SCHEMBL1457558

SCHEMBL1457558

CCCCCCCCC=CCCCCCCCC(=O)C=C(C)C(N)=O

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FAAH O00519 5/20 0.64
SOAT1 P35610 2/20 0.64
CYP1A2 P05177 2/20 0.64
CYP2C19 P33261 2/20 0.64
KMT2A Q03164 2/20 0.64
MEN1 O00255 1/20 0.64
TP53 P04637 1/20 0.64
CYP3A4 P08684 1/20 0.64
KDM4E B2RXH2 2/20 0.58
TERT O14746 3/20 0.54
PTPN1 P18031 3/20 0.54
PPARG P37231 3/20 0.54
PPARD Q03181 3/20 0.54
PPARA Q07869 3/20 0.54
MAPT P10636 2/20 0.54
BLM P54132 2/20 0.54
HSD17B10 Q99714 2/20 0.54
FABP4 P15090 2/20 0.54
GMNN O75496 1/20 0.54
USP2 O75604 1/20 0.54

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
SCHEMBL1226253 0.92 FAAH (0.49) FAAHSOAT1CYP1A2CYP2C19KMT2A
SCHEMBL1226250 0.92 FAAH (0.49) FAAHSOAT1CYP1A2CYP2C19KMT2A
SCHEMBL28183919 0.92 FAAH (0.49) FAAHSOAT1CYP1A2CYP2C19KMT2A
SCHEMBL28280440 0.85 PPARG (0.61) FAAHSOAT1CYP1A2CYP2C19KMT2A
SCHEMBL8029314 0.85 PPARG (0.61) FAAHSOAT1CYP1A2CYP2C19KMT2A
SCHEMBL3790005 0.84 CES1 (0.41) FAAHSOAT1CYP1A2CYP2C19KMT2A
SCHEMBL3790002 0.84 CES1 (0.41) FAAHSOAT1CYP1A2CYP2C19KMT2A
SCHEMBL2339651 0.80 FAAH (0.61) FAAHSOAT1CYP1A2CYP2C19KMT2A
SCHEMBL2339648 0.80 FAAH (0.61) FAAHSOAT1CYP1A2CYP2C19KMT2A
SCHEMBL23528231 0.79 FAAH (1.00) FAAHSOAT1CYP1A2CYP2C19KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20010021739-A1 Latex compositions containing ethylenically unsaturated esters of fatty compounds and applications thereof THE UNIVERSITY OF SOUTHERN MISSISSIPPI (US) 2001-09-13 US claimed
US-6174948-B1 ADDITION POLYMERS WITH ESTER AND ETHER GROUPS THE UNIVERSITY OF SOUTHERN MISSISSIPPI 2001-01-16 US claimed
US-8003738-B2 Method of producing aqueous secondary dispersions of water-insoluble polymers BASF SE (DE) 2011-08-23 US disclosed
US-7910680-B2 UV curable coatings, inks, sealants, adhesives; derived from renewable raw materials such as unsaturated vegetable oils; acrylated amide, ester or triglyceride moiety; acrylation to prepare monomers; an amide triacrylate from diethanolamine and methyl 11-hydroxyundecanoate and acryloyl chloride DOW GLOBAL TECHNOLOGIES LLC (US) 2011-03-22 US disclosed
EP-2121581-A2 HYDROXYL-TERMINATED OR CARBOXYLIC ACID- TERMINATED REACTIVE MONOMER COMPOSITIONS, THEIR PREPARATION AND THEIR USE Dow Global Technologies Inc. (US) 2009-11-25 EP disclosed
EP-1971652-A1 REACTIVE (METH)ACRYLATE MONOMER COMPOSITIONS AND PREPARATION AND USE THEREOF Dow Global Technologies Inc. (US) 2008-09-24 EP disclosed
WO-2008088624-A2 HYDROXYL-TERMINATED OR CARBOXYLIC ACID- TERMINATED REACTIVE MONOMER COMPOSITIONS, THEIR PREPARATION AND THEIR USE DOW GLOBAL TECHNOLOGIES INC. (US) 2008-07-24 WO disclosed
US-20080108728-A1 Reactive (meth)acrylate monomer compositions and preparation and use thereof DOW GLOBAL TECHNOLOGIES LLC 2008-05-08 US disclosed
WO-2007081429-A1 REACTIVE (METH)ACRYLATE MONOMER COMPOSITIONS AND PREPARATION AND USE THEREOF DOW GLOBAL TECHNOLOGIES INC. (US) 2007-07-19 WO disclosed
US-20060122321-A1 Method of producing aqueous secondary dispersions of water-insoluble polymers BASF AKTIENGESELLSCHAFT (DE) 2006-06-08 US disclosed
US-6599972-B2 Water soluble; low volatility solvents; odorless UNIVERSITY OF SOUTHERN MISSISSIPPI 2003-07-29 US disclosed
US-20010021739-A1 Latex compositions containing ethylenically unsaturated esters of fatty compounds and applications thereof THE UNIVERSITY OF SOUTHERN MISSISSIPPI (US) 2001-09-13 US disclosed
US-6174948-B1 ADDITION POLYMERS WITH ESTER AND ETHER GROUPS THE UNIVERSITY OF SOUTHERN MISSISSIPPI 2001-01-16 US disclosed