4-Aminophenol

4-Aminophenol

SCHEMBL3358484

CC(=O)O.Nc1ccc(O)cc1

nearest known ligand 0.68

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of 4-Aminophenol. 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
ESR1 known ✓ P03372 3/20 0.56
ESR2 known ✓ Q92731 3/20 0.56
CA3 P07451 4/20 0.68
CA14 Q9ULX7 4/20 0.68
ALDH1A1 P00352 3/20 0.68
CYP3A4 P08684 3/20 0.68
CA6 P23280 2/20 0.68
THRB P10828 2/20 0.68
ALOX15 P16050 2/20 0.68
HIF1A Q16665 2/20 0.68
HSD17B10 Q99714 2/20 0.68
CASP1 P29466 1/20 0.68
CYP19A1 P11511 2/20 0.56
APP P05067 3/20 0.52
CA12 O43570 3/20 0.46
CA1 P00915 3/20 0.46
CA2 P00918 3/20 0.46
CA4 P22748 3/20 0.46
CA9 Q16790 3/20 0.46
CA7 P43166 2/20 0.46

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
4-Aminophenol SCHEMBL27782121 0.92 ALDH1A1 (0.72) CA3CA14ALDH1A1CYP3A4CA6
4-Aminophenol SCHEMBL27835004 0.89 ALDH1A1 (0.77) CA3CA14ALDH1A1CYP3A4CA6
Acetic Acid SCHEMBL7113664 0.89 MAPT (0.53) CA3CA14ALDH1A1CYP3A4CA6
Acetic Acid SCHEMBL8968769 0.89 MAPT (0.53) CA3CA14ALDH1A1CYP3A4CA6
Acetic Acid SCHEMBL2043001 0.89 MAPT (0.53) CA3CA14ALDH1A1CYP3A4CA6
4-Aminophenol SCHEMBL28102190 0.86 ALDH1A1 (0.93) CA3CA14ALDH1A1CYP3A4CA6
Hydroquinone SCHEMBL1746628 0.86 CA2 (0.58) CA3CA14ALDH1A1CYP3A4CA6
Hydroquinone SCHEMBL2505159 0.86 CA2 (0.58) CA3CA14ALDH1A1CYP3A4CA6
4-Aminophenol SCHEMBL31598822 0.85 ALDH1A1 (0.62) CA3CA14ALDH1A1CYP3A4CA6
4-Aminophenol SCHEMBL28749694 0.85 ALDH1A1 (0.62) CA3CA14ALDH1A1CYP3A4CA6

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1848815-B1 ESTERASES FOR MONITORING PROTEIN BIOSYNTHESIS IN VITRO UNIV BAYREUTH (DE) 2010-05-19 EP claimed
US-11422106-B2 Using 4-acetoxyphenol as a substrate for modular hydrolase biosensors United States Government, as represented by the Administrator of the U.S. EPA (US) 2022-08-23 US disclosed
US-20200264124-A1 USING 4-ACETOXYPHENOL AS A SUBSTRATE FOR MODULAR HYDROLASE BIOSENSORS US GOVERNMENT, AS REPRESENTED BY THE ADMINISTRATOR OF THE EPA 2020-08-20 US disclosed
EP-0769573-B1 Process for reducing aluminium corrosion and use of a corrosion inhibitor in antifreeze compositions BP CHEM INT LTD (GB) 2000-03-22 EP disclosed
EP-0769573-A1 Anticorrosion agent and antifreeze composition containing the anticorrosion agent BP Chemicals Limited (GB) 1997-04-23 EP disclosed