SCH58261

1 1

Selleck Chemicals

S8104-5MG

€144,00 EUR
€144,00 EUR
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SCH58261 is an antagonist of Adenosine Receptors used in studies of GPCR Signaling. It is especially relevant when investigators need a named chemical input and interpretable readouts connected to receptor-driven second-messenger signaling and desensitization dynamics in cardiovascular and inflammation models.

By blocking Adenosine Receptors, SCH58261 can be used to examine receptor-driven second-messenger signaling and desensitization dynamics. The gpcr annotation adds relevance to GPCR pharmacology, ligand-binding, and signaling assays, together with downstream-response mapping in the same experimental setting. In cardiovascular and inflammation 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 Adenosine Receptors
  • Pathway perturbation studies connected to GPCR Signaling
  • Receptor-blockade and ligand-competition studies
  • GPCR pharmacology, ligand-binding, and signaling assays

Overall, SCH58261 is appropriate when a defined chemical perturbant is needed to connect Adenosine Receptors with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in cardiovascular and inflammation models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.

Targets:
Adenosine Receptors
Target Class:
GPCR
Pathways:
GPCR Signaling
Research Area:
Cardiovascular • Inflammation
CAS No.:
160098-96-4
Molecular Weight:
345.36
Formula:
C₁₈H₁₅N₇O
SMILES:
C1=CC=C(C=C1)CCN2C3=C(C=N2)C4=NC(=NN4C(=N3)N)C5=CC=CO5
Storage Temperature:
-20°C

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