ChemicalBook--->CAS DataBase List--->1557397-51-9

1557397-51-9

1557397-51-9 Structure

1557397-51-9 Structure
IdentificationBack Directory
[Name]

DB1976
[CAS]

1557397-51-9
[Synonyms]

DB1976
[Molecular Formula]

C20H16N8Se
[MDL Number]

MFCD34469954
[MOL File]

1557397-51-9.mol
[Molecular Weight]

447.35
Chemical PropertiesBack Directory
[Boiling point ]

796.5±70.0 °C(Predicted)
[pka]

9.42±0.10(Predicted)
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 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 (IC50 of 10 nM) and strongly inhibits the PU.1/DNA complex (with high DB1976-λB affinity, KD of 12 nM) in vitro. DB1976 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
Spectrum DetailBack Directory
[Spectrum Detail]

DB1976(1557397-51-9)1HNMR
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