HPI-1
CAS No. 599150-20-6
HPI-1 ( HPI1 )
产品货号. M15228 CAS No. 599150-20-6
HPI-1 是一种 Hedgehog (Hh) 通路抑制剂,可抑制通过 Shh 的信号传导 (IC50=1.5 uM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥563 | 有现货 |
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| 5MG | ¥907 | 有现货 |
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| 10MG | ¥1321 | 有现货 |
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| 25MG | ¥2213 | 有现货 |
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| 50MG | ¥3283 | 有现货 |
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| 100MG | ¥4437 | 有现货 |
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| 500MG | ¥8883 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥945 | 有现货 |
|
生物学信息
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产品名称HPI-1
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述HPI-1 是一种 Hedgehog (Hh) 通路抑制剂,可抑制通过 Shh 的信号传导 (IC50=1.5 uM)。
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产品描述HPI-1 is a Hedgehog (Hh) pathway inhibitor that suppresses signaling through Shh (IC50=1.5 uM) without significantly affecting Wnt signaling (IC50>30 uM); suppresses Hh activation induced by loss of Suppressor of Fused or by Gli overexpression; inhibits signaling through the oncogenic Smoothened (Smo) mutant SmoM2 in neuron precursors, preventing cell proliferation.
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体外实验GLI antagonist-1 (compound HPI-1) (0-25 μM; 72 h) shows anti-proliferative activity with IC50 values of 29, >25, 20.5 μM for SUM149, MDA-MB-231, SUM159 cells, respectively.GLI antagonist-1 (10 μM; 72 h) decreases the GLI1 mRNA expression in SUM149 cells.GLI antagonist-1 (5, 10, 20 μM) inhibits colony formation in a dose-dependent manner in SUM149 and MDA-MB-231 cells.Cell Proliferation Assay Cell Line:SUM149, MDA-MB-231, SUM159 cellsConcentration:0-25 μM Incubation Time:72 h Result:Showed anti-proliferative activity with IC50 values of 29, >25, 20.5 μM for SUM149, MDA-MB-231, SUM159 cells, respectively.
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体内实验——
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同义词HPI1
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通路GPCR/G Protein
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靶点Hedgehog (Hh)
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受体Hedgehog (Hh)
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研究领域——
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适应症——
化学信息
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CAS Number599150-20-6
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分子量463.5
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分子式C27H29NO6
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纯度>98% (HPLC)
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溶解度——
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SMILESCC1=C(C(C2=C(N1)CC(CC2=O)C3=CC=CC=C3OC)C4=CC(=CC=C4)O)C(=O)OCCOC
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化学全称1,4,5,6,7,8-Hexahydro-4-(3-hydroxyphenyl)-7-(2-methoxyphenyl)-2-methyl-5-oxo-3-quinolinecarboxylic acid 2-methoxyethyl ester
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Hyman JM, et al. Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):14132-7.
2. Xu Y, et al. Clin Cancer Res. 2012 Mar 1;18(5):1291-302.
3. Chenna V, et al. Mol Cancer Ther. 2012 Jan;11(1):165-73.
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