Mifepristone-d3

目录号: GC47674纯度: >99.00%同义词: RU486-d3; RU 38486-d3
A neuropeptide with diverse biological activities

Mifepristone-d3
Cas No.: N/A
规格价格库存数量操作
500 μg¥3,203.00现货
1
1 mg¥6,049.00现货
1

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产品描述 Description

Mifepristone-d3 is intended for use as an internal standard for the quantification of mifepristone by GC- or LC-MS. Mifepristone is an antagonist of glucocorticoid, progesterone, and androgen receptors (Kis = 0.1, 0.64, and 0.65 nM, respectively).1,2,3 It is selective for these receptors over the mineralocorticoid receptor (MR), estrogen receptor α (ERα), and ERβ (Kis = 640, >200, and >750 nM, respectively).1 In cell-based assays, mifepristone inhibits alkaline phosphatase activity stimulated by the progesterone receptor agonist R5020 as well as reporter transcription stimulated by either dexamethasone or R5020 (IC50s = 7, 5.9, and 1.3 nM, respectively).3 It also inhibits synthetic androgen R1881-stimulated reporter transcription in a concentration-dependent manner.2 Mifepristone (10 µM) inhibits growth of 4-OHT-resistant MCF-7 breast cancer cells in vitro.4 It also inhibits tumor growth in an SKOV3 ovarian cancer nude mouse xenograft model when administered at doses of 0.5 or 1 mg per day.5 Formulations containing mifepristone have been used for the induction of medical abortions.

1.von Gerldern, T.W., Tu, N., Kym, P.R., et al.Liver-selective glucocorticoid antagonists: A novel treatment for type 2 diabetesJ. Med. Chem.47(17)4213-4230(2004) 2.Song, L.-N., Coghlan, M.J., and Gelmann, E.P.Antiandrogen effects of mifepristone on coactivator and corepressor interactions with the androgen receptorMol. Endocrinol.18(1)70-85(2004) 3.Attardi, B.J., Burgenson, J., Hild, S.A., et al.In vitro antiprogestational/antiglucocorticoid activity and progestin and glucocorticoid receptor binding of the putative metabolites and synthetic derivatives of CDB-2914, CDB-4124, and mifepristoneJ. Steroid Biochem. Mol. Biol.88(3)277-288(2004) 4.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 cellsClinical Cancer Research105215-5225(2004) 5.Goyeneche, A.A., CarÓn, R.W., and Telleria, C.M.Mifepristone inhibits ovarian cancer cell growth in vitro and in vivoClin. Cancer Res.13(11)3370-3379(2007)

产品文档 Product Documents

Purity:>99.00%Appearance:A solid

化学性质Chemical Properties

CAS 号
N/A
同义词
RU486-d3; RU 38486-d3
SMILES
O=C1CCC(C(CC2)=C1)=C([C@]2([H])[C@@](CC[C@]3(C#CC)O)([H])[C@]3(C)C4)[C@H]4C5=CC=C(N(C([2H])([2H])[2H])C)C=C5
分子式
C29H32D3NO2
分子量
432.6 g/mol
溶解性
Chloroform: Soluble,Methanol: Soluble
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol