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[(1R,4S,12S,13R,16R,17S)-17-hydroxy-12-methyl-8-oxapentacyclo[14.2.1.0^{1,13}.0^{4,12}.0^{5,9}]nonadeca-5(9),6,10-trien-17-yl]methyl hexadecanoate
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ChemBase ID:
105690
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Molecular Formular:
C36H56O4
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Molecular Mass:
552.82744
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Monoisotopic Mass:
552.41786027
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SMILES and InChIs
SMILES:
O=C(OC[C@]1(O)C[C@@]23[C@H]([C@]4([C@@H](c5ccoc5C=C4)CC2)C)CC[C@H]1C3)CCCCCCCCCCCCCCC
Canonical SMILES:
CCCCCCCCCCCCCCCC(=O)OC[C@]1(O)C[C@]23C[C@@H]1CC[C@H]3[C@]1([C@H](CC2)c2ccoc2C=C1)C
InChI:
InChI=1S/C36H56O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-33(37)40-27-36(38)26-35-23-19-30-29-21-24-39-31(29)20-22-34(30,2)32(35)18-17-28(36)25-35/h20-22,24,28,30,32,38H,3-19,23,25-27H2,1-2H3/t28-,30-,32+,34-,35-,36-/m1/s1
InChIKey:
UMZARYXKQBKPOL-XCPWRNKKSA-N
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Cite this record
CBID:105690 http://www.chembase.cn/molecule-105690.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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[(1R,4S,12S,13R,16R,17S)-17-hydroxy-12-methyl-8-oxapentacyclo[14.2.1.0^{1,13}.0^{4,12}.0^{5,9}]nonadeca-5(9),6,10-trien-17-yl]methyl hexadecanoate
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IUPAC Traditional name
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[(1R,4S,12S,13R,16R,17S)-17-hydroxy-12-methyl-8-oxapentacyclo[14.2.1.0^{1,13}.0^{4,12}.0^{5,9}]nonadeca-5(9),6,10-trien-17-yl]methyl hexadecanoate
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Synonyms
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CAS 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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13.752199
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H Acceptors
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2
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H Donor
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1
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LogD (pH = 5.5)
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9.474768
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LogD (pH = 7.4)
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9.474768
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Log P
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9.474768
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Molar Refractivity
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163.1041 cm3
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Polarizability
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64.35598 Å3
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Polar Surface Area
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59.67 Å2
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Rotatable Bonds
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17
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Lipinski's Rule of Five
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false
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PROPERTIES
PROPERTIES
Safety Information
Product Information
Bioassay(PubChem)
Storage Condition
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-20°C, Protect from light
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Show
data source
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MSDS Link
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DETAILS
DETAILS
MP Biomedicals
MP Biomedicals -
02193764
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From Green Coffee Beans A natural extract which inhibits chemically induced carcinogenesis. |
PATENTS
PATENTS
PubChem Patent
Google Patent