SCHEMBL2600375

SCHEMBL2600375

CCCCCCCCCC(CCCCCCCC(=O)O)C(CCCCCCCCC)CCCCCCCC(=O)O

nearest known ligand 0.74

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FFAR4 Q5NUL3 2/20 0.74
FFAR1 O14842 2/20 0.74
GPR84 Q9NQS5 7/20 0.74
PPARG P37231 7/20 0.74
PPARD Q03181 7/20 0.74
PPARA Q07869 7/20 0.74
HDAC11 Q96DB2 5/20 0.74
TSHR P16473 4/20 0.74
PTPN1 P18031 3/20 0.74
ALDH1A1 P00352 3/20 0.74
TLR2 O60603 2/20 0.74
TDP1 Q9NUW8 2/20 0.74
FABP4 P15090 2/20 0.74
KMT2A Q03164 2/20 0.74
ALOX15 P16050 2/20 0.74
HSD17B10 Q99714 2/20 0.74
SLC22A6 Q4U2R8 1/20 0.74
SLC22A8 Q8TCC7 1/20 0.74
MEN1 O00255 1/20 0.74
ESR1 P03372 1/20 0.74

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
SCHEMBL16023553 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD
SCHEMBL516197 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD
SCHEMBL2354538 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD
SCHEMBL16131158 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD
SCHEMBL13069503 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD
SCHEMBL23128413 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD
SCHEMBL1358545 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD
SCHEMBL10448425 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD
SCHEMBL19076153 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD
SCHEMBL14213379 1.00 FFAR4 (0.74) FFAR4FFAR1GPR84PPARGPPARD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10738204-B2 Printing process for preparing controlled scattering effects XEROX CORPORATION (US) 2020-08-11 US disclosed
US-20190322881-A1 Printing Process For Preparing Controlled Scattering Effects XEROX CORPORATION 2019-10-24 US disclosed
US-9980898-B2 Polymer composition for high-heat application comprising thermo-releasable substance DSM IP ASSETS B.V. (NL) 2018-05-29 US disclosed
US-20170210922-A1 3D PRINTING SYSTEM COMPRISING SOLID BUILD INK COMPRISING COLORANT XEROX CORPORATION 2017-07-27 US disclosed
US-20170210922-A1 3D PRINTING SYSTEM COMPRISING SOLID BUILD INK COMPRISING COLORANT XEROX CORPORATION 2017-07-27 US disclosed
US-9676952-B2 3D printing system comprising solid build ink comprising colorant XEROX CORPORATION (US) 2017-06-13 US disclosed
EP-2108683-B1 CURABLE OVERCOAT COMPOSITIONS XEROX CORP (US) 2017-04-12 EP disclosed
US-20160244628-A1 3D PRINTING SYSTEM COMPRISING SOLID BUILD INK COMPRISING COLORANT XEROX CORPORATION 2016-08-25 US disclosed
US-9096767-B2 Curable solid inks containing cyclohexyl-based crystalline gellants XEROX CORPORATION (US) 2015-08-04 US disclosed
US-9096767-B2 Curable solid inks containing cyclohexyl-based crystalline gellants XEROX CORPORATION (US) 2015-08-04 US disclosed
US-20070123642-A1 Phase change inks containing curable isocyanate-derived compounds XEROX CORPORATION 2007-05-31 US disclosed
US-20070123642-A1 Phase change inks containing curable isocyanate-derived compounds XEROX CORPORATION 2007-05-31 US disclosed
US-20060128903-A1 Process for the controlled increase in the molecular weight of polyethylenes ROTH MICHAEL 2006-06-15 US disclosed
EP-1282630-B1 Process for Reducing the Molecular Weight of Polypropylene Using Hydroxylamine Esters CIBA SC HOLDING AG (CH) 2006-05-10 EP disclosed
EP-1655303-A2 Hydroxylamine esters as polimerization initiators Ciba SC Holding AG (CH) 2006-05-10 EP disclosed
US-7030196-B2 Process for reducing the molecular weight of polypropylene CIBA SPECIALTY CHEMICALS CORPORATION (US) 2006-04-18 US disclosed
US-20030216494-A1 Hydroxylamine esters as polymerization initiators CIBA SPECIALTY CHEMICALS CORP. 2003-11-20 US disclosed
EP-1282630-A1 HYDROXYLAMINE ESTERS AS POLYMERIZATION INITIATORS Ciba SC Holding AG (CH) 2003-02-12 EP disclosed
WO-2001090113-A1 HYDROXYLAMINE ESTERS AS POLYMERIZATION INITIATORS CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2001-11-29 WO disclosed
EP-0963753-A2 Utilisation of C20-40 dialkyldimerate for increasing the light protection factor and/or the UV-A protection of cosmetic or dermatologic light protection agents Beiersdorf Aktiengesellschaft (DE) 1999-12-15 EP 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-20030216494-A1 Hydroxylamine esters as polymerization initiators PNMT, HPGDS, HAAO FFAR4 328/4885FFAR1 407/4885GPR84 824/4885

“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.