FAK
Gli inibitori della chinasi di adesione focale (FAK) prendono di mira la FAK, una chinasi coinvolta nell'adesione cellulare, nella migrazione e nell'angiogenesi. La FAK è frequentemente sovraespressa nei tumori e contribuisce alla formazione di nuovi vasi sanguigni che forniscono nutrienti al tumore. L'inibizione della FAK può interrompere questi processi, rendendo gli inibitori della FAK strumenti preziosi nella terapia del cancro e nella ricerca sull'angiogenesi. Presso CymitQuimica, offriamo una gamma completa di inibitori della FAK di alta qualità per supportare la tua ricerca in biologia cellulare, cancro e angiogenesi.
Trovati 72 prodotti di "FAK"
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Ifebemtinib FA
BI-853520 FA (Ifebemtinib FA) is an orally active inhibitor of adhesion patch kinase with anticancer and antiproliferative activity for ovarian and lung cancer.Formula:C29H30F4N6O6Purezza:98.05% - 99.73%Colore e forma:SolidPeso molecolare:634.58FAK-IN-27
FAK-IN-27 (compound 8A) is a potent and selective inhibitor of FAK, with an IC50 of 4.968 nM. It effectively inhibits the proliferation of H1299 cells, with an IC50 of 0.28 μM, and is applicable for research in non-small cell lung cancer (NSCLC).Formula:C32H28ClN5O6Colore e forma:SolidPeso molecolare:613.17281FAK-IN-10
CAS:<p>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.</p>Formula:C15H10BrN3O2SPurezza:99.78%Colore e forma:SoildPeso molecolare:376.23Defactinib analogue-1
CAS:Defactinib analogue-1 (Compound 7) serves as a ligand for the target protein FAK, and is utilized in the synthesis of PROTAC FAK degrader 1.Formula:C20H20F3N5O3SColore e forma:SolidPeso molecolare:467.47GSK215
CAS:GSK215: potent, selective PROTAC degrader of FAK (pDC50=8.4), combines FAK inhibitor VS-4718 and VHL E3 ligase binder, causes fast, lasting FAK degradation.Formula:C50H59F3N10O6SPurezza:99.3%Colore e forma:SoildPeso molecolare:985.13Anti-PTK2 Antibody (4T687)
Anti-PTK2 Antibody (4T687) is an antibody targeting PTK2. Anti-PTK2 Antibody (4T687) can be used in ELISA, IHC.Colore e forma:Odour LiquidConteltinib tetrahydrochloride
Conteltinibtetrahydrochloride (CT-707 tetrahydrochloride) is the tetrahydrochloride form of Conteltinib. It acts as an inhibitor for FAK (IC50=1.6 nM), ALK, and Pyk2. When used in combination with Cabozantinib, Conteltinib tetrahydrochloride exhibits a synergistic antitumor effect.Formula:C32H49Cl4N9O3SColore e forma:SolidPeso molecolare:781.667BI-3663
CAS:<p>BI-3663 is a selective PTK2/FAK PROTAC with cereblon ligands, degrading PTK2 (IC50: 18 nM), and shows anti-cancer properties.</p>Formula:C44H42F3N7O12Purezza:98%Colore e forma:SolidPeso molecolare:917.84Defactinib
CAS:Defactinib (VS-6063) is a second-generation inhibitor of FAK. Defactinib has potential antitumor activity. Cost-effective and quality-assured.Formula:C20H21F3N8O3SPurezza:98% - 99.71%Colore e forma:SolidPeso molecolare:510.49SU6656
CAS: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.Formula:C19H21N3O3SPurezza:98.21% - 98.73%Colore e forma:SolidPeso molecolare:371.45Masitinib
CAS:Masitinib (AB1010) is a tyrosine-kinase inhibitor used in the treatment of mast cell tumors in animals, specifically dogs.Formula:C28H30N6OSPurezza:97.56% - >99.99%Colore e forma:SolidPeso molecolare:498.64Y15
CAS:<p>Y15 (1,2,4,5-Benzenetetramine tetrahydrochlor) is a potent and specificsmall-molecule FAK scaffolding inhibitor that inhibits its autophosphorylation activity,</p>Formula:C6H14Cl4N4Purezza:98% - 99.32%Colore e forma:Dark Brown CrystalsPeso molecolare:284.01PF-431396
CAS:PF-431396 is a dual PYK2/FAK inhibitor (IC50: 11/2 nM).Formula:C22H21F3N6O3SPurezza:98.83% - 99.82%Colore e forma:SolidPeso molecolare:506.5Fangchinoline
CAS:Fangchinoline (Tetrandrine B) is extracted from Stephania tetrandra S. Moore.Formula:C37H40N2O6Purezza:99.86% - >99.99%Colore e forma:SolidPeso molecolare:608.72AMP-945
CAS:AMP-945 is a proprietary focal adhesion kinase (FAK) inhibitor.Formula:C28H32F3N5O2Purezza:99.76%Colore e forma:SolidPeso molecolare:527.58PF-562271 hydrochloride
CAS:<p>PF-562271 hydrochloride (PF-562271 HCl) is a potent, ATP-competitive, reversible inhibitor of FAK with IC50 of 1.5 nM, ~10-fold less potent for Pyk2 than FAK.</p>Formula:C21H20F3N7O3SHClPurezza:97.08%Colore e forma:SolidPeso molecolare:543.95PF-573228
CAS:PF-573228 is an ATP-competitive FAK inhibitor. In a cell-free assay, the IC50 of FAK is 4 nM.Formula:C22H20F3N5O3SPurezza:96.58% - 99.51%Colore e forma:SolidPeso molecolare:491.49Nitidine chloride
CAS:1.Formula:C21H18ClNO4Purezza:96.59% - 99.55%Colore e forma:SolidPeso molecolare:383.82BI-4464
CAS:<p>BI-4464 is a highly selective ATP competitive inhibitor of PTK2/FAK, with an IC50 of 17 nM. A PTK2 ligand for PROTAC</p>Formula:C28H28F3N5O4Purezza:97.43%Colore e forma:SolidPeso molecolare:555.55Batatasin III
CAS:Batatasin III inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition and FAK-AKT signals and possesses anti-cancerFormula:C15H16O3Purezza:99.16%Colore e forma:SolidPeso molecolare:244.29
