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Join us! · InformexUSA 2012 · New Orleans, Louisiana · February 14-17, 2012 · Booth 2514

Mifepristone

Cayman Chemical Item Number 10006317

RU-486 (CAS 84371-65-3)

Mifepristone (CAS 84371-65-3)

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Description

Progesterone is responsible for preparing the uterine lining for implantation of a fertilized ovum and to maintain pregnancy, eliciting its action through the nuclear progesterone receptor (PR). Mifepristone is a potent PR and glucocorticoid receptor (GR) antagonist with Ki values of approximately 1 nM.1 It is used in combination with misoprostol for the oral induction of first trimester abortions.1 Mifepristone promotes efficient binding of PR to hormone response elements (HRE) on DNA, but prevents transcriptional activation of the receptor.2,3,4 The IC50 of mifepristone for PR dimerization and activation is 0.6 nM; the IC50 for mifepristone-induced competitive binding of wild-type PR with a constitutively active PR for HRE is 0.01 nM.2 In anti-estrogen-resistant breast cancer cells, mifepristone induces growth arrest, caspase activation, and cell death, indicating the effectiveness of PR antagonism as a novel approach to treatment of select cancers.5

1 Cadepond, F., Ulmann, A., and Baulieu, E. RU486 (mifepristone): Mechanisms of action and clinical uses. Annu Rev Med 48 129-156 (1997).

2 Delabre, K., Guiochon-Mantel, A., and Milgrom, E. In vivo evidence against the existence of antiprogestins disrupting receptor binding to DNA. Proc Natl Acad Sci USA 90 4421-4425 (1993).

3 Beck, C.A., Estes, P.A., Bona, B.J., et al. The steroid antagonist RU486 exerts different effects on the glucocorticoid and progesterone receptors. Endocrinology 133(2) 728-740 (1993).

4 Edwards, D.P., Altmann, M., DeMarzo, A., et al. Progesterone receptor and the mechanism of action of progesterone antagonists. J Steroid Biochem Mol Biol 53(1-6) 449-458 (1995).

5 Gaddy, V.T., Barrett, J.T., Delk, J.N., et al. Mifepristone induces growth arrest, caspase activation, and apoptosis of estrogen receptor-expressing, antiestrogen-resistant breast cancer cells. Clin Cancer Res 10 5215-5225 (2004).

Synonyms
  • RU-486
Formal Name 11β-​[4-​(dimethylamino)phenyl]-​17β-​hydroxy-​17-​(1-​propynyl)-​estra-​4,​9-​dien-​3-​one
CAS Number 84371-65-3
Molecular Formula C29H35NO2
Formula Weight 429.6
Formulation A crystalline solid
Purity >98%
λmax 204, 261, 303 nm
Stability 2 years
Storage -20°C
Shipping Room temperature in continental US; may vary elsewhere
SMILES
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CN(C)​C1=CC=C(C=C1)​[C@H]​2C[C@@]​3(C)​[C@]​(CC[C@]​3(C#CC)​O)​([H]​)​[C@]​4([H]​)​CCC5=CC(CCC5=C42)​=O

Background Reading

Delabre, K., Guiochon-Mantel, A., and Milgrom, E. In vivo evidence against the existence of antiprogestins disrupting receptor binding to DNA. Proc Natl Acad Sci USA 90 4421-4425 (1993).

Edwards, D.P., Altmann, M., DeMarzo, A., et al. Progesterone receptor and the mechanism of action of progesterone antagonists. J Steroid Biochem Mol Biol 53(1-6) 449-458 (1995).

Beck, C.A., Estes, P.A., Bona, B.J., et al. The steroid antagonist RU486 exerts different effects on the glucocorticoid and progesterone receptors. Endocrinology 133(2) 728-740 (1993).

Cadepond, F., Ulmann, A., and Baulieu, E. RU486 (mifepristone): Mechanisms of action and clinical uses. Annu Rev Med 48 129-156 (1997).

Gaddy, V.T., Barrett, J.T., Delk, J.N., et al. Mifepristone induces growth arrest, caspase activation, and apoptosis of estrogen receptor-expressing, antiestrogen-resistant breast cancer cells. Clin Cancer Res 10 5215-5225 (2004).

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Mifepristone is available in the following screening library:

Size Price Quantity Subtotal
100 mg $19.00 $0.00
500 mg $86.00 $0.00
1 g $152.00 $0.00
5 g $665.00 $0.00
Bulk Contact
Cart Total $0.00

This product is available in custom sizes and/or larger quantities.

Please contact our Sales Department for a quote or to purchase.

Pricing updated 2012-02-12. Prices are subject to change without notice.

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Warning This product is not for human or veterinary use.

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