SCHEMBL3293447

SCHEMBL3293447

CCCCCCCCCCCCCCCCCCc1cc(C(=O)O)cc(C(=O)O)c1

nearest known ligand 0.68

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
RARB P10826 9/20 0.62
MEN1 O00255 1/20 0.62
ALDH1A1 P00352 1/20 0.62
RARA P10276 1/20 0.62
MAPT P10636 1/20 0.62
MTOR P42345 1/20 0.62
KMT2A Q03164 1/20 0.62
PTGS2 P35354 3/20 0.55
GPR84 Q9NQS5 2/20 0.55
PLA2G2A P14555 1/20 0.54
KAT8 Q9H7Z6 2/20 0.54
PPARA Q07869 1/20 0.54
CYP3A4 P08684 1/20 0.52

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
SCHEMBL17060014 1.00 RARB (0.62) RARBMEN1ALDH1A1RARAMAPT
SCHEMBL28032028 1.00 RARB (0.62) RARBMEN1ALDH1A1RARAMAPT
SCHEMBL8413501 0.98 RARB (0.61) RARBMEN1ALDH1A1RARAMAPT
SCHEMBL27760653 0.96 RARB (0.62) RARBMEN1ALDH1A1RARAMAPT
SCHEMBL14118049 0.96 RARB (0.62) RARBMEN1ALDH1A1RARAMAPT
SCHEMBL27782228 0.94 GPR84 (0.61) RARBMEN1ALDH1A1RARAMAPT
SCHEMBL914005 0.92 RARB (0.59) RARBMEN1ALDH1A1RARAMAPT
SCHEMBL9701286 0.88 RARB (0.59) RARBMEN1ALDH1A1RARAMAPT
Heptane SCHEMBL29220036 0.86 PLA2G2A (0.63) RARBMEN1ALDH1A1RARAMAPT
Hexane SCHEMBL29263834 0.85 PLA2G2A (0.62) RARBMEN1ALDH1A1RARAMAPT

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7732625-B2 Colorant compounds XEROX CORPORATION (US) 2010-06-08 US claimed
US-7311767-B2 Forming a salt of a liquid phase change ink carrier of stearyl stearamide, an amine substituted Xanthene, acridine, anthracene or thioxanthene chromogen, and a metal salt capable of forming a compound with two chromogens XEROX CORPORATION (US) 2007-12-25 US claimed
US-7033424-B2 Phase change inks XEROX CORPORATION (US) 2006-04-25 US claimed
US-20060021546-A1 Processes for preparing phase change inks XEROX CORPORATION 2006-02-02 US claimed
US-20060020141-A1 Metallized dye XEROX CORPORATION 2006-01-26 US claimed
US-20060016369-A1 PHASE CHANGE INKS XEROX CORPORATION 2006-01-26 US claimed
EP-1956054-B1 Phase change ink XEROX CORP (US) 2010-11-24 EP disclosed
US-7732625-B2 Colorant compounds XEROX CORPORATION (US) 2010-06-08 US disclosed
EP-1958993-A1 Phase change inks containing colorant compounds Xerox Corporation (US) 2008-08-20 EP disclosed
EP-1956054-A2 Colorant compounds Xerox Corporation (US) 2008-08-13 EP disclosed
US-20080187664-A1 Phase change inks containing colorant compounds XEROX CORPORATION 2008-08-07 US disclosed
US-20080184910-A1 Mixture of basic dye and wax XEROX CORPORATION 2008-08-07 US disclosed
US-7311767-B2 Forming a salt of a liquid phase change ink carrier of stearyl stearamide, an amine substituted Xanthene, acridine, anthracene or thioxanthene chromogen, and a metal salt capable of forming a compound with two chromogens XEROX CORPORATION (US) 2007-12-25 US disclosed
US-20060021546-A1 Processes for preparing phase change inks XEROX CORPORATION 2006-02-02 US disclosed
US-20060020141-A1 Metallized dye XEROX CORPORATION 2006-01-26 US disclosed
US-20060016369-A1 PHASE CHANGE INKS XEROX CORPORATION 2006-01-26 US disclosed
US-6706823-B2 A CROSSLINKED COPOLYMER HAVING ALKENYL MONOMER UNITS AND MALEIMIDE MONOMER UNITS, IN A ELECTROLYTE SOLUTION; USED TO ELECTROLYTE CELLS BRIDGESTONE CORPORATION (JP) 2004-03-16 US disclosed
US-20030130397-A1 A crosslinked copolymer having alkenyl monomer units and maleimide monomer units, in a electrolyte solution; used to electrolyte cells BRIDGESTONE CORP. 2003-07-10 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 (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-20060020141-A1 Metallized dye CDYL, CDY1; CDY1B, CDYL2 RARB 316/4885MEN1 685/4885ALDH1A1 1569/4885

“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.