SCHEMBL3662634

SCHEMBL3662634

CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC(C)C

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CNR1 P21554 4/20 0.73
ALDH1A1 P00352 3/20 0.73
MAPT P10636 3/20 0.73
FAAH O00519 3/20 0.73
HPGD P15428 2/20 0.73
CNR2 P34972 2/20 0.73
LMNA P02545 3/20 0.64
MGLL Q99685 1/20 0.61
PPARG P37231 2/20 0.60
THRB P10828 1/20 0.60
KDM4E B2RXH2 1/20 0.60
MEN1 O00255 1/20 0.60
USP2 O75604 1/20 0.60
TP53 P04637 1/20 0.60
CYP3A4 P08684 1/20 0.60
HSPD1 P10809 1/20 0.60
CYP19A1 P11511 1/20 0.60
FABP4 P15090 1/20 0.60
ALOX15 P16050 1/20 0.60
CASP1 P29466 1/20 0.60

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
SCHEMBL3662637 1.00 CNR1 (0.73) CNR1ALDH1A1MAPTFAAHHPGD
SCHEMBL8706806 0.97 LMNA (0.69) CNR1ALDH1A1MAPTFAAHHPGD
SCHEMBL27860052 0.95 LMNA (0.72) CNR1ALDH1A1MAPTFAAHHPGD
SCHEMBL43113 0.95 LMNA (0.72) CNR1ALDH1A1MAPTFAAHHPGD
SCHEMBL29380166 0.95 LMNA (0.72) CNR1ALDH1A1MAPTFAAHHPGD
SCHEMBL27450484 0.95 LMNA (0.72) CNR1ALDH1A1MAPTFAAHHPGD
SCHEMBL14899321 0.95 LMNA (0.70) CNR1ALDH1A1MAPTFAAHHPGD
SCHEMBL11051839 0.95 LMNA (0.70) CNR1ALDH1A1MAPTFAAHHPGD
Iodide SCHEMBL28774884 0.94 LMNA (0.70) CNR1ALDH1A1MAPTFAAHHPGD
Iodide SCHEMBL28278305 0.92 LMNA (0.68) CNR1ALDH1A1MAPTFAAHHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8425784-B2 Ozonolysis reactions in liquid CO2 and CO2-expanded solvents UNIVERSITY OF KANSAS (US) 2013-04-23 US claimed
US-20120213715-A1 Method and composition for the prevention and treatment of early childhood dental caries Huang, Chifu (US) 2012-08-23 US claimed
US-20260144726-A1 POLYOL-FREE COSMETIC COMPOSITION COMPRISING ALPHA HYDROXY ACID ESTER L'OREAL (FR) 2026-05-28 US disclosed
EP-4733360-A1 VULCANIZING AGENT COMPOSITION AND PRODUCTION METHOD FOR SAME, RUBBER COMPOSITION AND PRODUCTION METHOD FOR SAME, AND VULCANIZED RUBBER AND PRODUCTION METHOD FOR SAME SHIKOKU CHEMICALS CORPORATION (JP) 2026-04-29 EP disclosed
WO-2024262346-A1 VULCANIZING AGENT COMPOSITION AND PRODUCTION METHOD FOR SAME, RUBBER COMPOSITION AND PRODUCTION METHOD FOR SAME, AND VULCANIZED RUBBER AND PRODUCTION METHOD FOR SAME 四国化成工業株式会社 2024-12-26 WO disclosed
WO-2023027021-A1 NOVEL PLASMALOGEN DERIVATIVE 株式会社レオロジー機能食品研究所 2023-03-02 WO disclosed
EP-2209547-B1 OZONOLYSIS REACTIONS IN LIQUID CO2 AND CO2-EXPANDED SOLVENTS UNIV KANSAS (US) 2018-06-20 EP disclosed
CN-101909729-B Ozonolysis reactions in liquid CO2 and CO2-expanded solvents UNIVERSITY OF KANSAS (US) 2014-10-22 CN disclosed
US-8801939-B2 Ozonolysis reactions in liquid CO2 and CO2-expanded solvents UNIVERSITY OF KANSAS (US) 2014-08-12 US disclosed
CN-102100668-B Advanced fatty acid derivative micro emulsion and preparation method and application thereof UNIV GUANGXI 2013-12-18 CN disclosed
US-20130240781-A1 Ozonolysis Reactions in Liquid CO2 and CO2-Expanded Solvents ARCHER DANIELS MIDLAND COMPANY (US) 2013-09-19 US disclosed
US-8425784-B2 Ozonolysis reactions in liquid CO2 and CO2-expanded solvents UNIVERSITY OF KANSAS (US) 2013-04-23 US disclosed
CN-102100668-A Advanced fatty acid derivative micro emulsion and preparation method and application thereof UNIV GUANGXI 2011-06-22 CN disclosed
EP-2209547-A2 OZONOLYSIS REACTIONS IN LIQUID CO2 AND CO2-EXPANDED SOLVENTS University Of Kansas (US) 2010-07-28 EP disclosed
WO-2009061806-A2 OZONOLYSIS REACTIONS IN LIQUID CO2 AND CO2-EXPANDED SOLVENTS UNIVERSITY OF KANSAS (US) 2009-05-14 WO disclosed
US-20090118498-A1 OZONOLYSIS REACTIONS IN LIQUID CO2 AND CO2-EXPANDED SOLVENTS ARCHER DANIELS MIDLAND COMPANY 2009-05-07 US disclosed
EP-1539892-B1 FAST DRYING COATINGS VOCFREE INC (US) 2007-11-14 EP disclosed
US-20030054103-A1 Curable coating composition, curable ink, printing method thereof and printed matter TOYO INK MFG. CO., LTD. (JP) 2003-03-20 US disclosed
US-4364743-A ESTER AND MIDDLE OIL ERNER WILLIAM E 1982-12-21 US 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-20260144726-A1 POLYOL-FREE COSMETIC COMPOSITION COMPRISING ALPHA HYDROXY ACID ESTER HAO2, HADH, LDHA CNR1 1575/4885ALDH1A1 202/4885MAPT 2477/4885

“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.