Oleic Acid

Oleic Acid

SCHEMBL12470952

CC(C)Cc1ccc(C(C)C(=O)O)cc1.CCCCCCCC/C=C\CCCCCCCC(=O)O

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGS1PTGS2

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
PTGS1 known ✓ P23219 5/20 0.59
PTGS2 known ✓ P35354 3/20 0.59
LMNA P02545 4/20 0.59
CYP2C9 P11712 3/20 0.59
AKR1C3 P42330 3/20 0.59
BLM P54132 3/20 0.59
CXCR1 P25024 2/20 0.59
CXCR2 P25025 2/20 0.59
TSHR P16473 2/20 0.59
ALB P02768 1/20 0.59
ESR1 P03372 1/20 0.59
ALOX5 P09917 1/20 0.59
RARB P10826 1/20 0.59
ADRB3 P13945 1/20 0.59
NFKB1 P19838 1/20 0.59
HTR2A P28223 1/20 0.59
NR1I3 Q14994 1/20 0.59
SLC22A6 Q4U2R8 1/20 0.59
CXCL8 P10145 1/20 0.59
AKR1C2 P52895 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
Linoleic Acid SCHEMBL12471256 0.98 ALDH1A1 (0.59) PTGS1LMNAPTGS2CYP2C9AKR1C3
Stearic Acid SCHEMBL12470629 0.93 PTGS1 (0.69) PTGS1LMNAPTGS2CYP2C9AKR1C3
Palmitic Acid SCHEMBL7702151 0.93 PTGS1 (0.69) PTGS1LMNAPTGS2CYP2C9AKR1C3
Ricinoleic Acid SCHEMBL9559032 0.91 FFAR1 (0.65) PTGS1LMNAPTGS2CYP2C9AKR1C3
Linolenic Acid SCHEMBL12470710 0.91 ALDH1A1 (0.59) PTGS1LMNAPTGS2CYP2C9AKR1C3
Ibuprofen SCHEMBL10523173 0.85 PTGS1 (0.58) PTGS1LMNAPTGS2CYP2C9AKR1C3
Ibuprofen SCHEMBL9302599 0.84 PTGS1 (0.83) PTGS1LMNAPTGS2CYP2C9AKR1C3
Glyceryl Monooleate SCHEMBL6369049 0.83 DGKA (0.64) PTGS1LMNAPTGS2CYP2C9AKR1C3
Ibuprofen SCHEMBL3428176 0.81 PTGS1 (0.68) PTGS1LMNAPTGS2CYP2C9AKR1C3
Ibuprofen SCHEMBL942351 0.80 PTGS1 (0.86) PTGS1LMNAPTGS2CYP2C9AKR1C3

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
EP-2673370-A1 PRODUCTION OF ALCOHOL ESTERS IN SITU USING ALCOHOLS AND FATTY ACIDS PRODUCED BY MICROORGANISMS E.I. Du Pont De Nemours And Company (US) 2013-12-18 EP disclosed
US-20130040340-A1 PRODUCTION OF ALCOHOL ESTERS IN SITU USING ALCOHOLS AND FATTY ACIDS PRODUCED BY MICROORGANISMS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2013-02-14 US disclosed
WO-2012109221-A1 PRODUCTION OF ALCOHOL ESTERS IN SITU USING ALCOHOLS AND FATTY ACIDS PRODUCED BY MICROORGANISMS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2012-08-16 WO disclosed