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164228873 molecular structure
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(14S,15S)-4-(2H3)methoxy-15-methyltetracyclo[8.7.0.02,7.011,15]heptadeca-2(7),3,5-triene-5,14-diol

ChemBase ID: 172963
Molecular Formular: C19H26O3
Molecular Mass: 302.40794
Monoisotopic Mass: 302.18819469
SMILES and InChIs

SMILES:
c1c(c(cc2c1C1C(CC2)C2[C@](CC1)([C@H](CC2)O)C)O)OC
Canonical SMILES:
COc1cc2c(cc1O)CCC1C2CC[C@]2(C1CC[C@@H]2O)C
InChI:
InChI=1S/C19H26O3/c1-19-8-7-12-13(15(19)5-6-18(19)21)4-3-11-9-16(20)17(22-2)10-14(11)12/h9-10,12-13,15,18,20-21H,3-8H2,1-2H3/t12?,13?,15?,18-,19-/m0/s1
InChIKey:
CQOQDQWUFQDJMK-WRWXEFHESA-N

Cite this record

CBID:172963 http://www.chembase.cn/molecule-172963.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(14S,15S)-4-(2H3)methoxy-15-methyltetracyclo[8.7.0.02,7.011,15]heptadeca-2(7),3,5-triene-5,14-diol
IUPAC Traditional name
(14S,15S)-4-(2H3)methoxy-15-methyltetracyclo[8.7.0.02,7.011,15]heptadeca-2(7),3,5-triene-5,14-diol
Synonyms
(17β)-2-Methoxy-d3-estra-1,3,5(10)-triene-3,17-diol
2-Hydroxyestradiol 2-Methyl-d3 Ether
2-Methoxy-d3-estra-1,3,5(10)-triene-3,17β-diol
2-Methoxy-d3-estradiol
NSC 659853-d3
Panzem-d3
2-Methoxy-d3 17β-Estradiol
PubChem SID
164228873
PubChem CID
71750082

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC M262627 external link Add to cart
PubChem 71750082 external link
Data Source Data ID Price
TRC
M262627 external link Add to cart Please log in.
Data Source Data ID
PubChem 71750082 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 10.290903  H Acceptors
H Donor LogD (pH = 5.5) 3.587823 
LogD (pH = 7.4) 3.5872755  Log P 3.58783 
Molar Refractivity 86.3679 cm3 Polarizability 33.825172 Å3
Polar Surface Area 49.69 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
Dichloromethane expand Show data source
Apperance
Crystalline Solid expand Show data source
Melting Point
188-190°C expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
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DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - M262627 external link
A natural metabolite of 17β-Estradiol which is devoid of estrogenic activity. Inhibits cell proliferation and angiogenesis. Binds to the colchicine binding site of tubulin, and has been suggested to function as a natural regulator of microtubule assembl

REFERENCES

REFERENCES

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  • • Cushman, M., et al.: J. Med. Chem., 38, 2041 (1995)
  • • D’Amato, R.J., et al.: Proc. Natl. Acad. Sci. USA, 91, 3964 (1995)
  • • Forsis, T., et al.: Nature, 368, 237 (1994)
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PATENTS

PATENTS

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INTERNET

INTERNET

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