TC-E 5008

Discontinued Product

5244 has been discontinued.

View all Isocitrate Dehydrogenase 1 (IDH1) products.
说明: Selective mutant isocitrate dehydrogenase 1 (mIDH1) inhibitor; phenotypically lethal
别名: SYC 435
化学名: 1-Hydroxy-4-methyl-6-(phenylmethyl)-2-(1H)pyridinone
说明书
引用文献
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文献 (4)

生物活性 for TC-E 5008

TC-E 5008 is a selective mutant isocitrate dehydrogenase 1 (mIDH1) inhibitor (Ki = 120-190 nM). Displays >60-fold selectivity for mIDH1 (found in ~75% of gliomas) over wild type IDH1. Also inhibits D-2-hydroxyglutaric acid in cells expressing mIDH1 (EC50 = 2.4 μM). Does not display cytotoxicity towards non-cancerous human cells. Phenotypically lethal.

技术数据 for TC-E 5008

分子量 215.25
公式 C13H13NO2
储存 Store at +4°C
CAS Number 50405-58-8
PubChem ID 13590964
InChI Key AVLZAVSZOAQKRC-UHFFFAOYSA-N
Smiles O=C1C=C(C)C=C(CC2=CC=CC=C2)N1O

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

参考文献 for TC-E 5008

参考文献是支持产品生物活性的出版物。

Zheng et al (2013) Crystallographic investigation and selective inhibition of mutant isocitrate dehydrogenase. ACS Med.Chem.Lett. 4 542 PMID: 23795241

关键词: TC-E 5008, TC-E 5008 supplier, TC-E5008, selective, mutant, isocitrate, dehydrogenase, 1, (IDH1), inhibitors, inhibits, phenotypically, lethal, cancer, gliomas, D-2-hydroxyglutaric, acid, SYC435, SYC, 435, Isocitrate, 5244, Tocris Bioscience

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