SCHEMBL673602

SCHEMBL673602

CCCCCCCCCCOP(=O)([O-])CCCCCCCCCC.CCCCCCCCCCOP(=O)([O-])CCCCCCCCCC.CCCCCCCCCCOP(=O)([O-])CCCCCCCCCC.[Cr+3]

nearest known ligand 0.53

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LPAR3 Q9UBY5 9/20 0.53
LPAR2 Q9HBW0 6/20 0.53
LPAR1 Q92633 2/20 0.53
AKT1 P31749 2/20 0.51
CDC25A P30304 2/20 0.51
LMNA P02545 1/20 0.51
ESR1 P03372 1/20 0.51
ADORA3 P0DMS8 1/20 0.51
AGTR1 P30556 1/20 0.51
ADRA1A P35348 1/20 0.51
KCNH2 Q12809 1/20 0.51
CYP3A4 P08684 1/20 0.45
TERT O14746 1/20 0.43
UCHL3 P15374 1/20 0.43
MAPK14 Q16539 1/20 0.43
FAAH O00519 1/20 0.42
TRPM8 Q7Z2W7 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
SCHEMBL672571 1.00 LPAR3 (0.53) LPAR3LPAR2LPAR1AKT1CDC25A
SCHEMBL672075 1.00 LPAR3 (0.53) LPAR3LPAR2LPAR1AKT1CDC25A
SCHEMBL673600 1.00 LPAR3 (0.53) LPAR3LPAR2LPAR1AKT1CDC25A
SCHEMBL673734 1.00 LPAR3 (0.53) LPAR3LPAR2LPAR1AKT1CDC25A
SCHEMBL673478 1.00 LPAR3 (0.53) LPAR3LPAR2LPAR1AKT1CDC25A
SCHEMBL673175 0.98 LPAR3 (0.50) LPAR3LPAR2LPAR1AKT1CDC25A
SCHEMBL640088 0.96 LPAR3 (0.53) LPAR3LPAR2LPAR1AKT1CDC25A
SCHEMBL3959389 0.96 LPAR3 (0.53) LPAR3LPAR2LPAR1AKT1CDC25A
SCHEMBL3961532 0.96 LPAR3 (0.53) LPAR3LPAR2LPAR1AKT1CDC25A
SCHEMBL149217 0.96 LPAR3 (0.53) LPAR3LPAR2LPAR1AKT1CDC25A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120252979-A1 Process for Producing Blends of Syndiotactic, 1,2-Polybutadiene and Rubbery Elastomers RADEMACHER CHRISTINE (US) 2012-10-04 US disclosed
US-8067503-B2 Process for producing blends of syndiotactic, 1,2-polybutadiene and rubbery elastomers BRIDGESTONE CORPORATION (JP) 2011-11-29 US disclosed
US-20070161748-A1 PROCESS FOR PRODUCING BLENDS OF SYNDIOTACTIC, 1,2-POLYBUTADIENE AND RUBBERY ELASTOMERS BRIDGESTONE CORPORATION 2007-07-12 US disclosed
US-20040242780-A1 using a catalyst that is based on a chromium-containing compound, a hydrogen phosphite, and an organomagnesium compound, or a catalyst based on a molybdenum or iron-compound, a hydrogen phosphite and organoaluminum compound; tire sidewalls; obviates the need for high-temperature mixing BRIDGESTONE CORPORATION (JP) 2004-12-02 US disclosed
WO-2003040231-A1 PROCESS FOR PRODUCING BLENDS OF SYNDIOTACTIC 1,2-POLYBUTADIENE AND RUBBERY ELASTOMERS BRIDGESTONE CORPORATION (JP) 2003-05-15 WO disclosed
US-6528588-B2 Polymerization of 1,3-butadiene in the presence of a catalyst made of a chromium compound, a hydrogen phosphite, an organomagnesium compound, a molybdenum containing compound and an organoaluminum compound BRIDGESTONE CORPORATION (JP) 2003-03-04 US disclosed
US-6465585-B2 REACTION PRODUCT OF A CHROMIUM CONTAINING COMPOUND, AN ORGANOMAGNESIUM COMPOUND AND A SILYL PHOSPHONATE BRIDGESTONE CORPORATION (JP) 2002-10-15 US disclosed
US-20020115558-A1 CHROMIUM-BASED CATALYST COMPOSITION FOR PRODUCING CONJUGATED DIENE POLYMERS BRIDGESTONE CORP. 2002-08-22 US disclosed
US-20020037967-A1 Process for producing blends of syndiotactic 1,2-polybutadiene and rubbery elastomers with a chromium-based catalyst system BRIDGESTONE CORPORATION (JP) 2002-03-28 US disclosed
US-6291591-B1 PROVIDING MIXTURE OF RUBBER CEMENT AND 1,3-BUTADIENE; POLYMERIZING 1,3-BUTADIENE BY USING A CATALYST WHICH IS COMBINATION OF OR THE REACTION PRODUCT OF CHROMIUM COMPOUND, HYDROGEN PHOSPHITE, ORGANOMAGNESIUM COMPOUND BRIDGESTONE CORPORATION (JP) 2001-09-18 US disclosed