
CAS 104004-96-8: Metapristone
Formula:C28H33NO2
InChI:InChI=1S/C28H33NO2/c1-4-14-28(31)15-13-25-23-11-7-19-16-21(30)10-12-22(19)26(23)24(17-27(25,28)2)18-5-8-20(29-3)9-6-18/h5-6,8-9,16,23-25,29,31H,7,10-13,15,17H2,1-3H3/t23-,24+,25-,27-,28-/m0/s1
InChI key:InChIKey=IBLXOBHABOVXDY-WKWWZUSTSA-N
SMILES:C[C@@]12[C@]([C@]3(C([C@H](C1)C4=CC=C(NC)C=C4)=C5C(CC3)=CC(=O)CC5)[H])(CC[C@]2(C#CC)O)[H]
Synonyms:- (11,17)-17-Hydroxy-11-[4-(methylamino)phenyl]-17-(1-propyn-1-yl)-estra-4,9-dien-3-one
- (11Beta)-17-Hydroxy-11-[4-(Methylamino)Phenyl]-17-(Prop-1-Yn-1-Yl)Estra-4,9-Dien-3-One
- (11β,17β)-17-Hydroxy-11-[4-(methylamino)phenyl]-17-(1-propyn-1-yl)estra-4,9-dien-3-one
- Desmethylmifepristone
- Estra-4,9-dien-3-one, 17-hydroxy-11-[4-(methylamino)phenyl]-17-(1-propyn-1-yl)-, (11β,17β)-
- Estra-4,9-dien-3-one, 17-hydroxy-11-[4-(methylamino)phenyl]-17-(1-propynyl)-, (11β,17β)-
- Metapristone
- N-Demethyl Mifepristone
- N-Demethylmifepristone
- N-Desmethyl-RU 486
- N-Methylaminopristone
- See more synonyms
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Found 7 products.
N-Demethyl Mifepristone
CAS:Applications A metabolite of Mifepristone (M343975). References Ringler, I., et al.: Metabolism, 13, 37 (1964), Gagne, D., et al.: J. Steroid. Biochem., 25, 315 (1986), Jang, G., et al.: Biochem. Pharmacol., 52, 753 (1996), Hild, S., et al.: Hum. Reprod., 15, 822 (2000), Gainer, E., et al.: Steroids, 68, 1005 (2003),Formula:C28H33NO2Color and Shape:NeatMolecular weight:415.57N-Demethyl Mifepristone-d3
CAS:Formula:C28H30D3NO2Color and Shape:Yellow SolidMolecular weight:418.60N-Demethyl Mifepristone
CAS:N-Demethyl Mifepristone (RU 42633), an active metabolite of Mifepristone, exhibits 61% of the affinity for the glucocorticoid receptor relative to Mifepristone'Formula:C28H33NO2Purity:98%Color and Shape:SolidMolecular weight:415.57N-Demethyl Mifepristone-d3
CAS:Controlled ProductFormula:C28D3H30NO2Color and Shape:NeatMolecular weight:418.586N-Demethyl mifepristone
CAS:Controlled ProductN-Demethyl mifepristone is a synthetic steroidal antiprogestin that is structurally similar to the natural progesterone. It is a prodrug of the anti-progestin, mifepristone, which is responsible for the antiprogestational effects of the drug. N-Demethyl mifepristone has been shown to have significant cytotoxicity in skin cancer cells and to inhibit epidermal growth factor-induced cell proliferation in cervical cancer cells. This drug also has pharmacokinetic properties that are different from those of mifepristone and may be less toxic than its parent compound.Formula:C28H33NO2Purity:Min. 95%Molecular weight:415.57 g/mol