| CAS: | 1462249-75-7 | |||||
| 分子式: | C18H11F3N2O | |||||
| 分子量: | 328.29 | |||||
| 英文名称: |
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| 用途: | PFK-158是一种有效的选择性PFKFB3抑制剂,目前对晚期实体瘤研究处于临床一期阶段。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||
| P882268 | MACKLIN | PFK-158 | ≥98% | 639元/10mg; 1918元/50mg; | 咨询 | ||||||||||||||||||||||||||||||
储存:2-8℃ | |||||||||||||||||||||||||||||||||||
| P797686 | MACKLIN | PFK-158 | 10mM in DMSO | 520元/1ml; | 咨询 | ||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||
| SML3145 | Sigma-Aldrich | PFK-158 | ≥98% (HPLC) | 975.89元/5 MG; 3157.38元/25 MG; | 咨询 | ||||||||||||||||||||||||||||||
产品说明 生化/生理作用 PFK158 is a 3PO analog with improved PFKFB3 inhibitory potency (cell-free IC50 = 137 nM; Jurkat cellular IC50 = 1.62 μM/PFKFB3 activity, 847 nM/2-deoxyglucose uptake, 328 nM/toxicity) and pharmacokinetic properties. PFK158 markedly sensitizes BRAF(V600E)-positive A375 melanoma cells to apoptosis induction by vemurafenib in cultures and causes ~80% growth inhibition in several murine models of human-derived tumors in vivo (60 mg/kg qod. ip.). 基本信息
产品性质
安全信息
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