Chemical Structure : Olaparib
CAS No.: 763113-22-0
货号: PC-42410Not For Human Use, Lab Use Only.
Olaparib (AZD2281, KU-0059436) is a potent, specific, and orally active PARP inhibitor with IC50 of 5 and 1 nM for PARP1 and PARP2, respectively.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
50 mg | ¥980 | In stock | |
100 mg | ¥1580 | In stock | |
250 mg | ¥2580 | In stock | |
1 g | Get quote |
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Olaparib (AZD2281, KU-0059436) is a potent, specific, and orally active PARP inhibitor with IC50 of 5 and 1 nM for PARP1 and PARP2, respectively.
Olaparib (AZD2281, KU-0059436) displays 300-fold selectivity over tankyrase (TNKS-1 IC50=1.5 uM).
Olaparib (AZD2281, KU-0059436) shows standalone activity against BRCA1-deficient breast cancer cell lines.
Olaparib (AZD2281, KU-0059436) regresses autochthonous Brca2/p53-mutant mammary tumors in vivo and delays tumor relapse in combination with carboplatin.
分子量 | 434.4628 | |
分子式 | C24H23FN4O3 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: 29 mg/mL |
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Chemical Name/SMILES |
1(2H)-Phthalazinone, 4-[[3-[[4-(cyclopropylcarbonyl)-1-piperazinyl]carbonyl]-4-fluorophenyl]methyl]- |
1. Menear KA, et al. J Med Chem. 2008 Oct 23;51(20):6581-91.
2. Evers B, et al. Clin Cancer Res. 2008 Jun 15;14(12):3916-25.
3. Rottenberg S, et al. Proc Natl Acad Sci U S A. 2008 Nov 4;105(44):17079-84.
4. Hay T, et al. Cancer Res. 2009 May 1;69(9):3850-5.
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