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L-779450 是一种有效的选择性 B-Raf 抑制剂,Kd 为 2.4 nM。
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更新时间:2026/10/7 8:42:16关注度:2493
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CAS No. : 303727-31-3
MCE 国际站:L⁻⁷79450
产品活性:L⁻⁷79450 是一种有效的选择性 B-Raf 抑制剂,Kd 为 2.4 nM。
研究领域:MAPK/ERK Pathway | Autophagy
In Vitro: L⁻⁷79450 (L⁻⁷79,450) shows a high degree of specificity towards Raf. The only other tested kinase inhibited is p38MAPK, which has a kinase domain structurally related to Raf. L⁻⁷79450 inhibits anchorage-independent growth of human tumor lines at doses ranging from 0.3 to 2 µM. The effects of L⁻⁷79450 (L⁻⁷79,450) on TRAIL sensitivity are investigated here in melanoma cell lines with high TRAIL sensitivity (A-375 and SK-Mel-147), moderate sensitivity (Mel-HO, SK-Mel-13, and SK-Mel-28), and permanent resistance (MeWo, Mel-2a, and SK-Mel-103), as well as in TRAIL-selected cell lines with acquired resistance (A-375-TS and Mel-HO-TS). Despite only moderate direct effects of L⁻⁷79450 on apoptosis, it strongly enhances TRAIL-induced apoptosis in sensitive melanoma cells and overrules TRAIL resistance in Mel-2a, SK-Mel-103, A-375-TS, and Mel-HO-TS. At 24 hours, 16-35% apoptosis induction is obtained.
相关产品:Bioactive Compound Library Plus | Immunology/Inflammation Compound Library | Kinase Inhibitor Library | MAPK Compound Library | Anti-Cancer Compound Library | CNS-Penetrant Compound Library | Autophagy Compound Library | Anti-Aging Compound Library | Oxygen Sensing Compound Library | Ferroptosis Compound Library | Glutamine Metabolism Compound Library | Anti-Lung Cancer Compound Library | Anti-Pancreatic Cancer Compound Library | Doramapimod | GW 5074 | Ro 5126766 | AZ 628 | GDC-0879 | ZM 336372 | Agerafenib | Raf inhibitor 1 | AZ304 | MCP110 | Sorafenib (D3) | Raf inhibitor 2
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