SCHEMBL672799

SCHEMBL672799

CCCCOP(=O)(O)OCCCC.[Mo]

nearest known ligand 0.61

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 2/20 0.61
LPAR3 Q9UBY5 8/20 0.58
LPAR2 Q9HBW0 6/20 0.58
LPAR1 Q92633 3/20 0.58
TSHR P16473 1/20 0.46
P2RY10 O00398 4/20 0.42
GPR34 Q9UPC5 2/20 0.42
GGPS1 O95749 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
SCHEMBL29177519 0.97 CYP3A4 (0.64) CYP3A4LPAR3LPAR2LPAR1TSHR
SCHEMBL15389152 0.97 CYP3A4 (0.64) CYP3A4LPAR3LPAR2LPAR1TSHR
SCHEMBL26559 0.97 CYP3A4 (0.64) CYP3A4LPAR3LPAR2LPAR1TSHR
SCHEMBL945567 0.95 CYP3A4 (0.61) CYP3A4LPAR3LPAR2LPAR1TSHR
Methane SCHEMBL11359992 0.95 CYP3A4 (0.61) CYP3A4LPAR3LPAR2LPAR1TSHR
SCHEMBL4631198 0.95 CYP3A4 (0.61) CYP3A4LPAR3LPAR2LPAR1TSHR
SCHEMBL11677508 0.95 CYP3A4 (0.61) CYP3A4LPAR3LPAR2LPAR1TSHR
SCHEMBL641061 0.95 CYP3A4 (0.61) CYP3A4LPAR3LPAR2LPAR1TSHR
Ammonia Solution, Strong SCHEMBL5519376 0.95 CYP3A4 (0.61) CYP3A4LPAR3LPAR2LPAR1TSHR
Bromide SCHEMBL11430321 0.95 CYP3A4 (0.61) CYP3A4LPAR3LPAR2LPAR1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8530542-B2 Forming polymer from urethane and/or acrylic monomer while adding solar control component(s) of metal oxide semiconductor selected from gold, silver, indium tin oxide, antimony tin oxide, zinc oxide, lanthanum hexaboride and zinc stannate; curing; laminated; reaction injection molding PPG INDUSTRIES OHIO, INC. (US) 2013-09-10 US claimed
WO-2008089017-A1 AUTOMOTIVE WINDOW INTERLAYER WITH SOLAR CONTROL PROPERTIES PPG INDUSTRIES OHIO, INC. (US) 2008-07-24 WO claimed
US-20080171808-A1 Automotive window interlayer with solar control properties VITRO FLAT GLASS LLC 2008-07-17 US claimed
US-8530542-B2 Forming polymer from urethane and/or acrylic monomer while adding solar control component(s) of metal oxide semiconductor selected from gold, silver, indium tin oxide, antimony tin oxide, zinc oxide, lanthanum hexaboride and zinc stannate; curing; laminated; reaction injection molding PPG INDUSTRIES OHIO, INC. (US) 2013-09-10 US disclosed
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
WO-2008089017-A1 AUTOMOTIVE WINDOW INTERLAYER WITH SOLAR CONTROL PROPERTIES PPG INDUSTRIES OHIO, INC. (US) 2008-07-24 WO disclosed
US-20080171808-A1 Automotive window interlayer with solar control properties VITRO FLAT GLASS LLC 2008-07-17 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
EP-1183283-B1 MOLYBDENUM-BASED CATALYST COMPOSITION FOR POLYMERIZING CONJUGATED DIENES BRIDGESTONE CORP (JP) 2003-06-11 EP 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-6545107-B2 Reaction product of an molybdenum- containing compound, a silyl phosphonate; and an organoaluminum compound catalyst used for polymerizing conjugated diene monomer BRIDGESTONE CORPORATION (JP) 2003-04-08 US 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-20020198337-A1 Molydenum-based catalyst composition for producing syndiotactic 1,2-polybutadiene BRIDGESTONE CORP. 2002-12-26 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
EP-1183283-A1 MOLYBDENUM-BASED CATALYST COMPOSITION FOR POLYMERIZING CONJUGATED DIENES BRIDGESTONE CORPORATION (JP) 2002-03-06 EP disclosed
US-6348550-B1 ADDITION POLYMERIZATION OF 1,3-BUTADIENE TO SYNDIOTACTIC 1,2-POLYBUTADIENE USING COORDINATION CATALYST COMPRISING MOLYBDENUM COMPOUND, A HYDROGEN PHOSPHITE, AND MIXTURE OF (NON)STERICALLY HINDERED ORGANOALUMINUM COMPOUNDS BRIDGESTONE CORPORATION (JP) 2002-02-19 US disclosed
US-6303692-B1 PROVIDING MIXTURE OF RUBBER CEMENT AND 1,3-BUTADIENE; POLYMERIZING INTO SYNDIOTACTIC 1,2-POLYBUTADIENE BY USING CATALYST FORMULATION COMPRISING MOLYBDENUM COMPOUND, HYDROGEN PHOSPHITE COMPOUND AND ORGANOALUMINUM COMPOUND BRIDGESTONE CORPORATION (JP) 2001-10-16 US disclosed
WO-2000075201-A1 MOLYBDENUM-BASED CATALYST COMPOSITION FOR POLYMERIZING CONJUGATED DIENES BRIDGESTONE CORPORATION (JP) 2000-12-14 WO disclosed