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Hebeirubescensins G

PubChem CID: 44445764

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Compound Synonyms hebeirubescensins G, (1R,2S,5S,8R,9R,10S,11R,15R,16S,18R)-9,10,15,16,18-pentahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo(7.6.2.15,8.01,11.02,8)octadecan-7-one, (1R,2S,5S,8R,9R,10S,11R,15R,16S,18R)-9,10,15,16,18-pentahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one, CHEMBL400340
Topological Polar Surface Area 127.0
Hydrogen Bond Donor Count 5.0
Heavy Atom Count 27.0
Isotope Atom Count 0.0
Molecular Complexity 749.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 10.0
Iupac Name (1R,2S,5S,8R,9R,10S,11R,15R,16S,18R)-9,10,15,16,18-pentahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one
Prediction Hob 1.0
Xlogp -0.4
Molecular Formula C20H28O7
Prediction Swissadme 0.0
Inchi Key BTWFVPFIPDEZTE-NPAPHPRCSA-N
Fcsp3 0.85
Logs -3.741
Rotatable Bond Count 0.0
Logd 0.132
Compound Name Hebeirubescensins G
Prediction Hob Swissadme 0.0
Exact Mass 380.184
Formal Charge 0.0
Monoisotopic Mass 380.184
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 380.4
Covalent Unit Count 1.0
Total Atom Stereocenter Count 10.0
Total Bond Stereocenter Count 0.0
Esol -1.9215094
Inchi InChI=1S/C20H28O7/c1-8-9-4-5-10-18-11(21)6-7-17(2,3)12(18)15(24)20(26,27-16(18)25)19(10,13(8)22)14(9)23/h9-12,14-16,21,23-26H,1,4-7H2,2-3H3/t9-,10-,11+,12+,14+,15-,16-,18-,19-,20-/m0/s1
Smiles CC1(CC[C@H]([C@]23[C@@H]1[C@@H]([C@@]([C@]45[C@H]2CC[C@H]([C@H]4O)C(=C)C5=O)(O[C@@H]3O)O)O)O)C
Nring 6.0
Defined Bond Stereocenter Count 0.0

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