Oleic Acid

Oleic Acid

SCHEMBL2161441

CCCCCCCC/C=C\CCCCCCCC(=O)O.CN(C)C(CCCN)C(=O)O.C[N+](C)(C)CC(=O)[O-]

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

BHMTBHMT2

The experimentally established mechanism targets of Oleic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PPARG P37231 5/20 0.47
PPARD Q03181 5/20 0.47
PPARA Q07869 5/20 0.47
F7 P08709 5/20 0.47
F3 P13726 5/20 0.47
TERT O14746 3/20 0.47
PTPN1 P18031 3/20 0.47
HSD17B10 Q99714 3/20 0.47
FABP4 P15090 3/20 0.47
MAPT P10636 2/20 0.47
BLM P54132 2/20 0.47
LMNA P02545 2/20 0.47
ALOX15 P16050 2/20 0.47
DUSP3 P51452 2/20 0.47
CYP19A1 P11511 2/20 0.47
PTGS1 P23219 2/20 0.47
NR4A2 P43354 2/20 0.47
SIRT6 Q8N6T7 2/20 0.47
PTPN7 P35236 2/20 0.47
TDP1 Q9NUW8 2/20 0.47

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
Palmitic Acid SCHEMBL2161701 0.94 FFAR4 (0.40) PPARGPPARDPPARAPTPN1HSD17B10
Dodecanoate SCHEMBL14632965 0.94 FFAR4 (0.40) PPARGPPARDPPARAPTPN1HSD17B10
Stearic Acid SCHEMBL2160333 0.94 FFAR4 (0.40) PPARGPPARDPPARAPTPN1HSD17B10
Myristic Acid SCHEMBL2160003 0.94 FFAR4 (0.40) PPARGPPARDPPARAPTPN1HSD17B10
Glycinebetaine SCHEMBL2131980 0.88 FABP3 (0.46) PPARGPPARDPPARAF7F3
Palmitic Acid SCHEMBL20786789 0.82 GPR84 (0.52) PPARGPPARDPPARAPTPN1HSD17B10
Oleic Acid SCHEMBL3250070 0.82 PPARG (0.70) PPARGPPARDPPARAF7F3
Glycinebetaine SCHEMBL2135218 0.81 GPR84 (0.41) PPARDMAPTNPSR1FFAR1TSHR
Glycinebetaine SCHEMBL2133338 0.81 GPR84 (0.41) PPARDMAPTNPSR1FFAR1TSHR
Glycinebetaine SCHEMBL2131138 0.81 GPR84 (0.41) PPARDMAPTNPSR1FFAR1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130023591-A1 Phenyl-Containing Organopolysiloxane Composition, Raw Cosmetic Material, and Glossy Cosmetic Material DOW CORNING TORAY CO., LTD. (JP) 2013-01-24 US disclosed
EP-2519587-A1 PHENYL-CONTAINING ORGANOPOLYSILOXANE COMPOSITION, RAW COSMETIC MATERIAL, AND GLOSSY COSMETIC MATERIAL Dow Corning Toray Co., Ltd. (JP) 2012-11-07 EP disclosed
WO-2011081218-A1 PHENYL-CONTAINING ORGANOPOLYSILOXANE COMPOSITION, RAW COSMETIC MATERIAL, AND GLOSSY COSMETIC MATERIAL DOW CORNING TORAY CO., LTD. (JP) 2011-07-07 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-20130023591-A1 Phenyl-Containing Organopolysiloxane Composition, Raw Cosmetic Material, and Glossy Cosmetic Material MITF, XPA, FANCI PPARG 2286/4885PPARD 3143/4885PPARA 3381/4885

“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.