SCHEMBL910534

SCHEMBL910534

C=CCC(O)CCCCCC

nearest known ligand 0.52

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
FFAR1 O14842 3/20 0.52
FFAR4 Q5NUL3 2/20 0.52
GPR84 Q9NQS5 8/20 0.48
TSHR P16473 1/20 0.44
FAAH O00519 3/20 0.44
SPHK1 Q9NYA1 1/20 0.42
PSMD14 O00487 2/20 0.42
PLA2G1B P04054 2/20 0.42
MMP2 P08253 2/20 0.42
ATG4B Q9Y4P1 2/20 0.42
HSP90AA1 P07900 1/20 0.42
RAD52 P43351 1/20 0.42
LMNA P02545 1/20 0.41

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
SCHEMBL2397949 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH
SCHEMBL9334962 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH
SCHEMBL11748318 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH
SCHEMBL9200158 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH
SCHEMBL1712736 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH
SCHEMBL1712990 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH
SCHEMBL9685588 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH
SCHEMBL9685329 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH
SCHEMBL7065643 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH
SCHEMBL9200169 1.00 FFAR1 (0.52) FFAR1FFAR4GPR84TSHRFAAH

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 65 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-4779121-B2 2011-09-28 JP claimed
EP-1673328-B1 AN IMPROVED PROCESS FOR THE SYNTHESIS OF UNSATURATED ALCOHOLS DOW GLOBAL TECHNOLOGIES INC (US) 2008-07-09 EP claimed
JP-2007508300-A 2007-04-05 JP claimed
US-7176336-B2 Preparing 9-octadecene-7,12-diol by catalyzing methyl ricinoleate derived from a seed oil, in presence of a metathesis catalyst; improved yield; use in manufacture of surfactants and thermoplastic polyurethanes DOW GLOBAL TECHNOLOGIES INC. (US) 2007-02-13 US claimed
EP-1673328-A2 AN IMPROVED PROCESS FOR THE SYNTHESIS OF UNSATURATED ALCOHOLS Dow Global Technologies Inc. (US) 2006-06-28 EP claimed
WO-2005040077-A2 AN IMPROVED PROCESS FOR THE SYNTHESIS OF UNSATURATED ALCOHOLS DOW GLOBAL TECHNOLOGIES INC. (US) 2005-05-06 WO claimed
US-20050080301-A1 Process for the synthesis of unsaturated alcohols DOW GLOBAL TECHNOLOGIES LLC 2005-04-14 US claimed
US-20240417359-A1 PRECURSORS OF PHENOLIC FRAGRANT COMPOUNDS GIVAUDAN SA (CH) 2024-12-19 US disclosed
CN-117126906-B Modification method of soybean protein isolate, modified soybean protein isolate and application thereof 中国农业大学 2024-10-25 CN disclosed
EP-4419498-A1 PRECURSORS OF PHENOLIC FRAGRANT COMPOUNDS Givaudan SA (CH) 2024-08-28 EP disclosed
CN-118119589-A Phenol aromatic compound precursor 奇华顿股份有限公司 2024-05-31 CN disclosed
CN-117126906-A Modification method of soybean protein isolate, modified soybean protein isolate and application thereof 中国农业大学 2023-11-28 CN disclosed
WO-2023067040-A1 PRECURSORS OF PHENOLIC FRAGRANT COMPOUNDS GIVAUDAN SA (CH) 2023-04-27 WO disclosed
EP-0841090-A2 Catalyst and process for production of 2-buten-1-ol compounds BASF AKTIENGESELLSCHAFT (DE) 1998-05-13 EP disclosed
US-4310709-A SELENIUM OR TELLURIUM MODIFIED PALLADIUM CATALYST BASF AKTIENGESELLSCHAFT (DE) 1982-01-12 US disclosed
US-4219683-A USING A PALLADIUM-THORIUM OXIDE CATALYST PHILLIPS PETROLEUM COMPANY (US) 1980-08-26 US disclosed
EP-0002027-B1 PROCESS FOR THE PREPARATION OF 2-BUTENE-1-OL COMPOUNDS BY ISOMERIZATION OF THE CORRESPONDING 3-BUTENE-1-OL COMPOUNDS BASF Aktiengesellschaft (DE) 1980-07-23 EP disclosed
EP-0002027-A1 Process for the preparation of 2-butene-1-ol compounds by isomerization of the corresponding 3-butene-1-ol compounds BASF Aktiengesellschaft (DE) 1979-05-30 EP disclosed
US-4040977-A HALOACETAMIDE OR THIOCYANOACETAMIDE-ALCOHOL-FORMALDEHYDE CONDENSATES STERLING DRUG INC. (US) 1977-08-09 US disclosed
US-4039585-A Hydroformylation process UOP INC. (US) 1977-08-02 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 (2 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-20050080301-A1 Process for the synthesis of unsaturated alcohols FASN, SQLE, ALOX12 FFAR1 119/4885FFAR4 189/4885GPR84 1361/4885
US-20240417359-A1 PRECURSORS OF PHENOLIC FRAGRANT COMPOUNDS HAAO, FOS, HPD FFAR1 562/4885FFAR4 822/4885GPR84 1890/4885

“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.