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Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
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- Epigenetics
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GPCR/G Protein
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Protease/Metabolic Enzyme
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Research Areas
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Azaindazole
- Pyridazine Series
- Nucleoside Series
- Quinazoline
- Pyrazole Series
- Boric acid
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- Pyrrole Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Benzene Series
- Pyridine Series
Raw Materials
FAK
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP45896 | Ifebemtinib New | 1227948-82-4 | |
IN10018, a novel small chemical FAK inhibitor against ovarian cancer.
|
BCP48306 | Conteltinib New | 1384860-29-0 | |
Conteltinib is a tyrosine kinase inhibitor and an antineoplastic.
|
BCP46447 | GSK215 New | 2743427-26-9 | |
GSK215 is a potent and selective PROTAC focal adhesion kinase (FAK) degrader.
|
BCP45164 | AMP-945 New | 1393653-34-3 | |
AMP945 is an inhibitor of the enzyme focal adhesion kinase (FAK) that plays a key role in the formation of scar tissue (fibrosis) both in cancer and diseases like IPF.
|
BCP42811 | PF-562271 HCl New | 939791-41-0 | |
PF-562271 is an orally bioavailable small molecule and ATP-competitive focal adhesion kinase (FAK) inhibitor with potential antineoplastic and antiangiogenic activities.
|
BCP27854 | Y15 tetrahydrochloride New | 4506-66-5 | |
Y15 is a potent and specific inhibitor of focal adhesion kinase (FAK) that inhibits its autophosphorylation activity, decreases the viability of cancer cells, and blocks tumor growth.
|
BCP30859 | BI-4464 New | 1227948-02-8 | |
BI-4464 is a highly selective ATP competitive inhibitor of PTK2/FAK, with an IC50 of 17 nM. A PTK2 ligand for PROTAC.
|
BCP29572 | PF 4618433 | 1166393-85-6 | |
PF 4618433 is an inhibitor of proline-rich tyrosine kinase 2 (PYK2) and focal adhesion kinase (FAK).
|
BCP28812 | Y 11 | 1086639-59-9 | |
Y11 is a small molecule inhibitor targeting Y397 site of FAK.
|
BCP19778 | Repotrectinib New Hot | 1802220-02-5 | |
TPX-0005 is a potent ALK/ROS1/TRK inhibitor, with IC50 of 5.3 nM, 1.01 nM, 1.26 nM and 1.08 nM for SRC, WT ALK, ALK G1202R and ALK L1196M, respectively.
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