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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
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 | |||
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. | |||
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). | |||
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. | |||
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... | |||
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... | |||
T3041 | ALK inhibitor 2 | FAK , ALK | |
ALK inhibitor 2 is a new-type and selective inhibitor for the ALK kinase. | |||
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). | |||
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. | |||
T21768 | PF-562271 hydrochloride | PF-562271 HCl | FAK , PYK2 , CDK |
PF-562271 hydrochloride (PF-562271 HCl) is a potent, ATP-competitive, reversible inhibitor of FAK with IC50 of 1.5 nM in cell-free assays, ~10-fold less potent for Pyk2 than FAK and >100-fold selectivity against other pr... | |||
T10285 | ALK inhibitor 1 | FAK , IGF-1R , ALK | |
ALK inhibitor 1 is a selective ALK kinase inhibitor. | |||
T1950 | PND-1186 | PND1186,PND 1186,VS-4718,SR-2516 | Apoptosis , FAK |
PND-1186 (VS-4718) is a reversible and specific FAK inhibitor (IC50: 1.5 nM). | |||
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. | |||
T17543 | BI-3663 | Others | |
BI-3663 is a highly selective PTK2/FAK PROTAC, with cereblon ligands to hijack E3 ligases for PTK2 degradation. BI-3663 inhibits PTK2 with an IC50 of 18 nM. BI-3663 is a PROTAC that composes of BI-4464 linked to Pomalido... | |||
T17133 | Tos-PEG4-t-butyl ester | Tos-PEG4-Boc | Others |
Tos-PEG4-t-butyl ester (Tos-PEG4-Boc) is a PROTAC linker characterized by its PEG composition. This compound plays a crucial role in the synthesis of a range of PROTACs, including BI-3663, a highly selective PTK2/FAK PRO... | |||
T82385 | FMF-06-098-1 | PROTACs | |
FMF-06-098-1 is a multitargeted depressant capable of promoting the degradation of a wide array of kinases, including AAK1, ABL2, AURKA, AURKB, BUB1B, CDC7, CDK1, CDK12, CDK13, CDK2, CDK4, CDK6, CDK7, CDK9, CHEK1, CSNK1D... |
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-... | |||
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... | |||
T3122 | Fangchinoline | Tetrandrine B,(+)-Limacine,Hanfangichin B,(+)-Fangchinoline | Apoptosis , FAK , HIV Protease , Autophagy |
Fangchinoline (Tetrandrine B) is extracted from Stephania tetrandra S. Moore. |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-06064 | CD146/MCAM Protein, Human, Recombinant (His), Biotinylated | Human | HEK293 |
The CD146 antigen, also known as melanoma cell adhesion molecule (MCAM) and MUC18, is an integral membrane glycoprotein belonging to the immunoglobulin superfamily. CD146 contains the characteristic immunoglobulin-like d... | |||
TMPY-01034 | CD146/MCAM Protein, Human, Recombinant (His) | Human | HEK293 |
The CD146 antigen, also known as melanoma cell adhesion molecule (MCAM) and MUC18, is an integral membrane glycoprotein belonging to the immunoglobulin superfamily. CD146 contains the characteristic immunoglobulin-like d... | |||
TMPY-00879 | CD146/MCAM Protein, Human, Recombinant (hFc) | Human | HEK293 |
The CD146 antigen, also known as melanoma cell adhesion molecule (MCAM) and MUC18, is an integral membrane glycoprotein belonging to the immunoglobulin superfamily. CD146 contains the characteristic immunoglobulin-like d... | |||
TMPY-02502 | CD146/MCAM Protein, Mouse, Recombinant (His) | Mouse | HEK293 |
The CD146 antigen, also known as melanoma cell adhesion molecule (MCAM) and MUC18, is an integral membrane glycoprotein belonging to the immunoglobulin superfamily. CD146 contains the characteristic immunoglobulin-like d... | |||
TMPY-02270 | RET Protein, Human, Recombinant (His) | Human | HEK293 |
RET proto-oncogene, also known as RET, is a cell-surface molecule that transduce signals for cell growth and differentiation. It contains 1 cadherin domain and 1 protein kinase domain. RET proto-oncogene belongs to the p... | |||
TMPY-04418 | RET Protein, Human, Recombinant (aa 658-1114, His & GST) | Human | Baculovirus-Insect Cells |
RET proto-oncogene, also known as RET, is a cell-surface molecule that transduce signals for cell growth and differentiation. It contains 1 cadherin domain and 1 protein kinase domain. RET proto-oncogene belongs to the p... |