11A-HYDROXY-18-METHYL-ESTR-4-ENE-3,17-DIONE CAS#: 53067-82-6; 凯望编码 (ChemWhat Code): 1411632

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

英文名11A-HYDROXY-18-METHYL-ESTR-4-ENE-3,17-DIONE
IUPAC Name(8S,9S,10R,11R,13S,14S)-13-ethyl-11-hydroxy-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-dione 
分子结构structure of 11A-HYDROXY-18-METHYL-ESTR-4-ENE-3,17-DIONE CAS 53067-82-6
CAS编号 53067-82-6
别名11a-Hydroxy-18-methylestr-4-ene-3,17-dione
53067-82-6
(8S,9S,10R,11R,13S,14S)-13-ethyl-11-hydroxy-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-dione
SCHEMBL1422228
DTXSID10578104
11alpha-hydroxy-13-ethyl-gon-4-ene-3,17-dione
11alpha-Hydroxy-13-ethylgona-4-ene-3,17-dione
(8S,9S,11R,13S,14S)-13-Ethyl-11-hydroxy-7,8,9,10,11,12,13,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17(2H,6H)-dione (non-preferred name)
分子式C19H26O3
分子量302.4
InChIInChI=1S/C19H26O3/c1-2-19-10-16(21)18-13-6-4-12(20)9-11(13)3-5-14(18)15(19)7-8-17(19)22/h9,13-16,18,21H,2-8,10H2,1H3/t13-,14-,15-,16+,18+,19-/m0/s1  
InChI KeyJEMKJBGEAVUIOC-ZRTWPRGNSA-N 
Canonical SMILESCC[C@]12C[C@H]([C@H]3[C@H]([C@@H]1CCC2=O)CCC4=CC(=O)CC[C@H]34)O 

Physical Data

AppearanceOff-white crystalline powder
Melting Point, °C
192 – 193

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)Solvents (NMR Spectroscopy)
Chemical shifts1Hchloroform-d1
Chemical shifts, Spectrum13Cchloroform-d1
Description (IR Spectroscopy)Solvent (IR Spectroscopy)
Bandspotassium bromide
Description (UV/VIS Spectroscopy)
Absorption maxima

Route of Synthesis (ROS)

Route of Synthesis (ROS) of 11A-HYDROXY-18-METHYL-ESTR-4-ENE-3,17-DIONE CAS 53067-82-6

Route of Synthesis (ROS) of 11A-HYDROXY-18-METHYL-ESTR-4-ENE-3,17-DIONE CAS 53067-82-6

ConditionsYield
With hydrogenchloride In tetrahydrofuran; water for 2h; Reflux; Green chemistry;90%
Experimental Procedure
To a 250 ml reaction flask was added compound IV (5 g), 12N hydrochloric acid, tetrahydrofuran (100 ml).The temperature was raised to reflux, and the reaction was stirred for 2 hours; after completion of the reaction, it was neutralized with a saturated aqueous solution of sodium hydrogencarbonate.Neutral (pH=7-8), add ethyl acetate (100 ml), extract and separate,The organic phase was dried over anhydrous sodium sulfate (10 g), filtered, and evaporated to dryness. (4.5 g) Yield: 90%.

Safety and Hazards

No data available


Other Data

TransportationUnder the room temperature and away from light
HS Code
StorageUnder the room temperature and away from light
Shelf Life2 years
Market Price
Druglikeness
Lipinski rules component
分子量302.414
logP1.311
HBA3
HBD1
Matching Lipinski Rules4
Veber rules component
Polar Surface Area (PSA)54.37
Rotatable Bond (RotB)1
Matching Veber Rules2
Use Pattern
11A-HYDROXY-18-METHYL-ESTR-4-ENE-3,17-DIONE CAS:#53067-82-6 possesses antiandrogenic activity. It can bind to androgen receptors, inhibiting the action of androgens. This potential makes Mifepristone useful in the treatment of certain androgen-dependent tumors and conditions characterized by excessive androgen levels.
And 11A-HYDROXY-18-METHYL-ESTR-4-ENE-3,17-DIONE can bind to glucocorticoid receptors and display some glucocorticoid receptor antagonistic activity.

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