Diphenylamine

Diphenylamine

SCHEMBL3003404

c1ccc(Nc2ccccc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HSD17B10 Q99714 5/20 1.00
▸ ALDH1A1 P00352 8/20 0.92
▸ TDP1 Q9NUW8 8/20 0.92
▸ TSHR P16473 5/20 0.92
▸ ALOX12 P18054 3/20 0.92
▸ L3MBTL1 Q9Y468 3/20 0.92
▸ ALOX15 P16050 2/20 0.92
▸ PTGS2 P35354 2/20 0.92
▸ PTGS1 P23219 1/20 0.92
▸ SLC6A2 P23975 1/20 0.92
▸ MAPK1 P28482 1/20 0.92
▸ HTR2B P41595 1/20 0.92
▸ MAPT P10636 6/20 0.75
▸ MEN1 O00255 5/20 0.75
▸ KMT2A Q03164 5/20 0.75
▸ AR P10275 1/20 0.75
▸ CYP3A4 P08684 6/20 0.67
▸ CYP1A2 P05177 3/20 0.67
▸ CYP2C9 P11712 3/20 0.67
▸ CYP2C19 P33261 3/20 0.67

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
Diphenylamine SCHEMBL229 1.00 HSD17B10 (1.00) HSD17B10ALDH1A1TDP1TSHRALOX12
Diphenylamine SCHEMBL6828443 1.00 HSD17B10 (1.00) HSD17B10ALDH1A1TDP1TSHRALOX12
Diphenylamine SCHEMBL1619083 1.00 HSD17B10 (1.00) HSD17B10ALDH1A1TDP1TSHRALOX12
Diphenylamine SCHEMBL301493 1.00 HSD17B10 (1.00) HSD17B10ALDH1A1TDP1TSHRALOX12
Diphenylamine SCHEMBL23295988 0.96 HSD17B10 (0.92) HSD17B10ALDH1A1TDP1TSHRALOX12
Diphenylamine SCHEMBL233665 0.96 HSD17B10 (0.92) HSD17B10ALDH1A1TDP1TSHRALOX12
Diphenylamine SCHEMBL8602771 0.96 HSD17B10 (0.92) HSD17B10ALDH1A1TDP1TSHRALOX12
SCHEMBL7896372 0.96 ALDH1A1 (1.00) HSD17B10ALDH1A1TDP1TSHRALOX12
Diphenylamine SCHEMBL1555489 0.96 HSD17B10 (0.92) HSD17B10ALDH1A1TDP1TSHRALOX12
Diphenylamine SCHEMBL11684039 0.96 HSD17B10 (0.92) HSD17B10ALDH1A1TDP1TSHRALOX12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113981475-A Electrochemical method for preparing N-alkyl sulfoxide imide 常州工学院 2022-01-28 — — CN disclosed
CN-107018662-B 6, 7-dihydropyrazolo [1,5-a ] pyrazin-4 (5H) -one compounds and their use as negative allosteric modulators of MGLUR2 receptors 詹森药业有限公司 2020-01-07 — — CN disclosed
US-20100193979-A1 Advanced Thermoplastics for Orthodontics UNIVERSITY OF CONNECTICUT 2010-08-05 — — US disclosed
WO-2008088826-A2 TRANSLUCENT, ISOTROPIC ENDODONTIC POST UNIVERSITY OF CONNECTICUT (US) 2008-07-24 — — WO disclosed
US-20080171306-A1 Translucent, isotropic endodontic post CONNECTICUT, UNIVERSITY OF 2008-07-17 — — US disclosed
US-20070190478-A1 Advanced thermoplastics for orthodontics GOLDBERG ARTIE J 2007-08-16 — — US disclosed
US-7186115-B2 Advanced thermoplastics for orthodontics UNIVERSITY OF CONNECTICUT (US) 2007-03-06 — — US disclosed
EP-1539020-A4 ADVANCED THERMOPLASTICS FOR ORTHODONTICS UNIV CONNECTICUT (US) 2005-12-21 — — EP disclosed
US-6933068-B2 Polymer electrolyte membrane and solid polymer electrolyte fuel cell using same HONDA GIKEN KOGYO KABUSHIKI KAISHA (JP) 2005-08-23 — — US disclosed
EP-1539020-A1 ADVANCED THERMOPLASTICS FOR ORTHODONTICS The University of Connecticut (US) 2005-06-15 — — EP disclosed
US-20040013994-A1 Advanced thermoplastics for orthodontics UNIVERSITY OF CONNECTICUT 2004-01-22 — — US disclosed
WO-2004004592-A1 ADVANCED THERMOPLASTICS FOR ORTHODONTICS UNIVERSITY OF CONNECTICUT (US) 2004-01-15 — — WO disclosed
US-20020172850-A1 Polymer electrolyte membrane and solid polymer electrolyte fuel cell using same HONDA GIKEN KOGYO KABUSHIKI KAISHA, JSR CORPORATION 2002-11-21 — — US disclosed
EP-0773249-B1 Polyphenylene co-polymers MISSISSIPPI POLYMER TECHNOLOGI (US) 2002-10-02 — — EP disclosed
US-6416834-B1 Composition for improving adhesion of elastomers to polymer compositions E. I. DU PONT DE NEMOURS AND COMPANY 2002-07-09 — — US disclosed
US-5886130-A THE CO-POLYMERS ARE USEFUL AS MOLDING RESINS, AND COMPOSITE MATRIX RESINS, AND WHERE AR IS HETEROARYLENE AS ION EXCHANGE RESINS. MAXDEM INCORPORATED (US) 1999-03-23 — — US disclosed
EP-0773249-A1 Polyphenylene co-polymers MAXDEM INCORPORATED (US) 1997-05-14 — — EP disclosed
EP-0387194-B1 N-substituted aminoalkane-diphosphonic acids CIBA GEIGY AG (CH) 1995-01-18 — — EP disclosed
US-5036058-A Regulates calcium metabolism CIBA-GEIGY CORPORATION (US) 1991-07-30 — — US disclosed
EP-0387194-A1 N-substituted aminoalkane-diphosphonic acids CIBA-GEIGY AG (CH) 1990-09-12 — — EP disclosed
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