| CAS: | 129-56-6 | ||||||
| 分子式: | C14H8N2O | ||||||
| 分子量: | 220.23 | ||||||
| 沸点: | 489.3ºC | ||||||
| 熔点: | 281~282 °C | ||||||
| 英文名称: |
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| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||||||||||
| H859104 | MACKLIN | 吡唑蒽酮 | 98% | 270元/250mg; 445元/1g; 1450元/5g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
储存:室温,干燥 状态:黄色固体 | |||||||||||||||||||||||||||||||||||||||||||||||
| H794775 | MACKLIN | 吡唑蒽酮 | 10mM in DMSO | 339元/1ml; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||||||||||||||
| A2548 | TCI | Anthra[1,9-cd]pyrazol-6(2H)-one | >95.0%(HPLC) | 590元/25MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
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| 983585 | J&K | Anthra[1,9-cd]pyrazol-6(2H)-one | 98% | 575元/25MG; 1437元/100MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
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| 420119 | Sigma-Aldrich | JNK Inhibitor II-CAS 129-56-6-Calbiochem | JNK Inhibitor II. SP600125, CAS 129-56-6, is a potent, cell-permeable, selective, and ATP competitive inhibitor of c-Jun N-terminal kinase (JNK; IC₅₀ = 40 nM for JNK-1 & JNK-2 & 90 | 1271.18元/5 MG; 3945.15元/25 MG; 6127.99元/50 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 A potent, cell-permeable, selective, and reversible inhibitor of c-Jun N-terminal kinase (JNK) (IC50 = 40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3). The inhibition is competitive with respect to ATP. Exhibits over 300-fold greater selectivity for JNK as compared to ERK1 and p38-2 MAP kinases. Inhibits the phosphorylation of c-Jun and blocks the expression of IL-2, IFN-γ, TNF-α, and COX-2 in cells. Blocks IL-1-induced accumulation of phospho-Jun and induction of c-Jun transcription. 包装 5, 25, 50 mg in Plastic ampoule 生化/生理作用 Target IC50: 40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3 警告 Toxicity: Standard Handling (A) 制备说明 For every 10 µM concentration of JNK Inhibitor II, include 0.1% DMSO in the culture medium. Pre-warming of culture medium and addition of BSA to the medium may enhance its solubility. 重悬 Following reconstitution, aliquot and freeze at -20°C. Stock solutions are stable for up to 2 months at -20°C. 其他说明 Shin, M., and Boyd, Y.D. 2002. Biochim. Biophys. Acta1589, 311. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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| S5567 | Sigma-Aldrich | SP600125 | ≥98% (HPLC) | 1521.75元/10 MG; 6419.98元/50 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
产品说明 应用 C2C12肌原细胞经过SP600125处理后,被用来测试肌生成激细胞活。11它用于处理HepG2处理,测试在氧化胆固醇诱导坏死效果。12 生化/生理作用 SP600125是一种JNK的吡唑蒽酮抑制剂,和ATP竞争性抑制c-Jun的磷酸化。它能够避免炎症基因比如, COX-2, IL-2 IFN-γ和TNF-α.8,9活化。在脑缺血后它能够避免JNK激活,对缺血性中风有治疗作用。10 基本信息
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| M02529 | Fluorochem | 1,9-Pyrazoloanthrone | >98% | 550元/1g; 1496元/5g; 2442元/10g; 4620元/25g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
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