| CAS: | 1986-47-6 | |
| 分子式: | C9H11N·HCl | |
| 分子量: | 169.65 | |
| 熔点: | 162-169℃ | |
| 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 | ||||||||||||||||||||||||||||||||||||||||||||||||
| P832943 | MACKLIN | 反式-2-苯基环丙胺盐酸盐 | 97% | 39元/250mg; 149元/1g; 725元/5g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
储存:2~8℃,干燥,密封 状态:白色到灰白色到黄色粉末或晶体 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| P797078 | MACKLIN | 反式-2-苯基环丙胺盐酸盐 | 10mM in DMSO | 185元/1ml; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
储存:-20°C, 密封, 干燥 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| C13047 | Alfa Aesar | trans-2-Phenylcyclopropylamine hydrochloride | 97% | 1245元/250mg; 2989元/1g; 12942元/5g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
基本信息 Ref# MDL 分子式 分子量 安全信息 危险等级 包装组 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| P8511 | Sigma-Aldrich | trans-2-Phenylcyclopropylamine hydrochloride | 650.91元/250 MG; 1572.9元/1 G; 6268.49元/5 G; | 展开 | |||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 包装 250 mg in glass insert 生化/生理作用 非选择性 MAO-A/B 抑制剂。 特点和优势 这种化合物是 ADME 毒性研究的特色产品。点击此处发现更多特色 ADME 毒性产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。 基本信息
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| P22370 | Sigma-Aldrich | trans-2-Phenylcyclopropylamine hydrochloride | 97% | 1146.58元/1 G; 2723.01元/2.5 G; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 包装 1, 2.5 g in glass bottle 生化/生理作用 非选择性 MAO-A/B 抑制剂。 基本信息
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| 616431 | Sigma-Aldrich | Tranylcypromine, HCl-CAS 1986-47-6-Calbiochem | A cell-permeable phenylcyclopropylamine that inhibits the monoamine oxidase and histone demethylase activities. | 1730.3元/500 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable phenylcyclopropylamine that inhibits the monoamine oxidase and histone demethylase activities, respectively, of MAO A/B (Ki = 101.9 and 16.0 M, respectively) and LSD1/2 (Ki = 242.7 and 180.0 M, respectively), four members of a flavin-dependent amine oxidase family enzymes, by a covalent adduct formation with the enzyme-bound FAD. In addition to preventing LSD1-CoREST (Corepressor of RE1-Silencing Transcription factor) complex-mediated H3K4 demethylation (IC50<2 M), TCP also inhibits LSD1-HCF-1 (Host Cell Factor-1) complex-mediated H3K9 demethylase activity, which is demonstrated to be an essential mechanism for the replication and latent infection of the α-herpesviruses HSV and VZV. The combined treatment of 2 M TCP and 10 M CHIR99061 is reported to enable the reprogramming of Oct4/Klf4-transduced primary HNEKs (Human Neonatal Epidermal Keratinocytes) into iPS (induced Pluripotent Stem) cells, albeit at a 100-time lower efficiency as seen in cultures transduced with 4-TFs (Oct44, Klf4, Sox2, and c-Myc). 包装 500 mg in Glass bottle 警告 Toxicity: Standard Handling (A) 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 Liang, Y., et al. 2009. Nat. Med.15, 1312. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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| 390375 | Fluorochem | (1S,2R)-2-PHENYLCYCLOPROPANAMINE HCL | 95% | 2112元/1g; 6182元/5g; 11132元/10g; 22286元/25g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
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