6 results for "Focal Adhesion Kinase Inhibitors" in 产品

Focal Adhesion Kinase Inhibitors

FAK (Focal Adhesion Kinase) is a non-receptor protein tyrosine kinase involved in signal transduction from integrin-enriched focal adhesion sites that mediate cell contact with the extracellular matrix. FAK-enhanced signals have been shown to mediate the survival of anchorage-dependent cells and are critical for efficient cell migration in response to growth factor receptor and integrin stimulation. Elevated expression of FAK in human tumors has been correlated with increased malignancy and invasiveness.

Selective FAK inhibitor

Alternate Names: Y15,NSC 677249
Chemical Name: 1,2,4,5-Benzenetetramine tetrahydrochloride
Selective FAK inhibitor
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Potent and selective FAK inhibitor

Chemical Name: 3,4-Dihydro-6-[[4-[[[3-(methylsulfonyl)phenyl]methyl]amino]-5-(trifluoromethyl)-2-pyrimidinyl]amino]-2(1H)-quinolinone
Purity: ≥98%
Potent and selective FAK inhibitor
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Potent focal adhesion kinase (FAK) inhibitor

Chemical Name: 2-[[5-Chloro-2-[[3-methyl-1-(1-methylethyl)-1H-pyrazol-5-yl]amino]-4-pyridinyl]amino]-N-methoxybenzamide
Purity: ≥98%
Potent focal adhesion kinase (FAK) inhibitor
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Dual FAK/PYK2 inhibitor

Chemical Name: N-Methyl-N-[2-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)amino]-5-(trifluoromethyl)-4-pyrimidinyl]amino]methyl]phenyl]methanesulfonamide
Purity: ≥98%
Dual FAK/PYK2 inhibitor
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Potent and selective FAK and Pyk2 inhibitor

Chemical Name: N-Methyl-4-[[4-[[[3-[methyl(methylsulfonyl)amino]-2-pyrazinyl]methyl]amino]-5-(trifluoromethyl)-2-pyrimidinyl]amino]benzamide
Purity: ≥98%
Potent and selective FAK and Pyk2 inhibitor
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Potent FAK inhibitor; orally bioavailable

Chemical Name: 2-[[2-[[2-Methoxy-4-(4-morpholinyl)phenyl]amino]-5-(trifluoromethyl)-4-pyridinyl]amino]-N-methylbenzamide
Purity: ≥98%
Potent FAK inhibitor; orally bioavailable
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