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(1S,2R,10R,11S,14S,15S)-14,15-diethyl-14-hydroxytetracyclo[8.7.0.02,7.011,15]heptadec-6-en-5-one
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ChemBase ID:
175576
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Molecular Formular:
C21H32O2
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Molecular Mass:
316.47758
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Monoisotopic Mass:
316.24023026
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SMILES and InChIs
SMILES:
C1C(=O)C=C2[C@H](C1)[C@@H]1[C@@H](CC2)[C@H]2[C@](CC1)([C@](CC2)(O)CC)CC
Canonical SMILES:
CC[C@]1(O)CC[C@@H]2[C@]1(CC)CC[C@H]1[C@H]2CCC2=CC(=O)CC[C@H]12
InChI:
InChI=1S/C21H32O2/c1-3-20-11-9-17-16-8-6-15(22)13-14(16)5-7-18(17)19(20)10-12-21(20,23)4-2/h13,16-19,23H,3-12H2,1-2H3/t16-,17+,18+,19-,20-,21-/m0/s1
InChIKey:
FTBJKONNNSKOLX-XUDSTZEESA-N
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Cite this record
CBID:175576 http://www.chembase.cn/molecule-175576.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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(1S,2R,10R,11S,14S,15S)-14,15-diethyl-14-hydroxytetracyclo[8.7.0.02,7.011,15]heptadec-6-en-5-one
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IUPAC Traditional name
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Synonyms
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(17α)-(+/-)-13-Ethyl-17-hydroxy-18,19-dinorpregn-4-en-3-one
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(+/-)-17α-Ethyl-18-homo-19-nortestosterone
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Genabol
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Norbolethone
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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
Data Source
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Data ID
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Price
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TRC
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CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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19.27863
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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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4.313043
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LogD (pH = 7.4)
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4.313044
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Log P
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4.313044
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Molar Refractivity
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93.7179 cm3
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Polarizability
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36.94731 Å3
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Polar Surface Area
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37.3 Å2
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Rotatable Bonds
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2
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
TRC
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Zierau, O., et al.: Steroids, 73, 1143 (2008)
- • McRobb, L., et al.: J. Steroid Biochem. Mol. Biol., 110, 39 (2008)
- • Baldwin, W., et al.: Toxicol. Sci., 107, 93 (2008)
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PATENTS
PATENTS
PubChem Patent
Google Patent