Phenazopyridine

drug
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Also known as FenazopiridinaNSC-145895SID104171363PHENAZOPYRIDINE HYDROCHLORIDE

Summary

Phenazopyridine (CHEMBL1242) is an approved small molecule (ATC G04BX06); indicated across 3 conditions.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: G04BX06
  • Indications: 3 conditions
  • Clinical trials: 15
  • Chemistry: 213.24 Da · C11H11N5

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1242
NamePhenazopyridine
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID4756
ATCG04BX06
Molecular formulaC11H11N5
Molecular weight213.24
InChIKeyQPFYXYFORQJZEC-UHFFFAOYSA-N

SMILES: C1=CC=C(C=C1)N=NC2=C(N=C(C=C2)N)N

IUPAC name: 3-phenyldiazenylpyridine-2,6-diamine

Also known as: Fenazopiridina, NSC-145895, Phenazopyridine, SID104171363, PHENAZOPYRIDINE, PHENAZOPYRIDINE HYDROCHLORIDE, phenazopyridine

Parent form; salt/anhydrous children: CHEMBL1201022

Patent coverage: 1,589 distinct patent families (4,686 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: 23 (assay-derived). Sample: 5-hydroxytryptamine receptor 2B, 5-hydroxytryptamine receptor 3A, Alpha-2C adrenergic receptor, Alpha-2B adrenergic receptor, D(1A) dopamine receptor, Thromboxane A2 receptor, Muscarinic acetylcholine receptor M1, D(2) dopamine receptor, Prostaglandin G/H synthase 1, Sodium-dependent noradrenaline transporter.

Bioactivity

ChEMBL activities: 14 potent at pChembl ≥ 5 of 24 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
HTR2C5.72AC501908nMCHEMBL_ACT_25131641
OPRD15.54AC502900nMCHEMBL_ACT_25153899
DRD35.51AC503100nMCHEMBL_ACT_25193359
ADRA2B5.5AC503200nMCHEMBL_ACT_25143534
OPRK15.48AC503300nMCHEMBL_ACT_25129274
DRD25.48AC503300nMCHEMBL_ACT_25140160
HTR3A5.48AC503300nMCHEMBL_ACT_25148956
CHRM35.44AC503600nMCHEMBL_ACT_25136528
ADRA2C5.43AC503700nMCHEMBL_ACT_25147704
SLC6A25.42AC503850nMCHEMBL_ACT_25146009
CHRM15.39AC504100nMCHEMBL_ACT_25135280
HRH15.35AC504500nMCHEMBL_ACT_25212338
SLC6A35.33AC504710nMCHEMBL_ACT_25124968
DRD15.03AC509350nMCHEMBL_ACT_25115219

Target pathways

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

Indications & clinical

Indications

3 indications (0 at ChEMBL trial phase 4).

The 3 indication records carry no mapped disease name (EFO/MeSH-only); none shown.

Clinical trials

Total trials: 15.

Phase distribution

PhaseTrials
PHASE35
Not specified5
PHASE44
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06577493PHASE4ACTIVE_NOT_RECRUITINGEffectiveness of Phenazopyridine for Pain Following Urodynamics
NCT03302936PHASE4COMPLETEDAssessing Pyridium for Post-Sling Urinary Retention
NCT03755089PHASE4UNKNOWNOral vs Intravesical Analgesia for Office Bladder Botox Injections
NCT06514430PHASE4WITHDRAWNProphylactic Analgesia for Bladder Botox Injections
NCT01064024PHASE3COMPLETEDEvaluate the Safety and Efficacy of Phenazopyridine Hydrochloride Tablets, USP 200 mg vs. Placebo
NCT01650051PHASE3COMPLETEDSafety and Efficacy of Phenazopyridine Hydrochloride Tablets, USP 200 mg as an Analgesic for Short-Term Treatment in Female Subjects Suffering From Moderate-to-Severe Pain and Burning Upon Urination Associated With Uncomplicated Urinary Tract Infections (uUTI)
NCT01657448PHASE3COMPLETEDEfficacy Study of Methenamine + Methylthioninium Chloride vs Phenazopyridine for the Symptomatic Control of Dysuria
NCT02806713PHASE3COMPLETEDThe Effect of Oral PhenazopyrIdine on Perioperative Voiding After Mid-urethral sliNg (EPIPhANy Study)
NCT03065075PHASE3COMPLETEDEffect of Phenazopyridine on Prolapse Surgery Voiding Trials
NCT02380573PHASE2COMPLETEDEffects of Methylene Blue in Healthy Aging, Mild Cognitive Impairment and Alzheimer’s Disease
NCT02424149Not specifiedCOMPLETEDPhenazopyridine for Confirmation of Ureteral Patency
NCT02476448Not specifiedCOMPLETEDEvaluation of Ureteral Jets on Cystoscopy
NCT02703558Not specifiedWITHDRAWNEvaluation of Fluorescein Use During Cystoscopy
NCT02715648Not specifiedUNKNOWNUsing Phenazopyridine for In-office Cystoscopy
NCT02757417Not specifiedWITHDRAWNIntravenous Sodium Fluorescein Versus Oral Phenazopyridine for Ureteral Patency

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

PharmGKB dosing guidelines (1) — CPIC / DPWG genotype-guided dosing for this drug (drug × pharmacogene):

GuidelineSourceGene(s)DosingRecommendation
Annotation of CPIC Guideline for aminosalicylic acid, chloramphenicol,CPICG6PD

PharmGKB also curates 1 clinical and 3 variant annotation(s) for this drug (gene-keyed; see PharmGKB).

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

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.