Evidence map›Paper›PMID 36876155›Full record

ArticleDrugs in context2023

Tissue distribution and abuse potential of prucalopride: findings from non-clinical and clinical studies.

Katayoun Derakhchan, Zhen Lou, Hong Wang, Robert Baughman

Open access · goldAbstract read
In one paragraph

Article in Drugs in context, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Chronic, combinatorial targeting of NMDARs and 5-HTNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Katayoun DerakhchanTakeda Development Center Americas, Inc., Cambridge, MA, USA.
Zhen LouTakeda Development Center Americas, Inc., Cambridge, MA, USA.
Hong WangTakeda Development Center Americas, Inc., Cambridge, MA, USA.
Robert BaughmanTakeda Development Center Americas, Inc., Lexington, MA, USA.
Takeda (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Prucalopride is a selective serotonin type 4 (5-HT Methods: In vitro receptor-ligand binding studies were performed to assess the affinity of prucalopride (≤1 mM) for peptide receptors, ion channels, monoamine neurotransmitters and 5-HT receptors. The tissue distribution of Results: Prucalopride showed no appreciable affinity for the receptors and ion channels investigated; its affinity (at ≤100 μM) for other 5-HT receptors was 150-10,000 times lower than that for the 5-HT Conclusion: This series of non-clinical and clinical studies suggest low abuse potential for prucalopride.

Indexed as

central nervous systemconstipationdrug abusedrug toxicitypharmacokineticspharmacologyprucalopridetoxicology

Identifiers

PMID36876155
PMCPMC9983627
OpenAlexW4322500793

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.