SCHEMBL7064626

SCHEMBL7064626

CCCCCCCCCCCCCCOOOC(=O)OOOCCCCCCCCCCCCCC

nearest known ligand 0.47

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
NAAA Q02083 1/20 0.47
CES2 O00748 5/20 0.45
EPHX1 P07099 1/20 0.44
TSHR P16473 3/20 0.42
LPAR3 Q9UBY5 3/20 0.42
LPAR1 Q92633 2/20 0.42
LPAR2 Q9HBW0 2/20 0.42
DGKA P23743 1/20 0.42
HCAR2 Q8TDS4 1/20 0.40
RAD52 P43351 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
CES1 P23141 3/20 0.39
FAAH O00519 1/20 0.39

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
SCHEMBL6333647 1.00 NAAA (0.47) NAAACES2EPHX1TSHRLPAR3
SCHEMBL8057242 0.98 NAAA (0.45) NAAACES2EPHX1TSHRLPAR3
SCHEMBL6856910 0.92 NAAA (0.48) NAAACES2EPHX1TSHRLPAR3
SCHEMBL21834086 0.92 NAAA (0.48) NAAACES2EPHX1TSHRLPAR3
SCHEMBL5808059 0.91 ALDH1A1 (0.44) NAAACES2EPHX1TSHRDGKA
SCHEMBL11477129 0.88 NAAA (0.50) NAAAEPHX1TSHRDGKAHCAR2
SCHEMBL10710530 0.88 NAAA (0.50) NAAAEPHX1TSHRDGKAHCAR2
SCHEMBL6442583 0.88 NAAA (0.38) NAAACES2EPHX1TSHRLPAR3
SCHEMBL6856916 0.87 NAAA (0.44) NAAACES2EPHX1TSHRHCAR2
SCHEMBL21834087 0.87 NAAA (0.44) NAAACES2EPHX1TSHRHCAR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3380552-B1 BCHPC HAVING A REDUCED BURNING RATE UNITED INITIATORS GMBH (DE) 2019-11-13 EP claimed
US-12600885-B2 Composition including monomer with a carboxylic acid group, monomer with a hydroxyl group, an alkyl monomer, and crosslinker and related article and method 3M INNOVATIVE PROPERTIES COMPANY (US) 2026-04-14 US disclosed
US-12398301-B2 Adhesives comprising cyclic imide addition-fragmentation and adhesion agents 3M INNOVATIVE PROPERTIES COMPANY (US) 2025-08-26 US disclosed
US-12378340-B2 Crosslinkers and curable compositions including the same 3M INNOVATIVE PROPERTIES COMPANY (US) 2025-08-05 US disclosed
US-20250034289-A1 POLYMERIZABLE COMPOSITIONS INCLUDING A POLYMERIZABLE COMPONENT AND A REDOX INITIATION SYSTEM CONTAINING A PHOTOLABILE REDUCING AGENT, AND A PHOTOLABILE REDUCING AGENT 3M INNOVATIVE PROPERTIES COMPANY 2025-01-30 US disclosed
US-20250011633-A1 Adhesives Comprising Cyclic Imide Addition-Fragmentation And Adhesion Agents 3M INNOVATIVE PROPERTIES COMPANY 2025-01-09 US disclosed
US-20240343951-A1 COMPOSITION INCLUDING MONOMER WITH A CARBOXYLIC ACID GROUP, MONOMER WITH A HYDROXYL GROUP, AN ALKYL MONOMER, AND CROSSLINKER AND RELATED ARTICLE AND METHOD 3M INNOVATIVE PROPERTIES COMPANY 2024-10-17 US disclosed
EP-4377367-A1 COMPOSITION INCLUDING MONOMER WITH A CARBOXYLIC ACID GROUP, MONOMER WITH A HYDROXYL GROUP, AN ALKYL MONOMER, AND CROSSLINKER AND RELATED ARTICLE AND METHOD 3M Innovative Properties Company (US) 2024-06-05 EP disclosed
US-20240084060-A1 COMPOSITION INCLUDING AN ACRYLIC MONOMER WITH A CARBOXYLIC ACID GROUP, AN ACRYLIC MONOMER WITH A HYDROXYL GROUP, AN ALKYL (METH)ACRYLATE MONOMER AND CROSSLINKER, AND RELATED ARTICLES AND METHODS 3M INNOVATIVE PROPERTIES COMPANY 2024-03-14 US disclosed
US-20240076523-A1 FREE-RADICALLY POLYMERIZABLE CROSSLINKER, CURABLE COMPOSITION, AND ADHESIVE THEREFROM 3M INNOVATIVE PROPERTIES COMPANY 2024-03-07 US disclosed
CN-102653616-B Propylene resin composition SUMITOMO CHEMICAL CO., LTD. (JP) 2016-02-03 CN disclosed
US-20150038630-A1 STRUCTURAL ACRYLIC ADHESIVE 3M INNOVATIVE PROPERTIES COMPANY 2015-02-05 US disclosed
EP-2817378-A1 STRUCTURAL ACRYLIC ADHESIVE 3M Innovative Properties Company (US) 2014-12-31 EP disclosed
WO-2013126377-A1 STRUCTURAL ACRYLIC ADHESIVE 3M INNOVATIVE PROPERTIES COMPANY (US) 2013-08-29 WO disclosed
US-20040002569-A1 Composite material of polyolefin resin and filler and molded article made from the same SUMITOMO CHEMICAL COMPANY, LIMITED 2004-01-01 US disclosed
US-5597853-A IMPROVED CREPE HARDENING AND SHELF STABILITY SHIN-ETSU CHEMICAL CO., LTD. (JP) 1997-01-28 US disclosed
US-5346932-A Silicone rubber composition and method for curing the same SHIN-ETSU CHEMICAL CO., LTD. (JP) 1994-09-13 US disclosed
EP-0449651-B1 Silicone rubber composition and its manufacture SHINETSU CHEMICAL CO (JP) 1994-08-10 EP disclosed
US-5194479-A Acid Strength Adjuster, Fatigue Resistance SHIN-ETSU CHEMICAL CO., LTD. (JP) 1993-03-16 US disclosed
EP-0449651-A1 Silicone rubber composition and its manufacture SHIN-ETSU CHEMICAL CO., LTD. (JP) 1991-10-02 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 (2 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-20250034289-A1 POLYMERIZABLE COMPOSITIONS INCLUDING A POLYMERIZABLE COMPONENT AND A REDOX INITIATION SYSTEM CONTAINING A PHOTOLABILE REDUCING AGENT, AND A PHOTOLABILE REDUCING AGENT PPOX, CYBA, SQOR NAAA 2820/4885CES2 2378/4885EPHX1 2027/4885
US-12600885-B2 Composition including monomer with a carboxylic acid group, monomer with a hydroxyl group, an alkyl monomer, and crosslinker and related article and method RAD51, HACL2, COL2A1 NAAA 950/4885CES2 126/4885EPHX1 1801/4885

“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.