Phenazopyridine

Phenazopyridine

SCHEMBL19357

Cl.Nc1ccc(/N=N/c2ccccc2)c(N)n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9A

The experimentally established mechanism targets of Phenazopyridine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 9/20 1.00
MEN1 O00255 8/20 1.00
KMT2A Q03164 8/20 1.00
MAPK1 P28482 6/20 1.00
TDP1 Q9NUW8 5/20 1.00
CYP3A4 P08684 3/20 1.00
SMN1; SMN2 Q16637 3/20 1.00
HBB P68871 2/20 1.00
KDM4E B2RXH2 2/20 1.00
TSHR P16473 2/20 1.00
ALOX15 P16050 2/20 1.00
SARM1 Q6SZW1 1/20 1.00
HSD17B10 Q99714 1/20 1.00
LMNA P02545 3/20 0.96
CYP1A2 P05177 2/20 0.96
HIF1A Q16665 2/20 0.96
USP2 O75604 1/20 0.96
CHRM1 P11229 1/20 0.96
CYP2C9 P11712 1/20 0.96
DRD2 P14416 1/20 0.96

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Phenazopyridine SCHEMBL14687482 1.00 MAPT (1.00) MAPTMEN1KMT2AMAPK1TDP1
Phenazopyridine SCHEMBL29392321 1.00 MAPT (1.00) MAPTMEN1KMT2AMAPK1TDP1
Phenazopyridine SCHEMBL26499 1.00 MAPT (1.00) MAPTMEN1KMT2AMAPK1TDP1
Phenazopyridine SCHEMBL28796595 1.00 MAPT (1.00) MAPTMEN1KMT2AMAPK1TDP1
Phenazopyridine SCHEMBL215655 1.00 MAPT (1.00) MAPTMEN1KMT2AMAPK1TDP1
Phenazopyridine SCHEMBL301672 0.98 MAPT (0.96) MAPTMEN1KMT2AMAPK1TDP1
Phenazopyridine SCHEMBL5973732 0.98 MAPT (0.96) MAPTMEN1KMT2AMAPK1TDP1
Phenazopyridine SCHEMBL302506 0.98 MAPT (0.96) MAPTMEN1KMT2AMAPK1TDP1
Phenazopyridine SCHEMBL6661856 0.98 MAPT (0.96) MAPTMEN1KMT2AMAPK1TDP1
Phenazopyridine SCHEMBL9151827 0.98 MAPT (0.96) MAPTMEN1KMT2AMAPK1TDP1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Appears in 6736 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12617874-B2 Cyclodextrin-polyoxometalate ionic liquid inclusion complex flame retardant additive for making a low smoke zero halogen compound CORNING INCORPORATED (US) 2026-05-05 US claimed
US-12486235-B2 Metal oxide nanoparticle with alkylsiloxane ligands bonded thereto CUBICPV INC. (US) 2025-12-02 US claimed
US-20250243357-A1 ULTRA-STRETCHABLE HOP-RING HYDROGELS TRUSTEES OF DARTMOUTH COLLEGE (US) 2025-07-31 US claimed
CN-119735984-B Antireflective composition, antireflective film, patterning process, patterned substrate, semiconductor device, and method for manufacturing the same 珠海基石科技有限公司 2025-05-23 CN claimed
US-20250134946-A1 SELF-ASSEMBLING AMPHIPHILIC PEPTIDE HYDROGELS FOR TREATMENT OF NERVE INJURY GEL4MED, INC. 2025-05-01 US claimed
US-20250113829-A1 HIGH MOLECULAR WEIGHT MODIFIED RNA COMPOSITIONS nanoSUR LLC 2025-04-10 US claimed
CN-119735984-A Antireflective composition, antireflective film, patterning process, patterned substrate, semiconductor device, and method for manufacturing the same 珠海基石科技有限公司 2025-04-01 CN claimed
US-20250090501-A1 METHODS OF TREATING GUT MOTILITY DISORDERS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2025-03-20 US claimed
WO-2025037759-A1 IONIC ORGANIC FRAMEWORK ELECTROLYTE FOR ALL-SOLID-STATE SECONDARY BATTERY, COMPRISING MULTIPLE COMPONENTS, PREPARATION METHOD THEREFOR, AND ALL-SOLID-STATE SECONDARY BATTERY COMPRISING SAME 한양대학교 에리카산학협력단 2025-02-20 WO claimed
US-RE50250-E1 Process for the preparation of cis-alpha,beta substituted cyclopentanones FIRMENICH SA (CH) 2024-12-31 US claimed
EP-0353474-A2 Glycerin derivative and its pharmacological use Eisai Co., Ltd. (JP) 1990-02-07 EP claimed
EP-0313684-A1 Solution for eliminating intra-abdominal infections GENECO, INC. (US) 1989-05-03 EP claimed
US-4704102-A Method of eliminating intra abdominal infections GENECO INC. (US) 1987-11-03 US claimed
US-4544615-A POLYACETYLENE, POLYPYRROLES, AROMATIC RESINS SHOWA DENKO KABUSHIKI KAISHA (JP) 1985-10-01 US claimed
EP-0034228-B1 REFORMING PROCESS MOBIL OIL CORPORATION (US) 1984-10-10 EP claimed
US-4455147-A COLORING TEXTILES, ANIONIC AND CATIONIC SURFACTANTS I.W.S. NOMINEE COMPANY, LIMITED (GB) 1984-06-19 US claimed
EP-0005569-B1 RESIN-LIGAND-TRANSITION METAL COMPLEX COMPOSITION AND PROCESSES FOR USING THIS COMPOSITION AS CATALYST SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1981-11-04 EP claimed
US-4226863-A BACTERICIDES, ANTIBIOTICS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1980-10-07 US claimed
US-4056609-A Article for diagnosis of achlorhydria GUNN, KIRCHUBEL & MILLER (US) 1977-11-01 US claimed
US-4017501-A Process for preparing pyridinium chloride salts of alkyl esters of 2-chloro-N-2-hydroxyethylacetamide AMERICAN CYANAMID COMPANY (US) 1977-04-12 US claimed