Secnidazole

drug
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Also known as DeprozolFlagentylNSC-759812Ornidazole metabolite m4PM-185184RP 14539RP-14539SecnidalSecnidazolSecnidazole anhydrousSolosecSYM-1219SabimaSecnolSID14742762SID26719698SID50086443SID144205010SID174007190

Summary

Secnidazole (CHEMBL498847) is an approved small-molecule antiprotozoal drug (ATC P01AB07); indicated across 4 conditions including bacterial vaginosis and trichomoniasis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: P01AB07
  • Indications: 4 conditions
  • Clinical trials: 10
  • Chemistry: 185.18 Da · C7H11N3O3

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL498847
NameSecnidazole
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID71815
ChEBICHEBI:140628
ATCP01AB07
Molecular formulaC7H11N3O3
Molecular weight185.18
InChIKeyKPQZUUQMTUIKBP-UHFFFAOYSA-N

SMILES: CC1=NC=C(N1CC(C)O)[N+](=O)[O-]

IUPAC name: 1-(2-methyl-5-nitroimidazol-1-yl)propan-2-ol

ChEBI definition: A C-nitro compound that is 5-nitroimidazole in which the hydrogens at positions 1 and 2 are replaced by 2-hydroxypropyl and methyl groups, respectively. It is a drug used for the treatment of trichomoniasis caused by Trichomonas vaginalis.

Pharmacological roles (ChEBI): epitope, antiprotozoal drug, antibacterial agent.

Also known as: Deprozol, Flagentyl, NSC-759812, Ornidazole metabolite m4, PM-185184, RP 14539, RP-14539, Secnidal, Secnidazol, Secnidazole, Secnidazole anhydrous, Solosec

Patent coverage: 644 distinct patent families (1,851 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 2 (assay-derived). Sample: Serine-protein kinase ATM, Mitogen-activated protein kinase 1.

Bioactivity

ChEMBL activities: 2 potent at pChembl ≥ 5 of 2 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
MAPK15.3Potency5012nMCHEMBL_ACT_4725558
ATM5.15Potency7080nMCHEMBL_ACT_4863360

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

4 indications (3 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
bacterial vaginosis4MONDO:0005316EFO:0003932
trichomoniasis4MONDO:0002154DOID:1947
amebiasis4MONDO:0005644EFO:0007144
vaginal discharge3MONDO:0002770EFO:0009365

Clinical trials

Total trials: 10.

Phase distribution

PhaseTrials
PHASE35
PHASE42
PHASE2/PHASE31
PHASE1/PHASE21
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06261840PHASE4RECRUITINGRefining Treatment Options for Trichomonas Vaginalis Infection: A Comparative Analysis of Metronidazole and Secnidazole
NCT03937869PHASE4COMPLETEDEvaluate the Safety of a Single Oral Dose of Solosec™ (Secnidazole) 2g for the Treatment of Adolescent Girls With BV
NCT01733966PHASE3TERMINATEDA Multicentre, Randomized as a Double Blind Study, Triple Placebo, Comparative of the Efficacy and Safety of an Association Secnidazol-Ciprofloxacin Compared With Amoxicillin-Clavulanic Acid for the Treatment of Uncomplicated Episode of Diverticular Sigmoïditis Among Adults
NCT02111629PHASE3COMPLETEDSafety and Clinical and Microbiological Efficacy of the Combination of Fluconazole and Secnidazole for the Treatment of Symptomatic Vaginal Discharge
NCT02418845PHASE3COMPLETEDA Phase 3 Study of SYM-1219 Treatment of Women and Post-Menarchal Adolescent Girls With Bacterial Vaginosis
NCT02452866PHASE3COMPLETEDOpen-Label Study to Evaluate Safety of A Single Dose of SYM-1219
NCT03935217PHASE3COMPLETEDA Phase 3 Study of Solosec® for the Treatment of Trichomoniasis
NCT05033743PHASE2/PHASE3COMPLETEDSuppressive Antibacterial Therapy With Once-Weekly Secnidazole Granules to Prevent Recurrent Bacterial Vaginosis; A Pilot Study
NCT01019083PHASE1/PHASE2COMPLETEDStudies of Immune Responses to Orally Administered Vaccines in Developing Country
NCT02147899PHASE2COMPLETEDA Phase 2 Study of SYM-1219 to Treat Bacterial Vaginosis

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).