Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10287 |
ALK2-IN-2
|
ALK; TGF-beta/Smad | Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors |
ALK2-IN-2是一种强效且具有选择性激活素受体样激酶2(ALK2)的抑制剂(IC50:9 nM),对 ALK2的抑制作用比 ALK3高700倍。 | |||
T39764 |
ALK2-IN-4
ALK2-IN-4 |
||
ALK2-IN-4, a highly effective ALK2 inhibitor. | |||
T40065 |
ALK2-IN-4 succinate
ALK2-IN-4 succinate |
||
ALK2-IN-4 succinate is a robust and effective inhibitor of ALK2. | |||
T79393 | ALK/EGFR-IN-2 | ||
ALK/EGFR-IN-2 是一种高效的 ALK 和 EGFR 双重抑制剂,能够诱导癌细胞凋亡及 G0/G1 细胞周期停滞。此化合物在 H1975、PC9 和 Baf3-EML4-ALK 癌熙胞株的增殖抑制实验中,其 IC50 值分别为0.0034、0.0065 和 0.0018 μM,表明其对这些癌熙胞系具有显著的抑制作用。 | |||
T3059 |
ALK-IN-1
AP26113,Brigatinib,AP26113-analog |
EGFR; IGF-1R; ALK | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
ALK-IN-1 (AP26113) 是一种高效的、选择性的 ALK 激酶抑制剂。 | |||
T62546 |
ALK5-IN-27
|
||
ALK5-IN-27 (Compound EX-04) 是一种 ALK-5 的有效抑制剂 (IC50≤10 nM)。ALK5-IN-27 对 ALK-2 也具有抑制作用。 | |||
T62393 |
ALK5-IN-25
|
||
ALK5-IN-25 (compound EX-02) 是一种 ALK-5 的有效抑制剂 (IC50<10 nM),也能够抑制 ALK-2。ALK5-IN-25 能够用于研究癌症。 | |||
T13139 |
TP-008
TGFβRI-IN-2 |
Others | Others |
TGFβRI-IN-2 is a selective, potent and orally active inhibitor of (Activin-Like Kinase 5) ALK 5(pIC50 and pEC50 values of 7.6 and 6.63, respectively). |