Cisapride Monohydrate
FDA-approved product (tablet, oral), marketed as Propulsid, Propulsid Quicksolv.
- Registered studies
- 5
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Gastrointestinal disease
Indications ChEMBL records as approved, from FDA and DailyMed labels.
- WHO therapeutic group
- Propulsives
- Anti-infective classification
- Not classified as an anti-infective.
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against E. coli, MRSA and M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA56.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli56.3% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae34.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis66.5% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
5registered studies name this medicine, for any condition. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredAutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.
Other medicines to investigate
AI prediction · nothing measuredOther repurposing candidates: approved medicines besides Cisapride Monohydrate with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.
Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.
- VenetoclaxExisting use: Cancer, Chronic lymphocytic leukemia, Neoplasm55.0% AI-predicted activityagainst E. coli50+ registered studies
- RepotrectinibExisting use: Cancer, Neoplasm55.0% AI-predicted activityagainst E. coli17 registered studies
- Telotristat EtiprateExisting use: Carcinoid tumor, Diarrhea, Neuroendocrine neoplasm54.9% AI-predicted activityagainst E. coli27 registered studies
- Prasugrel HydrochlorideExisting use: Acute coronary syndrome, Hemorrhage, Intermediate coronary syndrome and 1 more54.8% AI-predicted activityagainst E. coli50+ registered studies
- Bosutinib MonohydrateExisting use: Chronic myelogenous leukemia, Myeloid leukemia54.6% AI-predicted activityagainst E. coli2 registered studies
- Ribociclib SuccinateExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 1 more54.5% AI-predicted activityagainst E. coli1 registered study
- Ergoloid MesylatesExisting use: Cardiovascular disease54.5% AI-predicted activityagainst E. coli2 registered studies
- CabotegravirExisting use: HIV infection, HIV-1 infection, Viral disease54.4% AI-predicted activityagainst E. coli50+ registered studies
- RisperidoneExisting use: Aggressive behavior, Autism, Bipolar disorder and 4 more54.2% AI-predicted activityagainst E. coli50+ registered studies
- LorlatinibExisting use: Cancer, Lymphoma, Neoplasm and 1 more54.1% AI-predicted activityagainst E. coli50+ registered studies
- TelaprevirExisting use: Chronic hepatitis C virus infection, Viral disease53.9% AI-predicted activityagainst E. coli50+ registered studies
- EverolimusExisting use: Adenoma sebaceum, Anaplastic astrocytoma, Angiomyolipoma and 18 more53.9% AI-predicted activityagainst E. coli50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
A Study of Cisapride in Patients With Symptomatic Gastro-Oesophageal Reflux Disease
NCT01281553 · start 2003-09
Registered record
- Registry ID
- NCT01281553
- Conditions
- Gastroesophageal Reflux
- Interventions
- Placebo; Cisapride
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2003-09
- Completion
- 2003-10
- Enrolment
- 6
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastroesophageal RefluxInterventionPlacebo; CisapridePhasePhase 4Registry statusTerminatedAn Efficacy and Safety Study of Cisapride for Improving Symptoms Associated With Gastroparesis in Patients With Diabetes Mellitus
NCT01286090 · start 2003-07
Registered record
- Registry ID
- NCT01286090
- Conditions
- Gastroparesis; Diabetes Mellitus
- Interventions
- Cisapride; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2003-07
- Completion
- 2003-10
- Enrolment
- 4
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastroparesis; Diabetes MellitusInterventionCisapride; PlaceboPhasePhase 4Registry statusTerminatedAn Efficacy and Safety Study of Cisapride in Patients With Chronic Gastroparesis After Failure of Other Treatment Options
NCT01281540 · start 2003-05
Registered record
- Registry ID
- NCT01281540
- Conditions
- Gastroparesis
- Interventions
- Cisapride; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2003-05
- Completion
- 2003-11
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastroparesisInterventionCisapride; PlaceboPhasePhase 4Registry statusTerminatedA Study of Cisapride in Premature Infants With Feeding Problems
NCT01281566 · start 2003-03
Registered record
- Registry ID
- NCT01281566
- Conditions
- Infant, Premature; Infant, Newborn
- Interventions
- Placebo; Cisapride
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2003-03
- Completion
- 2003-07
- Enrolment
- 8
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfant, Premature; Infant, NewbornInterventionPlacebo; CisapridePhasePhase 4Registry statusTerminatedLimited Access Protocol for the Use of Oral Cisapride
NCT02524496 · start 2001-03
Registered record
- Registry ID
- NCT02524496
- Conditions
- Gastroparesis
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2001-03
- Completion
- 2011-03
- Enrolment
- 3
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastroparesisInterventionNot recordedPhaseNot recordedRegistry statusCompleted