货号	规格	价格	上海	北京	珠海	重庆	武汉
V48757-1mg	≥90%	￥1570.00 V48757-1mg ￥1570.00 3-5天	0 货期：3-5天	-	-	-	-
V48757-2mg	≥90%	￥2110.00 V48757-2mg ￥2110.00 3-5天	0 货期：3-5天	-	-	-	-
V48757-5mg	≥90%	￥3150.00 V48757-5mg ￥3150.00 3-5天	0 货期：3-5天	-	-	-	-
V48757-10mg	≥90%	￥4850.00 V48757-10mg ￥4850.00 3-5天	0 货期：3-5天	-	-	-	-
V48757-25mg	≥90%	￥9010.00 V48757-25mg ￥9010.00 3-5天	0 货期：3-5天	-	-	-	-
V48757-50mg	≥90%	￥11900.00 V48757-50mg ￥11900.00 3-5天	0 货期：3-5天	-	-	-	-
V48757-100mg	≥90%	￥19000.00 V48757-100mg ￥19000.00 3-5天	0 货期：3-5天	-	-	-	-

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产品描述：

SM-164 hydrochloride is a cell-permeable Smac mimetic compound. SM-164 binds to XIAP protein containing both the BIR2 and BIR3 domains with an IC50 value of 1.39 nM and functions as an extremely potent antagonist of XIAP.

靶点：

cIAP-1:0.31 nM (Ki);cIAP-2:1.1 nM (Ki);cIAP

体外研究：

SM-164 is evaluated for its ability to inhibit tumor growth. SM-164 is highly effective in inhibition of tumor growth and capable of achieving tumor regression in the MDA-MB-231 xenograft model. Treatment with SM-164 at 1 mg/kg completely inhibits tumor growth during the treatment. Treatment with SM-164 at 5 mg/kg reduces the tumor volume from 147±54 mm3 at the beginning of the treatment (day 25) to 54±32 mm3 at the end of the treatment (day 36), a reduction of 65%. The strong antitumor activity by SM-164 is long lasting and not transient. SM-164 at 5 mg/kg is statistically more effective than Taxotere at the end of the treatment (P<0.01) or when the tumor size in the control group reaches 750 mm3 (P<0.02).

体内研究：

SM-164 is a non-peptide, cell-permeable, bivalent small-molecule, which mimics Smac protein for targeting XIAP. SM-164 binds to XIAP containing both BIR domains with an IC50 value of 1.39 nM, being 300 and 7000-times more potent than its monovalent counterparts and the natural Smac AVPI peptide, respectively. SM-164 concurrently interacts with both BIR domains in XIAP and functions as an ultra-potent antagonist of XIAP in both cell-free functional and cell-based assays. SM-164 targets cellular XIAP and effectively induces apoptosis at concentrations as low as 1 nM in leukemia cancer cells, while having a minimal toxicity to normal human primary cells at 10,000 nM[1]. The binding affinities of SM-164 to XIAP, cIAP-1, and cIAP-2 proteins are determined using fluorescence-polarization based assays. SM-164 has a Ki value of 0.56 nM to XIAP protein containing both BIR2 and BIR3 domains. SM-164 has a Ki value of 0.31 nM to cIAP-1 protein containing both BIR2 and BIR3 domains. SM-164 binds to cIAP-2 BIR3 protein with Ki values of 1.1 nM. Addition of exogenous TNFα can significantly enhance the activity of these Smac mimetics, especially for SM-164, in resistant cancer cell lines such as HCT116 and MDA-MB-453[2].

参考文献：

1. Sun H, et al. Design, synthesis, and characterization of a potent, nonpeptide, cell-permeable, bivalent Smac mimetic that concurrently targets both the BIR2 and BIR3 domains in XIAP. J Am Chem Soc. 2007 Dec 12;129(49):15279-94.
2. Lu J, et al. SM-164: a novel, bivalent Smac mimetic that induces apoptosis and tumor regression by concurrent removal of the blockade of cIAP-1/2 and XIAP. Cancer Res. 2008 Nov 15;68(22):9384-93.

保存条件：

2-8°C, 干燥

配置溶液浓度参考：

	1mg	5mg	10mg
1 mM	0.864 ml	4.318 ml	8.636 ml
5 mM	0.173 ml	0.864 ml	1.727 ml
10 mM	0.086 ml	0.432 ml	0.864 ml
50 mM	0.017 ml	0.086 ml	0.173 ml

注意：

部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。

参考文献

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