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Search Results for " focal adhesion kinase "

20

Compounds

Cat No. Product Name Synonyms Targets
TN1433 Batatasin III FAK , Others , Akt
Batatasin III inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition and FAK-AKT signals and possesses anti-cancer activities. Batatasin III has a long-term inhibitory effect on whole-...
T3041 ALK inhibitor 2 FAK , ALK
ALK inhibitor 2 is a new-type and selective inhibitor for the ALK kinase.
T10285 ALK inhibitor 1 FAK , IGF-1R , ALK
ALK inhibitor 1 is a selective ALK kinase inhibitor.
T9576 AMP-945 FAK
AMP-945 is a proprietary focal adhesion kinase (FAK) inhibitor.
T2001 PF-573228 PF 573228 Apoptosis , FAK
PF-573228 is an ATP-competitive FAK inhibitor. In a cell-free assay, the IC50 of FAK is 4 nM.
T9973 FAK-IN-7 FAK
FAK-IN-7 has potential antiproliferative activity and is a FAK inhibitor.
T6997 SU6656 FAK , Akt , Src
SU 6656 is a selective inhibitor of Src family kinases, with IC50 of 280 nM, 20 nM, 130 nM, and 170 nM for Src, Yes, Lyn, and Fyn, respectively.
T2314 PF-431396 FAK , PYK2
PF-431396 is a dual PYK2/FAK inhibitor (IC50: 11/2 nM).
T2281 GSK2256098 GSK 2256098,GSK-2256098,GTPL7939 Apoptosis , FAK
GSK2256098 (GTPL7939) is a small molecule FAK kinase inhibitor.
T5480 BI-4464 FAK , Ligands for Target Protein for PROTAC
BI-4464 is a highly selective ATP competitive inhibitor of PTK2/FAK, with an IC50 of 17 nM. A PTK2 ligand for PROTAC
T2465 PF-562271 PF562271,PF 562271 FAK , PYK2 , CDK
PF-562271 is an effective ATP-competitive, reversible inhibitor of FAK(IC50=1.5 nM) and Pyk2 kinase(IC50=13 nM).
T1996 Defactinib PF-04554878,VS-6063 FAK
Defactinib (VS-6063) is an orally bioavailable, small-molecule focal adhesion kinase (FAK) inhibitor with potential antiangiogenic and antineoplastic activities.
T2655 CEP-37440 CEP37440 FAK , ALK
CEP-37440 is an effective and specific Dual FAK/ALK inhibitor with IC50s of 120 nM(ALK cellular in 75% human plasma) and 2.3 nM (FAK).
T6177 PF-562271 besylate PF-00562271 Besylate FAK , PYK2 , CDK
PF-562271 besylate (PF-00562271 Besylate) is a potent, ATP-competitive, reversible inhibitor of FAK with IC50 of 1.5 nM, ~10-fold less potent for Pyk2 than FAK and >100-fold selectivity against other protein kinases, exc...
T5S0761 Nitidine chloride Apoptosis , ERK , FAK , p38 MAPK , NF-κB , Topoisomerase , STAT , Parasite
1. Nitidine chloride has inhibitory effects on various tumors, such as renal cancer , breast cancer. 2. Nitidine chloride inhibits the proliferation of SMMC-7721 cells in vitro in a time- and dose-dependent manner and id...
T24730 Roslin 2 bromide Roslin-2,Benzylhexamethylenetetramine bromide,Roslin2 FAK , p53
Roslin 2 bromide (Benzylhexamethylenetetramine bromide) is a p53 reactivator that disrupts the binding of FAK and p5. Roslin 2 bromide exhibits anticancer effects.
T0263 Chloropyramine hydrochloride Nilfan,Alergosan,Halopyramine hydrochloride FAK , VEGFR , Histamine Receptor
Chloropyramine hydrochloride (Alergosan) is a histamine receptor H1 antagonist.
T3122 Fangchinoline Tetrandrine B,(+)-Limacine,Hanfangichin B,(+)-Fangchinoline Apoptosis , FAK , HIV Protease , Autophagy
Fangchinoline (Tetrandrine B) is extracted from Stephania tetrandra S. Moore.
T1918 NVP-TAE 226 TAE226 Apoptosis , FAK , c-Met/HGFR , PYK2 , IGF-1R
NVP-TAE 226 (TAE226) is an effective FAK inhibitor (IC50: 5.5 nM) and most effective to Pyk2(IC50: 3.5 nM); 10- to 100-fold less effective against IGF-1R, InsR, c-Met, and ALK.
T2609 Masitinib AB1010 Apoptosis , FAK , c-Fms , FGFR , Bcr-Abl , PDGFR , Src , c-Kit , Hck
Masitinib (AB1010) is a tyrosine-kinase inhibitor used in the treatment of mast cell tumors in animals, specifically dogs. Since its introduction in November 2008 it has been distributed under the commercial name Masivet...
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