| CAS: | 6960-45-8 | ||
| 分子式: | C9H6N2O4 | ||
| 分子量: | 206.15 | ||
| 熔点: | 260-264℃ | ||
| 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 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| N859038 | MACKLIN | 7-硝基吲哚-2-甲酸 | 98% | 43元/250mg; 145元/1g; 494元/5g; 2362元/25g; 7086元/100g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||
储存:室温,干燥 状态:橙色到棕色粉末或晶体 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| N795864 | MACKLIN | 7-硝基吲哚-2-甲酸 | 10mM in DMSO | 684元/1ml; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| B20786 | Alfa Aesar | 7-Nitroindole-2-carboxylic acid | 96% | 1502元/1g; 5953元/5g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||
基本信息 MDL EINECS 分子式 分子量 熔点 形态 GHS危害和防范说明 GHS符号 Hazard Statements Precautionary Statements 安全信息 危险类别 安全等级 TSCA | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| C0496 | Sigma-Aldrich | CRT0044876 | ≥98% (HPLC) | 860.47元/10 MG; 3353.99元/50 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 包装 10, 50 mg in glass bottle 生化/生理作用 APE1 的作用靶点是脱嘌呤核酸内切酶 (APE1),抑制其 3′-磷酸二酯酶和 3′-磷酸酶活性——切除修复的基本步骤——即使在浓度高达 100 μg 时,对核酸内切酶 IV、BamH1 限制性内切酶或拓扑异构酶 I 的影响极小在非细胞毒性浓度下,CRT0044876 可增强几种 DNA 碱基靶向化合物的细胞毒性,使脱嘌呤位点蓄积。 基本信息
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| 262015 | Sigma-Aldrich | DNA Base Excision Repair Pathway Inhibitor-CAS 6960-45-8-Calbiochem | The DNA Base Excision Repair Pathway Inhibitor, also referenced under CAS 6960-45-8, controls the biological activity of APE1 (human apurinic/apyrimidinic endonuclease. | 1709.38元/25 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable, potent, specific, and nontoxic inhibitor of the DNA repair enzyme, APE1 (human apurinic/apyrimidinic endonuclease; IC50 = ~3 µM). Shown to target the APE1 active site and inhibit its 3′-phosphodiesterase and 3′-phosphatase activities. Exhibits minimal effects on endonuclease IV, BamH1 restriction endonuclease, or topoisomerase I even at concentration as high as 100 µM. Also shown to potentiate the cytotoxicity of several DNA damaging agents, such as MMS, temozolomide, Zeocin, and H2O2 in HeLa, HT1080, and MDA-MB-231 cells. 包装 25 mg in Plastic ampoule 生化/生理作用 Cell permeable: yes 警告 Toxicity: Irritant (B) 重悬 Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C. 其他说明 Madhusudan, S., et al. 2005. Nucl. Acids Res.33, 4711. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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| 066301 | Fluorochem | 7-Nitro-1H-indole-2-carboxylic acid | 97% | 572元/250mg; 1056元/1g; 3080元/5g; 9284元/25g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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