Bromosporine

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Selleck Chemicals

S7233-5MG

€144,00 EUR
€144,00 EUR
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Bromosporine is an inhibitor of BET used in studies of Epigenetic Regulation. It is especially relevant in cancer and epigenetics models, where defined compound exposure can be linked to chromatin-state control, histone modification, and transcriptional regulation.

By inhibiting BET, Bromosporine can be used to examine chromatin-state control, histone modification, and transcriptional regulation. The epigenetic regulator annotation adds relevance to chromatin, epigenetic, and gene-expression profiling, together with downstream-response mapping in the same experimental setting. In cancer and epigenetics models, these readouts can be combined with viability, reporter, localization, biochemical conversion, or morphology endpoints to refine experimental interpretation.

Research Applications

  • Target-focused assays involving BET
  • Pathway perturbation studies connected to Epigenetic Regulation
  • Concentration-response inhibition and target-dependence studies
  • Chromatin, epigenetic, and gene-expression profiling

Overall, Bromosporine is appropriate when a defined chemical perturbant is needed to connect BET with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in cancer and epigenetics models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.

Targets:
BET
Target Class:
Epigenetic Regulator
Pathways:
Epigenetic Regulation
Research Area:
Cancer • Epigenetics
CAS No.:
1619994-69-2
Molecular Weight:
404.44
Formula:
C₁₇H₂₀N₆O₄S
SMILES:
CCOC(=O)NC1=CC(=NN2C1=NN=C2C)C3=CC(=C(C=C3)C)NS(=O)(=O)C
InChIKey:
UYBRROMMFMPJAN-UHFFFAOYSA-N
PubChem:
72943187
Storage Temperature:
-20°C

For Research Use Only. Not intended for diagnostic or therapeutic use.
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