

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)






Size | Price / USD | Stock | Quantity |
5MG | 222 | Get Quote |
![]() ![]() |
10MG | 357 | Get Quote |
![]() ![]() |
25MG | 597 | Get Quote |
![]() ![]() |
50MG | 851 | Get Quote |
![]() ![]() |
100MG | 1152 | Get Quote |
![]() ![]() |
500MG | 2313 | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameEthyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate
-
NoteResearch use only, not for human use.
-
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.
-
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.
-
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.
-
In Vivo——
-
SynonymsDC-S239
-
PathwayChromatin/Epigenetic
-
TargetHistone Demethylase
-
RecptorD1
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number303141-21-1
-
Formula Weight349.36
-
Molecular FormulaC15H15N3O5S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 125 mg/mL (357.80 mM)
-
SMILESCCOC(c1c(N)sc(C(Nc2cc([N+]([O-])=O)ccc2)=O)c1C)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog



related products
-
TC-E 5003
TC-E 5003 is a selective inhibitor of PRMT1 with IC50 of 1.5 μM.
-
Daminozide
Daminozide(DMASA; DIMG; B 995), a plant growth regulator, selectively inhibits the KDM2/7 JmjC subfamily.
-
KDM5A covalent inhib...
KDM5A covalent inhibitor N73 is the the isopropyl ester derivative of N71.