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(1R,3R,6R,7S,8S,10R,11R,12R,13S,16S,17R)-8-tert-butyl-6,12,17-trihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.01,11.03,7.07,11.013,17]nonadecane-5,15,18-trione
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ChemBase ID:
133501
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Molecular Formular:
C20H24O10
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Molecular Mass:
424.39856
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Monoisotopic Mass:
424.13694697
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SMILES and InChIs
SMILES:
C[C@@H]1C(=O)O[C@@H]2[C@]1([C@@]13C(=O)O[C@H]4[C@]1([C@H]2O)[C@@]1([C@@H](C4)C(C)(C)C)[C@H](C(=O)O[C@H]1O3)O)O
Canonical SMILES:
O=C1O[C@@H]2[C@@]([C@@H]1C)(O)[C@@]13[C@]4([C@H]2O)[C@H](OC3=O)C[C@H]([C@@]24[C@H](O1)OC(=O)[C@@H]2O)C(C)(C)C
InChI:
InChI=1S/C20H24O10/c1-6-12(23)28-11-9(21)18-8-5-7(16(2,3)4)17(18)10(22)13(24)29-15(17)30-20(18,14(25)27-8)19(6,11)26/h6-11,15,21-22,26H,5H2,1-4H3/t6-,7+,8-,9+,10+,11+,15+,17+,18+,19-,20-/m1/s1
InChIKey:
SQOJOAFXDQDRGF-MMQTXUMRSA-N
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Cite this record
CBID:133501 http://www.chembase.cn/molecule-133501.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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(1R,3R,6R,7S,8S,10R,11R,12R,13S,16S,17R)-8-tert-butyl-6,12,17-trihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.01,11.03,7.07,11.013,17]nonadecane-5,15,18-trione
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IUPAC Traditional name
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Synonyms
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BN-52021
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Ginkgolide B from Ginkgo biloba leaves
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Ginkgolide B
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银杏内酯 B 来源于银杏 叶
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银杏内酯 B
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CAS Number
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MDL Number
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Beilstein Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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11.709941
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H Acceptors
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7
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H Donor
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3
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LogD (pH = 5.5)
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-0.5822128
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LogD (pH = 7.4)
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-0.5822338
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Log P
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-0.58221257
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Molar Refractivity
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91.382 cm3
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Polarizability
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38.405952 Å3
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Polar Surface Area
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148.82 Å2
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Rotatable Bonds
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1
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
Sigma Aldrich
Sigma Aldrich -
G6910
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Biochem/physiol Actions Primary constituent of Ginkgo biloba. Potential anticancer agent and neuroprotective. Protocols & Applications Ginkgo (Ginkgo biloba) Plant Profile: bioactives, mechanism of action, references |
PATENTS
PATENTS
PubChem Patent
Google Patent