Dabrafenib
CAS No. 1195765-45-7
Dabrafenib ( GSK2118436 )
产品货号. M10687 CAS No. 1195765-45-7
Dabrafenib (GSK2118436) 是一种突变型 BRAFV600 特异性抑制剂,在无细胞测定中 IC50 为 0.8 nM,对 B-Raf(wt) 和 c-Raf 的效力分别降低 4 倍和 6 倍。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥332 | 有现货 |
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| 10MG | ¥462 | 有现货 |
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| 25MG | ¥583 | 有现货 |
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| 50MG | ¥689 | 有现货 |
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| 100MG | ¥948 | 有现货 |
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| 200MG | ¥1280 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Dabrafenib
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Dabrafenib (GSK2118436) 是一种突变型 BRAFV600 特异性抑制剂,在无细胞测定中 IC50 为 0.8 nM,对 B-Raf(wt) 和 c-Raf 的效力分别降低 4 倍和 6 倍。
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产品描述Dabrafenib (GSK2118436) is a mutant BRAFV600 specific inhibitor with IC50 of 0.8 nM in cell-free assays, with 4- and 6-fold less potency against B-Raf(wt) and c-Raf, respectively.(In Vitro):Dabrafenib (GSK2118436, 1 μM) with 0.01 μM GSK1120212 inhibits more than 90% of cell growth in the NRAS mutant clones. GSK2118436 is sufficient to reduce S6P phosphorylation in A375. Dabrafenib suppresses the PolyP-mediated vascular barrier permeability, upregulation of inflammatory biomarkers, adhesion/migration of leukocytes, and activation and/or production of nuclear factor-κB, tumor necrosis factor-α, and interleukin-6. Dabrafenib inhibits the release of HMGB1 and downregulates HMGB1-dependent inflammatory responses by enhancing the expressions of cell adhesion molecules (CAMs) in human endothelial cells.(In Vivo):Dabrafenib-treated females have mostly immature reproductive tracts with no evidence of ovulation, similar to age-matched controls; however, DAB-treated females have keratinized and histologically open vaginas.
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体外实验Dabrafenib (GSK2118436, 1 μM) with 0.01 μM GSK1120212 inhibits more than 90% of cell growth in the NRAS mutant clones. GSK2118436 is sufficient to reduce S6P phosphorylation in A375. Dabrafenib suppresses the PolyP-mediated vascular barrier permeability, upregulation of inflammatory biomarkers, adhesion/migration of leukocytes, and activation and/or production of nuclear factor-κB, tumor necrosis factor-α, and interleukin-6. Dabrafenib inhibits the release of HMGB1 and downregulates HMGB1-dependent inflammatory responses by enhancing the expressions of cell adhesion molecules (CAMs) in human endothelial cells.
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体内实验Dabrafenib-treated females have mostly immature reproductive tracts with no evidence of ovulation, similar to age-matched controls; however, DAB-treated females have keratinized and histologically open vaginas.
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同义词GSK2118436
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通路MAPK/ERK Signaling
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靶点Raf
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受体B-Raf| B-Raf (V600E)| C-Raf
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研究领域Cancer
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适应症——
化学信息
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CAS Number1195765-45-7
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分子量519.56
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分子式C23H20F3N5O2S2
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纯度>98% (HPLC)
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溶解度DMSO: 30 mg/mL (57.74 mM)
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SMILESCC(C)(C)C1=NC(=C(S1)C1=NC(N)=NC=C1)C1=C(F)C(NS(=O)(=O)C2=C(F)C=CC=C2F)=CC=C1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Sylvie Laquerre, et al. 2009, EORTC International Conference. Abst B88.
产品手册
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