Tyrosine Kinase
- Bcr-Abl(27)
- Ack1(2)
- Axl(10)
- ALK(27)
- BMX Kinase(1)
- Broad Spectrum Protein Kinase Inhibitor(9)
- c-FMS(3)
- c-Kit(12)
- c-MET(34)
- c-RET(7)
- CSF-1R(3)
- DDR1/DDR2 Receptor(1)
- EGFR(85)
- EphB4(1)
- FAK(15)
- FGFR(21)
- FLT3(23)
- HER2(19)
- IGF1R(13)
- Insulin Receptor(6)
- IRAK(6)
- ITK(3)
- Lck(1)
- LRRK2(10)
- PDGFR(31)
- PTKs/RTKs(4)
- Pyk2(3)
- ROR(6)
- Spleen Tyrosine Kinase (Syk)(16)
- Src(36)
- Tie-2 (2)
- Trk(12)
- VEGFR(64)
- Kinase(0)
- Cat.No. Product Name Information
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B6054
EAI045
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B5843
CTX0294885
CTx-0294885 is a novel bisanilino pyrimidine. It has inhibitory activity towards a wild range of kinases in vitro.
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A8706
BLU9931
BLU9931 is a potent and irreversible inhibitor of FGFR4.
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B3553
GS-9973
GS-9973 is an orally bioavailable, selective Syk inhibitor with IC50 of 7.7 nM. Phase 2.
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B5621
Y 11
New Product
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B7400
FAK Inhibitor 14
New Product
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B3688
ML347
ML347 is a potent and selective inhibitor of bone morphogenetic protein (BMP) receptor with IC50 value of 32nM against ALK2 .
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B3687
LDN-212854
LDN-212854 is a selective inhibitor of bone morphogenetic protein (BMP) signaling with IC50 value of 1.2nM .
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B3383
DDR1-IN-1
DDR1-IN-1 is a potent and selective DDR1 receptor tyrosine kinase inhibitor with IC50/EC50 of 105 nM/87 nM; 4-fold less potent for DDR2 (IC50= 413 nM).
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B1544
Tyrphostin AG 879
Tyrphostin AG 879 potently inhibits HER2/ErbB2 with IC50 of 1 μM, 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR.
