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Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate
Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate
CAS No. 303141-21-1
Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate( DC-S239 )
Catalog No. M28480 CAS No. 303141-21-1
Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate is a selective inhibitor of histone methyltransferase SETD7 (IC50 = 4.59 μM) with anticancer activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 67 | In Stock |
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| 2MG | 36 | In Stock |
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| 5MG | 61 | In Stock |
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| 10MG | 98 | In Stock |
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| 25MG | 198 | In Stock |
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| 50MG | 313 | In Stock |
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| 100MG | 498 | In Stock |
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| 200MG | 681 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameEthyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate
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NoteResearch use only, not for human use.
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Brief DescriptionEthyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate is a selective inhibitor of histone methyltransferase SETD7 (IC50 = 4.59 μM) with anticancer activity.
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DescriptionEthyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate is a selective inhibitor of histone methyltransferase SETD7 (IC50 = 4.59 μM) with anticancer activity.(In Vitro):Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate (0-100 μM) inhibits the proliferation of MCF7, HL60 and MV4-11 cells in a dose-dependent manner with the IC50 values of 10.93 μM and 16.43 μM, respectively. Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate inhibits DNMT1, DOT1L, EZH2, NSD1, SETD8 and G9a by less than 45%, whereas it inhibits SET7 by 90% at concentrations of 100 μM.
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In VitroDC-S239 inhibits DNMT1, DOT1L, EZH2, NSD1, SETD8 and G9a by less than 45%, while it inhibits SET7 by 90% at concentrations of 100 μM.DC-S239 (0-100 μM, 120 h) can inhibit the proliferation of MCF7, HL60 and MV4-11 cells in a dose-dependent manner but no significant effect on the activity of HCT116 and DHL4 cells.Cell Viability Assay Cell Line:MCF7, HL60, DHL4, MV4-11 and HCT116 cell lines Concentration:0-100 μM Incubation Time:120 h Result:Inhibited MCF7 and HL60 with the IC50 values of 10.93 μM and 16.43 μM, respectively.
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In Vivo——
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SynonymsDC-S239
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PathwayChromatin/Epigenetic
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TargetHistone Demethylase
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RecptorD1
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Research Area——
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Indication——
Chemical Information
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CAS Number303141-21-1
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Formula Weight349.36
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Molecular FormulaC15H15N3O5S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 125 mg/mL (357.80 mM)
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SMILESCCOC(c1c(N)sc(C(Nc2cc([N+]([O-])=O)ccc2)=O)c1C)=O
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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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