ChemicalBook--->CAS DataBase List--->2369663-93-2

2369663-93-2

2369663-93-2 Structure

2369663-93-2 Structure
IdentificationBack Directory
[Name]

DB1976 hydrochloride
[CAS]

2369663-93-2
[Synonyms]

DB1976 hydrochloride
DB1976 dihydrochloride
[Molecular Formula]

C20H17ClN8Se
[MDL Number]

MFCD32857162
[MOL File]

2369663-93-2.mol
[Molecular Weight]

483.83
Chemical PropertiesBack Directory
[form ]

Solid
[color ]

Brown to black
Hazard InformationBack Directory
[Description]

DB1976 is a selenophene analog of DB270 and a potent and cell-permeable fully efficacious transcription factor PU.1 inhibitor. DB1976 potently inhibits PU.1 binding and strongly inhibits the PU.1/DNA complex in vitro. DB1976 has apoptosis-inducing effect.
[Uses]

DB1976 dihydrochloride is a selenophene analog of DB270 and a potent and cell-permeable fully efficacious transcription factor PU.1 inhibitor. DB1976 dihydrochloride potently inhibits PU.1 binding (IC50 of 10 nM) and strongly inhibits the PU.1/DNA complex (with high DB1976-λB affinity, KD of 12 nM) in vitro. DB1976 dihydrochloride has apoptosis-inducing effect[1][2][3].
[References]

[1] Munde M, et al. Structure-dependent inhibition of the ETS-family transcription factor PU.1 by novel heterocyclic diamidines. Nucleic Acids Res. 2014 Jan;42(2):1379-90. DOI:10.1093/nar/gkt955
[2] Stephens DC, et al. Pharmacologic efficacy of PU.1 inhibition by heterocyclic dications: a mechanistic analysis. Nucleic Acids Res. 2016 May 19;44(9):4005-13. DOI:10.1093/nar/gkw229
[3] Antony-Debré I, et al. Pharmacological inhibition of the transcription factor PU.1 in leukemia. J Clin Invest. 2017 Dec 1;127(12):4297-4313. DOI:10.1172/JCI92504
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