目錄:MedChemExpress LLC>>生化試劑>> 5Z-7-Oxozeaenol | MCE
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更新時(shí)間:2023-06-08 11:38:53瀏覽次數(shù):116評(píng)價(jià)
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CAS | 253863-19-3 | 純度 | 99.60% |
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分子量 | 362.37 | 分子式 | C??H??O? |
供貨周期 | 現(xiàn)貨 | 貨號(hào) | HY-12686 |
應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 253863-19-3
產(chǎn)品活性:5Z-7-Oxozeaenol is a natural anti-protozoan compound from fungal origin, acting as a potent irreversible and selective inhibitor of TAK1 and VEGF-R2, with IC50s of 8 nM and 52 nM, respectively.
研究領(lǐng)域:MAPK/ERK Pathway | Protein Tyrosine Kinase/RTK | Anti-infection
作用靶點(diǎn):MAP3K | VEGFR | Antibiotic
結(jié)構(gòu)分類:酚類 | 單酚類 | 其他類 | 結(jié)構(gòu)分類
In Vitro: 5Z-7-Oxozeaenol is a potent irreversible and selective inhibitor of transforming growth factor (TGF)-β-activated kinase 1 (TAK1, IC50, 8.1 nM), less active on MEK1 (IC50, 411 nM). 5Z-7-Oxozeaenol prevents inflammation by inhibiting the catalytic activity of TAK1 MAPK kinase kinase. 5Z-7-Oxozeaenol is also an inhibitor of VEGF-R2, with an IC50 of 52 nM. 5Z-7-Oxozeaenol has inhibitory activity against VEGF-R3, FLT3, PDGFR-β, B-RAF VE and SRC, with IC50s of 110, 170, 340, 6300 and 6600 nM, respectively. 5Z-7-Oxozeaenol inhibits JNK/p38 paythway, but it is not a direct inhibitor and is signal specific. 5Z-7-Oxozeaenol suppresses the PMA-induced AP-1 activity almost to the basal level in the KT cells, but has no effects on IL-1-induced NF-kB activity in the KK cells.
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