Phenazopyridine

Phenazopyridine

SCHEMBL960940

Cl.Nc1ccc(/N=N/c2ccccc2)c(N)n1.O=[Cr](=O)(O)O[Cr](=O)(=O)O

nearest known ligand 0.73

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
MEN1 O00255 9/20 0.73
KMT2A Q03164 9/20 0.73
MAPT P10636 8/20 0.73
MAPK1 P28482 6/20 0.73
TDP1 Q9NUW8 5/20 0.73
CYP3A4 P08684 3/20 0.73
HBB P68871 2/20 0.73
KDM4E B2RXH2 2/20 0.73
TSHR P16473 2/20 0.73
SMN1; SMN2 Q16637 2/20 0.73
ALOX15 P16050 2/20 0.73
SARM1 Q6SZW1 1/20 0.73
HSD17B10 Q99714 1/20 0.73
CYP1A2 P05177 4/20 0.70
HIF1A Q16665 3/20 0.70
LMNA P02545 2/20 0.70
USP2 O75604 1/20 0.70
CHRM1 P11229 1/20 0.70
CYP2C9 P11712 1/20 0.70
DRD2 P14416 1/20 0.70

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 SCHEMBL18534 0.92 MEN1 (0.82) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL7406346 0.91 MEN1 (0.71) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL270 0.89 MEN1 (0.77) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL5948996 0.89 MEN1 (0.77) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL19357 0.85 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL28796595 0.85 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL26499 0.85 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL14687482 0.85 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL29392321 0.85 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL215655 0.85 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1

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

Claimed or disclosed in 195 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1373245-B1 INTERMEDIATES FOR PRODUCING SPINOSYNS BAYER CROPSCIENCE AG (DE) 2006-12-27 EP claimed
WO-2004106343-A2 AGELASTATIN DERIVATIVES OF ANTITUMOUR AND GSK-3BETA-INHIBITING ALKALOIDS UFC LIMITED (GB) 2004-12-09 WO claimed
US-20040147766-A1 Intermediates for producing spinosyns BAYER CROPSCIENCE AG (DE) 2004-07-29 US claimed
US-5750794-A Process for preparing chiral tetralone PFIZER INC. (US) 1998-05-12 US claimed
JP-5339252-A None JP disclosed
US-20240060096-A1 COMPOSITIONS AND METHODS FOR PRODUCING 1,8-DIHYDROXYNAPHTHALENE AND CYCLIC HYDROCARBONS FROM 1,8-DIHYDROXYNAPHTHALENE TECH HOLDING LLC (US) 2024-02-22 US disclosed
US-20220033435-A1 Cyclic Di-Nucleotide Compounds as STING Agonists MERCK SHARP & DOHME CORP. (US) 2022-02-03 US disclosed
US-20220033431-A1 Cyclic Di-Nucleotide Compounds as STING Agonists MERCK SHARP & DOHME CORP. (US) 2022-02-03 US disclosed
US-20220024964-A1 Cyclic Di-Nucleotide Compounds as STING Agonists MERCK SHARP & DOHME CORP. (US) 2022-01-27 US disclosed
EP-3891165-A1 CYCLIC DI-NUCLEOTIDE COMPOUNDS AS STING AGONISTS Merck Sharp & Dohme Corp. (US) 2021-10-13 EP disclosed
EP-3891166-A1 CYCLIC DI-NUCLEOTIDE COMPOUNDS AS STING AGONISTS Merck Sharp & Dohme Corp. (US) 2021-10-13 EP disclosed
EP-3891164-A1 CYCLIC DI-NUCLEOTIDE COMPOUNDS AS STING AGONISTS Merck Sharp & Dohme Corp. (US) 2021-10-13 EP disclosed
US-4707489-A TERMITES, CRICKETS CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 1987-11-17 US disclosed
EP-0161921-A2 Improvements relating to pesticides BTG INTERNATIONAL LIMITED (GB) 1985-11-21 EP disclosed
EP-0161492-A2 Estrogen synthesis inhibitors THE ROCKEFELLER UNIVERSITY (US) 1985-11-21 EP disclosed
US-4546098-A ANTIESTROGENS; HORMONE INHIBITORS THE ROCKEFELLER UNIVERSITY (US) 1985-10-08 US disclosed
EP-0072111-B1 SYNTHETIC PHOSPHOLIPID COMPOUNDS AND THEIR PREPARATION LIPID SPECIALTIES, INC. (US) 1985-10-02 EP disclosed
EP-0145875-A2 Gamma-aminobutyric acid transaminase inhibitors and processes for their preparation MERRELL DOW PHARMACEUTICALS INC. (US) 1985-06-26 EP disclosed
US-4426330-A Synthetic phospholipid compounds LIPID SPECIALTIES, INC. (US) 1984-01-17 US disclosed
EP-0072111-A1 Synthetic phospholipid compounds and their preparation LIPID SPECIALTIES, INC. (US) 1983-02-16 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20040147766-A1 Intermediates for producing spinosyns SPIN4, SPIN3, FDPS MEN1 2196/4885KMT2A 3432/4885MAPT 2180/4885
US-20220033431-A1 Cyclic Di-Nucleotide Compounds as STING Agonists STING1, CGAS, IFNAR1 MEN1 1602/4885KMT2A 3097/4885MAPT 4830/4885
US-20220024964-A1 Cyclic Di-Nucleotide Compounds as STING Agonists STING1, CGAS, IFNAR1 MEN1 1573/4885KMT2A 3101/4885MAPT 4828/4885
US-20220033435-A1 Cyclic Di-Nucleotide Compounds as STING Agonists STING1, CGAS, IFNAR1 MEN1 1605/4885KMT2A 3091/4885MAPT 4827/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.