目錄:MedChemExpress LLC>>生化試劑>> Dabrafenib | MCE
CAS | 1195765-45-7 | 純度 | 99.91% |
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分子量 | 519.56 | 分子式 | C??H??F?N?O?S? |
供貨周期 | 現貨 | 規(guī)格 | 5 mg |
貨號 | HY-14660 | 應用領域 | 醫(yī)療衛(wèi)生,化工,生物產業(yè),制藥/生物制藥 |
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CAS No. : 1195765-45-7
產品活性:Dabrafenib (GSK2118436A) is an ATP-competitive inhibitor of Raf with IC50s of 5 nM and 0.6 nM for C-Raf and B-RafV600E, respectively.
研究領域:MAPK/ERK Pathway
作用靶點:Raf
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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