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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T77718 | FAK-IN-10 | FAK | |
FAK-IN-10 is an inhibitor of FAK (IC50:76.3 μM).FAK-IN-10 z MCF-7 and A431 cell lines showed antitumor activity with IC50 of 4.23 and 0.78 μM, respectively. | |||
T9973 | FAK-IN-7 | FAK | |
FAK-IN-7 has potential antiproliferative activity and is a FAK inhibitor. | |||
T7119 | Y15 | 1,2,4,5-Benzenetetramine tetrahydrochlor,FAK Inhibitor 14 | FAK |
Y15 (1,2,4,5-Benzenetetramine tetrahydrochlor) is a potent and specificsmall-molecule FAK scaffolding inhibitor that inhibits its autophosphorylation activity, blocks tumor growth. | |||
T40183 | FAK-IN-1 | ||
FAK-IN-1 is a FAK inhibitor with anticancer activities (WO2020231726 (Example 27)). | |||
T11260 | FAK inhibitor 2 | FAK | |
FAK inhibitor 2, antitumor and anti-angiogenesis activitiesis ,is a potent focal adhesion kinase (FAK) inhibitor with an IC50 of 0.07 nM . | |||
T11261 | FAK inhibitor 5 | Others | |
FAK inhibitor 5 is a novel allosteric FAK inhibitor, with IC50 values in the low micromolar range. | |||
T13840 | PROTAC FAK degrader 1 | Others | |
PROTAC FAK degrader 1 is a selective and potent degrader of focal adhesion kinase (Fak) (IC50 of 6.5 nM). | |||
T17943 | FAK ligand-Linker Conjugate 1 | Others | |
FAK ligand-Linker Conjugate 1 is a chemical compound designed to facilitate PROTAC-mediated protein degradation. This compound consists of a ligand specifically targeting FAK and a PROTAC linker module, which acts as a r... | |||
T63545 | FAK-IN-3 | ||
FAK-IN-3 is a potent inhibitor of adherens spot kinase (FAK). FAK-IN-3 reduces migration and invasion of PA-1 cells and inhibits the expression of MMP-2 and MMP-9. FAK-IN-3 inhibits tumor growth and metastasis with no si... | |||
T79688 | FAK-IN-11 | FAK | |
FAK-IN-11 (Compound 4l), a FAK inhibitor, specifically targets the ATP binding pocket of FAK to prevent its phosphorylation. It exhibits cytotoxic effects on MDA-MB-231 cells, achieving an IC50 value of 13.73 μM, and ind... | |||
T61019 | FAK-IN-4 | ||
FAK-IN-4 (Compound 7d) has anticancer activities that can induce cell apoptosis. FAK-IN-4 is potential inhibitor of FAK [1]. | |||
T64077 | FAK-IN-5 | ||
FAK-IN-5 is a FAK signaling inhibitor that induces apoptosis and autophagy. | |||
T64207 | FAK-IN-6 | ||
FAK-IN-6 is a potent inhibitor of FAK (IC50: 1.415 nM). FAK-IN-6 exhibits anti-proliferative effects on certain cancer cell lines and can be used to study pancreatic cancer. | |||
T74802 | FAK-IN-9 | ||
FAK-IN-9 (Compound 8f) is a potent, orally active inhibitor of FAK, demonstrating an IC50 value of 27.44 nM. This compound effectively induces apoptosis in triple-negative breast cancer (TNBC) cells [1]. | |||
T63978 | FAK-IN-2 | ||
FAK-IN-2 is a potent, orally active adherens spot kinase (FAK) inhibitor (IC50: 35 nM) that exhibits antitumour effects. FAK-IN-2 covalently inhibits FAK autophosphorylation in a dose-dependent manner and also inhibits t... | |||
T61410 | FAK-IN-8 | ||
FAK-IN-8 (compound 5h), a FAK inhibitor with an IC50 of 5.32 μM, exhibits potent anti-proliferative activity, making it suitable for use in cancer research [1]. | |||
T74281 | FAK PROTAC B5 | ||
Compound B5 (FAK PROTAC B5) is a FAK PROTAC degrader exhibiting potent FAK degradation and antiproliferative activities, with an IC50 of 14.9 nM. It also shows excellent plasma stability, moderate membrane permeability, ... | |||
T82420 | FAK-IN-12 | FAK | |
FAK-IN-12 (Compound 12S) is a selective FAK inhibitor with an IC50 of 47 nM. It effectively suppresses proliferation of MGC-803, HCT-116, and KYSE30 cells with IC50 values of 0.24, 0.45, and 0.44 μM, respectively. Additi... | |||
T63123 | FAK inhibitor 6 | ||
Compound 26F effectively optimizes enzyme inhibition (IC50 = 28.2 nM) while demonstrating relatively low cytotoxicity (IC50 = 3.32 μM). It induces apoptosis in MDA-MB-231 cells in a dose-dependent manner and efficiently ... | |||
T9576 | AMP-945 | FAK | |
AMP-945 is a proprietary focal adhesion kinase (FAK) inhibitor. |