Palmitic Acid

Palmitic Acid

SCHEMBL2161701

CCCCCCCCCCCCCCCC(=O)O.CN(C)C(CCCN)C(=O)O.C[N+](C)(C)CC(=O)[O-]

nearest known ligand 0.40

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

BHMTBHMT2

The experimentally established mechanism targets of Palmitic 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
FFAR4 Q5NUL3 2/20 0.40
FFAR1 O14842 2/20 0.40
GPR84 Q9NQS5 7/20 0.40
PPARG P37231 7/20 0.40
PPARD Q03181 7/20 0.40
PPARA Q07869 7/20 0.40
HDAC11 Q96DB2 5/20 0.40
TSHR P16473 4/20 0.40
ALDH1A1 P00352 4/20 0.40
PTPN1 P18031 3/20 0.40
KMT2A Q03164 3/20 0.40
TLR2 O60603 2/20 0.40
TDP1 Q9NUW8 2/20 0.40
FABP4 P15090 2/20 0.40
MEN1 O00255 2/20 0.40
ALOX15 P16050 2/20 0.40
SLC22A6 Q4U2R8 1/20 0.40
SLC22A8 Q8TCC7 1/20 0.40
ESR1 P03372 1/20 0.40
PDE4A P27815 1/20 0.40

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
Myristic Acid SCHEMBL2160003 1.00 FFAR4 (0.40) FFAR4FFAR1GPR84PPARGPPARD
Stearic Acid SCHEMBL2160333 1.00 FFAR4 (0.40) FFAR4FFAR1GPR84PPARGPPARD
Dodecanoate SCHEMBL14632965 1.00 FFAR4 (0.40) FFAR4FFAR1GPR84PPARGPPARD
Oleic Acid SCHEMBL2161441 0.94 PPARG (0.47) FFAR4FFAR1PPARGPPARDPPARA
Palmitic Acid SCHEMBL20786789 0.88 GPR84 (0.52) FFAR4FFAR1GPR84PPARGPPARD
Glycinebetaine SCHEMBL2132643 0.86 GPR84 (0.41) FFAR1GPR84PPARDTSHRMAPT
Glycinebetaine SCHEMBL3889766 0.86 GPR84 (0.41) FFAR1GPR84PPARDTSHRMAPT
Glycinebetaine SCHEMBL2133338 0.86 GPR84 (0.41) FFAR1GPR84PPARDTSHRMAPT
Glycinebetaine SCHEMBL2135218 0.86 GPR84 (0.41) FFAR1GPR84PPARDTSHRMAPT
Glycinebetaine SCHEMBL2131138 0.86 GPR84 (0.41) FFAR1GPR84PPARDTSHRMAPT

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 FFAR4 2605/4885FFAR1 1413/4885GPR84 701/4885

“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.