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R1530
Chemical Information
M.Wt
356.78
Storage
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CGI1746
Chemical Information
M.Wt
579.71
Storage
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KX1-004
Chemical Information
M.Wt
284.29
Storage
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GS9973
Chemical Information
M.Wt
411.46
Storage
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BMS-754807
Chemical Information
M.Wt
461.49
Storage
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DMH1
Chemical Information
M.Wt
380.44
Storage
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WP 1130 (degrasyn)
WP-1130 (degrasyn) is a selective deubiquitinase (DUB: USP5, UCH-L1, USP9x, USP14, and UCH37) inhibitor and also inhibits Bcr/Abl with IC50 of 1.8 &mu...
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Brigatinib (Synonyms: AP-26113)
AP-26113 is a potent ALK inhibitor for ALK, FER, ROS/ROS1, FLT3 and FES/FPS with IC50 of 0.62 nM, 1.3 nM, 1.9 nM, 2.1 nM and 3.4 nM, respectively. Dua...
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RN 486
RN-486 is a Bruton's tyrosine kinase (Btk) inhibitor. RN486 not only potently and selectively inhibited the Btk enzyme, but also displayed functional ...
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LY2801653
LY-2801653 is an orally available, small molecule inhibitor of the proto-oncogene c-Met (mesenchymal-epithelial transition, also known as hepatocyte g...
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Varlitinib (ARRY 334543)
Varlitinib (ARRY-334543) is a selective and potent ErbB1 and ErbB2 inhibitor with IC50 of 7 nM and 2 nM, respectively. Varlitinib selectively and reve...
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E 3810
E-3810 is a novel dual inhibitor targeting human vascular endothelial growth factor receptors (VEGFRs) and fibroblast growth factor receptors (FGFRs) ...
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LY 2874455
LY2874455 is a novel and potent FGF/FGFR Inhibitor. LY-2874455 exhibits a potent activity against FGF/FGFR-mediated signaling in several cancer cell l...
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ZM 306416
ZM-306416 is a VEGFR inhibitor, inhibiting Src, VEGFR1 and Abl with IC50 of 0.33 μM, 0.33 μM and 1.3 μM, respectively. [1][2]
Refere...
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ZM323881 hydrochloride
ZM-323881 is a potent and selective inhibitor of VEGF-R2 tyrosine kinase in vitro (IC(50) < 2 nM), compared with other receptor tyrosine kinases, i...
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Apoptosis
Btk
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