Chromatin/Epigenetik
Chromatin-/Epigenetik-Inhibitoren sind Verbindungen, die die Struktur und Funktion des Chromatins modulieren oder epigenetische Modifikationen wie DNA-Methylierung und Histonmodifikation beeinträchtigen. Diese Inhibitoren sind wesentliche Werkzeuge zur Untersuchung der Genexpressionsregulation und der Rolle der Epigenetik bei Krankheiten wie Krebs, neurologischen Störungen und Entwicklungsanomalien. Durch die gezielte Beeinflussung epigenetischer Prozesse können diese Inhibitoren Genexpressionsmuster verändern und neue therapeutische Ansätze bieten. Bei CymitQuimica bieten wir eine breite Auswahl an hochwertigen Chromatin-/Epigenetik-Inhibitoren zur Unterstützung Ihrer Forschung in Molekularbiologie, Genetik und Epigenetik an.
Unterkategorien von "Chromatin/Epigenetik"
2592 Produkte aus dem Bereich "Chromatin/Epigenetik" gefunden
Sortieren nach
Reinheit (%)
0
100
|
0
|
50
|
90
|
95
|
100
JAK2 Inhibitor V
CAS:JAK2 Inhibitor V (JAK2 Inhibitor V Z3) is a novel specific inhibitor of Jak2, inhibiting Jak2-V617F and Jak2-WT autophosphorylation in a dose-dependent manner.Formel:C23H24N2OReinheit:98.36% - 99.15%Farbe und Form:SolidMolekulargewicht:344.45Ref: TM-T3042
2mg37,00€5mg54,00€10mg80,00€25mg148,00€50mg259,00€100mg477,00€500mg1.063,00€1mL*10mM (DMSO)59,00€SNDX-5613
CAS:Revumenib (SNDX-5613) is a potent and selective oral inhibitor of menin-KMT2A interaction.Cost-effective and quality-assured.Formel:C32H47FN6O4SReinheit:99.12% - 99.74%Farbe und Form:SolidMolekulargewicht:630.82Ref: TM-T12943
1mg73,00€2mg97,00€5mg160,00€10mg274,00€25mg542,00€50mg778,00€100mg1.074,00€1mL*10mM (DMSO)217,00€VTP50469
CAS:VTP50469 is a highly selective and orally active small molecule inhibitor of the Menin-MLL protein-protein interaction.Cost-effective and quality-assured.Formel:C32H47FN6O4SReinheit:98.31% - 99.55%Farbe und Form:SolidMolekulargewicht:630.82Ref: TM-T13336
1mg164,00€5mg334,00€10mg401,00€25mg560,00€50mg715,00€100mg964,00€1mL*10mM (DMSO)465,00€Fenbendazole
CAS:Fenbendazole (Fenbendazol) is an antinematodal benzimidazole used in veterinary medicine.Formel:C15H13N3O2SReinheit:99.74%Farbe und Form:White To Yellowish PowderMolekulargewicht:299.35GNE-781
CAS:GNE-781: potent CBP inhibitor (IC50: 0.94 nM), also targets BRET/BRD4(1) (IC50: 6.2/5100 nM).Formel:C27H33F2N7O2Reinheit:99.25% - 99.64%Farbe und Form:SolidMolekulargewicht:525.59Ref: TM-T15405
1mg138,00€5mg298,00€10mg485,00€25mg808,00€50mg1.093,00€100mg1.483,00€1mL*10mM (DMSO)343,00€Glucosamine hydrochloride
CAS:Glucosamine hydrochloride (Chitosamine hydrochloride) is commonly used as a treatment for osteoarthritis, although its acceptance as a medical therapy varies.Formel:C6H13NO5·HClReinheit:99.77%Farbe und Form:White Solid CrystallineMolekulargewicht:215.63Minocycline hydrochloride
CAS:Minocycline HCl: tetracycline antibiotic, treats bacterial infections and acne, may cause acute or chronic hepatitis.Formel:C23H28ClN3O7Reinheit:99.28% - >99.99%Farbe und Form:Bright Yellow-Orange Amorphous Solid Crystalline YellowMolekulargewicht:493.94Oltipraz
CAS:Oltipraz (RP 35972) is a synthetic dithiolethione with potential chemopreventive and anti-angiogenic properties.Formel:C8H6N2S3Reinheit:98.79% - 99.77%Farbe und Form:SolidMolekulargewicht:226.34A-395
CAS:A-395 blocks PRC2 (EZH2-EED-SUZ12) interactions, strongly inhibiting the complex with an IC50 of 18 nM.
Formel:C26H35FN4O2SReinheit:98.43%Farbe und Form:SolidMolekulargewicht:486.65Golidocitinib
CAS:Golidocitinib (AZD4205) is a selective JAK1 inhibitor (IC50: 73 nM) and weakly inhibits JAK2/JAK3 (IC50: >14.7, >30 μM).Formel:C25H31N9O2Reinheit:98.87% - 99.88%Farbe und Form:SolidMolekulargewicht:489.57TRIM24/BRPF1-IN-2
CAS:TRIM24/BRPF1-IN-2 is a TRIM24/BRPF1 dual inhibitor with anticancer activity that inhibits the proliferation of prostate cancer cells.Formel:C20H22N2O4SReinheit:98.69% - 99.13%Farbe und Form:SoildMolekulargewicht:386.47Uzansertib phosphate
CAS:Uzansertib phosphate (INCB053914 phosphate) is an orally active, ATP-competitive inhibitor of pan-PIM kinase, inhibiting PIM1, PIM2 and PIM3.Formel:C26H29F3N5O7PReinheit:99.75% - 99.79%Farbe und Form:SolidMolekulargewicht:611.51ODM-207
CAS:ODM-207 (BET-IN-4) is a potent BRD4 inhibitor.Formel:C22H21N3O3Reinheit:99.75%Farbe und Form:SolidMolekulargewicht:375.42Ref: TM-T10521
1mg44,00€5mg92,00€10mg133,00€25mg235,00€50mg339,00€100mg480,00€200mg660,00€1mL*10mM (DMSO)90,00€Levetiracetam
CAS:Levetiracetam (SIB-S1) is a relatively unique anticonvulsant that is typically used in combination with other antiepileptic medications for partial onsetFormel:C8H14N2O2Reinheit:99.67% - 99.86%Farbe und Form:White Crystalline PowderMolekulargewicht:170.21Lin28-let-7a antagonist 1
CAS:Lin28-let-7a antagonist 1, with an IC50 of 4.03 μM for Lin28A-let-7a-1 interaction，and shows a clear antagonistic effect against the Lin28-let-7a interaction.Formel:C31H29N5O7Reinheit:99.44%Farbe und Form:SolidMolekulargewicht:583.59Ref: TM-T11851
1mg96,00€5mg205,00€10mg313,00€25mg562,00€50mg845,00€100mg1.243,00€1mL*10mM (DMSO)266,00€MS402
CAS:MS402 is a novel BD1-selective BET BrD inhibitor.Formel:C20H19ClN2O3Reinheit:99.72%Farbe und Form:SolidMolekulargewicht:370.83LIN28 inhibitor LI71
CAS:LIN28 inhibitor LI71 is a potent and cell-permeable LIN28 inhibitor, which abolishes LIN28-mediated oligouridylation with an IC50 of 7 uM.Formel:C21H21NO3Reinheit:95.88%Farbe und Form:SolidMolekulargewicht:335.4Ref: TM-T11850
1mg107,00€5mg255,00€10mg414,00€25mg745,00€50mg1.063,00€100mg1.459,00€1mL*10mM (DMSO)341,00€BMS-986158
CAS:BMS-986158: BET inhibitor, IC50 of 6.6 nM in SCLC, 5 nM in TNBC cells.Formel:C30H33N5O2Reinheit:98.78%Farbe und Form:SolidMolekulargewicht:495.62Ref: TM-T14685
1mg87,00€5mg259,00€10mg465,00€25mg745,00€50mg1.026,00€100mg1.388,00€1mL*10mM (DMSO)283,00€MAK683
CAS:MAK683 is an inhibitor of embryonic ectoderm development (EED) (IC50s: 59, 89, 26 nM in EED Alphascreen binding, LC-MS and ELISA assay).Formel:C20H17FN6OReinheit:98.25% - 99.92%Farbe und Form:SolidMolekulargewicht:376.39Ref: TM-T15201
1mg52,00€5mg107,00€10mg188,00€25mg411,00€50mg607,00€100mg847,00€500mg1.758,00€1mL*10mM (DMSO)95,00€Pulrodemstat benzenesulfonate
CAS:Pulrodemstat benzenesulfonate (CC-90011 benzenesulfonate) is a potent and orally inhibitor of lysine specific demethylase-1 (LSD1) with anticancer effect.Formel:C30H29F2N5O5SReinheit:97.67%Farbe und Form:SolidMolekulargewicht:609.64Ref: TM-T11882
1mg60,00€2mg86,00€5mg124,00€10mg188,00€25mg329,00€50mg490,00€100mg710,00€1mL*10mM (DMSO)170,00€
