SCHEMBL4410974

SCHEMBL4410974

O=C(O)CCCCCCCc1ccc(O)cc1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 1/20 0.71
▸ RXFP1 Q9HBX9 1/20 0.71
▸ LTB4R Q15722 1/20 0.68
▸ ACHE P22303 3/20 0.60
▸ SGMS1 Q86VZ5 2/20 0.60
▸ SGMS2 Q8NHU3 2/20 0.60
▸ DPP4 P27487 1/20 0.59
▸ SLC6A3 Q01959 3/20 0.59
▸ HDAC3 O15379 1/20 0.59
▸ MAPK1 P28482 1/20 0.59
▸ ADRA1A P35348 1/20 0.59
▸ HDAC4 P56524 1/20 0.59
▸ HDAC1 Q13547 1/20 0.59
▸ SMN1; SMN2 Q16637 1/20 0.59
▸ HDAC7 Q8WUI4 1/20 0.59
▸ HDAC2 Q92769 1/20 0.59
▸ HDAC10 Q969S8 1/20 0.59
▸ HDAC11 Q96DB2 1/20 0.59
▸ HDAC8 Q9BY41 1/20 0.59
▸ HDAC6 Q9UBN7 1/20 0.59

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
SCHEMBL9662554 1.00 MAPT (0.71) MAPTRXFP1LTB4RACHESGMS1
SCHEMBL31522354 1.00 MAPT (0.71) MAPTRXFP1LTB4RACHESGMS1
SCHEMBL1832377 1.00 MAPT (0.71) MAPTRXFP1LTB4RACHESGMS1
SCHEMBL2516030 1.00 MAPT (0.71) MAPTRXFP1LTB4RACHESGMS1
SCHEMBL9138858 1.00 MAPT (0.71) MAPTRXFP1LTB4RACHESGMS1
SCHEMBL503636 1.00 MAPT (0.71) MAPTRXFP1LTB4RACHESGMS1
SCHEMBL418561 0.98 MAPT (0.68) MAPTRXFP1LTB4RACHESGMS1
SCHEMBL28968198 0.96 MAPT (0.66) MAPTRXFP1LTB4RACHESGMS1
SCHEMBL284671 0.92 SMN1; SMN2 (0.69) MAPTRXFP1LTB4RDPP4SLC6A3
SCHEMBL3814880 0.92 MAPT (0.83) MAPTRXFP1LTB4RSLC6A3HDAC3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1691845-A4 COMPOUNDS CONTAINING MATRIX METALLOPROTEINASE SUBSTRATES AND METHODS OF THEIR USE BRISTOL MYERS SQUIBB PHARMA CO (US) 2009-02-25 — — EP disclosed
EP-1086160-B1 CARBOXY-FUNCTIONALIZED POLYPHENYLENE ETHERS AND BLENDS CONTAINING THEM GEN ELECTRIC (US) 2006-10-04 — — EP disclosed
EP-1691845-A1 COMPOUNDS CONTAINING MATRIX METALLOPROTEINASE SUBSTRATES AND METHODS OF THEIR USE Bristol-Myers Squibb Pharma Company (US) 2006-08-23 — — EP disclosed
US-20050106100-A1 Compounds containing matrix metalloproteinase substrates and methods of their use LANTHEUS MEDICAL IMAGING, INC. 2005-05-19 — — US disclosed
WO-2005023314-A1 COMPOUNDS CONTAINING MATRIX METALLOPROTEINASE SUBSTRATES AND METHODS OF THEIR USE BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2005-03-17 — — WO disclosed
US-6552133-B2 Copolymerization or redistribution of o-hydroxyaromatic substituted aliphatic carboxylic acids into polyphenylene ethers; thermoplastic engineering resins with excellent hydrolytic stability, dimensional stability and toughness GENERAL ELECTRIC COMPANY 2003-04-22 — — US disclosed
EP-0895519-B1 REDISTRIBUTION OF POLYPHENYLENE ETHERS AND POLYPHENYLENE ETHERS WITH NOVEL STRUCTURE GEN ELECTRIC (US) 2002-10-16 — — EP disclosed
US-20010034430-A1 Carboxy-functionalized polyphenylene ethers and blends containing them SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2001-10-25 — — US disclosed
US-20010034418-A1 Carboxy-functionalized polyphenylene ethers and blends containing them YEAGER GARY WILLIAM (US) 2001-10-25 — — US disclosed
US-6268463-B1 POLYPHENYLENE ETHERS WITH CARBOXY GROUPS GENERAL ELECTRIC COMPANY 2001-07-31 — — US disclosed
EP-1086160-A1 CARBOXY-FUNCTIONALIZED POLYPHENYLENE ETHERS AND BLENDS CONTAINING THEM GENERAL ELECTRIC COMPANY (US) 2001-03-28 — — EP disclosed
US-6063875-A CONTAIN STRUCTURAL UNITS WITH A CARBOXYETHYL GROUP IN THE 2-POSITION; USEFUL AS COMPATIBILIZING COPOLYMERS WITH POLYMERS CONTAINING CARBOXYLIC ACID-REACTIVE GROUPS, SUCH AS POLYESTERS AND POLYAMIDES GENERAL ELECTRIC COMPANY (US) 2000-05-16 — — US disclosed
WO-1999064494-A1 CARBOXY-FUNCTIONALIZED POLYPHENYLENE ETHERS AND BLENDS CONTAINING THEM GENERAL ELECTRIC COMPANY (US) 1999-12-16 — — WO disclosed
US-5880221-A POLY(2,6-DIMETHYLPHENYL ETHER) REACTED WITH PHENOLIC COMPOUNDS GENERAL ELECTRIC COMPANY (US) 1999-03-09 — — US disclosed
EP-0895519-A1 REDISTRIBUTION OF POLYPHENYLENE ETHERS AND POLYPHENYLENE ETHERS WITH NOVEL STRUCTURE GENERAL ELECTRIC COMPANY (US) 1999-02-10 — — EP disclosed
WO-1998036015-A1 REDISTRIBUTION OF POLYPHENYLENE ETHERS AND POLYPHENYLENE ETHERS WITH NOVEL STRUCTURE GENERAL ELECTRIC COMPANY (US) 1998-08-20 — — WO 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-20050106100-A1 Compounds containing matrix metalloproteinase substrates and methods of their use MMP1, MMP10, MMP8 MAPT 2533/4885RXFP1 2548/4885LTB4R 1419/4885

“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.

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