SCHEMBL246629

SCHEMBL246629

CC(=CCCOC(N)=O)C(=O)O

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM2 P08172 2/20 0.41
CHRM4 P08173 2/20 0.41
CHRM5 P08912 2/20 0.41
CHRM1 P11229 2/20 0.41
CHRM3 P20309 2/20 0.41
CHRNB2 P17787 2/20 0.41
CHRNA4 P43681 2/20 0.41
LMNA P02545 2/20 0.41
HTR1A P08908 1/20 0.41
TSHR P16473 1/20 0.41
CYP2C19 P33261 1/20 0.41
CHRNA7 P36544 1/20 0.41
ALOX15 P16050 2/20 0.38
CHRNB4 P30926 1/20 0.36
CHRNA3 P32297 1/20 0.36
CD81 P60033 2/20 0.35
PPARG P37231 1/20 0.31
GRIK1 P39086 1/20 0.30
GRIK2 Q13002 1/20 0.30
BACE1 P56817 1/20 0.30

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
SCHEMBL289046 1.00 CHRM2 (0.41) CHRM2CHRM4CHRM5CHRM1CHRM3
Methacrylic Acid SCHEMBL21775702 0.93 CHRM2 (0.36) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL6252919 0.89 ALOX15 (0.40) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL6252916 0.89 ALOX15 (0.40) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL6250929 0.87 LMNA (0.39) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL6250935 0.87 LMNA (0.39) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL6363352 0.83 CD81 (0.37) CHRM5CHRM1CHRM3TSHRCYP2C19
SCHEMBL406199 0.83 ALOX15 (0.47) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL1696441 0.83 ALOX15 (0.47) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL16244314 0.81 ALOX15 (0.48) CHRM2CHRM4CHRM5CHRM1CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2427421-A1 METHOD AND SYSTEM FOR PURIFYING MONOMERS Evonik Röhm GmbH (DE) 2012-03-14 EP claimed
WO-2010127909-A1 METHOD AND SYSTEM FOR PURIFYING MONOMERS EVONIK RÖHM GMBH (DE) 2010-11-11 WO claimed
EP-1474454-B1 THERMOSETTING COMPOSITIONS CONTAINING ALTERNATING COPOLYMERS OF ISOBUTYLENE TYPE MONOMERS PPG IND OHIO INC (US) 2009-11-18 EP claimed
EP-1474479-B1 POWDER COATING COMPOSITIONS HAVING IMPROVED MAR AND ACID RESISTANCE PPG IND OHIO INC (US) 2008-08-06 EP claimed
EP-4004125-B1 MIXING SYSTEM FOR PREPARING LOW VOC AQUEOUS COATING AGENTS BASF COATINGS GMBH (DE) 2023-09-06 EP disclosed
EP-4004125-A1 MIXING SYSTEM FOR PRODUCING AQUEOUS COATING AGENTS WITH A LOW VOC BASF Coatings GmbH (DE) 2022-06-01 EP disclosed
WO-2021018594-A1 MIXING SYSTEM FOR PRODUCING AQUEOUS COATING AGENTS WITH A LOW VOC BASF COATINGS GMBH (DE) 2021-02-04 WO disclosed
EP-1773760-B1 CATALYTIC METHODS FOR THE PRODUCTION OF (METH)ACRYLATES FROM N-HYDROXYALKYLATED AMIDES BASF SE (DE) 2017-01-11 EP disclosed
US-9221738-B2 Method and system for purifying monomers EVONIK RÖHM GMBH (DE) 2015-12-29 US disclosed
EP-2430173-B1 METHOD FOR PRODUCING (METH)ACRYLIC ACID ESTERS CONTAINING URETHANE GROUPS BASF SE (DE) 2015-08-12 EP disclosed
WO-2012038197-A1 COATING AGENT HAVING (METH)ACRYLIC POLYMERS AND COALESCENCE ADDITIVES EVONIK RÖHM GMBH (DE) 2012-03-29 WO disclosed
EP-2430071-A1 METHOD FOR THE CONTINUOUS PRODUCTION OF (METH)ACRYLIC ACID ESTERS CONTAINING URETHANE GROUPS BASF SE (DE) 2012-03-21 EP disclosed
EP-1651684-A1 ETHERIFIED CARBAMATE FUNCTIONAL COPOLYMERS OF ISOBUTYLENE TYPE MONOMERS, AND THEIR USE IN CURABLE COMPOSITIONS PPG Industries Ohio, Inc. (US) 2006-05-03 EP disclosed
WO-2006012980-A1 CATALYTIC METHODS FOR THE PRODUCTION OF (METH)ACRYLATES FROM N-HYDROXYALKYLATED AMIDES BASF AKTIENGESELLSCHAFT (DE) 2006-02-09 WO disclosed
EP-1570065-A1 ENZYMATIC PRODUCTION OF (METH)ACRYLIC ESTERS THAT CONTAIN URETHANE GROUPS BASF AKTIENGESELLSCHAFT (DE) 2005-09-07 EP disclosed
WO-2005047234-A1 METHOD FOR PRODUCING CARBAMATE GROUP-CONTAINING (METH)ACRYLIC ESTERS Röhm GmbH & Co. KG (DE) 2005-05-26 WO disclosed
WO-2005016979-A1 ETHERIFIED CARBAMATE FUNCTIONAL COPOLYMERS OF ISOBUTYLENE TYPE MONOMERS, AND THEIR USE IN CURABLE COMPOSITIONS PPG INDUSTRIES OHIO, INC. (US) 2005-02-24 WO disclosed
US-20050032978-A1 Etherified carbamate functional copolymers of isobutylene type monomers, and their use in curable compositions PPG INDUSTRIES OHIO, INC. 2005-02-10 US disclosed
US-6780897-B1 COATING MATERIALS, ADHESIVES OR SEALING COMPOUNDS WHICH CAN BE CROSSLINKED THERMALLY AND/OR WITH ACTINIC RADIATION BASF COATING AG (DE) 2004-08-24 US disclosed
WO-2004050888-A1 ENZYMATIC PRODUCTION OF (METH)ACRYLIC ESTERS THAT CONTAIN URETHANE GROUPS BASF AKTIENGESELLSCHAFT (DE) 2004-06-17 WO disclosed