Outgoing r'ship FOUND_IN to/from Isodon Eriocalyx (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all