c-Kit
Los inhibidores de c-Kit son compuestos que bloquean la actividad del Receptor del Factor de Células Madre (c-Kit), una tirosina quinasa que desempeña un papel crucial en la supervivencia, proliferación y diferenciación celular, particularmente en células hematopoyéticas. Las mutaciones en c-Kit están vinculadas a varios tipos de cáncer, incluidos los tumores del estroma gastrointestinal (GIST) y la leucemia. En CymitQuimica, ofrecemos inhibidores de c-Kit para apoyar su investigación en oncología, hematología y biología de células madre.
Se han encontrado 116 productos para "c-Kit".
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APcK110
CAS:"APcK110, a potent novel Kit inhibitor, outperforms imatinib/dasatinib in halting OCI/AML3 and HMC1.2 cell growth, also inhibiting Kit-signaling."Fórmula:C20H16FN3O2Forma y color:SolidPeso molecular:349.36KBP-7018
CAS:KBP-7018 is a selective TKI targeting c-KIT, RET, and PDGFR for mechanistic studies of fibrotic signaling and kinase-driven diseases.Fórmula:C31H30N4O5Pureza:99.73%Forma y color:Yellow SolidPeso molecular:538.59c-Kit-IN-2
CAS:c-Kit-IN-2 is a c-KIT inhibitor (IC₅₀=82 nM) with anti-proliferative effects on GIST882, GIST430, GIST48 (GI₅₀=3,1,2 nM respectively).Fórmula:C25H29N9O2SPureza:98.95%Forma y color:White SolidPeso molecular:519.62Bezuclastinib
CAS:Bezuclastinib (CGT9486) is a novel, potent and highly selective tyrosine kinase and c-kit D816V inhibitor for the study of advanced mastocytosis.Fórmula:C19H17N5OPureza:99.55%Forma y color:SolidPeso molecular:331.37c-Kit-IN-3
CAS:c-Kit-IN-3 is a selective inhibitor of c-KIT kinase with IC50s of 4 nM and 8 nM for c-Kit (wt) and c-Kit (T670I).Fórmula:C26H20ClF3N2O4Pureza:99.94%Forma y color:SolidPeso molecular:516.9Ref: TM-T10651
1mg82,00€5mg154,00€10mg240,00€1mL*10mM (DMSO)316,00€25mg396,00€50mg532,00€100mg745,00€500mg1.494,00€Tafetinib
CAS:Tafetinib (SIM-010603) is a novel potent and orally available tyrosine kinase inhibitor with anti-angiogenic and anti-tumour activity.Fórmula:C24H29FN4O2Pureza:96.23%Forma y color:SolidPeso molecular:424.51Chiauranib
CAS:Chiauranib, a potent anticancer agent, inhibits angiogenesis kinases (VEGFR1-3, PDGFRα, c-Kit), Aurora B, and CSF1R with IC50 values of 1-9 nM.Fórmula:C27H21N3O3Pureza:99.22%Forma y color:SolidPeso molecular:435.47Ref: TM-T35570
1mg66,00€5mg144,00€1mL*10mM (DMSO)157,00€10mg245,00€25mg492,00€50mg710,00€100mg973,00€Henatinib
CAS:Henatinib: orally active multi-kinase inhibitor targeting VEGFR-2, c-kit, PDGFR with antitumor effects.Fórmula:C25H29FN4O4Forma y color:SolidPeso molecular:468.52N-desmethyl Regorafenib N-oxide
CAS:N-Desmethyl Regorafenib N-oxide, an active metabolite of the multi-kinase inhibitor regorafenib, originates through the action of the cytochrome P450 (CYP) isoform CYP3A4. This compound demonstrates efficacy in vitro by inhibiting key enzymes such as VEGFR2, Tie2, c-Kit, and B-RAF, and it exhibits tumor growth inhibition in HT-29 and MDA-MB-231 mouse xenograft models at a dosage of 1 mg/kg.Fórmula:C20H13ClF4N4O4Forma y color:SolidPeso molecular:484.79SIM010603
CAS:SIM010603, an oral RTK inhibitor, targets Kit, VEGFR-2, PDGFR-β, RET, FLT3 (IC50: 5.0-68.1 nmol/l), inhibits cell proliferation and angiogenesis.Fórmula:C22H25FN4O2Forma y color:SolidPeso molecular:396.46Agerafenib hydrochloride
CAS:Agerafenib hydrochloride is a highly potent inhibitor of BRAFV600E (Kd: 14 nM).Fórmula:C24H23ClF3N5O5Pureza:98%Forma y color:SolidPeso molecular:553.92Labuxtinib
CAS:Labutinib is a selective inhibitor of the c-kit tyrosine kinase [1].Fórmula:C20H16FN5O2Pureza:99.95%Forma y color:SolidPeso molecular:377.37Ref: TM-T79851
1mg88,00€5mg192,00€1mL*10mM (DMSO)212,00€10mg306,00€25mg610,00€50mg880,00€100mg1.179,00€Protein kinase inhibitor 10
CAS:Protein kinase inhibitor 10 is a protein kinase inhibitor with IC50 values of 28.9 μM, 13.6 μM, and 2.41 μM for TAM receptors, FAK, and KIT, respectively. It can inhibit abnormal and excessive cell proliferation, showing potential for research in the field of cancer treatment.Fórmula:C14H9FN6S2Forma y color:SolidPeso molecular:344.39AMG-25
CAS:AMG-25 (c-Kit-IN-5-1) is a c-Kit inhibitor that inhibits c-Kit, KDR, p38, Lck, and Src, and can be used for the study of mast cell-associated fibrotic diseases.Fórmula:C23H17N5O2Pureza:98.16%Forma y color:Yellow SolidPeso molecular:395.41c-Kit-IN-8
CAS:C-Kit-IN-8 (Compound 53) acts as an inhibitor of c-Kit kinase, hampering uKIT kinase activity with an IC50 greater than 1 μM. Additionally, it inhibits the proliferation of both wild-type and mutant GIST430 and BaF3 cancer cells, exhibiting an IC50 greater than 0.1 μM.Fórmula:C24H26FN5O4Forma y color:SolidPeso molecular:467.49c-Kit-IN-7
CAS:c-Kit-IN-7 (compound 104) serves as an effective inhibitor of c-Kit, exhibiting an IC50 of 10 nM or less. It plays a crucial role in cancer research.Fórmula:C27H32FN7O3Forma y color:SolidPeso molecular:521.59
