
KDM5-C49
CAS No. 1596348-16-1
KDM5-C49( KDM5 inhibitor C49 )
Catalog No. M12279 CAS No. 1596348-16-1
KDM5-C49 is a potent, selective KDM5 inhibitor with IC50 of 25, 30 and 59 nM for KDM5A, B and C, respectively.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 873 | Get Quote |
![]() ![]() |
50MG | 1782 | Get Quote |
![]() ![]() |
100MG | 2250 | Get Quote |
![]() ![]() |
200MG | Get Quote | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameKDM5-C49
-
NoteResearch use only, not for human use.
-
Brief DescriptionKDM5-C49 is a potent, selective KDM5 inhibitor with IC50 of 25, 30 and 59 nM for KDM5A, B and C, respectively.
-
DescriptionKDM5-C49 is a potent, selective KDM5 inhibitor with IC50 of 25, 30 and 59 nM for KDM5A, B and C, respectively; displays 25-100-fold selectivity over KDM6B, 2-30-fold selectivity over KDM4 family, but with less cell-permeablity.
-
In Vitro——
-
In Vivo——
-
SynonymsKDM5 inhibitor C49
-
PathwayChromatin/Epigenetic
-
TargetHistone Demethylase
-
RecptorHistone Demethylase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1596348-16-1
-
Formula Weight308.382
-
Molecular FormulaC15H24N4O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(O)C1=CC=NC(CNCC(N(CCN(C)C)CC)=O)=C1
-
Chemical Name2-(((2-((2-(dimethylamino)ethyl)(ethyl)amino)-2-oxoethyl)amino)methyl)isonicotinic acid
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Johansson C, et. Nat Chem Biol. 2016 Jul;12(7):539-45.
2. Horton JR, et al. Cell Chem Biol. 2016 Jul 21;23(7):769-81.
molnova catalog



related products
-
Vafidemstat
Vafidemstat is a novel potent, selective lysine-specific histone demethylase (LSD1) inhibitor.
-
SGC-iMLLT
SGC-iMLLT is a potent and selective MLLT1/3-histone interactions inhibitor(IC50 = 0.26 μM),and is a first-in-class chemical probe displaying cellular target engagement of MLLT1(Kd = 0.129?μM) and MLLT3(Kd = 0.077?μM).
-
TC-E 5003
TC-E 5003 is a selective inhibitor of PRMT1 with IC50 of 1.5 μM.