SCHEMBL296867

SCHEMBL296867

[CH2]CCCCCCCOC(=O)CC

nearest known ligand 0.69

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
NAAA Q02083 1/20 0.69
HTT P42858 1/20 0.50
RAD52 P43351 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
FAAH O00519 1/20 0.43
TSHR P16473 3/20 0.42
DGKA P23743 1/20 0.42
HTR2C P28335 1/20 0.42
ALDH1A1 P00352 2/20 0.41
PRSS1 P07477 1/20 0.41
PRSS2 P07478 1/20 0.41
PRSS3 P35030 1/20 0.41
CYP3A4 P08684 1/20 0.40
EPHX1 P07099 1/20 0.39
DNM1 Q05193 1/20 0.39
ACHE P22303 3/20 0.38

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
SCHEMBL7839868 1.00 NAAA (0.69) NAAAHTTRAD52NPSR1FAAH
SCHEMBL130965 1.00 NAAA (0.69) NAAAHTTRAD52NPSR1FAAH
SCHEMBL15953232 1.00 NAAA (0.69) NAAAHTTRAD52NPSR1FAAH
SCHEMBL7843054 1.00 NAAA (0.69) NAAAHTTRAD52NPSR1FAAH
SCHEMBL128836 0.98 NAAA (0.65) NAAAHTTRAD52NPSR1FAAH
SCHEMBL128268 0.91
SCHEMBL12956536 0.89 NAAA (0.86) NAAAHTTRAD52NPSR1FAAH
SCHEMBL3993048 0.89 NAAA (0.86) NAAAHTTRAD52NPSR1FAAH
SCHEMBL14472850 0.89 NAAA (0.86) NAAAHTTRAD52NPSR1FAAH
SCHEMBL50185 0.86 NAAA (0.81) NAAAHTTRAD52NPSR1FAAH

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111278896-A Thermosetting resin composition and method for producing same 堺化学工业株式会社 2020-06-12 CN disclosed
EP-1501897-B1 METHOD FOR THE PRODUCTION OF PERYLEN-3,4:9,10-TETRACARBOXYLIC ACID DIIMIDES AND PERYLEN-3,4:9,10-TETRACARBOXYLIC ACID DIANHYDRIDE AND NAPHTALENE-1,8-DICARBOXYLIMIDES BASF SE (DE) 2012-03-14 EP disclosed
US-7807836-B2 Preparation of perylen-3,4:9,10-tetracarboxylic dianhydride and also of naphtalene-1,8-dicarboximides BASF AKTIENGESELLSCHAFT (DE) 2010-10-05 US disclosed
US-20080161569-A1 PREPARATION OF PERYLEN-3,4:9,10-TETRACARBOXYLIC DIANHYDRIDE AND ALSO OF NAPHTALENE-1,8-DICARBOXIMIDES BASF AKTIENGESELLSCHAFT (DE) 2008-07-03 US disclosed
US-7393956-B2 Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides BASF AKTIENGESELLSCHAFT (DE) 2008-07-01 US disclosed
CN-100341947-C Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides BASF AG (DE) 2007-10-10 CN disclosed
CN-1649967-A Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides BASF AG (DE) 2005-08-03 CN disclosed
US-20050131220-A1 Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides BASF AKTIENGESELLSCHAFT (DE) 2005-06-16 US disclosed
EP-1501897-A1 METHOD FOR THE PRODUCTION OF PERYLEN-3,4:9,10-TETRACARBOXYLIC ACID DIIMIDES AND PERYLEN-3,4:9,10-TETRACARBOXYLIC ACID DIANHYDRIDE AND NAPHTALENE-1,8-DICARBOXYLIMIDES BASF AKTIENGESELLSCHAFT (DE) 2005-02-02 EP disclosed
WO-2003091345-A1 METHOD FOR THE PRODUCTION OF PERYLEN-3,4:9,10-TETRACARBOXYLIC ACID DIIMIDES AND PERYLEN-3,4:9,10-TETRACARBOXYLIC ACID DIANHYDRIDE AND NAPHTALENE-1,8-DICARBOXYLIMIDES BASF AKTIENGESELLSCHAFT (DE) 2003-11-06 WO disclosed
WO-1994008934-A1 ENANTIOMERIC RESOLUTION ALBEMARLE CORPORATION (US) 1994-04-28 WO disclosed
WO-1994008935-A1 ENANTIOMERIC RESOLUTION ALBEMARLE CORPORATION (US) 1994-04-28 WO disclosed
WO-1994008936-A1 ENANTIOMERIC RESOLUTION ALBEMARLE CORPORATION (US) 1994-04-28 WO disclosed
WO-1994008937-A1 ENANTIOMERIC RESOLUTION ALBEMARLE CORPORATION (US) 1994-04-28 WO disclosed
US-5278337-A Enantiomeric resolution of aryl-substituted aliphatic carboxylic acids ETHYL CORPORATION (US) 1994-01-11 US disclosed
US-5260482-A Enantiomeric resolution ETHYL CORPORATION (US) 1993-11-09 US disclosed
US-5256816-A Enantiomeric resolution ETHYL CORPORATION (US) 1993-10-26 US disclosed
US-5248813-A Enantiomeric resolution ETHYL CORPORATION (US) 1993-09-28 US disclosed
US-4808620-A ANTIINFLAMMATORY, ANALGESICS, ANTIPYRETIC, ANTIALLERGENS, ANTIARTHRITIC, ANTIRHEUMATIC AGENTS YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD. (JP) 1989-02-28 US disclosed
EP-0254241-A1 Pyrazolopyridine compounds, their preparation and use Yoshitomi Pharmaceutical Industries, Ltd. (JP) 1988-01-27 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-20080161569-A1 PREPARATION OF PERYLEN-3,4:9,10-TETRACARBOXYLIC DIANHYDRIDE AND ALSO OF NAPHTALENE-1,8-DICARBOXIMIDES CLIC1, PNPO, CLIC4 NAAA 682/4885HTT 3060/4885RAD52 3203/4885
US-20050131220-A1 Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides CBR1, CBR3, SCO2 NAAA 1942/4885HTT 3673/4885RAD52 2196/4885

“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.