
Metiltransferasi del DNA
Le metiltransferasi del DNA (DNMT) sono enzimi che catalizzano l'aggiunta di gruppi metilici ai residui di citosina nel DNA, portando al silenziamento genico. Una metilazione aberrante del DNA è associata a varie malattie, incluso il cancro. Gli inibitori delle DNMT bloccano l'attività di questi enzimi, portando alla riattivazione dei geni silenziati e all'induzione dell'apoptosi nelle cellule tumorali. Gli inibitori delle DNMT sono ampiamente utilizzati nella ricerca epigenetica e nella terapia del cancro. Presso CymitQuimica, offriamo una gamma di inibitori delle DNMT di alta qualità per supportare la tua ricerca in epigenetica, metilazione del DNA e biologia del cancro.
Trovati 450 prodotti di "Metiltransferasi del DNA"
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
1-Hydrazinophthalazine Hydrochloride
CAS:Formula:C8H8N4·HClPurezza:>99.0%(T)(HPLC)Colore e forma:White to Almost white powder to crystalPeso molecolare:196.64Procaine Hydrochloride
CAS:Formula:C13H20N2O2·HClPurezza:>98.0%(T)(HPLC)Colore e forma:White to Almost white powder to crystalPeso molecolare:272.77Zebularine
CAS:Formula:C9H12N2O5Purezza:>98.0%(T)(HPLC)Colore e forma:White to Light yellow powder to crystalPeso molecolare:228.20(-)-Epigallocatechin Gallate Hydrate
CAS:Formula:C22H18O11·xH2OPurezza:>98.0%(HPLC)Colore e forma:White to Light yellow to Light orange powder to crystalPeso molecolare:458.38 (as Anhydrous)Chlorogenic Acid
CAS:Formula:C16H18O9Purezza:>98.0%(T)(HPLC)Colore e forma:White to Light yellow powder to crystalPeso molecolare:354.31N-Phthalyl-L-tryptophan
CAS:Formula:C19H14N2O4Purezza:>98.0%(T)(HPLC)Colore e forma:Light yellow to Amber to Dark green powder to crystalinePeso molecolare:334.33Genistein
CAS:Formula:C15H10O5Purezza:>98.0%(HPLC)Colore e forma:White to Light yellow to Light orange powder to crystalPeso molecolare:270.24Caffeic Acid
CAS:Formula:C9H8O4Purezza:>98.0%(T)(HPLC)Colore e forma:White to Orange to Green powder to crystalPeso molecolare:180.165-Azacytidine
CAS:Formula:C8H12N4O5Purezza:>98.0%(T)Colore e forma:White to Almost white powder to crystalPeso molecolare:244.21Diperodon hydrochloride
CAS:Diperodon hydrochloride (Diperocaine) is a local anesthetic that can be broken down by serolytic enzymes to produce local anesthetic effects.Formula:C22H28ClN3O4Purezza:99.91%Colore e forma:SolidPeso molecolare:433.934-amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydro-1,3,5-triazin-2-one
CAS:Formula:C8H12N4O5Purezza:98%Colore e forma:SolidPeso molecolare:244.2047(E)-3,4-dihydroxycinnamic acid
CAS:Formula:C9H8O4Purezza:98%Colore e forma:SolidPeso molecolare:180.15745-Azacytidine
CAS:5-Azacytidine (Ladakamycin) is a cytidine nucleoside analog, a DNA methylation inhibitor with specificity.Formula:C8H12N4O5Purezza:98% - 99.79%Colore e forma:Crystals From Methanol Physical Description White Crystalline Powder (Ntp 1992)Peso molecolare:244.2Decitabine
CAS:Decitabine (Deoxycytidine) is a deoxycytidine analog, a DNA methyltransferase inhibitor with oral activity.Formula:C8H12N4O4Purezza:98.06% - 99.87%Colore e forma:Physical Description Fine White Crystalline Powder Used As A DrugPeso molecolare:228.21A-395
CAS:<p>A-395 blocks PRC2 (EZH2-EED-SUZ12) interactions, strongly inhibiting the complex with an IC50 of 18 nM.</p>Formula:C26H35FN4O2SPurezza:98.43%Colore e forma:SolidPeso molecolare:486.65Amodiaquine dihydrochloride dihydrate
CAS:<p>Amodiaquine dihydrochloride dihydrate (Amodiaquin hydrochloride) is an orally active 4-aminoquinoline derivative with antimalarial and anti-inflammatory effects</p>Formula:C20H28Cl3N3O3Purezza:99.97%Colore e forma:SolidPeso molecolare:464.824H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-
CAS:Formula:C15H10O5Purezza:97%Colore e forma:SolidPeso molecolare:270.2369Ref: IN-DA00I8G3
1g26,00€5g24,00€10g31,00€1kg686,00€25g52,00€50g77,00€5kgPrezzo su richiesta100g114,00€10kgPrezzo su richiesta250g181,00€500g320,00€100mg26,00€Procaine Hydrochloride
CAS:Formula:C13H21ClN2O2Purezza:98%Colore e forma:SolidPeso molecolare:272.7710(1S,3R,4R,5R)-3-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid
CAS:Formula:C16H18O9Purezza:98%Colore e forma:SolidPeso molecolare:354.3087Ref: IN-DA00I681
1g30,00€5g52,00€10g75,00€1kgPrezzo su richiesta25g153,00€100g489,00€250gPrezzo su richiesta500gPrezzo su richiesta50kg41.345,00€250mg26,00€Phthalazine, 1-hydrazinyl-, hydrochloride (1:1)
CAS:Formula:C8H9ClN4Purezza:98%Colore e forma:SolidPeso molecolare:196.6369Dihydro-5-azacytidine FA
Dihydro-5-azacytidine FA (DHAC) is a pyrimidine analog that has antitumor activity, inhibits cell growth, inhibits DNA methylation, and may be used in the study of malignant mesothelioma.Formula:C9H16N4O7Purezza:>99.99%Colore e forma:SolidPeso molecolare:292.25(2R,3R)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate
CAS:Formula:C22H18O11Purezza:98%Colore e forma:SolidPeso molecolare:458.3717Ref: IN-DA00IK6L
1g22,00€5g24,00€10g31,00€1kg527,00€25g55,00€50g80,00€5kgPrezzo su richiesta100g114,00€250g177,00€500g302,00€EBI-2511
CAS:EBI-2511 is a highly potent and orally active inhibitor of EZH2 (IC50: 6 nM in Pfeffiera cell lines).Formula:C34H48N4O4Purezza:99.74%Colore e forma:SolidPeso molecolare:576.774-amino-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydro-1,3,5-triazin-2-one
CAS:Formula:C8H12N4O4Purezza:98%Colore e forma:SolidPeso molecolare:228.2053Ref: IN-DA002NLT
1g99,00€5g255,00€10g563,00€25gPrezzo su richiesta50gPrezzo su richiesta5mg30,00€100gPrezzo su richiesta100mg31,00€250mg53,00€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).Formula:C20H17FN6OPurezza:98.25% - 99.92%Colore e forma:SolidPeso molecolare:376.39BVT948
CAS:BVT948 is a protein tyrosine phosphatase (PTP) inhibitor.It can also inhibit lysine methyltransferase SETD8 (KMT5A) and several cytochrome P450 (P450) isoforms.Formula:C14H11NO3Purezza:98.87%Colore e forma:SolidPeso molecolare:241.24iso-Azalansta
CAS:(2R,4S)-Azalanstat (Iso-Azalansta) is a selective heme oxygenase (HO) inhibitor that is used in the study of cardiovascular disease.Formula:C22H24ClN3O2SPurezza:99.53% - 99.89%Colore e forma:SoildPeso molecolare:429.96N-Phthalyl-L-tryptophan
CAS:Formula:C19H14N2O4Purezza:95%Colore e forma:SolidPeso molecolare:334.3255Levetiracetam
CAS:Levetiracetam (SIB-S1) is a relatively unique anticonvulsant that is typically used in combination with other antiepileptic medications for partial onsetFormula:C8H14N2O2Purezza:99.67% - 99.86%Colore e forma:White Crystalline PowderPeso molecolare:170.21Tulmimetostat
CAS:Tulmimetostat (CPI-0209) is an orally active EZH1/EZH2 inhibitor.Tulmimetostat has antitumor activity and is used in the study of ovarian cancer and advancedFormula:C28H36ClN3O5SPurezza:98.04% - 99.872%Colore e forma:SolidPeso molecolare:562.12Valemetostat
CAS:Valemetostat (DS-3201) is a first-in-class EZH1/2 dual inhibitor, which can be used to study T-cell lymphoma.Cost-effective and quality-assured.Formula:C26H34ClN3O4Purezza:98.38% - 99.83%Colore e forma:SolidPeso molecolare:488.022(1H)-Pyrimidinone, 1-β-D-ribofuranosyl-
CAS:Formula:C9H12N2O5Purezza:98%Colore e forma:SolidPeso molecolare:228.2020DC-05
CAS:<p>DC-05 is an inhibitor of DNA methyltransferase 1 (DNMT1) (IC50 and a Kd: 10.3 μM and 1.09 μM, respectively).</p>Formula:C25H25N3OPurezza:98.95%Colore e forma:SolidPeso molecolare:383.49A-893
CAS:A-893 is a cell-active inhibitor of Methyltransferase SMYD2 (IC 50 = 2.8 nM) .Formula:C29H38Cl2N4O4Colore e forma:SolidPeso molecolare:577.54PROTAC EED degrader-1
PROTAC EED degrader-1 is a PROTAC targeting EED (pKD = 9.02), is a inhibitor of polycomb repressive complex 2 (PRC2) with pIC50 of 8.17.Formula:C55H60FN11O8SPurezza:98%Colore e forma:SolidPeso molecolare:1054.2PRMT5-IN-9
CAS:<p>PRMT5-IN-9 is a novel PRMT5 inhibitor for treating cancer, with an IC 50 of 0.01 μM.</p>Formula:C25H23F3N6OColore e forma:SolidPeso molecolare:480.495Larsucosterol Ammonium salt
CAS:Larsucosterol ammonium salt is a derivative of 25HC3S. It is a DNMT inhibitor, a LXR antagonist, an endogenous epigenetic modulator of lipid metabolism.Formula:C27H49NO5SPurezza:>99.99% - >99.99%Colore e forma:SoildPeso molecolare:499.75SW2_152F
<p>SW2_152F: Potent CBX2 ChD inhibitor, Kd 80 nM, 24-1000x selective over other CBXs in vitro.</p>Formula:C45H62Cl3N7O8Colore e forma:SolidPeso molecolare:935.37WDR5-47
CAS:WDR5-47 is a potent small molecule to disturb the interaction of MLL1-WDR5 with IC50 value of 0.3μM.Formula:C19H20ClFN4O3Purezza:98.15%Colore e forma:SoildPeso molecolare:406.84UNC6852
CAS:<p>UNC6852 contains an EED ligand (IC50 = 247 nM) and a von Hippel-Lindau ligand and is a selective polycomb repressive complex 2 (PRC2) degrader based on PROTAC.</p>Formula:C43H48N10O6SPurezza:96.64%Colore e forma:SolidPeso molecolare:832.97SAH-EZH2
CAS:<p>EZH2/EPP inhibitor, Kd 320 nM. Reduces EZH2, H3K27me3; halts MLL-AF9 leukemia growth; drives monocyte-macrophage differentiation.</p>Formula:C155H256N48O40Purezza:98%Colore e forma:SolidPeso molecolare:3432.05FTX-6058
CAS:FTX-6058 is an oral inhibitor of EED that induces HbF and may treat hemoglobinopathies like sickle cell and β-thalassemia.Formula:C22H18FN5O2Colore e forma:SolidPeso molecolare:403.417UNC2399
CAS:<p>UNC2399, a biotinylated version of UNC1999, functions as a selective degrader of EZH2 and exhibits strong in vitro efficacy against EZH2, demonstrated by its IC</p>Formula:C67H104N10O17SColore e forma:SolidPeso molecolare:1353.68PRMT5-IN-11
CAS:PRMT5-IN-11 demonstrates potent structure-dependent inhibition against the protein methyltransferase PRMT5:MEP50 complex at submicromolar concentrations.Formula:C13H17N5O4Colore e forma:SolidPeso molecolare:307.31ML234
ML234 is a dual inhibitor targeting EZH2/LSD1, with IC50 values of 0.09 and 0.12 μM, respectively. It demonstrates strong antiproliferative effects on prostate cancer cell lines LNCAP, PC3, and 22RV1. Additionally, ML234 inhibits tumor growth in a 22RV1 xenograft mouse model, showing potential as a research agent in prostate cancer therapeutics.Colore e forma:Odour SolidDot1L-IN-9
Dot1L-IN-9 (Compound 12) is a DOT1L inhibitor with an IC50 of 125 nM. It effectively reduces H3K79 dimethylation and is utilized in leukemia research.Colore e forma:Odour SolidBBDDL2204
BBDDL2204 (compound 13) is a potent and selective covalent inhibitor of EZH2, demonstrating an IC50 of 2.5 nM against EZH2Y641F.Formula:C37H47N5O5SColore e forma:SolidPeso molecolare:673.32979XF056-132
CAS:XF056-132 is a potent WDR5 (WD40 repeat domain protein 5) PROTAC degrader [1] .Formula:C51H57F4N9O7SColore e forma:SolidPeso molecolare:1016.11



