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Isoadenolin E

PubChem CID: 56673381

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Compound Synonyms isoadenolin E, (1S,2S,3S,5S,7R,8R,9S,10S,11R,16S,18R)-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo(7.6.2.15,8.01,11.02,8)octadecane-3,7,9,10,18-pentol, (1S,2S,3S,5S,7R,8R,9S,10S,11R,16S,18R)-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-3,7,9,10,18-pentol, CHEMBL1802170
Topological Polar Surface Area 120.0
Hydrogen Bond Donor Count 5.0
Heavy Atom Count 28.0
Isotope Atom Count 0.0
Molecular Complexity 724.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 11.0
Iupac Name (1S,2S,3S,5S,7R,8R,9S,10S,11R,16S,18R)-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-3,7,9,10,18-pentol
Prediction Hob 1.0
Xlogp -0.2
Molecular Formula C21H32O7
Prediction Swissadme 1.0
Inchi Key MQFOWMSWYZXMPL-OZJHOVKHSA-N
Fcsp3 0.9047619047619048
Logs -3.671
Rotatable Bond Count 1.0
Logd 1.016
Compound Name Isoadenolin E
Prediction Hob Swissadme 1.0
Exact Mass 396.215
Formal Charge 0.0
Monoisotopic Mass 396.215
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 396.5
Covalent Unit Count 1.0
Total Atom Stereocenter Count 11.0
Total Bond Stereocenter Count 0.0
Esol -2.1124760000000005
Inchi InChI=1S/C21H32O7/c1-9-10-8-11(22)12-19-7-5-6-18(2,3)13(19)16(25)21(26,28-17(19)27-4)20(12,14(9)23)15(10)24/h10-17,22-26H,1,5-8H2,2-4H3/t10-,11-,12-,13+,14+,15+,16-,17-,19-,20-,21+/m0/s1
Smiles CC1(CCC[C@@]23[C@@H]1[C@@H]([C@]([C@]45[C@H]2[C@H](C[C@H]([C@H]4O)C(=C)[C@H]5O)O)(O[C@@H]3OC)O)O)C
Nring 6.0
Defined Bond Stereocenter Count 0.0

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