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Angeloylgomisin Q

PubChem CID: 14992071

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Compound Synonyms Angeloylgomisin Q, 72561-28-5, UNII-HJE27L4CC0, HJE27L4CC0, 2-Butenoic acid, 2-methyl-, (5S,6S,7S,12aS)-5,6,7,8-tetrahydro-6-hydroxy-1,2,3,10,11,12-hexamethoxy-6,7-dimethyldibenzo(a,C)cycloocten-5-yl ester, (2Z)-, [(8S,9S,10S)-9-hydroxy-3,4,5,14,15,16-hexamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] (Z)-2-methylbut-2-enoate, CHEMBL2386337, DTXSID401349295, HY-N8260, DA-61060, MS-29809, CS-0142043, E88816, Q27279958
Topological Polar Surface Area 102.0
Hydrogen Bond Donor Count 1.0
Heavy Atom Count 38.0
Isotope Atom Count 0.0
Molecular Complexity 818.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 3.0
Uniprot Id n.a.
Iupac Name [(8S,9S,10S)-9-hydroxy-3,4,5,14,15,16-hexamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] (Z)-2-methylbut-2-enoate
Prediction Hob 0.0
Xlogp 4.7
Molecular Formula C29H38O9
Prediction Swissadme 0.0
Inchi Key RHABJANPSGWEFC-MRFZJNLZSA-N
Fcsp3 0.4827586206896552
Logs -4.404
Rotatable Bond Count 9.0
Logd 3.136
Compound Name Angeloylgomisin Q
Prediction Hob Swissadme 0.0
Exact Mass 530.252
Formal Charge 0.0
Monoisotopic Mass 530.252
Hydrogen Bond Acceptor Count 9.0
Molecular Weight 530.6
Covalent Unit Count 1.0
Total Atom Stereocenter Count 3.0
Total Bond Stereocenter Count 1.0
Esol -5.724191010526317
Inchi InChI=1S/C29H38O9/c1-11-15(2)28(30)38-27-18-14-20(33-6)24(35-8)26(37-10)22(18)21-17(12-16(3)29(27,4)31)13-19(32-5)23(34-7)25(21)36-9/h11,13-14,16,27,31H,12H2,1-10H3/b15-11-/t16-,27-,29-/m0/s1
Smiles C/C=C(/C)\C(=O)O[C@H]1C2=CC(=C(C(=C2C3=C(C(=C(C=C3C[C@@H]([C@]1(C)O)C)OC)OC)OC)OC)OC)OC
Nring 3.0
Defined Bond Stereocenter Count 1.0

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