SCHEMBL1029423

SCHEMBL1029423

O=C(O)OCCCCCCCCCOC(=O)O

nearest known ligand 0.48

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.48
ALDH1A1 P00352 2/20 0.48
CYP3A4 P08684 1/20 0.48
NAAA Q02083 1/20 0.44
TDP1 Q9NUW8 1/20 0.42
HCAR2 Q8TDS4 2/20 0.41
EPHX1 P07099 1/20 0.41
ACHE P22303 6/20 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
SCHEMBL8505216 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1
SCHEMBL6567582 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1
SCHEMBL8505895 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1
SCHEMBL2513161 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1
SCHEMBL8507336 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1
SCHEMBL1729891 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1
SCHEMBL8508151 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1
SCHEMBL8505503 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1
SCHEMBL284653 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1
SCHEMBL8505232 1.00 TSHR (0.48) TSHRALDH1A1CYP3A4NAAATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1778764-B1 COATINGS FOR IMPLANTABLE DEVICES COMPRISING POLY(HYDROXY-ALKANOATES) AND DIACID LINKAGES ABBOTT CARDIOVASCULAR SYSTEMS (US) 2011-01-19 EP claimed
US-6932974-B2 Method of preventing adhesions with absorbable polyoxaesters ETHICON, INC. (US) 2005-08-23 US disclosed
EP-1242505-B1 METHOD FOR THE CONTINUOUS PRODUCTION OF COPOLYAMIDES BASED ON A LACTAME (I), A DIAMINE (II) AND A DICARBOXYLIC ACID (III) BASF AG (DE) 2003-06-18 EP disclosed
EP-1280846-A1 METHOD FOR PRODUCING A POLYMER, USING CAPROLACTAM BASF AKTIENGESELLSCHAFT (DE) 2003-02-05 EP disclosed
EP-1242505-A1 METHOD FOR THE CONTINUOUS PRODUCTION OF COPOLYAMIDES BASED ON A LACTAME (I), A DIAMINE (II) AND A DICARBOXYLIC ACID (III) BASF AKTIENGESELLSCHAFT (DE) 2002-09-25 EP disclosed
US-6403655-B1 Method of preventing adhesions with absorbable polyoxaesters ETHICON, INC. 2002-06-11 US disclosed
WO-2001083589-A1 METHOD FOR PRODUCING A POLYMER, USING CAPROLACTAM BASF AKTIENGESELLSCHAFT (DE) 2001-11-08 WO disclosed
US-20010012511-A1 Method of preventing adhesions with absorbable polyoxaesters BEZWADA RAO S (US) 2001-08-09 US disclosed
WO-2001040355-A1 METHOD FOR THE CONTINUOUS PRODUCTION OF COPOLYAMIDES BASED ON A LACTAME (I), A DIAMINE (II) AND A DICARBOXYLIC ACID (III) BASF AKTIENGESELLSCHAFT (DE) 2001-06-07 WO disclosed
US-6224894-B1 MEDICAL EQUIPMENT ETHICON, INC. 2001-05-01 US disclosed
US-6147168-A Copolymers of absorbable polyoxaesters ETHICON, INC. (US) 2000-11-14 US disclosed
US-6100346-A Copolymers of polyoxaamides ETHICON, INC. (US) 2000-08-08 US disclosed
US-6074660-A Absorbable polyoxaesters containing amines and/ or amido groups ETHICON, INC. (US) 2000-06-13 US disclosed
US-5869421-A A MATRIX RESIN AND A DISPERSION RESIN HAVING A GLASS TRANSITION TEMPERATURE HIGHER AND DISPERSED IN THE MATRIX AS RESIN AGGREGATES; EXCELLENT ERASING; HEAT RESISTANCE; STORAGE STABILITY; DURABILITY RICOH COMPANY, LTD. (JP) 1999-02-09 US disclosed
EP-0082983-B1 CURABLE SYNTHETIC RESIN COMPOSITIONS AND AGENTS FOR CURABLE SYNTHETIC RESIN COMPOSITIONS BASED ON PREPOLYMERIC POLYETHER-URETHANE-UREA AMINES AND EPOXIDE RESINS AN/OR AROMATIC CARBAMIC-ACID ARYL ESTERS SCHERING AKTIENGESELLSCHAFT (DE) 1987-02-04 EP disclosed
EP-0084106-B1 CURABLE MIXTURES OF SYNTHETIC RESINS AND MEANS FOR CURABLE MIXTURES OF SYNTHETIC RESINS ON THE BASIS OF POLYETHERURETHANEUREA-AMINE PREPOLYMERS AND EPOXY RESINS SCHERING AKTIENGESELLSCHAFT (DE) 1986-09-10 EP disclosed
EP-0045383-B1 HOT MELT ADHESIVE FOR JOINING TEXTILES SCHERING AKTIENGESELLSCHAFT (DE) 1983-09-14 EP disclosed
EP-0084106-A1 Curable mixtures of synthetic resins and means for curable mixtures of synthetic resins on the basis of polyetherurethaneurea-amine prepolymers and epoxy resins SCHERING AKTIENGESELLSCHAFT (DE) 1983-07-27 EP disclosed
EP-0082983-A1 Curable synthetic resin compositions and agents for curable synthetic resin compositions based on prepolymeric polyether-urethane-urea amines and epoxide resins an/or aromatic carbamic-acid aryl esters SCHERING AKTIENGESELLSCHAFT (DE) 1983-07-06 EP disclosed
EP-0045383-A2 Hot melt adhesive for joining textiles SCHERING AKTIENGESELLSCHAFT (DE) 1982-02-10 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 (1 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-20010012511-A1 Method of preventing adhesions with absorbable polyoxaesters EPCAM, CDH1, DSC1 TSHR 4723/4885ALDH1A1 1799/4885CYP3A4 4472/4885

“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.