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81760-45-4 molecular structure
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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

ChemBase ID: 105690
Molecular Formular: C36H56O4
Molecular Mass: 552.82744
Monoisotopic Mass: 552.41786027
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

Cite this record

CBID:105690 http://www.chembase.cn/molecule-105690.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[(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
IUPAC Traditional name
[(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
Synonyms
KAHWEOL PALMITATE
CAS Number
81760-45-4
PubChem SID
162094207
PubChem CID
71299760

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
MP Biomedicals
02193764 external link Add to cart Please log in.
Data Source Data ID
PubChem 71299760 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 13.752199  H Acceptors
H Donor LogD (pH = 5.5) 9.474768 
LogD (pH = 7.4) 9.474768  Log P 9.474768 
Molar Refractivity 163.1041 cm3 Polarizability 64.35598 Å3
Polar Surface Area 59.67 Å2 Rotatable Bonds 17 
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
Storage Condition
-20°C, Protect from light expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
Download expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals
MP Biomedicals - 02193764 external link
From Green Coffee Beans
A natural extract which inhibits chemically induced carcinogenesis.

REFERENCES

REFERENCES

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  • • Lam, L.K.T., et al., Cancer Res. , 42 : 1193-98, (1982).
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PATENTS

PATENTS

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INTERNET

INTERNET

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