Drug intelligence / Profile preview

FP-TZTP

Development stage
Preclinical
Lead developer
National Institute of Mental Health
Modality
Alpha Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Beta Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

FP-TZTP is a small molecule muscarinic acetylcholine receptor agonist with high selectivity for the M2 subtype. It is primarily used as a radioligand in positron emission tomography (PET) imaging to study muscarinic M2 receptor distribution and function in the brain. The compound can be labeled with fluorine‑18 ([18F]FP-TZTP) or carbon‑11 for PET studies. Its main research application is in neurodegenerative diseases such as Alzheimer's disease, where it enables noninvasive measurement of cholinergic system integrity and function[1][7][10]. FP-TZTP binds selectively to M2 receptors and its binding can be competitively inhibited by endogenous acetylcholine or other muscarinic agonists[6][10]. It does not have approved therapeutic indications but serves as an important tool compound for neuroscience research.

Other names
424829-90-3C2LNI0YP8ZC-2LNI0YP8ZC 2LNI0YP8ZUNII-C2LNI0YP8ZUNII-C-2LNI0YP8ZUNII-C 2LNI0YP8ZDTXSID50435762DTXSID-50435762DTXSID 50435762
02

Targets

CHRM2 (M2)M1 (Muscarinic acetylcholine receptor M1)

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