PSFL1911

PSFL1911 : Negative Allosteric Modulator of P2RX7

Structure

Information

  • P2RX7
  • Negative Allosteric Modulator
  • up to 1 uM

In Vitro Validations

Uniprot ID: Q99572
Target Class: Ion Channel
Target SubClass: P2X Family
PDB ID for probe-target interaction (3D structure): 8Z1D
Target aliases:
P2X purinoceptor 7, P2RX7, P2RX7_HUMAN, P2X7, Puri ...

DOI Reference: 10.1038/s41467-025-65847-0

In Cell Validations

In Vivo Data

No in Vivo Validations

Off-Target Selectivity Assesments

Potency assay (off target): When tested against other P2X receptor subtypes, PSFL1191 showed inhibition rates of -8.35 ± 4.49% for hP2X1, 3.09 ± 7.46% for hP2X2, 20.6 ± 6.4% for hP2X3, and -17.6 ± 9.0% for hP2X4 at 30 μM highlighting PSFL1191’s selectivity for P2X7 receptors.
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SERP ratings and comments


SERP Ratings

In Cell Rating

SERP Comments:

Looks a useful probe but, as ever, independent corroboration of the direct binding activity against the human target would be valuable Structure not yet in PubChem but this should eventually be submitted via the PDB ligand structure. https://doi.org/10.2210/pdb8z1d/pdb A Cryo-EM structure of the panda P2X7 receptor in complex with PSFL1191 is available (n.b. not the human target)

(last updated: 7 Jan 2026 )