SCHEMBL2853552

SCHEMBL2853552

C1=CC2CCC1C2.CCCCCCCCC(C)CCC(=O)O

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.57
ACE2 Q9BYF1 1/20 0.47
FFAR4 Q5NUL3 2/20 0.44
FFAR1 O14842 2/20 0.44
ALOX5 P09917 1/20 0.42
GPR84 Q9NQS5 7/20 0.41
PPARG P37231 7/20 0.41
PPARD Q03181 7/20 0.41
PPARA Q07869 7/20 0.41
HDAC11 Q96DB2 5/20 0.41
TSHR P16473 4/20 0.41
PTPN1 P18031 3/20 0.41
ALDH1A1 P00352 2/20 0.41
TLR2 O60603 2/20 0.41
TDP1 Q9NUW8 2/20 0.41
FABP4 P15090 2/20 0.41
SLC22A6 Q4U2R8 1/20 0.41
SLC22A8 Q8TCC7 1/20 0.41
MEN1 O00255 1/20 0.41
ESR1 P03372 1/20 0.41

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
Decanoic Acid SCHEMBL14890324 0.83 GPR84 (0.61) MAPTFFAR4FFAR1ALOX5GPR84
SCHEMBL1134744 0.83 ACE2 (0.66) MAPTACE2FFAR4FFAR1GPR84
SCHEMBL8036038 0.83 ACE2 (0.66) MAPTACE2FFAR4FFAR1GPR84
SCHEMBL2545350 0.83 ACE2 (0.66) MAPTACE2FFAR4FFAR1GPR84
SCHEMBL16213113 0.83 ACE2 (0.66) MAPTACE2FFAR4FFAR1GPR84
SCHEMBL25275005 0.83 ACE2 (0.66) MAPTACE2FFAR4FFAR1GPR84
SCHEMBL3626201 0.83 ACE2 (0.66) MAPTACE2FFAR4FFAR1GPR84
SCHEMBL2222385 0.83 ACE2 (0.66) MAPTACE2FFAR4FFAR1GPR84
SCHEMBL13746761 0.83 ACE2 (0.66) MAPTACE2FFAR4FFAR1GPR84
SCHEMBL3623541 0.83 ACE2 (0.66) MAPTACE2FFAR4FFAR1GPR84

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7814713-B2 Catalyst system for polymerizing cyclic olefin having polar functional group, polymerizing method using the catalyst system, olefin polymer produced by the method and optical anisotropic film comprising the olefin polymer LG CHEM, LTD. (KR) 2010-10-19 US disclosed
US-20100174039-A1 Catalyst system for polymerizing cyclic olefin having polar functional group, polymerizing method using the catalyst system, olefin polymer produced by the method and optical anisotropic film comprising the olefin polymer LG CHEM, LTD. (KR) 2010-07-08 US disclosed
US-7648937-B2 Catalyst system for polymerizing cyclic olefin having polar functional group, polymerizing method using the catalyst system, olefin polymer produced by the method and optical anisotropic film comprising the olefin polymer LG CHEM, LTD. (KR) 2010-01-19 US disclosed
EP-1794197-A4 CATALYST SYSTEM FOR POLYMERIZING CYCLIC OLEFIN HAVING POLAR FUNCTIONAL GROUP, POLYMERIZING METHOD USING THE CATALYST SYSTEM, OLEFIN POLYMER PRODUCED BY THE METHOD AND OPTICAL ANISOTROPIC FILM COMPRISING THE OLEFIN POLYMER LG CHEMICAL LTD (KR) 2009-07-01 EP disclosed
EP-1794197-A1 CATALYST SYSTEM FOR POLYMERIZING CYCLIC OLEFIN HAVING POLAR FUNCTIONAL GROUP, POLYMERIZING METHOD USING THE CATALYST SYSTEM, OLEFIN POLYMER PRODUCED BY THE METHOD AND OPTICAL ANISOTROPIC FILM COMPRISING THE OLEFIN POLYMER LG Chemical Limited (KR) 2007-06-13 EP disclosed
WO-2006031067-A1 CATALYST SYSTEM FOR POLYMERIZING CYCLIC OLEFIN HAVING POLAR FUNCTIONAL GROUP, POLYMERIZING METHOD USING THE CATALYST SYSTEM, OLEFIN POLYMER PRODUCED BY THE METHOD AND OPTICAL ANISOTROPIC FILM COMPRISING THE OLEFIN POLYMER LG CHEM, LTD. (KR) 2006-03-23 WO disclosed
US-20060058477-A1 Catalyst system for polymerizing cyclic olefin having polar functional group, polymerizing method using the catalyst system, olefin polymer produced by the method and optical anisotropic film comprising the olefin polymer LG CHEM, LTD. (KR) 2006-03-16 US disclosed