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Updated: Aug 6, 2025

Proteomics to Identify Proteins Interacting with P2X2 Ligand-Gated Cation Channels
Published on: May 18, 2009
DT-0111: a novel P2X3 receptor antagonist
Amir Pelleg1, Elena Sirtori2, Jean-Francois Rolland2
1Danmir Therapeutics LLC, 24 Dartmouth Lane, Haverford, PA, 19041-1020, USA. Danmirusa@gmail.com.
A novel molecule, DT-0111, selectively targets P2X3 receptors, which are implicated in chronic cough. This research presents its receptor affinity data, offering potential for new cough treatments.
Area of Science:
- Pharmacology
- Neuroscience
- Respiratory Medicine
Background:
- Extracellular adenosine 5'-triphosphate (ATP) signals through P2 receptors (P2R), including P2X receptors (P2XRs).
- P2XRs are cationic channels, with P2X3 and P2X2/3 receptors on vagal nerve terminals mediating cough and bronchoconstriction.
- P2X3R and P2X2/3R antagonists are under development for chronic cough treatment.
Purpose of the Study:
- To present the receptor affinity data of a novel P2X3R antagonist, DT-0111.
- To evaluate DT-0111 as a potential therapeutic agent for conditions involving P2X3R activation.
Main Methods:
- Characterization of DT-0111 as a water-soluble small molecule.
- Assessment of DT-0111's affinity for P2X3 receptors.
Main Results:
- DT-0111 demonstrates selective antagonism of P2X3 receptors.
- The study provides quantitative receptor affinity data for DT-0111.
Conclusions:
- DT-0111 is a selective P2X3R antagonist with potential therapeutic applications.
- This compound warrants further investigation for the treatment of chronic cough and related conditions.
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