Phenazopyridine
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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
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1242 |
| Name | Phenazopyridine |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 4756 |
| ATC | G04BX06 |
| Molecular formula | C11H11N5 |
| Molecular weight | 213.24 |
| InChIKey | QPFYXYFORQJZEC-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):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| HTR2C | 5.72 | AC50 | 1908 | nM | CHEMBL_ACT_25131641 |
| OPRD1 | 5.54 | AC50 | 2900 | nM | CHEMBL_ACT_25153899 |
| DRD3 | 5.51 | AC50 | 3100 | nM | CHEMBL_ACT_25193359 |
| ADRA2B | 5.5 | AC50 | 3200 | nM | CHEMBL_ACT_25143534 |
| OPRK1 | 5.48 | AC50 | 3300 | nM | CHEMBL_ACT_25129274 |
| DRD2 | 5.48 | AC50 | 3300 | nM | CHEMBL_ACT_25140160 |
| HTR3A | 5.48 | AC50 | 3300 | nM | CHEMBL_ACT_25148956 |
| CHRM3 | 5.44 | AC50 | 3600 | nM | CHEMBL_ACT_25136528 |
| ADRA2C | 5.43 | AC50 | 3700 | nM | CHEMBL_ACT_25147704 |
| SLC6A2 | 5.42 | AC50 | 3850 | nM | CHEMBL_ACT_25146009 |
| CHRM1 | 5.39 | AC50 | 4100 | nM | CHEMBL_ACT_25135280 |
| HRH1 | 5.35 | AC50 | 4500 | nM | CHEMBL_ACT_25212338 |
| SLC6A3 | 5.33 | AC50 | 4710 | nM | CHEMBL_ACT_25124968 |
| DRD1 | 5.03 | AC50 | 9350 | nM | CHEMBL_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
| Phase | Trials |
|---|---|
| PHASE3 | 5 |
| Not specified | 5 |
| PHASE4 | 4 |
| PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06577493 | PHASE4 | ACTIVE_NOT_RECRUITING | Effectiveness of Phenazopyridine for Pain Following Urodynamics |
| NCT03302936 | PHASE4 | COMPLETED | Assessing Pyridium for Post-Sling Urinary Retention |
| NCT03755089 | PHASE4 | UNKNOWN | Oral vs Intravesical Analgesia for Office Bladder Botox Injections |
| NCT06514430 | PHASE4 | WITHDRAWN | Prophylactic Analgesia for Bladder Botox Injections |
| NCT01064024 | PHASE3 | COMPLETED | Evaluate the Safety and Efficacy of Phenazopyridine Hydrochloride Tablets, USP 200 mg vs. Placebo |
| NCT01650051 | PHASE3 | COMPLETED | Safety 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) |
| NCT01657448 | PHASE3 | COMPLETED | Efficacy Study of Methenamine + Methylthioninium Chloride vs Phenazopyridine for the Symptomatic Control of Dysuria |
| NCT02806713 | PHASE3 | COMPLETED | The Effect of Oral PhenazopyrIdine on Perioperative Voiding After Mid-urethral sliNg (EPIPhANy Study) |
| NCT03065075 | PHASE3 | COMPLETED | Effect of Phenazopyridine on Prolapse Surgery Voiding Trials |
| NCT02380573 | PHASE2 | COMPLETED | Effects of Methylene Blue in Healthy Aging, Mild Cognitive Impairment and Alzheimer’s Disease |
| NCT02424149 | Not specified | COMPLETED | Phenazopyridine for Confirmation of Ureteral Patency |
| NCT02476448 | Not specified | COMPLETED | Evaluation of Ureteral Jets on Cystoscopy |
| NCT02703558 | Not specified | WITHDRAWN | Evaluation of Fluorescein Use During Cystoscopy |
| NCT02715648 | Not specified | UNKNOWN | Using Phenazopyridine for In-office Cystoscopy |
| NCT02757417 | Not specified | WITHDRAWN | Intravenous 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):
| Guideline | Source | Gene(s) | Dosing | Recommendation |
|---|---|---|---|---|
| Annotation of CPIC Guideline for aminosalicylic acid, chloramphenicol, | CPIC | G6PD |
PharmGKB also curates 1 clinical and 3 variant annotation(s) for this drug (gene-keyed; see PharmGKB).
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.