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PKI-179

    
10mM in DMSO

源叶(MedMol)
V56987 一键复制产品信息
1197160-28-3
C25H28N8O3
488.54
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V56987-1ml
10mM in DMSO

¥2210.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: PKI-179 is a potent and orally active dual PI3K/mTOR inhibitor, with IC50s of 8 nM, 24 nM, 74 nM, 77 nM, and 0.42 nM for PI3K-α, PI3K-β, PI3K-γ, PI3K-δ and mTOR, respectively. PKI-179 also exhibits activity over E545K and H1047R, with IC50s of 14 nM and 11 nM, respectively. PKI-179 shows anti-tumor activity in vivo.
靶点: PI3Kα:8 nM (IC50); PI3Kβ:24 nM (IC50); PI3Kγ:74 nM (IC50); PI3Kδ:77 nM (IC50); mTOR:0.42 nM (IC50); E545K:14 nM (IC50); H1047R:11 nM (IC50)
体外研究: PKI-179 (5-50 mg/kg; p.o. once daily for 40 days) inhibits the tumor growth and is well tolerated in nude mice bearing MDA-361 human breast cancer tumors[1].
PKI-179 (50 mg/kg; p.o.) results in good inhibition of PI3K signaling in nude mice bearing MDA361 tumor xenografts[1].
PKI-179 exhibits good oral bioavailability (98% in nude mouse, 46% in rat, 38% in monkey, and 61% in dog) and a high half-life (>60 min) [1].
体内研究: PKI-179 inhibits the cell proliferation, with IC50s of 22 nM and 29 nM for MDA361 and PC3 cells, respectively.
PKI-179 shows inhibitory activity against a panel of 361 other kinases, hERG and cytochrome P450 (CYP) isoforms at concentrations up to >30 μM, but does have activity for CYP2C8 (IC50=3 μM).
参考文献: 1. Venkatesan AM, et, al. PKI-179: an orally efficacious dual phosphatidylinositol-3-kinase (PI3K)/mammalian target of rapamycin (mTOR) inhibitor. Bioorg Med Chem Lett. 2010 Oct 1;20(19):5869-73.
2. Rehan M. A structural insight into the inhibitory mechanism of an orally active PI3K/mTOR dual inhibitor, PKI-179 using computational approaches. J Mol Graph Model. 2015 Nov;62:226-234.
 
保存条件: -80°C 6个月;-20°C 1个月
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.047 ml 10.235 ml 20.469 ml
5 mM 0.409 ml 2.047 ml 4.094 ml
10 mM 0.205 ml 1.023 ml 2.047 ml
50 mM 0.041 ml 0.205 ml 0.409 ml
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参考文献

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摩尔浓度计算器

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