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2093401-33-1

2093401-33-1 Structure

2093401-33-1 Structure
IdentificationBack Directory
[Name]

OTS193320
[CAS]

2093401-33-1
[Synonyms]

OTS193320
cis-N1-(2-(5-Chloro-2,4-dimethoxyphenyl)imidazo[1,2-a]pyridin-7-yl)-N4-(4-nitrobenzyl)cyclohexane-1,4-diamine
1,4-Cyclohexanediamine, N1-[2-(5-chloro-2,4-dimethoxyphenyl)imidazo[1,2-a]pyridin-7-yl]-N4-[(4-nitrophenyl)methyl]-, cis-
[Molecular Formula]

C28H30ClN5O4
[MOL File]

2093401-33-1.mol
[Molecular Weight]

536.02
Chemical PropertiesBack Directory
[density ]

1.37±0.1 g/cm3(Predicted)
[form ]

Solid
[pka]

8.86±0.40(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

OTS193320, a imidazo[1,2-a]pyridine compound, is a SUV39H2 methyltransferase activity inhibitor. OTS193320 decreases global histone H3 lysine 9 tri-methylation levels in breast cancer cells and triggers apoptotic cell death. Combination of OTS193320 with Doxorubicin (DOX; HY-15142A) results in reduction of γ-H2AX levels as well as cancer cell viability compared to a single agent OTS193320 or DOX[1].
[IC 50]

SUV39H2/KMT1B
[References]

[1] Theodore Vougiouklakis, et al. Development of novel SUV39H2 inhibitors that exhibit growth suppressive effects in mouse xenograft models and regulate the phosphorylation of H2AX. Oncotarget. 2018 Aug 7;9(61):31820-31831. DOI:10.18632/oncotarget.25806
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