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2863635-05-4

2863635-05-4 Structure

2863635-05-4 Structure
IdentificationBack Directory
[Name]

4-Pyridinecarboxylic acid, 2-[[[2-[[2-(dimethylamino)ethyl]ethylamino]-2-oxoethyl]amino]methyl]-, 2,4-bis(1-methylethoxy)phenyl ester, hydrochloride (1:2)
[CAS]

2863635-05-4
[Synonyms]

4-Pyridinecarboxylic acid, 2-[[[2-[[2-(dimethylamino)ethyl]ethylamino]-2-oxoethyl]amino]methyl]-, 2,4-bis(1-methylethoxy)phenyl ester, hydrochloride (1:2)
[Molecular Formula]

C27H40N4O5.2ClH
[MOL File]

2863635-05-4.mol
[Molecular Weight]

573.55
Chemical PropertiesBack Directory
[solubility ]

Soluble to 50 mM in DMSO
Hazard InformationBack Directory
[Uses]

JQKD82 (JADA82) dihydrochloride is a cell-permeable and selective KDM5 inhibitor. JQKD82 dihydrochloride increases H3K4me3 and can be used for the research of multiple myeloma[1].
[Biological Activity]

JQKD 82 dihydrochloride is cell-permeable, selective inhibitor of lysine demethylase 5 (KDM5). JQKD 82 does not show activity toward other KDMs; and it has selectivity for KDM5A over other KDM5 isoforms. JQKD 82 causes hypermethylation of H3K4me3, downregulation of MYC targets and RNAPII phosphorylation; it suppresses multiple myeloma cell (MM.1S) growth (IC50 = 0.42 μmol/L). JQKD 82-treated tumors display an increase in H3K4me3 levels and results in a reduction of MYC immuno-staining in NSG mice.
[storage]

Store at -20°C
[References]

[1] Jun Qi, et al. Histone demethylase 5 inhibitors and uses thereof. WO2020033377A1.
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