Receptor de efrina
Los inhibidores de los receptores de efrinas (Eph) están dirigidos a los receptores Eph, una familia de tirosina quinasas receptoras que interactúan con ligandos de efrinas unidos a la membrana. La señalización de efrinas es crucial para la posición celular, el patrón de los tejidos y la angiogénesis. La desregulación de esta vía está implicada en el cáncer, enfermedades neurodegenerativas y trastornos del desarrollo. En CymitQuimica, ofrecemos inhibidores de los receptores de efrinas para apoyar su investigación en biología del desarrollo, oncología y neurobiología.
Se han encontrado 27 productos para "Receptor de efrina".
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ALW-II-49-7
CAS:ALW-II-49-7 is a selective and potent inhibitor of EphB2 kinase with an EC50 value of 40 nM in cell.Fórmula:C21H17F3N4O2Pureza:99.72%Forma y color:SolidPeso molecular:414.38Ref: TM-T67736
1mg67,00€5mg158,00€1mL*10mM (DMSO)167,00€10mg230,00€25mg416,00€50mg613,00€100mg873,00€500mg1.755,00€(123B9)2-L2-PTX
(123B9)2-L2-PTX is an EphA2 agonist peptide-drug conjugate (PDC). It consists of dimer 123B9 and Paclitaxel. This compound significantly reduces circulating tumor cells and inhibits lung metastasis in a breast cancer metastasis mouse model. (123B9)2-L2-PTX is applicable in cancer research, including studies on melanoma, ovarian cancer, and breast cancer.Forma y color:Odour SolidEphA2 agonist 1
CAS:Compound 7bg is a potent, selective EphA2 agonist targeting overexpressed glioblastoma cells.Fórmula:C50H58N12O12Forma y color:SolidPeso molecular:1019.07UniPR1449
UniPR1449 is an EphA2 receptor antagonist with a KD of 3.8±2.4 μM, which is significant in cancer pathophysiology [1].Pureza:98%Forma y color:Odour SolidAWL-II-38.3
CAS:AWL-II-38.3 is a highly potent EphA3 inhibitor with potent kinase inhibitory activity against EphA3.Cost-effective and quality-assured.Fórmula:C23H18F3N5O3Pureza:99.03% - 99.57%Forma y color:SolidPeso molecular:469.42Ref: TM-T38511
1mg77,00€5mg166,00€1mL*10mM (DMSO)167,00€10mg250,00€25mg515,00€50mg740,00€100mg1.018,00€500mg2.052,00€PKMYT1-IN-8
PKMYT1-IN-8 (Compound 137) is an inhibitor of PKMYT1, with an IC50 value of 9 nM. It also inhibits EPHB3, EPHA1, KIT, EPHB1, EPHA2, EPHA3, and EPHB2, exhibiting IC50 values of 1.79, 3.17, 4.29, 6.32, 6.83, 8.10, and 10.9 μM, respectively. Additionally, PKMYT1-IN-8 suppresses the proliferation of cancer cells OVCAR3 with a GI50 of 2.02 μM.Fórmula:C17H16F3N5O2Forma y color:SolidPeso molecular:379.336SA-PA
SA-PA, a self-assembled intracellular PROTAC leveraging azide-alkyne click chemistry, selectively degrades VEGFR-2, PDGFR-β, and EphB4 proteins within U87 cellsFórmula:C40H32ClF3N10O8Pureza:98%Forma y color:SolidPeso molecular:873.19AZ12672857
CAS:AZ12672857 is an inhibitor of EphB4 with IC50 of 1.3 nM.Fórmula:C26H30N8O2Pureza:98.99%Forma y color:Red SolidPeso molecular:486.57Ref: TM-T9650
1mg66,00€2mg87,00€5mg146,00€1mL*10mM (DMSO)158,00€10mg245,00€25mg403,00€50mg627,00€100mg847,00€KYL peptide
CAS:EphA4 inhibitor, Kd 0.8 μM, blocks EphA4-EphrinA5; avoids AβO damage, preserves spines & LTP; long half-life (8-12h), neuroprotective.Fórmula:C74H108N14O17Pureza:98%Forma y color:SolidPeso molecular:1465.75UniPR1454
UniPR1454 targets the EphA2 receptor and inhibits the interaction between EphA2 and ephrin A1, with an IC50 of 2.6 μM. Furthermore, UniPR1454 suppresses the proliferation of glioblastoma U251 cells.Forma y color:Odour SolidALW-II-41-27
CAS:ALW-II-41-27 (Eph receptor tyrosine kinase inhibitor), an Eph receptor tyrosine kinase inhibitor, is used for cancer therapy.Fórmula:C32H32F3N5O2SPureza:97.01% - 99.52%Forma y color:Yellow SolidPeso molecular:607.69Ref: TM-T4344
1mg63,00€5mg159,00€1mL*10mM (DMSO)216,00€10mg236,00€25mg371,00€50mg522,00€100mg713,00€200mg982,00€123C4
CAS:123C4 is a potent, selective and competitive agonist of the receptor tyrosine kinase EPHA4 (Ki=0.65 μM)[1].Fórmula:C43H47ClN8O6Pureza:98.94%Forma y color:SolidPeso molecular:807.34Ref: TM-TP1561
1mg137,00€5mg295,00€1mL*10mM (DMSO)480,00€10mg485,00€25mg772,00€50mg1.035,00€100mg1.395,00€NVP-BHG712 isomer
CAS:NVP-BHG712 isomer shows conserved non-bonded binding to EPHA2 and EPHB4.Fórmula:C26H20F3N7OPureza:99.14%Forma y color:White SolidPeso molecular:503.48Ref: TM-T19487
1mg40,00€2mg52,00€5mg84,00€1mL*10mM (DMSO)93,00€10mg142,00€25mg245,00€50mg356,00€100mg530,00€JI-101
CAS:JI-101 (CGI-1842) is an oral multi-kinase inhibitor that targets VEGFR-2, PDGFR-β, and EphB4.Fórmula:C22H20BrN5O2Pureza:99.41% - 99.97%Forma y color:SolidPeso molecular:466.33Tesevatinib
CAS:Tesevatinib (XL-647) is an oral, multi-targeted tyrosine kinase inhibitor.Cost-effective and quality-assured.Fórmula:C24H25Cl2FN4O2Pureza:97.89% - 99.99%Forma y color:White SolidPeso molecular:491.39NVP-BHG712
CAS:NVP-BHG712 is a specific EphB4 inhibitor with ED50 of 25 nM that discriminates between VEGFR and EphB4 inhibition; also shows activity against c-Raf, c-Src andFórmula:C26H20F3N7OPureza:97.32% - 98.63%Forma y color:SolidPeso molecular:503.48Ref: TM-T6348
1mg34,00€5mg74,00€1mL*10mM (DMSO)84,00€10mg105,00€25mg200,00€50mg371,00€100mg557,00€200mg790,00€Eph inhibitor 2
CAS:Eph inhibitor 2 is an Eph family tyrosine kinase inhibitor targeting Eph receptors.Fórmula:C18H15N5OPureza:99.01%Forma y color:White SolidPeso molecular:317.34KYL acetate(676657-00-4 free base)
EphA4 inhibitor, Kd: 0.8 μM, IC50: 6.34 μM. Protects synapses and spines, maintains LTP. Long half-life: 8-12h. Neuroprotective.Fórmula:C76H112N14O19Pureza:99.75%Forma y color:SolidPeso molecular:1525.78Tivozanib
CAS:Tivozanib (KRN951) is an oral VEGFRs 1-3 inhibitor with potential antiangiogenic and cancer-fighting properties.Fórmula:C22H19ClN4O5Pureza:98.08% - 99.67%Forma y color:SolidPeso molecular:454.86Ref: TM-T2456
2mg38,00€5mg57,00€1mL*10mM (DMSO)63,00€10mg79,00€25mg135,00€50mg226,00€100mg405,00€200mg597,00€Ehp-inhibitor-2
CAS:Ehp-inhibitor-2 is an Eph family tyrosine kinase inhibitor targeting Eph receptors.Fórmula:C17H13N5OPureza:97.88%Forma y color:SolidPeso molecular:303.32Ref: TM-T5452
2mg35,00€5mg55,00€1mL*10mM (DMSO)62,00€10mg96,00€25mg146,00€50mg210,00€100mg309,00€200mg444,00€
