Ulipristal Acetate

CAS : 126784-99-4

Ref. TR-U700810

Informations sur le produit

• Nom: Ulipristal Acetate
• Synonymes: [(8S,11R,13S,14S,17R)-17-acetyl-11-[4-(dimethylamino)phenyl]-13-methyl-3-oxo-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-yl] acetate, (11Beta,17Alpha)-17-Acetyl-11-[4-(Dimethylamino)Phenyl]-3-Oxoestra-4,9-Dien-17-Yl Acetate, (11β)-17-(Acetyloxy)-11-[4-(dimethylamino)phenyl]-19-norpregna-4,9-diene-3,20-dione, 17-Acetoxy-11β-[(4-(N,N-dimethylamino)phenyl]-19-norpregna-4,9-diene-3,20-dione, 17-Acetoxy-11β-[(4-(dimethylamino)phenyl]-19-norpregna-4,9-diene-3,20-dione, 17-Acetyloxy-11β-[(4-(N,N-dimethylamino)phenyl]-19-norpregna-4,9-diene-3,20-dione, 17α-Acetoxy-11β-(4-dimethylaminophenyl)-19-norpregna-4,9-dien-3,20-dione, 17α-Acetoxy-11β-[4-N,N-dimethylaminophenyl]-19-norpregna-4,9-diene-3,20-dione, 19-Norpregna-4,9-diene-3,20-dione, 17-(acetyloxy)-11-[4-(dimethylamino)phenyl]-, (11β)-, Cbd(Va) 2914, Cdb-2914, EllaOne, Esmya, Hrp 2000, Rti-3021-012, Ru 44675, Ulipristal,Ella, Va 2914

Description

Applications Ulipristal acetate is a selective progesterone receptor modulator. Ulipristal acetate is used during pregnancy.
References Gronemeijer, H., et al.: J. Steroid Biochem., 40, 271 (1991), Spitz, I., et al.: Contraception, 48, 403 (1993), Conneely, O., et al.: Steroids, 68, 771 (2003), Chwalisz, K., et al.: Endocr. Rev., 26, 423 (2005),

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 475.62
• Formule: C₃₀H₃₇NO₄
• Couleur/Forme: Neat
• InChI: InChI=1S/C30H37NO4/c1-18(32)30(35-19(2)33)15-14-27-25-12-8-21-16-23(34)11-13-24(21)28(25)26(17-29(27,30)3)20-6-9-22(10-7-20)31(4)5/h6-7,9-10,16,25-27H,8,11-15,17H2,1-5H3/t25-,26+,27-,29-,30-/m0/s1
• Code InChI: InChIKey=OOLLAFOLCSJHRE-ZHAKMVSLSA-N
• SMILES: CC(=O)O[C@]1(C(C)=O)CC[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(N(C)C)cc3)C[C@@]21C