Pamoic acid disodium

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Selleck Chemicals

E2660-100MG

€144,00 EUR
€144,00 EUR
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Pamoic acid disodium is an agonist of GPR and ERK1 used in studies of MAPK / ERK Signaling and GPCR Signaling. It is especially relevant when investigators need a named chemical input and interpretable readouts connected to mitogenic kinase cascades, proliferation control, and differentiation-linked signaling and receptor-driven second-messenger signaling and desensitization dynamics in cancer and cell signaling models.

By activating GPR and ERK1, Pamoic acid disodium can be used to examine mitogenic kinase cascades, proliferation control, and differentiation-linked signaling and 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 cancer and cell signaling 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 GPR and ERK1
  • Pathway perturbation studies connected to MAPK / ERK Signaling and GPCR Signaling
  • Agonist-response and downstream signaling studies
  • GPCR pharmacology, ligand-binding, and signaling assays

Overall, Pamoic acid disodium is appropriate when a defined chemical perturbant is needed to connect GPR and ERK1 with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in cancer and cell signaling models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.

Targets:
GPR • ERK1
Target Class:
GPCR
Pathways:
MAPK / ERK Signaling • GPCR Signaling
Research Area:
Cancer • Cell Signaling
CAS No.:
6640-22-8
Molecular Weight:
432.33
Formula:
C₂₃H₁₆O₆·2Na
Storage Temperature:
-20°C

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