Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 3/20 | 0.44 |
| ▸ | LPAR1 | Q92633 | 1/20 | 0.42 |
| ▸ | LPAR2 | Q9HBW0 | 1/20 | 0.42 |
| ▸ | LPAR3 | Q9UBY5 | 1/20 | 0.42 |
| ▸ | THRB | P10828 | 1/20 | 0.40 |
| ▸ | FAAH | O00519 | 3/20 | 0.40 |
| ▸ | TRPV1 | Q8NER1 | 1/20 | 0.39 |
| ▸ | GMNN | O75496 | 1/20 | 0.39 |
| ▸ | USP2 | O75604 | 1/20 | 0.39 |
| ▸ | LMNA | P02545 | 1/20 | 0.39 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.39 |
| ▸ | POLB | P06746 | 1/20 | 0.39 |
| ▸ | MAPT | P10636 | 1/20 | 0.39 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.39 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.39 |
| ▸ | APEX1 | P27695 | 1/20 | 0.39 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.39 |
| ▸ | RECQL | P46063 | 1/20 | 0.39 |
| ▸ | BLM | P54132 | 1/20 | 0.39 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.39 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL198889 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB | |
| SCHEMBL202073 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB | |
| SCHEMBL198971 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB | |
| SCHEMBL198755 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB | |
| SCHEMBL984915 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB | |
| SCHEMBL198374 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB | |
| SCHEMBL980876 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB | |
| SCHEMBL199294 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB | |
| SCHEMBL198324 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB | |
| SCHEMBL198791 | 1.00 | TSHR (0.44) | TSHRLPAR1LPAR2LPAR3THRB |
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 147 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-7429393-B2 | Graft polymer | BRIDGESTONE CORPORATION (JP) | 2008-09-30 | — | — | US | claimed |
| US-20030130398-A1 | Soft polymeric compounds including metal oxide fillers | BRIDGESTONE CORPORATION | 2003-07-10 | — | — | US | claimed |
| US-20030130426-A1 | Method of grafting polymaleimides to alkenyl butyl rubbers | BRIDGESTONE CORP. | 2003-07-10 | — | — | US | claimed |
| US-20030091527-A1 | Graft polymer | BRIDGESTONE CORPORATION (JP) | 2003-05-15 | — | — | US | claimed |
| WO-2003016398-A1 | THERMOPLASTIC ELASTOMERS AND METHOD OF MAKING THE SAME | BRIDGESTONE CORPORATION (US) | 2003-02-27 | — | — | WO | claimed |
| US-20020188064-A1 | Poly(alkenyl-co-maleimide) , an inorganic salt, and an extender | BRIDGESTONE/FIRESTONE RESEARCH, INC. | 2002-12-12 | — | — | US | claimed |
| WO-2002094893-A1 | CENTIPEDE IONOMERS | BRIDGESTONE CORPORATION (JP) | 2002-11-28 | — | — | WO | claimed |
| US-6403724-B1 | VIBRATION DAMPING; ALKENYL-MALEIC ANHYDRIDE COPOLYMER IMIDIZED WITH PRIMARY AMINE, A MALEATED POLYALKYLENE, AT LEAST ONE DENDRIMER, AND OPTIONALLY, AN EXTENDER. | BRIDGESTONE CORPORATION (JP) | 2002-06-11 | — | — | US | claimed |
| US-6369166-B1 | PLASTICIZED; TENSILE AND TEAR STRENGTH; ELONGATION; HIGH DAMPING; ETHYLENE-MALEIC ANHYDRIDE COPOLYMER REACTED WITH PRIMARY AMINE | BRIDGESTONE CORPORATION (JP) | 2002-04-09 | — | — | US | claimed |
| US-6359064-B1 | COMBINING POLY(ALKENYL-CO-MALEIMIDE), MALEATED POLYALKYLENE AND CROSSLINKING AGENT; REACTING TO CROSSLINK AND TO FORM A MALEATED POLYALKYLENE GRAFTED POLY(ALKENYL-CO-MALEIMIDE); COMBINING WITH WITH A POLYESTER TO PROVIDE THE ELASTOMER | BRIDGESTONE CORPORATION | 2002-03-19 | — | — | US | claimed |
| WO-2002020669-A1 | POLYESTER AND POLYALKYLENE-GRAFTED POLYMER COMPOSITION | BRIDGESTONE CORPORATION (JP) | 2002-03-14 | — | — | WO | claimed |
| US-6353054-B1 | Alkenyl-co-maleimide/diene rubber copolymers and applications | BRIDGESTONE CORPORATION (JP) | 2002-03-05 | — | — | US | claimed |
| WO-2001070822-A2 | PROCESS FOR FORMING CENTIPEDE POLYMER GELS | BRIDGESTONE CORPORATION (JP) | 2001-09-27 | — | — | WO | claimed |
| US-20010021743-A1 | Method of producing a graft copolymer | BRIDGESTONE CORPORATION (JP) | 2001-09-13 | — | — | US | claimed |
| US-6207763-B1 | A COPOLYMER OF SUBSTITUTED OR UNSUBSTITUTED 1-20 ALKYL GROUP DISUBSTITUTED ETHYLENE-MALEIMIDE COPOLYMER(A REACTION PRODUCT OF DISUBTITUTED ETHYLENE-MALEIC ANHYDRIDE IMIDIZED WITH PRIMARY AMINE) IS A PLASTICIZER FOR RUBBER; HIGH DAMPING | BRIDGESTONE CORPORATION (JP) | 2001-03-27 | — | — | US | claimed |
| US-6204354-B1 | DRY ENVIRONMENT | BRIDGESTONE CORPORATION (JP) | 2001-03-20 | — | — | US | claimed |
| US-6191217-B1 | REACTING POLY(ALKYL VINYLETHER-CO-MALEIMIDE) POLYMER WITH MALEATED POLYALKYLENE AND ALKYL DIAMINE UNDER SUBSTANTIALLY DRY CONDITIONS SUFFICIENT TO FORM POLYALKYLENE GRAFTED POLY(ALKYL VINYLETHER-CO-MALEIMIDE) POLYMER | BRIDGESTONE CORPORATION (JP) | 2001-02-20 | — | — | US | claimed |
| US-6133354-A | MIXING A POLY(DIALKYLSUBSTITUTED ETHYLENE-CO-MALEIMIDE) POLYMER SUCH AS POLYISOBUTYLENE-CO-MALEIMIDE, AND PLASTICIZERS OR EXTENDERS WITHIN A NON-VULCANIZED THERMOPLASTIC ELASTOMER TO FORM A DAMPING GEL; TENSILE STRENGTH AND TEAR STRENGTH | BRIDGESTONE CORPORATION (JP) | 2000-10-17 | — | — | US | claimed |
| EP-0955319-A1 | Soft compounds derived from polypropylene grafted disubstituted ethylene-maleimide copolymers | Bridgestone Corporation (JP) | 1999-11-10 | — | — | EP | claimed |
| WO-2023080257-A1 | METHOD FOR PRODUCING ISOCYANATE COMPOUNDS, METHOD FOR PRODUCING CARBAMATE COMPOUNDS, METHOD FOR RECOVERING AMINE COMPOUNDS, AND ISOCYANATE COMPOSITION | 旭化成株式会社 | 2023-05-11 | — | — | WO | disclosed |
| WO-2023080258-A1 | CARBONYL COMPOUND, METHOD FOR PRODUCING CARBONYL COMPOUND, METHOD FOR PRODUCING ISOCYANATE COMPOUND, AND ISOCYANATE COMPOSITION | 旭化成株式会社 | 2023-05-11 | — | — | WO | disclosed |
| EP-2275406-B1 | PROCESS FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2018-11-28 | — | — | EP | disclosed |
| EP-1655291-B1 | COMPOUNDS HAVING THROMBOPOIETIN RECEPTOR AGONISM | SHIONOGI & CO (JP) | 2016-08-03 | — | — | EP | disclosed |
| US-9233918-B2 | Isocyanate production process | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2016-01-12 | — | — | US | disclosed |
| CN-103130739-B | There is the compound of thrombopoietin receptor agonism | SHIONOGI & CO., LTD. (JP) | 2015-09-16 | — | — | CN | disclosed |
| CN-102796058-B | Compound having thrombopoietin receptor agonism | SHIONOGI & CO | 2015-05-13 | — | — | CN | disclosed |
| US-8481736-B2 | Liquid crystalline rylene tetracarboxylic acid derivatives and use thereof | BASF SE (DE) | 2013-07-09 | — | — | US | disclosed |
| CN-103130739-A | Compounds having thrombopoietin receptor agonism | SHIONOGI & CO | 2013-06-05 | — | — | CN | disclosed |
| EP-2088138-B1 | Process for producing isocyanate | ASAHI KASEI CHEMICALS CORP (JP) | 2013-02-27 | — | — | EP | disclosed |
| US-8362293-B2 | Process for producing isocyanates | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2013-01-29 | — | — | US | disclosed |
| US-8349964-B2 | Reversible polymer/metal nano-composites and method for manufacturing same | BRIDGESTONE CORPORATION (JP) | 2013-01-08 | — | — | US | disclosed |
| CN-102796058-A | Compound having thrombopoietin receptor agonism | SHIONOGI & CO | 2012-11-28 | — | — | CN | disclosed |
| US-8088922-B2 | Dibenzorylenetetracarboximides as infrared absorbers | BASF AKTIENGESELLSCHAFT (DE) | 2012-01-03 | — | — | US | disclosed |
| CN-102271732-A | Nanochannel devices and related methods | — | 2011-12-07 | — | — | CN | disclosed |
| EP-2029573-B1 | DIBENZORYLENETETRACARBOXIMIDES AS INFRARED ABSORBERS | BASF SE (DE) | 2011-10-26 | — | — | EP | disclosed |
| US-20110092731-A1 | ISOCYANATE PRODUCTION PROCESS | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2011-04-21 | — | — | US | disclosed |
| CN-102026965-A | Method for producing isocyanate | ASAHI CHEMICAL CORP (JP) | 2011-04-20 | — | — | CN | disclosed |
| US-20110042651-A1 | LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF | BASF SE (DE) | 2011-02-24 | — | — | US | disclosed |
| EP-2275406-A1 | PROCESS FOR PRODUCING ISOCYANATE | Asahi Kasei Chemicals Corporation (JP) | 2011-01-19 | — | — | EP | disclosed |
| WO-2010111822-A1 | OLIGOCONDENSED PERYLENE BISIMIDES | BASF SE (DE) | 2010-10-07 | — | — | WO | disclosed |
| WO-2010112452-A1 | OLIGOCONDENSED PERYLENE BISIMIDES | BASF SE (DE) | 2010-10-07 | — | — | WO | disclosed |
| US-20100069665-A1 | PROCESS FOR PRODUCING ISOCYANATES | AHAHI KASEI CHEMICALS CORPORATION (JP) | 2010-03-18 | — | — | US | disclosed |
| US-20100048904-A1 | DIBENZORYLENETETRACARBOXIMIDES AS INFRARED ABSORBERS | BASF AKTIENGESELLSCHAFT (DE) | 2010-02-25 | — | — | US | disclosed |
| US-20090318513-A1 | COMPOUNDS EXHIBITING THROMBOPOIETIN RECEPTOR AGONISM | SHIONOGI & CO., LTD. | 2009-12-24 | — | — | US | disclosed |
| US-7601746-B2 | Compounds exhibiting thrombopoietin receptor agonism | SHIONOGI & CO., LTD. (JP) | 2009-10-13 | — | — | US | disclosed |
| EP-2088138-A1 | PROCESS FOR PRODUCING ISOCYANATE | Asahi Kasei Chemicals Corporation (JP) | 2009-08-12 | — | — | EP | disclosed |
| CN-101467276-A | Liquid crystalline rylene tetracarboxylic acid derivatives and use thereof | MAX PLANCK GESELLSCHAFT (DE) | 2009-06-24 | — | — | CN | disclosed |
| EP-2029573-A1 | DIBENZORYLENETETRACARBOXIMIDES AS INFRARED ABSORBERS | BASF SE (DE) | 2009-03-04 | — | — | EP | disclosed |
| EP-2008319-A2 | LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF | BASF SE (DE) | 2008-12-31 | — | — | EP | disclosed |
| US-20080305336-A1 | Reversible Polymer/Metal Nano-Composites And Method For Manufacturing Same | BRIDGESTONE CORPORATION (JP) | 2008-12-11 | — | — | US | disclosed |
| US-7429393-B2 | Graft polymer | BRIDGESTONE CORPORATION (JP) | 2008-09-30 | — | — | US | disclosed |
| WO-2007138051-A1 | DIBENZORYLENETETRACARBOXIMIDES AS INFRARED ABSORBERS | BASF SE (DE) | 2007-12-06 | — | — | WO | disclosed |
| WO-2007116001-A2 | LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF | BASF SE (DE) | 2007-10-18 | — | — | WO | disclosed |
| EP-1843407-A1 | Liquid crystalline rylenetetracarboxylic acid derivatives and their use | BASF AKTIENGESELLSCHAFT (DE) | 2007-10-10 | — | — | EP | disclosed |
| US-20070043087-A1 | Such as 3-{2,6-difluoro-4-[4,5-dihydro-6-(3,3-dimethylbutyl)naphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid | EDDINGPHARM (HONG KONG) COMPANY LIMITED (CN) | 2007-02-22 | — | — | US | disclosed |
| CN-1863783-A | Compounds with Thrombopoietin Receptor Agonism | SHIONOGI & CO (JP) | 2006-11-15 | — | — | CN | disclosed |
| EP-1655291-A1 | COMPOUNDS HAVING THROMBOPOIETIN RECEPTOR AGONISM | SHIONOGI & CO., LTD. (JP) | 2006-05-10 | — | — | EP | disclosed |
| US-20050282956-A1 | Reversible polymer/metal nano-composites and method for manufacturing same | BRIDGESTONE CORPORATION (JP) | 2005-12-22 | — | — | US | disclosed |
| EP-0964006-B1 | Application of disubstituted ethylene-maleimide copolymers in rubber compounds | BRIDGESTONE CORP (JP) | 2004-05-19 | — | — | EP | disclosed |
| US-6706823-B2 | A CROSSLINKED COPOLYMER HAVING ALKENYL MONOMER UNITS AND MALEIMIDE MONOMER UNITS, IN A ELECTROLYTE SOLUTION; USED TO ELECTROLYTE CELLS | BRIDGESTONE CORPORATION (JP) | 2004-03-16 | — | — | US | disclosed |
| EP-1280830-B1 | HIGHLY FUNCTIONALIZED POLYMERS AND A PROCESS FOR MAKING THE SAME | BRIDGESTONE CORP (JP) | 2004-01-21 | — | — | EP | disclosed |
| US-20030130398-A1 | Soft polymeric compounds including metal oxide fillers | BRIDGESTONE CORPORATION | 2003-07-10 | — | — | US | disclosed |
| US-20030130426-A1 | Method of grafting polymaleimides to alkenyl butyl rubbers | BRIDGESTONE CORP. | 2003-07-10 | — | — | US | disclosed |
| US-20030130397-A1 | A crosslinked copolymer having alkenyl monomer units and maleimide monomer units, in a electrolyte solution; used to electrolyte cells | BRIDGESTONE CORP. | 2003-07-10 | — | — | US | disclosed |
| US-20030091527-A1 | Graft polymer | BRIDGESTONE CORPORATION (JP) | 2003-05-15 | — | — | US | disclosed |
| EP-1290040-A2 | POLYALKYLENE GRAFTED CENTIPEDE POLYMERS | Bridgestone Corporation (JP) | 2003-03-12 | — | — | EP | disclosed |
| WO-2003016398-A1 | THERMOPLASTIC ELASTOMERS AND METHOD OF MAKING THE SAME | BRIDGESTONE CORPORATION (US) | 2003-02-27 | — | — | WO | disclosed |
| EP-1280830-A2 | HIGHLY FUNCTIONALIZED POLYMERS AND A PROCESS FOR MAKING THE SAME | Bridgestone Corporation (JP) | 2003-02-05 | — | — | EP | disclosed |
| WO-2002098957-A1 | POLYMER GEL INCLUDING DENDRIMERS | BRIDGESTONE CORPORATION (JP) | 2002-12-12 | — | — | WO | disclosed |
| US-20020188064-A1 | Poly(alkenyl-co-maleimide) , an inorganic salt, and an extender | BRIDGESTONE/FIRESTONE RESEARCH, INC. | 2002-12-12 | — | — | US | disclosed |
| WO-2002094893-A1 | CENTIPEDE IONOMERS | BRIDGESTONE CORPORATION (JP) | 2002-11-28 | — | — | WO | disclosed |
| US-6476143-B2 | INITIATING FORMATION AND PROPAGATION OF AN ANIONICALLY-POLYMERIZED LIVING POLYMER, TERMINATING PROPAGATION BY REACTING WITH SULFENYL CHLORIDE TERMINATING AGENT SUCH AS TRIPHENYLMETHANE SULFENYL CHLORIDE | BRIDGESTONE CORPORATION (JP) | 2002-11-05 | — | — | US | disclosed |
| US-6451935-B1 | ANIONIC POLYMERIZATION OF MIXTURE OF LIVING POLYMERS AND LITHIUM ALKOXIDE STABILIZER | BRIDGESTONE CORPORATION (JP) | 2002-09-17 | — | — | US | disclosed |
| US-20020128426-A1 | HIGHLY FUNCTIONALIZED POLYMERS AND A PROCESS FOR MAKING THE SAME | BRIDGESTONE CORPORATION (JP) | 2002-09-12 | — | — | US | disclosed |
| US-6417259-B1 | POLYMER BLENDS OF POLYALKYLENE CO MALEIMIDE AND MALEATED POLYALKYLENE | BRIDGESTONE CORPORATION (JP) | 2002-07-09 | — | — | US | disclosed |
| US-6403724-B1 | VIBRATION DAMPING; ALKENYL-MALEIC ANHYDRIDE COPOLYMER IMIDIZED WITH PRIMARY AMINE, A MALEATED POLYALKYLENE, AT LEAST ONE DENDRIMER, AND OPTIONALLY, AN EXTENDER. | BRIDGESTONE CORPORATION (JP) | 2002-06-11 | — | — | US | disclosed |
| US-6401776-B1 | REACTION PRODUCT OF AN ELASTOMER CONTAINING AT LEAST ONE REACTIVE HALOGEN ATOM WITH A MALEIMIDE ADDITION COPOLYMER IN THE PRESENCE OF A COMPATIBILIZER; HARD AND SOFT DOMAINS ARE CHEMICALLY BONDED TO ONE ANOTHER; TIRE INNER LINERS | BRIDGESTONE CORPORATION (JP) | 2002-06-11 | — | — | US | disclosed |
| US-6369166-B1 | PLASTICIZED; TENSILE AND TEAR STRENGTH; ELONGATION; HIGH DAMPING; ETHYLENE-MALEIC ANHYDRIDE COPOLYMER REACTED WITH PRIMARY AMINE | BRIDGESTONE CORPORATION (JP) | 2002-04-09 | — | — | US | disclosed |
| US-6359064-B1 | COMBINING POLY(ALKENYL-CO-MALEIMIDE), MALEATED POLYALKYLENE AND CROSSLINKING AGENT; REACTING TO CROSSLINK AND TO FORM A MALEATED POLYALKYLENE GRAFTED POLY(ALKENYL-CO-MALEIMIDE); COMBINING WITH WITH A POLYESTER TO PROVIDE THE ELASTOMER | BRIDGESTONE CORPORATION | 2002-03-19 | — | — | US | disclosed |
| WO-2002020669-A1 | POLYESTER AND POLYALKYLENE-GRAFTED POLYMER COMPOSITION | BRIDGESTONE CORPORATION (JP) | 2002-03-14 | — | — | WO | disclosed |
| US-6353054-B1 | Alkenyl-co-maleimide/diene rubber copolymers and applications | BRIDGESTONE CORPORATION (JP) | 2002-03-05 | — | — | US | disclosed |
| US-20020022701-A1 | Sulfenyl halide polymerization terminators | BRIDGESTONE CORPORATION (JP) | 2002-02-21 | — | — | US | disclosed |
| WO-2002010224-A2 | ALKENYL-CO-MALEIMIDE/DIENE RUBBER COMPOSITION | BRIDGESTONE CORPORATION (JP) | 2002-02-07 | — | — | WO | disclosed |
| WO-2001094425-A2 | POLYALKYLENE GRAFTED CENTIPEDE POLYMERS | BRIDGESTONE CORPORATION (JP) | 2001-12-13 | — | — | WO | disclosed |
| EP-0435632-B1 | Phenylpyrimidine derivatives, process for preparing the same, liquid crystal compositions containing said derivatives as active ingredient, and liquid crystal elements using such compositions | SUMITOMO CHEMICAL CO (JP) | 2001-11-28 | — | — | EP | disclosed |
| WO-2001085805-A2 | HIGHLY FUNCTIONALIZED POLYMERS AND A PROCESS FOR MAKING THE SAME | BRIDGESTONE CORPORATION (JP) | 2001-11-15 | — | — | WO | disclosed |
| WO-2001070822-A2 | PROCESS FOR FORMING CENTIPEDE POLYMER GELS | BRIDGESTONE CORPORATION (JP) | 2001-09-27 | — | — | WO | disclosed |
| US-20010021743-A1 | Method of producing a graft copolymer | BRIDGESTONE CORPORATION (JP) | 2001-09-13 | — | — | US | disclosed |
| US-6274680-B1 | LIVING POLYMERS | BRIDGESTONE/FIRESTONE RESEARCH, INC. | 2001-08-14 | — | — | US | disclosed |
| US-6207763-B1 | A COPOLYMER OF SUBSTITUTED OR UNSUBSTITUTED 1-20 ALKYL GROUP DISUBSTITUTED ETHYLENE-MALEIMIDE COPOLYMER(A REACTION PRODUCT OF DISUBTITUTED ETHYLENE-MALEIC ANHYDRIDE IMIDIZED WITH PRIMARY AMINE) IS A PLASTICIZER FOR RUBBER; HIGH DAMPING | BRIDGESTONE CORPORATION (JP) | 2001-03-27 | — | — | US | disclosed |
| US-6204354-B1 | DRY ENVIRONMENT | BRIDGESTONE CORPORATION (JP) | 2001-03-20 | — | — | US | disclosed |
| US-6191217-B1 | REACTING POLY(ALKYL VINYLETHER-CO-MALEIMIDE) POLYMER WITH MALEATED POLYALKYLENE AND ALKYL DIAMINE UNDER SUBSTANTIALLY DRY CONDITIONS SUFFICIENT TO FORM POLYALKYLENE GRAFTED POLY(ALKYL VINYLETHER-CO-MALEIMIDE) POLYMER | BRIDGESTONE CORPORATION (JP) | 2001-02-20 | — | — | US | disclosed |
| EP-1067122-A2 | Phenylpyrimidine derivatives, process for preparing the same, liquid crystal compositions containing said derivatives as active ingredient, and liquid crystal elements using such compositions | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2001-01-10 | — | — | EP | disclosed |
| US-6133354-A | MIXING A POLY(DIALKYLSUBSTITUTED ETHYLENE-CO-MALEIMIDE) POLYMER SUCH AS POLYISOBUTYLENE-CO-MALEIMIDE, AND PLASTICIZERS OR EXTENDERS WITHIN A NON-VULCANIZED THERMOPLASTIC ELASTOMER TO FORM A DAMPING GEL; TENSILE STRENGTH AND TEAR STRENGTH | BRIDGESTONE CORPORATION (JP) | 2000-10-17 | — | — | US | disclosed |
| EP-1016674-A1 | Sulfenyl halide polymerization terminators | BRIDGESTONE/FIRESTONE, INC. (US) | 2000-07-05 | — | — | EP | disclosed |
| EP-0643119-B1 | Trans-olefin compounds, method for production thereof, liquid crystal composition containing the same as active ingredient, and liquid crystal element using said composition | SUMITOMO CHEMICAL CO (JP) | 2000-04-26 | — | — | EP | disclosed |
| EP-0549279-B1 | Optically active pyrimidine compound, process for producing the same and liquid crystal composition containing the same | SUMITOMO CHEMICAL CO (JP) | 2000-03-29 | — | — | EP | disclosed |
| EP-0806417-B1 | Novel optically active benzene derivatives, process for producing the same and liquid-crystalline composition containing said derivatives as liquid-crystalline compound and light switching elements | SUMITOMO CHEMICAL CO (JP) | 2000-03-08 | — | — | EP | disclosed |
| US-6030546-A | FERROELECTRIC PHASE; LOW VISCOSITY;, THERMOSENSITIVITY OVER A BROAD AND EXHIBITS A LARGE TILT ANGLE AND A HIGH-SPEED RESPONSE PROPERTY;CHEMICAL INTERMEDIATES FOR PESTICIDES, DRUGS AND LIQUID CRYSTALS; BORIDING AND HYDROLYSIS | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2000-02-29 | — | — | US | disclosed |
| EP-0964006-A1 | Application of disubstituted ethylene-maleimide copolymers in rubber compounds | Bridgestone Corporation (JP) | 1999-12-15 | — | — | EP | disclosed |
| EP-0955319-A1 | Soft compounds derived from polypropylene grafted disubstituted ethylene-maleimide copolymers | Bridgestone Corporation (JP) | 1999-11-10 | — | — | EP | disclosed |
| EP-0634469-B1 | Compound having unsaturated side-chain, process for preparing the same, liquid crystalline polymer prepared from the same, liquid crystal mixture and display element | SUMITOMO CHEMICAL CO (JP) | 1999-10-06 | — | — | EP | disclosed |
| EP-0360622-B1 | Novel optically active benzene derivatives, process for producing the same and liquid-crystalline composition containing said derivatives as liquid-crystalline compound and light switching elements | SUMITOMO CHEMICAL CO (JP) | 1999-07-28 | — | — | EP | disclosed |
| EP-0628530-B1 | ACETYLENE DERIVATIVES, PROCESS FOR PRODUCING THE SAME, LIQUID CRYSTAL COMPOSITION CONTAINING THE SAME AS ACTIVE INGREDIENT, AND LIQUID CRYSTAL ELEMENT MADE THEREFROM | SUMITOMO CHEMICAL CO (JP) | 1999-03-24 | — | — | EP | disclosed |
| US-5741438-A | Optically active biphenyl derivative, process for preparation thereof, liquid crystal composition containing the same as an effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1998-04-21 | — | — | US | disclosed |
| US-5723610-A | Alcohol reactants for forming phenylpyrimidine derivatives and process for preparing said alcohols | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1998-03-03 | — | — | US | disclosed |
| US-5707547-A | CONTAINING FLUORINATED BENZENE OR NAPHTHALENE RINGS AND/OR NITROGEN CONTAINING HETEROCYCLES | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1998-01-13 | — | — | US | disclosed |
| US-5693251-A | LIQUID CRYSTAL DISPLAYS; HIGH SPEED RESPONSE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1997-12-02 | — | — | US | disclosed |
| EP-0806417-A1 | Novel optically active benzene derivatives, process for producing the same and liquid-crystalline composition containing said derivatives as liquid-crystalline compound and light switching elements | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1997-11-12 | — | — | EP | disclosed |
| US-5662828-A | Compound having unsaturated side chain, process for preparing the same, liquid crystalline polymer prepared from the same, liquid crystal mixture and display element | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1997-09-02 | — | — | US | disclosed |
| EP-0434297-B1 | Optically active aromatic compounds, preparation process thereof, and liquid crystal compositions and elements | SUMITOMO CHEMICAL CO (JP) | 1996-10-16 | — | — | EP | disclosed |
| US-5554317-A | POLYSILOXANE LIQUID CRYSTALLINE POLYMERS FORMED BY GRAFT POLYMERIZING AT LEAST ONE UNSATURATED COMPOUND WITH ONE OR MORE AROMATIC OR HETEROAROMATIC RINGS, OPTIONAL ETHER GROUP AND OPTIONAL ASYMMETRIC C ON POLYALKYLHYDROSILOXANE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1996-09-10 | — | — | US | disclosed |
| US-5539115-A | FERROELECTRIC CRYSTALS FOR OPTICAL APPARATUS | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1996-07-23 | — | — | US | disclosed |
| US-5534188-A | Acetylene derivatives, process for producing the same, liquid crystal composition containing the same as an active ingredient, and liquid crystal element using said liquid crystal composition | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1996-07-09 | — | — | US | disclosed |
| US-5422038-A | Ferroelectric liquid crystal material with sufficient spontaneous polarization, high speed response capability, wide temperature range | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1995-06-06 | — | — | US | disclosed |
| EP-0643119-A1 | Trans-olefin compounds, method for production thereof, liquid crystal composition containing the same as active ingredient, and liquid crystal element using said composition | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1995-03-15 | — | — | EP | disclosed |
| US-5389293-A | Light switches | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1995-02-14 | — | — | US | disclosed |
| US-5385693-A | Having rapid response and low phase transition temperature | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1995-01-31 | — | — | US | disclosed |
| EP-0634469-A1 | Compound having unsaturated side-chain, process for preparing the same, liquid crystalline polymer prepared from the same, liquid crystal mixture and display element | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1995-01-18 | — | — | EP | disclosed |
| US-5374376-A | Optically active aromatic compounds, preparation process therefor, liquid crystal materials and a light switching element | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1994-12-20 | — | — | US | disclosed |
| EP-0628530-A1 | ACETYLENE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, LIQUID CRYSTAL COMPOSITION CONTAINING THE SAME AS ACTIVE INGREDIENT, AND LIQUID CRYSTAL ELEMENT MADE THEREFROM | SUMITOMO CHEMICAL COMPANY LIMITED (JP) | 1994-12-14 | — | — | EP | disclosed |
| EP-0357372-B1 | Optically active ester derivatives, preparation process thereof, liquid crystal materials and a light switching element | SUMITOMO CHEMICAL CO (JP) | 1994-11-17 | — | — | EP | disclosed |
| EP-0416946-B1 | Optically active naphthalene derivative, process for preparation thereof, liquid crystal composition containing the same as effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL CO (JP) | 1994-11-09 | — | — | EP | disclosed |
| EP-0395390-B1 | Optically active biphenyl derivative, process for preparation thereof, liquid crystal composition containing the same as effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL CO (JP) | 1994-09-28 | — | — | EP | disclosed |
| US-5332675-A | Liquid crystals | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1994-07-26 | — | — | US | disclosed |
| US-5326871-A | Optically active pyrimidine compound, process for producing the same and liquid crystal composition containing the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1994-07-05 | — | — | US | disclosed |
| EP-0357435-B1 | Optically active aromatic compounds, preparation process therefor, liquid crystal materials and a light switching element | SUMITOMO CHEMICAL CO (JP) | 1993-12-08 | — | — | EP | disclosed |
| US-5264151-A | Optically active ester derivatives, preparation process thereof, liquid crystal materials and a light switching element | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1993-11-23 | — | — | US | disclosed |
| US-5238598-A | Having trifluoromethyl group; high speed response | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1993-08-24 | — | — | US | disclosed |
| EP-0549279-A1 | Optically active pyrimidine compound, process for producing the same and liquid crystal composition containing the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1993-06-30 | — | — | EP | disclosed |
| EP-0288297-B1 | OPTICALLY ACTIVE BENZENE DERIVATIVES AND PROCESS FOR PREPARATION THEREOF | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1993-03-17 | — | — | EP | disclosed |
| EP-0289307-B1 | OPTICALLY ACTIVE AROMATIC CARBOXYLIC ACID DERIVATIVES AND PROCESS FOR PRODUCING THE SAME | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1992-07-08 | — | — | EP | disclosed |
| US-5124070-A | High speed response | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1992-06-23 | — | — | US | disclosed |
| EP-0297745-B1 | OPTICALLY ACTIVE ETHER DERIVATIVES, PREPARATION PROCESSES THEREFOR, LIQUID CRYSTAL MATERIALS AND AN OPTICAL SWITCHING ELEMENT | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1991-09-18 | — | — | EP | disclosed |
| EP-0435632-A2 | Phenylpyrimidine derivatives, process for preparing the same, liquid crystal compositions containing said derivatives as active ingredient, and liquid crystal elements using such compositions | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1991-07-03 | — | — | EP | disclosed |
| EP-0434297-A2 | Optically active aromatic compounds, preparation process thereof, and liquid crystal compositions and elements | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1991-06-26 | — | — | EP | disclosed |
| US-5019298-A | Optically active aromatic carboxylic acid derivatives and process for producing the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1991-05-28 | — | — | US | disclosed |
| US-5013479-A | Aromatic ether esters containing two or three benzene rings | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1991-05-07 | — | — | US | disclosed |
| EP-0416946-A2 | Optically active naphthalene derivative, process for preparation thereof, liquid crystal composition containing the same as effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1991-03-13 | — | — | EP | disclosed |
| US-4985590-A | Optically active benzene derivatives and process for preparation thereof | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1991-01-15 | — | — | US | disclosed |
| EP-0395390-A1 | Optically active biphenyl derivative, process for preparation thereof, liquid crystal composition containing the same as effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1990-10-31 | — | — | EP | disclosed |
| EP-0360622-A2 | Novel optically active benzene derivatives, process for producing the same and liquid-crystalline composition containing said derivatives as liquid-crystalline compound and light switching elements | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1990-03-28 | — | — | EP | disclosed |
| EP-0357372-A2 | Optically active ester derivatives, preparation process thereof, liquid crystal materials and a light switching element | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1990-03-07 | — | — | EP | disclosed |
| EP-0357435-A2 | Optically active aromatic compounds, preparation process therefor, liquid crystal materials and a light switching element | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1990-03-07 | — | — | EP | disclosed |
| EP-0297745-A1 | Optically active ether derivatives, preparation processes therefor, liquid crystal materials and an optical switching element | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1989-01-04 | — | — | EP | disclosed |
| EP-0289307-A2 | Optically active aromatic carboxylic acid derivatives and process for producing the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1988-11-02 | — | — | EP | disclosed |
| EP-0288297-A2 | Optically active benzene derivatives and process for preparation thereof | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1988-10-26 | — | — | EP | disclosed |
| EP-0288297-A2 | Optically active benzene derivatives and process for preparation thereof | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1988-10-26 | — | — | EP | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (7 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20100048904-A1 | DIBENZORYLENETETRACARBOXIMIDES AS INFRARED ABSORBERS | TDO2, C9, CYP3A43 | TSHR 1062/4885LPAR1 4094/4885LPAR2 3965/4885 |
| US-20030091527-A1 | Graft polymer | PARG, PARN, PCNA | TSHR 4752/4885LPAR1 2945/4885LPAR2 2729/4885 |
| US-20110042651-A1 | LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF | TPR, ROR1, CA3 | TSHR 1618/4885LPAR1 996/4885LPAR2 994/4885 |
| US-20110092731-A1 | ISOCYANATE PRODUCTION PROCESS | CPS1, PHGDH, APEH | TSHR 4853/4885LPAR1 3008/4885LPAR2 2136/4885 |
| US-20090318513-A1 | COMPOUNDS EXHIBITING THROMBOPOIETIN RECEPTOR AGONISM | MPL, TEK, GHRHR | TSHR 9/4885LPAR1 93/4885LPAR2 194/4885 |
| US-20070043087-A1 | Such as 3-{2,6-difluoro-4-[4,5-dihydro-6-(3,3-dimethylbutyl)naphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid | DHFR, NAT1, ACR | TSHR 757/4885LPAR1 819/4885LPAR2 1261/4885 |
| US-20100069665-A1 | PROCESS FOR PRODUCING ISOCYANATES | CPS1, IDH2, PHGDH | TSHR 4775/4885LPAR1 3140/4885LPAR2 2523/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.