SCHEMBL449789

SCHEMBL449789

CCCCCCC(O)CC=CCC(O)CCCCCC

nearest known ligand 0.64

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
FFAR1 O14842 3/20 0.64
FFAR4 Q5NUL3 2/20 0.64
FAAH O00519 2/20 0.54
GPR84 Q9NQS5 8/20 0.52
NFKB1 P19838 2/20 0.47
NFKB2 Q00653 1/20 0.47
RELA Q04206 1/20 0.47
SPHK1 Q9NYA1 1/20 0.45
LMNA P02545 1/20 0.44
PSMD14 O00487 2/20 0.44
PLA2G1B P04054 2/20 0.44
MMP2 P08253 2/20 0.44
ATG4B Q9Y4P1 2/20 0.44
HSP90AA1 P07900 1/20 0.44
RAD52 P43351 1/20 0.44

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
SCHEMBL449788 1.00 FFAR1 (0.64) FFAR1FFAR4FAAHGPR84NFKB1
SCHEMBL26091378 0.94 FFAR1 (0.58) FFAR1FFAR4FAAHGPR84NFKB1
SCHEMBL11864171 0.94 FFAR1 (0.58) FFAR1FFAR4FAAHGPR84NFKB1
SCHEMBL11864156 0.94 FFAR1 (0.58) FFAR1FFAR4FAAHGPR84NFKB1
SCHEMBL31216729 0.94 FFAR1 (0.58) FFAR1FFAR4FAAHGPR84NFKB1
SCHEMBL26088775 0.94 FFAR1 (0.58) FFAR1FFAR4FAAHGPR84NFKB1
SCHEMBL25132301 0.92 FFAR1 (0.76) FFAR1FFAR4FAAHGPR84NFKB1
SCHEMBL23092271 0.92 FFAR1 (0.76) FFAR1FFAR4FAAHGPR84NFKB1
SCHEMBL20021280 0.92 FFAR1 (0.76) FFAR1FFAR4FAAHGPR84NFKB1
SCHEMBL23092225 0.92 FFAR1 (0.76) FFAR1FFAR4FAAHGPR84NFKB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-4779121-B2 2011-09-28 JP claimed
US-7534917-B1 Method of producing dicarboxylic acids THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF AGRICULTURE (US) 2009-05-19 US 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
EP-4644996-A2 IMAGE FORMING METHOD Konica Minolta, Inc. (JP) 2025-11-05 EP disclosed
EP-3926408-B1 IMAGE FORMING METHOD AND IMAGE FORMING SYSTEM KONICA MINOLTA INC (JP) 2025-09-24 EP disclosed
US-12398095-B2 Photoresponsive compound, adhesive, switching material, and toner containing the photoresponsive compound, and image forming method using the toner Konica Minolta, Inc. (JP) 2025-08-26 US disclosed
US-20250237969-A1 RESIN, RESIN COMPOSITION, PRINTED IMAGE, ELECTROSTATIC CHARGE IMAGE DEVELOPING TONER, AND METHOD FOR PRODUCING ELECTROSTATIC CHARGE IMAGE DEVELOPING TONER Konica Minolta, Inc. (JP) 2025-07-24 US disclosed
US-12321132-B2 Resin composition, toner for developing electrostatic charge image, image forming method, photosensitive adhesive, and optical switching material Konica Minolta, Inc. (JP) 2025-06-03 US disclosed
US-20250138454-A1 IMAGE FORMING METHOD AND IMAGE FORMING SYSTEM Konica Minolta, Inc. (JP) 2025-05-01 US disclosed
EP-1673328-A2 AN IMPROVED PROCESS FOR THE SYNTHESIS OF UNSATURATED ALCOHOLS Dow Global Technologies Inc. (US) 2006-06-28 EP disclosed
WO-2005040077-A3 AN IMPROVED PROCESS FOR THE SYNTHESIS OF UNSATURATED ALCOHOLS DOW GLOBAL TECHNOLOGIES INC (US) 2005-08-04 WO disclosed
WO-2005040077-A2 AN IMPROVED PROCESS FOR THE SYNTHESIS OF UNSATURATED ALCOHOLS DOW GLOBAL TECHNOLOGIES INC. (US) 2005-05-06 WO disclosed
WO-2005040077-A2 AN IMPROVED PROCESS FOR THE SYNTHESIS OF UNSATURATED ALCOHOLS DOW GLOBAL TECHNOLOGIES INC. (US) 2005-05-06 WO disclosed
US-20050080301-A1 Process for the synthesis of unsaturated alcohols DOW GLOBAL TECHNOLOGIES LLC 2005-04-14 US disclosed
US-20050080301-A1 Process for the synthesis of unsaturated alcohols DOW GLOBAL TECHNOLOGIES LLC 2005-04-14 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-12398095-B2 Photoresponsive compound, adhesive, switching material, and toner containing the photoresponsive compound, and image forming method using the toner ACTR2, SUN2, ADGRF1 FFAR1 78/4885FFAR4 313/4885FAAH 871/4885
US-20050080301-A1 Process for the synthesis of unsaturated alcohols FASN, SQLE, ALOX12 FFAR1 119/4885FFAR4 189/4885FAAH 181/4885

“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.