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T10444TAK1/MAP4K2 inhibitor 1TAK1/MAP4K2 inhibitor 1
TAK1/MAP4K2 inhibitor 1 is a potent dual inhibitor of TGFβ-activated kinase 1 (TAK1) and MAP4K2 (IC50s: 41.1 nM and 18.2 nM).
价 格：￥电议型 号：T10444产 地：美洲
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T70741AZ-TAK1；化合物 AZ-TAK1AZ-TAK1
AZ-Tak1 is a potent and a relatively selective inhibitor of TAK1 kinase activity, with an IC50 of 0.009 mM. AZ-Tak1 treatment decreased the level of p38 and ERK in mantle cell lymphoma cells, and induced apoptosis in a dose and time dependent manner, with an IC50 of 0.1–0.5 mM. Using the annexin-V and PI staining and FACS analysis, After 48 hours of incubation, AZ-Tak1 (0.1 mM) induced apoptosis in 28%, 34% and 86% of Mino, SP53, and Jeko cells, respectively, which was increased to 32%, 42%, and
价 格：￥电议型 号：T70741产 地：中国大陆
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T67909TAK1 inhibitor；TAK1抑制剂compound 13a；compound 13a
TAK1 inhibitor is an inhibitor, which can inhibit MCF-7, A549, DU-145 and MDA MB-231, with IC50 of 0.021, 0.14, 0.064 and 0.19, respectively. TAK1 inhibitor showed good antibacterial activity with microphones ranging from 93.7 to 46.9μg/mL and from 7.8 to 5.8μg/mL.
价 格：￥电议型 号：T67909产 地：中国大陆
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T40577TAK1-IN-3；TAK1 抑制剂3TAK1-IN-3；TAK1-IN-3
TAK1-IN-3 is a novel ATP-competitive TAK1 inhibitor for the study of cancer.
价 格：￥电议型 号：T40577产 地：中国大陆
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T36782TAK1-IN-2；TAK1-IN-2TAK1-IN-2；TAK1-IN-2
TAK1-IN-2 is a potent and selective TAK1 inhibitor, with an IC50> of 2 nM[1].
价 格：￥电议型 号：T36782产 地：中国大陆
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T29203Zanapezil fumarate；化合物 T29203TAK 147|||TAK147|||TAK-147；TAK 147|||TAK147|||TAK-147
Zanapezil is an acetylcholinesterase (AChE) inhibitor. Zanapezil increases choline acetyltransferase activity in cultured rat septal cholinergic neurons.
价 格：￥电议型 号：T29203产 地：中国大陆
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T28914Tak 187；化合物 T28914Tak-187|||Tak187；Tak-187|||Tak187
Tak 187 is a long-lasting inhibitor of ergosterol biosynthesis.
价 格：￥电议型 号：T28914产 地：中国大陆
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T10444TAK1/MAP4K2 inhibitor 1；化合物 T10444TAK1/MAP4K2 inhibitor 1
TAK1/MAP4K2 inhibitor 1 is a potent dual inhibitor of TGFβ-activated kinase 1 (TAK1) and MAP4K2 (IC50s: 41.1 nM and 18.2 nM).
价 格：￥电议型 号：T10444产 地：中国大陆
