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(1S,2R,8R,10R,11S,14R,15S)-14-acetyl-8-(2H3)methyl-2,15-dimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadec-6-en-14-yl (2H3)acetate
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ChemBase ID:
172604
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Molecular Formular:
C24H34O4
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Molecular Mass:
386.52436
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Monoisotopic Mass:
386.24570957
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SMILES and InChIs
SMILES:
C1C(=O)C=C2[C@](C1)([C@@H]1[C@@H](C[C@H]2C)[C@H]2[C@](CC1)([C@](CC2)(C(=O)C)OC(=O)C)C)C
Canonical SMILES:
O=C1CC[C@]2(C(=C1)[C@H](C)C[C@@H]1[C@@H]2CC[C@]2([C@H]1CC[C@]2(OC(=O)C)C(=O)C)C)C
InChI:
InChI=1S/C24H34O4/c1-14-12-18-19(22(4)9-6-17(27)13-21(14)22)7-10-23(5)20(18)8-11-24(23,15(2)25)28-16(3)26/h13-14,18-20H,6-12H2,1-5H3/t14-,18-,19+,20+,22-,23+,24+/m1/s1
InChIKey:
PSGAAPLEWMOORI-BMHIUQAOSA-N
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Cite this record
CBID:172604 http://www.chembase.cn/molecule-172604.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
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IUPAC name
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(1S,2R,8R,10R,11S,14R,15S)-14-acetyl-8-(2H3)methyl-2,15-dimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadec-6-en-14-yl (2H3)acetate
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IUPAC Traditional name
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(1S,2R,8R,10R,11S,14R,15S)-14-acetyl-8-(2H3)methyl-2,15-dimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadec-6-en-14-yl (2H3)acetate
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Synonyms
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U 8839-d6
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Veramix-d6
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Medroxy Progesterone-d6 17-Acetate
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(6α)-17-(Acetyloxy)-6-methyl-pregn-4-ene-3,20-dione-d6
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17α-Acetoxy-6α-methylpregn-4-ene-3,20-dione-d6
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17α-Acetoxy-6α-methyl-progesterone-d6
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17α-Hydroxy-6α-methylprogesterone-d6 Acetate
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Meprate-d6
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Metigestrona-d6
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NSC 26386-d6
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Nadigest-d6
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Nidaxin-d6
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Novo-Medrone-d6
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Oragest-d6
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Prodasone-d6
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Progespon-d6
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Progestalfa-d6
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Progeston-d6
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Progevera-d6
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Provera-d6
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Ralovera-d6
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Repromap-d6
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Repromix-d6
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Sirprogen-d6
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Sodelut G-d6
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
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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
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Acid pKa
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17.821218
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H Acceptors
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3
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H Donor
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0
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LogD (pH = 5.5)
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4.129324
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LogD (pH = 7.4)
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4.129324
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Log P
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4.129324
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Molar Refractivity
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107.8054 cm3
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Polarizability
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42.687153 Å3
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Polar Surface Area
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60.44 Å2
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Rotatable Bonds
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3
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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
- • Tang, M., et al.: Endocrinol., 151, 1320 (2010)
- • Lee, K., et al.: Mol. Cell. Endocrinol., 319, 109 (2010)
- • Rodgers, A., et al.: Chem., Res. Toxicol., 23, 724 (2010)
- • Gohil, V., et al.: Nat. Biotechnol., 28, 249 (2010)
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PATENTS
PATENTS
PubChem Patent
Google Patent