CAS: | 40045-50-9 | ||
分子式: | C5H3N5O2S3 | ||
分子量: | 261.29 | ||
中文名称: |
| ||
英文名称: |
|
货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||
A869156 | MACKLIN | 2-氨基-5-[(5-硝基-2-噻唑基)硫代]-1,3,4-噻二唑 | 96% | 269元/10mg; 509元/50mg; 1206元/250mg; 3211元/1g; | 展开 | ||||||||||||||||||||||||||||||||||
储存:-20°C 状态:浅黄色到琥珀色到深绿色粉末到晶体 | |||||||||||||||||||||||||||||||||||||||
A2940 | TCI | 2-Amino-5-[(5-nitro-2-thiazolyl)thio]-1,3,4-thiadiazole | >96.0%(HPLC) | 995元/20MG; | 展开 | ||||||||||||||||||||||||||||||||||
基本信息
技术规格
物性(参考值)
安全信息
| |||||||||||||||||||||||||||||||||||||||
420144 | Sigma-Aldrich | JNK Inhibitor XIII-CAS 40045-50-9-Calbiochem | The JNK Inhibitor XIII, also referenced under CAS 40045-50-9, controls the biological activity of JNK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation appli | 1954.93元/10 MG; | 展开 | ||||||||||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable non-peptidyl thiazolyl-thiadiazole alternative to pepJIP1 (TI-JIP1153-163) and TAT-pepJIP1 (Cat. Nos. 420133 & 420134, respectively) as a JIP-docking site-targeting (IC50 = 239 nM against pepJIP1 binding to JNK1) and substrate-competitive JNK inhibitor (IC50 = 700 nM against ATF2 phosphorylation by JNK1), while exhibiting little activity (IC50 >50 µM) toward p38α, Akt, furin, or lethal factor. Shown to inhibit the phosphorylation of overexpressed GFP-c-Jun in HeLa cultures upon TNF-α stimulation (IC50 = 6.23 µM) in vitro and restore insulin sensitivity in a murine of type-2 diabetes model (25 mg/kg, i.p.) in vivo. Biostability analysis with rat liver microsome preparations results in a compound half-life of 27 min at 37.5°C. 包装 Packaged under inert gas 警告 Toxicity: Standard Handling (A) 其他说明 De, S.K., et al. 2009. J. Med. Chem.52, 1943. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
产品性质
安全信息
|