Linolenic Acid

Linolenic Acid

SCHEMBL12470710

CC(C)Cc1ccc(C(C)C(=O)O)cc1.CC/C=C\C/C=C\C/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 Linolenic 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 7/20 0.59
PTGS2 known ✓ P35354 4/20 0.59
ALDH1A1 P00352 8/20 0.59
F7 P08709 7/20 0.59
F3 P13726 7/20 0.59
PPARG P37231 5/20 0.59
PPARD Q03181 5/20 0.59
PPARA Q07869 5/20 0.59
LMNA P02545 4/20 0.59
CYP19A1 P11511 4/20 0.59
FFAR1 O14842 4/20 0.59
OXER1 Q8TDS5 3/20 0.59
MAPT P10636 2/20 0.59
BLM P54132 2/20 0.59
KMT2A Q03164 2/20 0.59
KDM4E B2RXH2 2/20 0.59
CYP3A4 P08684 2/20 0.59
HPGD P15428 2/20 0.59
ALOX15 P16050 2/20 0.59
FFAR4 Q5NUL3 2/20 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 0.93 ALDH1A1 (0.59) ALDH1A1PTGS1F7F3PPARG
Oleic Acid SCHEMBL12470952 0.91 PTGS1 (0.59) ALDH1A1PTGS1F7F3PPARG
Palmitic Acid SCHEMBL7702151 0.83 PTGS1 (0.69) ALDH1A1PTGS1PPARGPPARDPPARA
Stearic Acid SCHEMBL12470629 0.83 PTGS1 (0.69) ALDH1A1PTGS1PPARGPPARDPPARA
Ricinoleic Acid SCHEMBL9559032 0.82 FFAR1 (0.65) ALDH1A1PTGS1F7F3PPARG
Ibuprofen SCHEMBL3428176 0.79 PTGS1 (0.68) ALDH1A1PTGS1PTGS2LMNABLM
Ibuprofen SCHEMBL942351 0.78 PTGS1 (0.86) PTGS1PTGS2LMNABLMAKR1C3
SCHEMBL23698166 0.77 ALDH1A1 (1.00) ALDH1A1PTGS1F7F3PPARG
SCHEMBL23698135 0.77 ALDH1A1 (1.00) ALDH1A1PTGS1F7F3PPARG
SCHEMBL23698246 0.77 ALDH1A1 (1.00) ALDH1A1PTGS1F7F3PPARG

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