Valemetostat
CAS No. 1809336-39-7
Valemetostat( —— )
Catalog No. M21864 CAS No. 1809336-39-7
Valemetostat is a dual inhibitor of enhancer of zeste homolog 1 (EZH1) and EZH2.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 177 | In Stock |
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10MG | 312 | In Stock |
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25MG | 520 | In Stock |
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50MG | 743 | In Stock |
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100MG | 981 | In Stock |
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200MG | Get Quote | In Stock |
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Biological Information
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Product NameValemetostat
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NoteResearch use only, not for human use.
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Brief DescriptionValemetostat is a dual inhibitor of enhancer of zeste homolog 1 (EZH1) and EZH2.
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DescriptionValemetostat is a dual inhibitor of enhancer of zeste homolog 1 (EZH1) and EZH2.1 It inhibits polycomb repressive complex 2 (PRC2) containing EZH1 or EZH2 as the catalytic subunit in cell-free assays (IC50s = 8.4 and 2.5 nM, respectively). Valemetostat inhibits trimethylation of histone H3 lysine 27 in HCT116 cells (IC50 = 0.44 nM). It inhibits the growth of Karpas-422 diffuse large B cell lymphoma (DLBCL) cells (GI50 = 4.8 nM).(In Vitro):Valemetostat (1-1000 nM) strongly and specifically inhibits EZH1 and EZH2 with IC50 values <10 nM.Valemetostat (100 nM; 7 d) effectively removes H3K27me3 and also prevents unexpected gain of H3K27me3.Valemetostat (0.1-100 nM; 7 d) potently inhibits H3K27me3 by low-dose treatment in the sensitive lymphoma types.(In Vivo):Valemetostat (0.01 mg/g; i.p.; once) prevents the changes of H3K27me3 after exercise training.
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In VitroValemetostat (1-1000 nM) strongly and specifically inhibits EZH1 and EZH2 with IC50 values <10 nM.Valemetostat (100 nM; 7 d) effectively removes H3K27me3 and also prevents unexpected gain of H3K27me3. Valemetostat (0.1-100 nM; 7 d) potently inhibits H3K27me3 by low-dose treatmentin the sensitive lymphoma types.
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In VivoValemetostat (0.01 mg/g; i.p.; once) prevents the changes of H3K27me3 after exercise training. Animal Model:Male C57BL/6J mice with chronic and acute running exercise or without exercise Dosage:0.01 mg/g Administration:Intraperitoneal injection; 0.01 mg/g; 30 min before the start of running exercise Result:Significantly increased the level of H3K27me3 , slightly decresed EZH1 level , upregulated the EZH2 level and increased the level of phosphorylated AMPK after exercise. Repressed myonuclear H3K27me3 accumulation during training and caused a failure of adaptive changes.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorEZH1/2
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Research Area——
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Indication——
Chemical Information
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CAS Number1809336-39-7
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Formula Weight488.02
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Molecular FormulaC26H34ClN3O4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 70 mg/mL (143.44 mM)
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SMILESCC1=CC(=C(C(=O)N1)CNC(=O)C2=CC(=C3C(=C2C)OC(O3)(C)C4CCC(CC4)N(C)C)Cl)C
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
molnova catalog
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