Angiogénesis
Los inhibidores de la angiogénesis son compuestos que interfieren con la formación de nuevos vasos sanguíneos, un proceso crucial en el crecimiento y la metástasis del cáncer. Al inhibir la angiogénesis, estos compuestos pueden restringir el suministro de sangre a los tumores, ralentizando o deteniendo su crecimiento. Los inhibidores de la angiogénesis son esenciales en la investigación del cáncer y en el desarrollo terapéutico, proporcionando información sobre los mecanismos de progresión tumoral y ofreciendo posibles tratamientos para el cáncer y otras enfermedades relacionadas con la angiogénesis. En CymitQuimica, ofrecemos una amplia gama de inhibidores de la angiogénesis de alta calidad para apoyar su investigación en oncología y biología vascular.
Subcategorías de "Angiogénesis"
- BTK(166 productos)
- Bcr-Abl(117 productos)
- EGFR(553 productos)
- FAK(72 productos)
- FLT(88 productos)
- Receptor del factor de crecimiento de fibroblastos (FGFR)(176 productos)
- JAK(243 productos)
- PDGFR(127 productos)
- RAAS(86 productos)
- Src(82 productos)
- Syk(37 productos)
- Trombina(51 productos)
- VDA(2 productos)
- VEGFR(236 productos)
Mostrar 6 subcategorías más
Se han encontrado 2277 productos de "Angiogénesis"
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PKI-166
CAS:PKI-166: oral EGF-R tyrosine kinase inhibitor (IC50: 0.7 nM), halts growth & spread of many human cancers, including pancreatic.Fórmula:C20H18N4OPureza:99.2%Forma y color:SolidPeso molecular:330.38Ref: TM-T16549
2mg39,00€5mg75,00€10mg111,00€25mg215,00€50mg358,00€100mg572,00€200mg767,00€1mL*10mM (DMSO)84,00€A 419259 trihydrochloride
CAS:A 419259 trihydrochloride (RK 20449 trihydrochloride) is an Src family kinases inhibitor (IC50s: 9 nM, 3 nM and 3 nM for Src, Lck and Lyn).Fórmula:C29H37Cl3N6OPureza:99.75% - 99.96%Forma y color:SolidPeso molecular:592BMS-605541
CAS:BMS-605541 is a potent and selective inhibitor of vascular endothelial growth factor receptor-2 (VEGFR-2) kinase activity(Ki=49 nM).
Fórmula:C19H17F2N5OSPureza:98.07%Forma y color:SolidPeso molecular:401.43Tafetinib
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:424.51Cloperastine fendizoate
CAS:Cloperastine fendizoate (Hustazol) inhibits the hERG K+ currents in a concentration-dependent manner (IC50: 27 nM).Fórmula:C40H38ClNO5Pureza:99.97%Forma y color:SolidPeso molecular:648.19TG-89
CAS:TG-89 is an inhibitor of JAK2, JAK3, RET and FLT3, and has an IC50 value of 11.2 μM against JAK2, showing anticancer activity in the treatment of ovarian andFórmula:C26H34N6O3SPureza:98.68%Forma y color:SolidPeso molecular:510.65SI-2 hydrochloride
CAS:SI-2 hydrochloride, an SRC-3 inhibitor, induces breast cancer cell death (IC50: 3-20 nM) with good oral bioavailability.Fórmula:C15H16ClN5Pureza:98.6%Forma y color:SolidPeso molecular:301.77EMI1
CAS:EMI1 targets mutated EGFR in drug-resistant NSCLC research.Fórmula:C20H18N2O3Pureza:99.96%Forma y color:SolidPeso molecular:334.37(±)-Zanubrutinib
CAS:(±)-Zanubrutinib ((±)-BGB-3111) is a potent and orally available Bruton's tyrosine kinase (Btk) inhibitor that demonstrates superior oral bioavailability,Fórmula:C27H29N5O3Pureza:99.09%Forma y color:SolidPeso molecular:471.55Ref: TM-TQ0039
1mg47,00€5mg92,00€10mg145,00€25mg256,00€50mg409,00€100mg587,00€500mg1.215,00€1mL*10mM (DMSO)101,00€PPY A
CAS:PPY A is a potent inhibitor of T315l mutant and wild-type Abl kinase and inhibits the growth of Bcr-Abl T315l mutant or wild-type Bcr-Abl gene-transformed cellsFórmula:C22H20N4O2Pureza:98.77%Forma y color:SolidPeso molecular:372.42Sunvozertinib
CAS:Sunvozertinib (DZD9008) is a potent ErbBs and BTK inhibitor, with inhibitory effects on EGFR, Her2.Cost-effective and quality-assured.Fórmula:C29H35ClFN7O3Pureza:98.11% - 99.63%Forma y color:SolidPeso molecular:584.08Ref: TM-T64124
1mg34,00€5mg60,00€10mg85,00€25mg124,00€50mg200,00€100mg353,00€500mg1.314,00€1mL*10mM (DMSO)150,00€Epitinib succinate
CAS:Epitinib succinate (HMPL-813 succinate) is an orally active and brain penetration EGFR tyrosine kinase inhibitor and can be used in studies about cancer.Fórmula:C28H32N6O6Pureza:98.02% - 99.79%Forma y color:SolidPeso molecular:548.59Ref: TM-T35914
1mg75,00€2mg97,00€5mg170,00€10mg271,00€25mg449,00€50mg615,00€100mg843,00€500mg1.691,00€JAK-STAT-IN-1
CAS:JAK-STAT-IN-1 is a specific JAK-STAT inhibitor indicated for the study of autoimmune diseases.Fórmula:C21H21N5O2Pureza:99.59%Forma y color:SolidPeso molecular:375.42Dasatinib hydrochloride
CAS:Dasatinib hydrochloride is an oral Src/Bcr-Abl inhibitor with potent antitumor effects, Ki values of 16 pM (Src) and 30 pM (Bcr-Abl).Fórmula:C22H27Cl2N7O2SPureza:99.88% - 99.98%Forma y color:SolidPeso molecular:524.47SU16f
CAS:SU16f, a 3-substituted indolin-2-one, is a selective PDGFRβ inhibitor; IC50: 10 nM (PDGFRβ), 140 nM (PDGFR1), 2.29 μM (PDGFR2), halts GC cell growth.Fórmula:C24H22N2O3Pureza:97.69%Forma y color:SolidPeso molecular:386.44LY 456236 hydrochloride
CAS:LY 456236 hydrochloride (MPMQ hydrochloride) is an mGlu1 receptor antagonist with an ic50 value of 143 nM.Fórmula:C16H16ClN3O2Pureza:99.95%Forma y color:SolidPeso molecular:317.77CHMFL-EGFR-202
CAS:CHMFL-EGFR-202 is a potent, irreversible inhibitor of EGFR mutant kinase (IC50s: 5.3 nM and 8.3 nM for drug-resistant mutant EGFR T790M and WT EGFR kinases).Fórmula:C25H24ClN7O2Pureza:99.66%Forma y color:SolidPeso molecular:489.96Ref: TM-T10802
1mg109,00€2mg163,00€5mg241,00€10mg355,00€25mg532,00€50mg745,00€100mg1.018,00€1mL*10mM (DMSO)289,00€JNJ-49095397
CAS:JNJ-49095397 (RV568) is a p38 MAPK-α and p38 MAPK-γ kinase inhibitor for the study of respiratory syncytial virus infection.Fórmula:C34H36N6O4Pureza:98.33% - 99.04%Forma y color:SolidPeso molecular:592.69(R)-Zanubrutinib
CAS:(R)-Zanubrutinib ((R)-BGB-3111) is a selective inhibitor of Bruton tyrosine kinase (BTK).Fórmula:C27H29N5O3Pureza:99.55%Forma y color:SolidPeso molecular:471.55Ref: TM-T13447
1mg37,00€5mg80,00€10mg133,00€25mg215,00€50mg323,00€100mg442,00€200mg615,00€1mL*10mM (DMSO)85,00€AMPK-IN-3
CAS:AMPK-IN-3: potent, selective AMPK (α2/α1) & KDR inhibitor; IC50: 60.7/107/3820 nM; anticancer in K562 cells.Fórmula:C25H33N5O3Pureza:97.25%Forma y color:SolidPeso molecular:451.56
