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Gentian Violet

FDA-approved product (suppository, vaginal), marketed as Genapax, Gvs.

Registered studies
8
Lab records
0
Pathogens at ≥40%
1 of 4

Chemical structure

Chemical structure of Gentian Violet
A drawing shows what the molecule is, not what it does.

Existing / approved use

Documented · FDA, WHO, ChEMBL

No approved indication recorded

ChEMBL records no approved indication for Gentian Violet. Its therapeutic class is shown instead.

Anti-infective classification
Neither a WHO ATC code nor an FDA pharmacologic class was found for it, so whether it is already an antimicrobial is not established. It needs review and is not counted as a repurposing candidate.

Repurposing investigation

Gentian Violet reaches ≥40% AI-predicted activity against M. tuberculosis, but no WHO ATC code or FDA pharmacologic class says whether it is already an antimicrobial. It needs review, so it is not counted among the repurposing candidates.

AI-predicted activity

AI prediction · nothing measured
  • MRSA22.5% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
  • E. coli21.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
  • K. pneumoniae3.9% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
  • M. tuberculosis44.3% 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 evidence

Clinical

8registered 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 measured

Dihydrofolate reductase ↗ (E. coli)

Not yet docked: queued in the docking rundetails

KPC-2 carbapenemase ↗ (K. pneumoniae)

Not yet docked: queued in the docking rundetails

Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)

Not yet docked: queued in the docking rundetails

Dihydrofolate reductase ↗ (MRSA)

Not yet docked: queued in the docking rundetails

AutoDock 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 measured

Other repurposing candidates: approved medicines besides Gentian Violet 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.

Registered studies

A registration describes a study; it does not establish a positive result.

  • Antibiofilm Activity of Chitosan Nanoparticles Against Uropathogenic Escherichia Coli

    NCT07482553 · start 2026-05-01

    Registered record
    Registry ID
    NCT07482553
    Conditions
    Urinary Tract Infections (UTIs); Catheter-Associated Urinary Tract Infections (CAUTIs); Biofilm Formation by Uropathogenic Escherichia Coli (UPEC)
    Interventions
    chitosan nanoparticles
    Study type
    OBSERVATIONAL
    Phase
    Not recorded
    Registry status
    Not yet recruiting
    Start
    2026-05-01
    Completion
    2027-06
    Enrolment
    60

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionUrinary Tract Infections (UTIs); Catheter-Associated Urinary Tract Infections (CAUTIs); Biofilm Formation by Uropathogenic Escherichia Coli (UPEC)
    Interventionchitosan nanoparticles
    PhaseNot recorded
    Registry statusNot yet recruiting
  • Gentian Violet Treatment for Hidradenitis Suppurativa

    NCT04388163 · start 2025-08

    Registered record
    Registry ID
    NCT04388163
    Conditions
    Hidradenitis Suppurativa
    Interventions
    Gentian Violet
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Withdrawn
    Start
    2025-08
    Completion
    2026-12
    Enrolment
    0

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionHidradenitis Suppurativa
    InterventionGentian Violet
    PhasePhase 2
    Registry statusWithdrawn
  • Hidradenitis Suppurativa Wound Care

    NCT04354012 · start 2021-02-04

    Registered record
    Registry ID
    NCT04354012
    Conditions
    Hidradenitis Suppurativa (HS)
    Interventions
    methylene blue, gentian violet, and ovine forestomach wound dressings
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Completed
    Start
    2021-02-04
    Completion
    2024-08-28
    Enrolment
    5

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionHidradenitis Suppurativa (HS)
    Interventionmethylene blue, gentian violet, and ovine forestomach wound dressings
    PhasePhase 2
    Registry statusCompleted
  • Antibacterial and Anti-biofilm Activity of Frankincense Extract Against Porphyromonas Gingivalis

    NCT04705714 · start 2021-01-15

    Registered record
    Registry ID
    NCT04705714
    Conditions
    Periodontal Diseases
    Interventions
    Frankincense Extract
    Study type
    INTERVENTIONAL
    Phase
    Phase 1
    Registry status
    Completed
    Start
    2021-01-15
    Completion
    2021-03-01
    Enrolment
    30

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionPeriodontal Diseases
    InterventionFrankincense Extract
    PhasePhase 1
    Registry statusCompleted
  • Accuracy for Predicting Deep Submucosal Invasion

    NCT03748667 · start 2018-12-01

    Registered record
    Registry ID
    NCT03748667
    Conditions
    Colorectal Cancer; Colorectal Polyp
    Interventions
    White light endoscopy (WLE); NBI/BLI +/- chromoendoscopy (NBIBLI +/- CE)
    Study type
    OBSERVATIONAL
    Phase
    Not recorded
    Registry status
    Completed
    Start
    2018-12-01
    Completion
    2022-10-30
    Enrolment
    426

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionColorectal Cancer; Colorectal Polyp
    InterventionWhite light endoscopy (WLE); NBI/BLI +/- chromoendoscopy (NBIBLI +/- CE)
    PhaseNot recorded
    Registry statusCompleted
  • Investigation of Bacterial Adhesion and Bactericide Effect ex Vivo on Different Implant Restoration Materials

    NCT04657757 · start 2018-03-14

    Registered record
    Registry ID
    NCT04657757
    Conditions
    Dental Diseases
    Interventions
    Intraoral apparatus
    Study type
    INTERVENTIONAL
    Phase
    Not applicable
    Registry status
    Completed
    Start
    2018-03-14
    Completion
    2020-03-31
    Enrolment
    16

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionDental Diseases
    InterventionIntraoral apparatus
    PhaseNot applicable
    Registry statusCompleted
  • Gentian Violet Vs. Nystatin Oral Suspension for Treatment of Oropharyngeal Candidiasis

    NCT01427738 · start 2011-06

    Registered record
    Registry ID
    NCT01427738
    Conditions
    HIV-1 Infection
    Interventions
    Gentian Violet; Nystatin oral suspension
    Study type
    INTERVENTIONAL
    Phase
    Phase 3
    Registry status
    Completed
    Start
    2011-06
    Completion
    2014-01
    Enrolment
    221

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionHIV-1 Infection
    InterventionGentian Violet; Nystatin oral suspension
    PhasePhase 3
    Registry statusCompleted
  • A Comparison of Gentian Violet (GV) Mouth Washes, Nystatin, and Ketoconazole Tabs in Treating Oropharyngeal Candidiasis

    NCT00128323 · start 2002-11

    Registered record
    Registry ID
    NCT00128323
    Conditions
    Candidiasis, Oral
    Interventions
    Gentian violet 1% solution; Gentian violet 0.00165% solution; Nystatin solution
    Study type
    INTERVENTIONAL
    Phase
    Phase 3
    Registry status
    Completed
    Start
    2002-11
    Completion
    2005-04
    Enrolment
    558

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionCandidiasis, Oral
    InterventionGentian violet 1% solution; Gentian violet 0.00165% solution; Nystatin solution
    PhasePhase 3
    Registry statusCompleted