Phenazopyridine

Phenazopyridine

SCHEMBL270

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

nearest known ligand 0.77

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 0.77
KMT2A Q03164 9/20 0.77
MAPT P10636 8/20 0.77
MAPK1 P28482 6/20 0.77
TDP1 Q9NUW8 5/20 0.77
CYP3A4 P08684 3/20 0.77
HBB P68871 2/20 0.77
KDM4E B2RXH2 2/20 0.77
TSHR P16473 2/20 0.77
SMN1; SMN2 Q16637 2/20 0.77
ALOX15 P16050 2/20 0.77
SARM1 Q6SZW1 1/20 0.77
HSD17B10 Q99714 1/20 0.77
CYP1A2 P05177 3/20 0.74
HIF1A Q16665 3/20 0.74
LMNA P02545 2/20 0.74
USP2 O75604 1/20 0.74
CHRM1 P11229 1/20 0.74
CYP2C9 P11712 1/20 0.74
DRD2 P14416 1/20 0.74

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 SCHEMBL5948996 1.00 MEN1 (0.77) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL18534 0.94 MEN1 (0.82) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL7406346 0.91 MEN1 (0.71) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL960940 0.89 MEN1 (0.73) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL26499 0.88 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL28796595 0.88 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL215655 0.88 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL29392321 0.88 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL14687482 0.88 MAPT (1.00) MEN1KMT2AMAPTMAPK1TDP1
Phenazopyridine SCHEMBL19357 0.88 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 315 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6833459-B2 Reducing thiazole ester to thiazole alcohol using sodium borohydride in the presence of aluminum chloride in a solvent and oxidising the thiazole alcohol to obtain 4-methyl-5-formyl-thiazole ORCHID CHEMICALS & PHARMACEUTICALS LIMITED (IN) 2004-12-21 US claimed
US-5750794-A Process for preparing chiral tetralone PFIZER INC. (US) 1998-05-12 US claimed
US-20230373954-A1 NOVEL ACID SECRETION INHIBITOR AND USE THEREOF ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-11-23 US disclosed
US-11767311-B2 Acid secretion inhibitor and use thereof ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-09-26 US disclosed
EP-4212533-A1 PROCESS FOR PREPARING PURINE DERIVATIVES Cyclacel Limited (GB) 2023-07-19 EP disclosed
US-20230192650-A1 NOVEL ACID SECRETION INHIBITOR AND USE THEREOF ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-06-22 US disclosed
US-20230098332-A1 HETEROCYCLIC DERIVATIVES AS TRMP8 ANTAGONISTS GIVAUDAN SA (CH) 2023-03-30 US disclosed
EP-4148050-A1 NOVEL ACID SECRETION INHIBITOR AND USE THEREOF Ildong Pharmaceutical Co., Ltd. (KR) 2023-03-15 EP disclosed
EP-3573988-B1 PROCESS FOR PREPARING PURINE DERIVATIVES CYCLACEL LTD (GB) 2022-12-28 EP disclosed
WO-2021256861-A1 NOVEL ACID SECRETION INHIBITOR AND USE THEREOF 일동제약(주) 2021-12-23 WO disclosed
US-10927113-B2 Process for preparing purine derivatives CYCLACEL LIMITED (GB) 2021-02-23 US disclosed
EP-0145434-A2 Novel dihydropyridine derivatives and process for preparing the same OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1985-06-19 EP disclosed
US-4510331-A ISOMERIZATION OF 2,7-OCTADIENE-1-OL USING A COPPER CHROMIUM AND/OR ZINC OXIDE CATALYST KURARAY COMPANY, LTD. (JP) 1985-04-09 US disclosed
EP-0113101-A1 6-(1-Hydroxyethyl)-2-SR8-1-methyl-1-carbadethiapen-2-em-3-carboxylic acid esters MERCK & CO. INC. (US) 1984-07-11 EP disclosed
EP-0069339-A2 Process for producing 7-octen-1-al and derivatives thereof KURARAY CO., LTD. (JP) 1983-01-12 EP disclosed
US-4244874-A ANTICARCINOGENIC AGENTS BRISTOL-MYERS COMPANY (US) 1981-01-13 US disclosed
US-4232036-A 6-, 1- and 2-Substituted-1-carbadethiapen-2-em-3-carboxylic acids MERCK & CO., INC. (US) 1980-11-04 US disclosed
US-4218462-A 6-(1-Hydroxyethyl)-2-(2-aminoethylthio)-1-substituted-1-carbade-thiapen-2-em-3-carboxylic acids MERCK & CO., INC. (US) 1980-08-19 US disclosed
US-4208422-A ANTIBIOTICS, BACTERICIDES MERCK & CO., INC. (US) 1980-06-17 US disclosed
EP-0010317-A1 6-, 1- and 2-substituted-1-carbapen-2-em-3-carboxylic acids, processes for the preparation of such compounds and pharmaceutical composition comprising such compounds MERCK & CO. INC. (US) 1980-04-30 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 (5 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-11767311-B2 Acid secretion inhibitor and use thereof SLC10A2, SLC10A1, ASIC1 MEN1 1938/4885KMT2A 3688/4885MAPT 4359/4885
US-20230098332-A1 HETEROCYCLIC DERIVATIVES AS TRMP8 ANTAGONISTS TRPM8, TRPM7, TRPM5 MEN1 3144/4885KMT2A 2737/4885MAPT 2450/4885
US-10927113-B2 Process for preparing purine derivatives CTR9, PNP, C5 MEN1 4360/4885KMT2A 4625/4885MAPT 4586/4885
US-20230373954-A1 NOVEL ACID SECRETION INHIBITOR AND USE THEREOF SLC10A2, SLC10A1, ASIC1 MEN1 2339/4885KMT2A 3786/4885MAPT 4517/4885
US-20230192650-A1 NOVEL ACID SECRETION INHIBITOR AND USE THEREOF SLC10A2, SLC10A1, ASIC1 MEN1 2339/4885KMT2A 3786/4885MAPT 4517/4885

“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.