e-Drug3D 781 |
MIFEPRISTONE
|
cas 84371-65-3 |
CLASS GENITO |
ROUTE (list) ORAL |
PK parameters F 69 PERCENT Solubility POORLY SOLUBLE IN WATER |
Target TARGET PROGESTERONE RECEPTOR PDB Ligand code = 486 (link to the list of PDB complexes) Download experimental 3D coordinates of 486 with added hydrogens |
DrugCentral Glucocorticoid receptor UNIPROT P04150 NR3C1 Progesterone receptor UNIPROT P06401 PGR |
Download SDF file | (8S,11R,13S,14S,17S)-11-(4-dimethylaminophenyl)-17-hydroxy-13-methyl-17-prop-1-ynyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one Formula: Calculated chemical properties: MW 429.58 NB_atoms 32 XLogP 5.41 PSA 40.9 NB_HD 1 NB_HA 3 fsp3 0.55 Lipinski(0=no;1=yes) 0 |
FDA NDA 020687 (pdf not found) INN (MIFEPRISTONE) MIFEPREX (DANCO LABS LLC) APPROVAL= AP YEAR= 2000 NDA 202107 (pdf not found) INN (MIFEPRISTONE) KORLYM (CORCEPT THERAP) APPROVAL= AP YEAR= 2012 NDA 091178 (pdf not found) INN (MIFEPRISTONE) MIFEPRISTONE (GENBIOPRO) APPROVAL= AP YEAR= 2019 NDA 211436 (pdf not found) INN (MIFEPRISTONE) MIFEPRISTONE (TEVA PHARMS USA INC) APPROVAL= AP YEAR= 2020 |
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