Recettore del fattore di crescita dei fibroblasti (FGFR)
Gli inibitori dei recettori del fattore di crescita dei fibroblasti (FGFR) sono terapie mirate che bloccano l'attività dei FGFR, coinvolti nella proliferazione cellulare, differenziazione e angiogenesi. La segnalazione FGFR contribuisce alla formazione di nuovi vasi sanguigni nei tumori, promuovendo la loro crescita e sopravvivenza. Inibire i FGFR può quindi ridurre l'angiogenesi e la progressione del tumore. Presso CymitQuimica, offriamo una gamma di inibitori FGFR di alta qualità per supportare la tua ricerca in oncologia, biologia dello sviluppo e angiogenesi.
Trovati 183 prodotti per "Recettore del fattore di crescita dei fibroblasti (FGFR)".
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FGFR4-IN-19
FGFR4-IN-19 (compound 8B) is a potent covalent inhibitor of fibroblast growth factor receptor 4 (FGFR4) with an IC50 value of 1.2 nM. It achieves high efficiency and selectivity by covalently targeting the rare cysteine (C552) in the FGFR4 kinase domain. FGFR4-IN-19 is applicable for hepatocellular carcinoma (HCC) research.Formula:C21H14Cl3N5O4Colore e forma:SolidPeso molecolare:505.01114FGFR4-IN-20
FGFR4-IN-20 (comp 11) is an orally active and selective FGFR4 inhibitor, demonstrating IC50 values of 19 nM against Huh7 cells and 36 nM for FGFR4 kinase. It is utilized in hepatocellular carcinoma research.Formula:C26H22Cl2N4O3Peso molecolare:508.1069FGFR1 inhibitor 7
FGFR1 Inhibitor 7 (compound 5), a potent FGFR1 tyrosine kinase inhibitor, exhibits an IC50 of 0.33 nM against its target and demonstrates broad-spectrumFormula:C25H16ClNO4Purezza:98%Colore e forma:SolidPeso molecolare:429.85PKCε (85-92)
CAS:PKCε (85-92) (ψεRACK) is a peptide and selective PKCε activator, induces a pro-angiogenic response, promotes FGF-2 cytosolization, regulates VEGF activity.Formula:C39H54N10O14Purezza:98.71%Colore e forma:SolidPeso molecolare:886.91PD 173074
CAS:Formula:C28H41N7O3Purezza:>95.0%(HPLC)Colore e forma:White to Yellow to Orange powder to crystalPeso molecolare:523.68(Z)-Orantinib
CAS:(Z)-Orantinib ((Z)-SU6668) is an orally active ATP-competitive inhibitor of Flk-1/KDR, PDGFRβ, and FGFR1, acting as a potent anti-angiogenic and anti-tumor agent.Formula:C18H18N2O3Purezza:98.05%Colore e forma:Orange SolidPeso molecolare:310.35Methyl 1-Acetyl-3-(ethoxyphenylmethylene)-2,3-dihydro-2-oxo-1H-indole-6-carboxylate
CAS:Formula:C21H19NO5Purezza:>95.0%(HPLC)(qNMR)Colore e forma:White to Light yellow to Light orange powder to crystalPeso molecolare:365.39NSC 12
CAS:NSC 12 is an orally active pan-FGF trap that binds FGF2 and interferes with its interaction with FGFR1 with potential FGF-dependent antitumor activity.Formula:C24H34F6O3Purezza:99.51%Colore e forma:White SolidPeso molecolare:484.52Regorafenib
CAS:Formula:C21H15ClF4N4O3Purezza:>98.0%(HPLC)Colore e forma:White to Light yellow to Light orange powder to crystalPeso molecolare:482.82SM27
CAS:SM27 is a fibroblast growth factor 2 (FGF2) inhibitor with anti-angiogenic activity and can be used to study tumours.Formula:C21H16N2O9S2Purezza:98.83%Colore e forma:SolidPeso molecolare:504.49Nintedanib
CAS:Formula:C31H33N5O4Purezza:>95.0%(T)(HPLC)Colore e forma:White to Yellow to Yellow green powder to crystalPeso molecolare:539.64PD-161570
CAS:Formula:C26H35Cl2N7OPurezza:>98.0%(HPLC)Colore e forma:White to Light yellow powder to crystalPeso molecolare:532.51PRN1371
CAS:PRN1371 is a specific and potent FGFR1-4 and CSF1R inhibitor (IC50s: 0.6/1.3/4.1/19.3/8.1 nM for FGFR1/2/3/4 and CSF1R).Formula:C26H30Cl2N6O4Purezza:98.65%Colore e forma:SolidPeso molecolare:561.46Ref: TM-TQ0015
1mg77,00€2mg100,00€5mg166,00€1mL*10mM (DMSO)200,00€10mg289,00€25mg492,00€50mg710,00€100mg973,00€R1530
CAS:R1530 is a multikinase inhibitor with antineoplastic and antiangiogenesis activities.Formula:C18H14ClFN4OPurezza:98.42%Colore e forma:SolidPeso molecolare:356.78Ref: TM-TQ0317
1mg39,00€2mg52,00€5mg84,00€1mL*10mM (DMSO)93,00€10mg130,00€25mg264,00€50mg423,00€100mg640,00€FGFR2-IN-3 hydrochloride
CAS:FGFR2-IN-3 hydrochloride is a selective, orally active FGFR2 inhibitor.Formula:C28H25ClFN7O2Colore e forma:SolidPeso molecolare:546.0KHS 101
CAS:KHS101 is a novel inhibitor of transforming acidic coiled-coil protein 3 (TACC3). It is a selective inducer of neuronal differentiation.Formula:C18H21N5SPurezza:99.63%Colore e forma:SolidPeso molecolare:339.46SU4984
CAS:SU4984 is a cell-permeable, ATP-competitive and reversible inhibitor of the fibroblast growth factor receptor 1 (FGFR1).Formula:C20H19N3O2Purezza:97.20%Colore e forma:SolidPeso molecolare:333.38PF 477736
CAS:PF 477736 (PF-736,PF-00477736) is a specifc, effective and ATP-competitive Chk1 inhibitor (Ki: 0.49 nM ) and also inhibits FGFR3, Aurora-A, VEGFR2, Flt3, Fms (Formula:C22H25N7O2Purezza:97.58% - 99.94%Colore e forma:Yellow SolidPeso molecolare:419.48Ferulic acid sodium
CAS:Ferulic acid sodium (Sodium ferulic) is an agent used in the treatment of cardiovascular and cerebrovascular diseases and to prevent thrombosis.Formula:C10H9NaO4Purezza:99.58%Colore e forma:SolidPeso molecolare:216.16GW786034B
CAS:Pazopanib HCl (Votrient) inhibits VEGFR1-3, PDGFR, FGFR, c-Kit, c-Fms with IC50 range 10-146 nM in cell-free assays.Formula:C21H23N7O2S·HClPurezza:99.87%Colore e forma:SolidPeso molecolare:473.98
