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MedKoo product information:

Mifepristone

MedKoo Code#: 201870

Name: Mifepristone

CAS#:  84371-65-3

 

Synonym:  Mifegyne;Mifepriston;Pictovir;Mifepristonum;Prestwick_570;Mifepristona C-1073 ;RU-486。 Corlux™;MifeprexŇ。11β-[p-(Dimethylamino)phenyl]-17β-hydroxy-17-(1-propynyl)estra-4,9-dien-3-one

 

IUPAC/Chemical name: 

(8S,11R,13S,14S,17S)-11-(4-(dimethylamino)phenyl)-17-hydroxy-13-methyl-17-(prop-1-yn-1-yl)-6,7,8,11,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one

 

Chemical structure: Theoretical analysis

 

 

Chemical Formula: C29H35NO2

Exact Mass: 429.26678

Molecular Weight: 429.59

m/z: 429.26678 (100.0%), 430.27013 (31.4%), 431.27349 (4.7%)

 Elemental Analysis: C, 81.08; H, 8.21; N, 3.26; O, 7.45

 

Availability and price:

This agent is not in stock, which may be available through custom synthesis. To inquire quotation and lead time or to ask questions, please send email to sales@medkoo.com to describe your needs. A representative will respond your email shortly. We offer big discount for orders of bulk quantities.

 

Quality control data:

Product will be shipped with supporting analytical data.

 

 

Information about this agent

Mifepristone is a synthetic steroid compound used as a pharmaceutical. It is used as an abortifacient in the first two months of pregnancy, and in smaller doses as an emergency contraceptive. During early trials, it was known as RU-486, its designation at the Roussel Uclaf company, which designed the drug. The drug was initially made available in France, and other countries then followed—often amid controversy. It is marketed under tradenames Mifegyne and Mifeprex.

 

According to http://en.wikipedia.org/wiki/Mifepristone, the compound was discovered by researchers at Roussel Uclaf of France in 1980 (the "RU" in RU-486) while they were studying glucocorticoid receptor antagonists. Étienne-Émile Baulieu recognized its anti-progesterone activities and saw its potential for the induction of a medical abortion. Clinical testing began in 1982. The drug was first licensed in France in 1988, for use in combination with a prostaglandin, under the name Mifegyne.

 

Mifegyne is sold outside the U.S. by Exelgyn Laboratories, made in France, and is approved for:
1. Medical termination of intrauterine pregnancies of up to 49 days gestation (up to 63 days gestation in Britain and Sweden); 2. Softening and dilatation of the cervix prior to mechanical cervical dilatation for pregnancy termination; 3. Use in combination with gemeprost for termination of pregnancies between 13 and 24 weeks gestation; 4. Labor induction in fetal death in utero.

Mifeprex is sold in the U.S. by Danco Laboratories, made in China, and is U.S. Food and Drug Administration-approved to terminate intrauterine pregnancies of up to 49 days gestation.  see http://en.wikipedia.org/wiki/Mifepristone.  

 

 

Other medical applications of mifepristone that have been studied in Phase II clinical trials include regular long-term use as an oral contraceptive, and treatment of: uterine fibroids, endometriosis, major depression with psychotic features, glaucoma, meningiomas, breast cancer, ovarian cancer, and prostate cancer. Mifepristone has been used to treat Cushing's syndrome with treatment durations being as long as 10 years without noticeable adverse effect.

Current developer:    Corcept Therapeutics Inc

 

References

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25: Obert M, Pleuger H, Hanagarth HG, Schulte-Mönting J, Wiesmüller KH, Braun DG, Brandner G, Hess RD. Protection of mice against SV40 tumours by Pam3Cys, MTP-PE and Pam3Cys conjugated with the SV40 T antigen-derived peptide, K(698)-T(708). Vaccine. 1998 Jan-Feb;16(2-3):161-9. PubMed PMID: 9607025.

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28: Dieter P, Ambs P, Fitzke E, Schwende H. Lipopolysaccharide and liposome-encapsulated MTP-PE-induced cytotoxicity and release of eicosanoids, tumor necrosis factor- alpha and nitric oxide in liver macrophages. Adv Exp Med Biol. 1997;407:485-90. PubMed PMID: 9321995.

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43: Galligioni E, Favaro D, Santarosa M, Quaia M, Spada A, Freschi A, Alberti D.

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57: Bui T, Dykers T, Hu SL, Faltynek CR, Ho RJ. Effect of MTP-PE liposomes and interleukin-7 on induction of antibody and cell-mediated immune responses to a recombinant HIV-envelope protein. J Acquir Immune Defic Syndr. 1994 Aug;7(8):799-806. PubMed PMID: 8021814.

58: Ding JW, Andersson R, Soltesz VL, Pärsson H, Johansson K, Wang W, Bengmark S. Inhibition of bacterial translocation in obstructive jaundice by muramyl tripeptide phosphatidylethanolamine in the rat. J Hepatol. 1994 Jun;20(6):720-8.

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72: Asano T, Fujimaki W, McWatters A, An T, Matsushima K, Kleinerman ES. Effect of Adriamycin on liposomal muramyl tripeptide's ability to up-regulate monocyte cytokine expression. Cancer Immunol Immunother. 1993 Nov;37(6):408-11. PubMed PMID: 8242665.

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77: Maeda M, Asano T, Kleinerman ES. Anti-(tumor necrosis factor) alters the response of human monocytes to liposomal muramyl tripeptide. Cancer Immunol Immunother. 1993 Aug;37(3):203-8. PubMed PMID: 8334682.

78: Seger M, Gold D, Lengy J, Pauli H, Keisari Y. The schistosomulicidal activity and the production of IL-1 and TNF-alpha by peritoneal macrophages from infected

mice and their potentiation by muramyl tripeptide-phosphatidyl ethanolamine (MTP-PE) treatment. Parasite Immunol. 1993 Jun;15(6):339-47. PubMed PMID: 8361776.

79: Hoedemakers RM, Vossebeld PJ, Daemen T, Scherphof GL. Functional characteristics of the rat liver macrophage population after a single intravenous injection of liposome-encapsulated muramyl peptides. J Immunother Emphasis Tumor

Immunol. 1993 May 4;13(4):252-60. PubMed PMID: 8334109.

80: Teske E, Rutteman GR. Liposome-enhanced tumour therapy in canine mammary gland tumours. Tijdschr Diergeneeskd. 1993 Mar;118 Suppl 1:32S-33S. Review. PubMed PMID: 8480312.

81: Fujimaki W, Griffin JR, Kleinerman ES. Effect of ibuprofen on monocyte activation by liposome-encapsulated muramyl tripeptide phosphatidylethanolamine (CGP 19835A): can ibuprofen reduce fever and chills without compromising immune stimulation? Cancer Immunol Immunother. 1993;36(1):45-51. PubMed PMID: 8422667.

82: Melissen PM, van Vianen W, Bidjai O, van Marion M, Bakker-Woudenberg IA. Free versus liposome-encapsulated muramyl tripeptide phosphatidylethanolamide (MTPPE)

and interferon-y (IFN-y) in experimental infection with Listeria monocytogenes. Biotherapy. 1993;6(2):113-24. PubMed PMID: 8398570.

83: Macková NO, Fedorocko P. Pre- and postirradiation hemopoietic effects of liposomal muramyl tripeptide phosphatidylethanolamine (MTP-PE) administered to C57Bl/6 mice before irradiation. Neoplasma. 1993;40(6):379-85. PubMed PMID: 8289971.

84: Keitel W, Couch R, Bond N, Adair S, Van Nest G, Dekker C. Pilot evaluation of influenza virus vaccine (IVV) combined with adjuvant. Vaccine. 1993;11(9):909-13. PubMed PMID: 8212835.

85: Kleinerman ES, Maeda M, Jaffe N. Liposome-encapsulated muramyl tripeptide: a

new biologic response modifier for the treatment of osteosarcoma. Cancer Treat Res. 1993;62:101-7. Review. PubMed PMID: 8096724.

86: Melissen PM, van Vianen W, Leenen PJ, Bakker-Woudenberg IA. Tissue distribution and cellular distribution of liposomes encapsulating muramyltripeptide phosphatidyl ethanolamide. Tissue and cellular distribution of

LE-MTPPE. Biotherapy. 1993;7(1):71-8. Erratum in: Biotherapy 1994;8(1):85. PubMed PMID: 8068486.

87: Landmann R, Obrist R, Denz H, Ludwig C, Frost H, Wesp M, Rordorf C, Towbin H, Gygax D, Tarcsay L, et al. Pharmacokinetics and immunomodulatory effects on monocytes during prolonged therapy with liposomal muramyltripeptide. Biotherapy.

1993;7(1):1-12. PubMed PMID: 8068481.

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