Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | IDO1 | P14902 | 2/20 | 0.50 |
| ▸ | HTR3E | A5X5Y0 | 1/20 | 0.50 |
| ▸ | HTR3B | O95264 | 1/20 | 0.50 |
| ▸ | HTR3A | P46098 | 1/20 | 0.50 |
| ▸ | HTR3D | Q70Z44 | 1/20 | 0.50 |
| ▸ | HTR3C | Q8WXA8 | 1/20 | 0.50 |
| ▸ | KDR | P35968 | 1/20 | 0.50 |
| ▸ | TMPRSS4 | Q9NRS4 | 1/20 | 0.49 |
| ▸ | TP53 | P04637 | 1/20 | 0.48 |
| ▸ | NOTUM | Q6P988 | 6/20 | 0.47 |
| ▸ | CCR2 | P41597 | 2/20 | 0.45 |
| ▸ | RAPGEF4 | Q8WZA2 | 1/20 | 0.44 |
| ▸ | PDK1 | Q15118 | 1/20 | 0.44 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.44 |
| ▸ | TSHR | P16473 | 1/20 | 0.44 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.44 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.44 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.44 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.44 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.44 |
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 | |
|---|---|---|---|---|
| SCHEMBL29649700 | 1.00 | IDO1 (0.50) | IDO1HTR3EHTR3BHTR3AHTR3D | |
| SCHEMBL3789153 | 0.82 | CYP3A4 (0.52) | TMPRSS4TP53CYP3A4TSHRMAPK1 | |
| Benzonitrile SCHEMBL10444954 | 0.80 | TSHR (0.45) | NOTUMTSHRKDM4E | |
| SCHEMBL30867127 | 0.80 | TSHR (0.54) | TMPRSS4CYP3A4TSHRMAPK1TDP1 | |
| SCHEMBL107751 | 0.80 | TSHR (0.62) | TMPRSS4TP53NOTUMCYP3A4TSHR | |
| SCHEMBL31303886 | 0.80 | SLC6A4 (0.46) | IDO1CYP3A4TSHRMAPK1TDP1 | |
| SCHEMBL2698021 | 0.80 | NOTUM (0.61) | IDO1HTR3EHTR3BHTR3AHTR3D | |
| SCHEMBL657298 | 0.80 | SLC6A4 (0.46) | IDO1CYP3A4TSHRMAPK1TDP1 | |
| SCHEMBL29403188 | 0.80 | TSHR (0.62) | TMPRSS4TP53NOTUMCYP3A4TSHR | |
| Bromide SCHEMBL9619767 | 0.79 | IDO1 (0.46) | IDO1HTR3EHTR3BHTR3AHTR3D |
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 181 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-112174878-B | Method and device for preparing 2, 6-dichloropyridine by fractional photochlorination of pyridine | 浙江埃森化学有限公司 | 2023-05-26 | — | — | CN | claimed |
| CN-114920655-A | Preparation method of 2-fluoro-3-trifluoromethylaniline | 南京正荣医药化学有限公司 | 2022-08-19 | — | — | CN | claimed |
| CN-109134355-B | Method for preparing 2, 6-dichloropyridine by liquid-phase photochlorination of pyridine | 浙江埃森化学有限公司 | 2022-04-12 | — | — | CN | claimed |
| CN-109516948-B | Method and production line for preparing 2, 6-dichloropyridine by gas-phase photochlorination of pyridine | 浙江埃森化学有限公司 | 2022-01-11 | — | — | CN | claimed |
| CN-113831214-A | Method for synthesizing 2, 5-dichlorotrifluorotoluene by continuous flow catalytic chlorination | 爱斯特（成都）生物制药股份有限公司 | 2021-12-24 | — | — | CN | claimed |
| CN-112174878-A | Method and device for preparing 2, 6-dichloropyridine by stepwise photochlorination of pyridine | 浙江埃森化学有限公司 | 2021-01-05 | — | — | CN | claimed |
| US-10851060-B2 | Method for preparing 2,6-dichloropyridine through liquid phase photochlorination of pyridine | ZHEJIANG AVILIVE CHEMICAL CO., LTD. (CN) | 2020-12-01 | — | — | US | claimed |
| US-20200131128-A1 | METHOD FOR PREPARING 2,6-DICHLOROPYRIDINE THROUGH LIQUID PHASE PHOTOCHLORINATION OF PYRIDINE | ZHEJIANG AVILIVE CHEMICAL CO., LTD. (CN) | 2020-04-30 | — | — | US | claimed |
| US-10577326-B1 | Method for preparing 2-chloro-6-trichloromethylpyridine through liquid phase photochlorination of 2-methylpyridine | Zhejiang Avilive Chemical, Co., Ltd. (CN) | 2020-03-03 | — | — | US | claimed |
| US-10442766-B1 | Method and production line for preparing 2,6-dichloropyridine through gas phase photochlorination of pyridine | ZHEJIANG AVILIVE CHEMICAL CO., LTD. (CN) | 2019-10-15 | — | — | US | claimed |
| CN-109694346-A | The method that 2- picoline liquid phase Light chlorimation prepares N-serve | 浙江埃森化学有限公司 | 2019-04-30 | — | — | CN | claimed |
| CN-109516948-A | A kind of pyridine gas phase Light chlorimation prepares the method and production line of 2,6- dichloropyridine | 浙江埃森化学有限公司 | 2019-03-26 | — | — | CN | claimed |
| CN-109134355-A | A kind of method that pyridine liquid phase Light chlorimation prepares 2,6- dichloropyridine | 浙江埃森化学有限公司 | 2019-01-04 | — | — | CN | claimed |
| JP-3266260-B2 | — | — | 2002-03-18 | — | — | JP | claimed |
| EP-0632825-B1 | METHOD OF CLEANING EPOXY ARTICLES | OCCIDENTAL CHEM CO (US) | 1996-07-10 | — | — | EP | claimed |
| EP-0632825-A1 | METHOD OF CLEANING EPOXY ARTICLES. | OCCIDENTAL CHEM CO (US) | 1995-01-11 | — | — | EP | claimed |
| WO-1993019153-A1 | METHOD OF CLEANING EPOXY ARTICLES | OCCIDENTAL CHEMICAL CORPORATION (US) | 1993-09-30 | — | — | WO | claimed |
| US-5244507-A | Chlorobenzotrifluorides, printed circuits | OCCIDENTAL CHEMICAL CORPORATION (US) | 1993-09-14 | — | — | US | claimed |
| US-4289909-A | Process for preparing 1-dichloroacyl-4-substituted phenoxy benzene and intermediates therefor | CHEVRON RESEARCH (US) | 1981-09-15 | — | — | US | claimed |
| CN-119143664-A | Preparation method of 2-chloro-5-trichloromethyl pyridine | 宁夏瑞泰科技股份有限公司 | 2024-12-17 | — | — | CN | disclosed |
| CN-112174878-B | Method and device for preparing 2, 6-dichloropyridine by fractional photochlorination of pyridine | 浙江埃森化学有限公司 | 2023-05-26 | — | — | CN | disclosed |
| CN-116008331-A | Method for measuring content of liquid electrolyte component of battery | 清华大学 | 2023-04-25 | — | — | CN | disclosed |
| CN-114920655-A | Preparation method of 2-fluoro-3-trifluoromethylaniline | 南京正荣医药化学有限公司 | 2022-08-19 | — | — | CN | disclosed |
| CN-114920655-A | Preparation method of 2-fluoro-3-trifluoromethylaniline | 南京正荣医药化学有限公司 | 2022-08-19 | — | — | CN | disclosed |
| CN-109134355-B | Method for preparing 2, 6-dichloropyridine by liquid-phase photochlorination of pyridine | 浙江埃森化学有限公司 | 2022-04-12 | — | — | CN | disclosed |
| CN-109516948-B | Method and production line for preparing 2, 6-dichloropyridine by gas-phase photochlorination of pyridine | 浙江埃森化学有限公司 | 2022-01-11 | — | — | CN | disclosed |
| CN-113831214-A | Method for synthesizing 2, 5-dichlorotrifluorotoluene by continuous flow catalytic chlorination | 爱斯特（成都）生物制药股份有限公司 | 2021-12-24 | — | — | CN | disclosed |
| CN-113831214-A | Method for synthesizing 2, 5-dichlorotrifluorotoluene by continuous flow catalytic chlorination | 爱斯特（成都）生物制药股份有限公司 | 2021-12-24 | — | — | CN | disclosed |
| CN-113831214-A | Method for synthesizing 2, 5-dichlorotrifluorotoluene by continuous flow catalytic chlorination | 爱斯特（成都）生物制药股份有限公司 | 2021-12-24 | — | — | CN | disclosed |
| EP-3326715-B1 | OXALIC ACID MONOAMIDE LIGAND, AND USES THEREOF IN COUPLING REACTION OF COPPER-CATALYZED ARYL HALOGEN SUBSTITUTE | CE PHARM CO LTD (CN) | 2021-09-15 | — | — | EP | disclosed |
| CN-112174878-A | Method and device for preparing 2, 6-dichloropyridine by stepwise photochlorination of pyridine | 浙江埃森化学有限公司 | 2021-01-05 | — | — | CN | disclosed |
| US-10851060-B2 | Method for preparing 2,6-dichloropyridine through liquid phase photochlorination of pyridine | ZHEJIANG AVILIVE CHEMICAL CO., LTD. (CN) | 2020-12-01 | — | — | US | disclosed |
| US-10759765-B2 | Heterocyclic carboxylic acid amide ligand and applications thereof in copper catalyzed coupling reaction of aryl halogeno substitute | CE PHARM CO., LTD. (CN) | 2020-09-01 | — | — | US | disclosed |
| US-20200131128-A1 | METHOD FOR PREPARING 2,6-DICHLOROPYRIDINE THROUGH LIQUID PHASE PHOTOCHLORINATION OF PYRIDINE | ZHEJIANG AVILIVE CHEMICAL CO., LTD. (CN) | 2020-04-30 | — | — | US | disclosed |
| US-10577326-B1 | Method for preparing 2-chloro-6-trichloromethylpyridine through liquid phase photochlorination of 2-methylpyridine | Zhejiang Avilive Chemical, Co., Ltd. (CN) | 2020-03-03 | — | — | US | disclosed |
| EP-3052536-B1 | SYNTHESIS OF CHLOROTRIFLUOROETHYLENE-BASED BLOCK COPOLYMERS BY IODINE TRANSFER POLYMERIZATION | HONEYWELL INT INC (US) | 2019-11-06 | — | — | EP | disclosed |
| US-10442766-B1 | Method and production line for preparing 2,6-dichloropyridine through gas phase photochlorination of pyridine | ZHEJIANG AVILIVE CHEMICAL CO., LTD. (CN) | 2019-10-15 | — | — | US | disclosed |
| EP-2956496-B1 | FLUOROPOLYMERS CONTAINING A COPOLYMERIZED FLUOROMONOMER AND A FUNCTIONAL HYDROCARBON COMONOMER AND ARTICLES MADE FROM SUCH FLUOROPOLYMERS | HONEYWELL INT INC (US) | 2019-10-09 | — | — | EP | disclosed |
| CN-109912502-A | A kind of method that pyridine liquid phase Light chlorimation prepares 2,6- dichloropyridine | 浙江埃森化学有限公司 | 2019-06-21 | — | — | CN | disclosed |
| CN-105555846-B | Fluoropolymers containing copolymerized fluoromonomers and functional hydrocarbon comonomers and articles made from such fluoropolymers | 霍尼韦尔国际公司 | 2019-06-18 | — | — | CN | disclosed |
| US-20190127337-A1 | HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE | CE PHARM CO., LTD. (CN) | 2019-05-02 | — | — | US | disclosed |
| CN-109516948-A | A kind of pyridine gas phase Light chlorimation prepares the method and production line of 2,6- dichloropyridine | 浙江埃森化学有限公司 | 2019-03-26 | — | — | CN | disclosed |
| US-20180207628-A1 | OXALIC ACID MONOAMIDE LIGAND, AND USES THEREOF IN COUPLING REACTION OF COPPER-CATALYZED ARYL HALOGEN SUBSTITUTE | SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY, CHINESE ACADEMY OF SCIENCES (CN) | 2018-07-26 | — | — | US | disclosed |
| US-20180207628-A1 | OXALIC ACID MONOAMIDE LIGAND, AND USES THEREOF IN COUPLING REACTION OF COPPER-CATALYZED ARYL HALOGEN SUBSTITUTE | SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY, CHINESE ACADEMY OF SCIENCES (CN) | 2018-07-26 | — | — | US | disclosed |
| EP-3326715-A1 | OXALIC ACID MONOAMIDE LIGAND, AND USES THEREOF IN COUPLING REACTION OF COPPER-CATALYZED ARYL HALOGEN SUBSTITUTE | Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences (CN) | 2018-05-30 | — | — | EP | disclosed |
| US-9969899-B2 | Fluoropolymers containing a copolymerized fluoromonomer and a functional hydrocarbon comonomer and articles made from such fluoropolymers | HONEYWELL INTERNATIONAL INC. (US) | 2018-05-15 | — | — | US | disclosed |
| CN-105439943-B | A kind of industrialized preparing process of 2 chlorine, 5 trichloromethyl pyridine | 连云港埃森化学有限公司 | 2018-04-13 | — | — | CN | disclosed |
| CN-105439943-B | A kind of industrialized preparing process of 2 chlorine, 5 trichloromethyl pyridine | 连云港埃森化学有限公司 | 2018-04-13 | — | — | CN | disclosed |
| WO-2017177979-A1 | HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE | 中国科学院上海有机化学研究所 | 2017-10-19 | — | — | WO | disclosed |
| WO-2017012379-A1 | OXALIC ACID MONOAMIDE LIGAND, AND USES THEREOF IN COUPLING REACTION OF COPPER-CATALYZED ARYL HALOGEN SUBSTITUTE | 中国科学院上海有机化学研究所 | 2017-01-26 | — | — | WO | disclosed |
| EP-2006274-B1 | METHOD FOR PRODUCING 3,3,3-TRIFLUOROPROPIONIC ACID CHLORIDE | CENTRAL GLASS CO LTD (JP) | 2016-12-21 | — | — | EP | disclosed |
| CN-105940027-A | Synthesis of chlorotrifluoroethylene-based block copolymers by iodine transfer polymerization | 霍尼韦尔国际公司 | 2016-09-14 | — | — | CN | disclosed |
| EP-3052536-A1 | SYNTHESIS OF CHLOROTRIFLUOROETHYLENE-BASED BLOCK COPOLYMERS BY IODINE TRANSFER POLYMERIZATION | Honeywell International Inc. (US) | 2016-08-10 | — | — | EP | disclosed |
| US-9394394-B2 | Synthesis of chlorotrifluoroethylene-based block copolymers by iodine transfer polymerization | HONEYWELL INTERNATIONAL INC. (US) | 2016-07-19 | — | — | US | disclosed |
| EP-2326621-B1 | SUBSTITUTED 1,2,3,4- TETRAHYDROCYCLOPENTA[b]INDOL-3-YL) ACETIC ACID DERIVATIVES USEFUL IN THE TREATMENT OF AUTOIMMUNE AND INFLAMMATORY DISORDERS | ARENA PHARM INC (US) | 2016-06-08 | — | — | EP | disclosed |
| CN-105555846-A | Fluoropolymers containing copolymerized fluoromonomers and functional hydrocarbon comonomers and articles made from such fluoropolymers | HONEYWELL INT INC | 2016-05-04 | — | — | CN | disclosed |
| CN-105439943-A | Industrial production method of 2-chloro-5-trichloromethyl pyridine | LIANYUNGANG AVILIVE CHEMICAL CO LTD | 2016-03-30 | — | — | CN | disclosed |
| CN-105439943-A | Industrial production method of 2-chloro-5-trichloromethyl pyridine | LIANYUNGANG AVILIVE CHEMICAL CO LTD | 2016-03-30 | — | — | CN | disclosed |
| EP-2956496-A1 | FLUOROPOLYMERS CONTAINING A COPOLYMERIZED FLUOROMONOMER AND A FUNCTIONAL HYDROCARBON COMONOMER AND ARTICLES MADE FROM SUCH FLUOROPOLYMERS | Honeywell International Inc. (US) | 2015-12-23 | — | — | EP | disclosed |
| CN-102812016-B | Organic electronic devices and polymers including photovoltaic cells and diketone-based polymers | SOLVAY USA INC. (US) | 2015-12-09 | — | — | CN | disclosed |
| EP-2900645-A1 | 3-PHENYLISOXAZOLIN DERIVATIVES WITH HERBICIDAL ACTION | Bayer CropScience AG (DE) | 2015-08-05 | — | — | EP | disclosed |
| WO-2015047749-A1 | SYNTHESIS OF CHLOROTRIFLUOROETHYLENE-BASED BLOCK COPOLYMERS BY IODINE TRANSFER POLYMERIZATION | HONEYWELL INTERNATIONAL INC. (US) | 2015-04-02 | — | — | WO | disclosed |
| US-20150094428-A1 | SYNTHESIS OF CHLOROTRIFLUOROETHYLENE-BASED BLOCK COPOLYMERS BY IODINE TRANSFER POLYMERIZATION | SOLSTICE ADVANCED MATERIALS US, INC. | 2015-04-02 | — | — | US | disclosed |
| US-8968885-B2 | Organic electronic devices and polymers, including photovoltaic cells and diketone-based polymers | SOLVAY USA, INC. (US) | 2015-03-03 | — | — | US | disclosed |
| US-20140234630-A1 | FLUOROPOLYMERS CONTAINING A COPOLYMERIZED FLUOROMONOMER AND A FUNCTIONAL HYDROCARBON COMONOMER AND ARTICLES MADE FROM SUCH FLUOROPOLYMERS | SOLSTICE ADVANCED MATERIALS US, INC. | 2014-08-21 | — | — | US | disclosed |
| WO-2014127197-A1 | FLUOROPOLYMERS CONTAINING A COPOLYMERIZED FLUOROMONOMER AND A FUNCTIONAL HYDROCARBON COMONOMER AND ARTICLES MADE FROM SUCH FLUOROPOLYMERS | HONEYWELL INTERNATIONAL INC. (US) | 2014-08-21 | — | — | WO | disclosed |
| US-8735391-B2 | Synthesis of functionalized octahydro-isoquinolin-1-one-8-carboxamides, octahydro-isoquinolin-1-one-8-carboxylic esters and analogs, and therapeutic methods | UNIVERSITY OF KANSAS (US) | 2014-05-27 | — | — | US | disclosed |
| US-8735391-B2 | Synthesis of functionalized octahydro-isoquinolin-1-one-8-carboxamides, octahydro-isoquinolin-1-one-8-carboxylic esters and analogs, and therapeutic methods | UNIVERSITY OF KANSAS (US) | 2014-05-27 | — | — | US | disclosed |
| US-20140128560-A1 | PROCESS TO PREPARE CROSSLINKABLE TRIFLUOROSTYRENE POLYMERS AND MEMBRANES | E I DU PONT DE NEMOURS AND COMPANY (US) | 2014-05-08 | — | — | US | disclosed |
| US-8664282-B2 | Process to prepare crosslinkable trifluorostyrene polymers and membranes | E I DU PONT DE NEMOURS AND COMPANY (US) | 2014-03-04 | — | — | US | disclosed |
| US-8440785-B2 | Compositions, methods and polymers | PLEXTRONICS, INC. (US) | 2013-05-14 | — | — | US | disclosed |
| EP-1914263-B1 | SINGLE-CRYSTALLINE ORGANIC CARBOXYLIC ACID METAL COMPLEX, PROCESS FOR PRODUCING THE SAME, AND USE THEREOF | UNIV YOKOHAMA CITY (JP) | 2012-12-05 | — | — | EP | disclosed |
| EP-2112133-B1 | Halogenated aromatic compound, polymer thereof, and proton-conductive membrane comprising same | JSR CORP (JP) | 2012-07-04 | — | — | EP | disclosed |
| EP-2467371-A2 | ORGANIC ELECTRONIC DEVICES AND POLYMERS, INCLUDING PHOTOVOLTAIC CELLS AND DIKETONE-BASED POLYMERS | Plextronics, Inc. (US) | 2012-06-27 | — | — | EP | disclosed |
| EP-2449561-A2 | POLYMERS COMPRISING AT LEAST ONE BITHIOPHENE REPEAT UNIT, METHODS SYNTHETISING SAID POLYMERS AND COMPOSITIONS COMPRISING THE SAME | Plextronics, Inc. (US) | 2012-05-09 | — | — | EP | disclosed |
| US-8034165-B2 | Single-crystalline organic carboxylic acid metal complex, process for producing the same, and use thereof | YOKOHAMA CITY UNIVERSITY (JP) | 2011-10-11 | — | — | US | disclosed |
| US-20110230575-A1 | CROSSLINKABLE TRIFLUOROSTYRENE POLYMERS AND MEMBRANES | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2011-09-22 | — | — | US | disclosed |
| US-20110204341-A1 | ORGANIC ELECTRONIC DEVICES AND POLYMERS, INCLUDING PHOTOVOLTAIC CELLS AND DIKETONE-BASED POLYMERS | PLEXTRONICS, INC. | 2011-08-25 | — | — | US | disclosed |
| WO-2011028827-A2 | ORGANIC ELECTRONIC DEVICES AND POLYMERS, INCLUDING PHOTOVOLTAIC CELLS AND DIKETONE-BASED POLYMERS | PLEXTRONICS, INC. (US) | 2011-03-10 | — | — | WO | disclosed |
| US-20110046247-A1 | CROSSLINKABLE MONOMER | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2011-02-24 | — | — | US | disclosed |
| US-20110028644-A1 | NOVEL COMPOSITIONS, METHODS AND POLYMERS | PLEXTRONICS, INC. | 2011-02-03 | — | — | US | disclosed |
| WO-2011002927-A2 | NOVEL COMPOSITIONS, METHODS AND POLYMERS | PLEXTRONICS, INC. (US) | 2011-01-06 | — | — | WO | disclosed |
| EP-2260032-A2 | FUNGICIDAL HETERCYCLIC COMPOUNDS | E. I. du Pont de Nemours and Company (US) | 2010-12-15 | — | — | EP | disclosed |
| US-20100292351-A1 | PROCESS TO PREPARE CROSSLINKABLE TRIFLUOROSTYRENE POLYMERS AND MEMBRANES | E.I DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-18 | — | — | US | disclosed |
| US-20100256142-A1 | SYNTHESIS OF FUNCTIONALIZED OCTAHYDRO-ISOQUINOLIN-1-ONE-8- CARBOXAMIDES, OCTAHYDRO-ISOQUINOLIN-1-ONE-8-CARBOXYLIC ESTERS AND ANALOGS, AND THERAPEUTIC METHODS | UNIVERSITY OF NORTH CAROLINA | 2010-10-07 | — | — | US | disclosed |
| US-20100256142-A1 | SYNTHESIS OF FUNCTIONALIZED OCTAHYDRO-ISOQUINOLIN-1-ONE-8- CARBOXAMIDES, OCTAHYDRO-ISOQUINOLIN-1-ONE-8-CARBOXYLIC ESTERS AND ANALOGS, AND THERAPEUTIC METHODS | UNIVERSITY OF NORTH CAROLINA | 2010-10-07 | — | — | US | disclosed |
| EP-2222761-A1 | PROCESS TO PREPARE CROSSLINKABLE TRIFLUOROSTYRENE POLYMERS AND MEMBRANES | E. I. du Pont de Nemours and Company (US) | 2010-09-01 | — | — | EP | disclosed |
| EP-2222733-A1 | CROSSLINKABLE TRIFLUOROSTYRENE POLYMERS AND MEMBRANES | E. I. du Pont de Nemours and Company (US) | 2010-09-01 | — | — | EP | disclosed |
| US-7754927-B2 | Method for producing 3,3,3-trifluoropropionyl chloride | CENTRAL GLASS COMPANY, LIMITED (JP) | 2010-07-13 | — | — | US | disclosed |
| CN-1800228-B | Amorphous tetrafluoroethylene (TFE) - hexafluoropropylene (HFP) copolymers | DU PONT | 2010-06-16 | — | — | CN | disclosed |
| US-20100113834-A1 | chlorinating 3,3,3-trifluoropropionaldehyde with a radical initiator; also producing 3,3,3-trifluoropropionic acid by hydrolysis; useful as an intermediate of medicines and agricultural chemicals and a fluoropolymer | CENTRAL GLASS COMPANY LIMITED (JP) | 2010-05-06 | — | — | US | disclosed |
| EP-2112133-A1 | Halogenated aromatic compound, polymer thereof, and proton-conductive membrane comprising same | JSR Corporation (JP) | 2009-10-28 | — | — | EP | disclosed |
| EP-1245555-B1 | Halogenated aromatic compound, polymer thereof, and proton-conductive membrane comprising same | JSR CORP (JP) | 2009-08-19 | — | — | EP | disclosed |
| WO-2009094445-A2 | FUNGICIDAL HETERCYCLIC COMPOUNDS | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-07-30 | — | — | WO | disclosed |
| WO-2009082663-A1 | PROCESS TO PREPARE CROSSLINKABLE TRIFLUOROSTYRENE POLYMERS AND MEMBRANES | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-07-02 | — | — | WO | disclosed |
| WO-2009082661-A1 | CROSSLINKABLE TRIFLUOROSTYRENE POLYMERS AND MEMBRANES | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-07-02 | — | — | WO | disclosed |
| US-20090139401-A1 | Single-crystalline organic carboxylic acid metal complex, process for producing the same, and use thereof | YOKOHAMA CITY UNIVERSITY (JP) | 2009-06-04 | — | — | US | disclosed |
| EP-1482589-B1 | Manufacturing process of membrane-electrode assemblies | JSR CORP (JP) | 2009-02-18 | — | — | EP | disclosed |
| EP-2006274-A1 | METHOD FOR PRODUCING 3,3,3-TRIFLUOROPROPIONIC ACID CHLORIDE | Central Glass Co., Ltd. (JP) | 2008-12-24 | — | — | EP | disclosed |
| US-7396607-B2 | Manufacturing process for membrane-electrode assemblies | JSR CORPORATION (JP) | 2008-07-08 | — | — | US | disclosed |
| EP-1914263-A1 | SINGLE-CRYSTALLINE ORGANIC CARBOXYLIC ACID METAL COMPLEX, PROCESS FOR PRODUCING THE SAME, AND USE THEREOF | Yokohama City University (JP) | 2008-04-23 | — | — | EP | disclosed |
| US-20080032184-A1 | Stable Trifluorostyrene Containing Compounds, And Their Use In Polymer Electroyte Membranes | U.S. DEPARTMENT OF ENERGY | 2008-02-07 | — | — | US | disclosed |
| CN-1302030-C | amorphous tetrafluoroethylene-hexafluoropropylene copolymer | DU PONT (US) | 2007-02-28 | — | — | CN | disclosed |
| CN-1290879-C | amorphous tetrafluoroethylene-hexafluoropropylene copolymer, preparation method and application thereof | DU PONT (US) | 2006-12-20 | — | — | CN | disclosed |
| US-20060269655-A1 | Process for producing electrolyte membrane-bonded electrode and varnish composition used therein | JSR CORPORATION | 2006-11-30 | — | — | US | disclosed |
| CN-1800228-A | Amorphous hexafluoropropylene (HFP) / tetrafluoroethylene (TFE) copolymers | DU PONT (US) | 2006-07-12 | — | — | CN | disclosed |
| US-20060135715-A1 | Trifluorostyrene containing compounds, and their use in polymer electrolyte membranes | E. I. DU PONT DE NEMOURS AND COMPANY | 2006-06-22 | — | — | US | disclosed |
| US-7001929-B2 | Proton conductive membrane having improved thermal stability | JSR CORPORATION (JP) | 2006-02-21 | — | — | US | disclosed |
| EP-1138712-B1 | Polyarylene copolymers and proton-conductive membrane | JSR CORP (JP) | 2006-01-18 | — | — | EP | disclosed |
| WO-2005113491-A1 | STABLE TRIFLUOROSTYRENE CONTAINING COMPOUNDS, AND THEIR USE IN POLYMER ELECTROLYTE MEMBRANES | E.I. DUPONT DE NEMOURS AND COMPANY (US) | 2005-12-01 | — | — | WO | disclosed |
| US-6933068-B2 | Polymer electrolyte membrane and solid polymer electrolyte fuel cell using same | HONDA GIKEN KOGYO KABUSHIKI KAISHA (JP) | 2005-08-23 | — | — | US | disclosed |
| EP-1245554-B1 | Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same | JSR CORP (JP) | 2005-01-26 | — | — | EP | disclosed |
| WO-2005003083-A1 | TRIFLUOROSTYRENE CONTAINING COMPOUNDS, AND THEIR USE IN POLYMER ELECTROLYTE MEMBRANES | E.I. DUPONT DE NEMOURS AND COMPANY (US) | 2005-01-13 | — | — | WO | disclosed |
| EP-1482589-A2 | Manufacturing process for membrane-electrode assemblies | JSR Corporation (JP) | 2004-12-01 | — | — | EP | disclosed |
| US-6825310-B2 | POLYETHER KETONE POLYMERS PROVIDE STABLE MECHANICAL AND THERMAL PROPERTIES (DURABILITY) WHEN SULFONATED; FOR USE IN BATTERIES/FUEL CELLS | JSR CORPORATION (JP) | 2004-11-30 | — | — | US | disclosed |
| US-6812290-B2 | FOR USE AS ELECTROLYTES | JSR CORPORATION (JP) | 2004-11-02 | — | — | US | disclosed |
| US-6794480-B2 | POLYARYLENE-BASED COPOLYMER USEFUL AS PROTON-CONDUCTIVE MEMBRANE WHICH CAN BE USED AS ELECTRON FOR PRIMARY BATTERY, ELECTROLYTE FOR SECONDARY BATTERY, HIGH MOLECULAR SOLID ELECTROLYTE FOR FUEL CELL | JSR CORPORATION (JP) | 2004-09-21 | — | — | US | disclosed |
| US-20040163760-A1 | Manufacturing process for membrane-electrode assemblies | JSR CORPORATION AND HONDA MOTOR CO., LTD. | 2004-08-26 | — | — | US | disclosed |
| US-20040151984-A1 | Proton conductive membrane having improved thermal stability | JSR CORPORATION | 2004-08-05 | — | — | US | disclosed |
| US-20040110053-A1 | Proton conductive composition and proton conductive membrane | JSR CORPORATION (JP) | 2004-06-10 | — | — | US | disclosed |
| EP-0889066-B1 | Amorphous copolymers containing hexafluoropropylene | DU PONT (US) | 2004-06-09 | — | — | EP | disclosed |
| EP-1408517-A2 | Proton conductive composition and proton conductive membrane | JSR Corporation (JP) | 2004-04-14 | — | — | EP | disclosed |
| US-20040043297-A1 | Proton conductive resin composition, method for preparing the same, and proton conductive membrane comprising the composition | JSR CORPORATION | 2004-03-04 | — | — | US | disclosed |
| EP-1391480-A1 | Proton conductive resin composition, method for preparing the same, and proton conductive membrane comprising the composition | JSR Corporation (JP) | 2004-02-25 | — | — | EP | disclosed |
| US-20040028806-A1 | Process for producing electrolyte membrane-bonded electrode and varnish composition used therein | THE RELIABLE AUTOMATIC SPRINKLER CO. INC. | 2004-02-12 | — | — | US | disclosed |
| US-6685984-B2 | FORMING FUEL CELL COMPRISED OF NONPENETRATING ELECTROLYTE MEMBRANE ON ELECTRODE | JSR CORPORATION (JP) | 2004-02-03 | — | — | US | disclosed |
| US-20030228421-A1 | Method for the production of multilayers | JSR CORPORATION | 2003-12-11 | — | — | US | disclosed |
| US-20030195301-A1 | Polyarylene copolymers and proton-conductive membrane | JSR CORPORATION (JP) | 2003-10-16 | — | — | US | disclosed |
| US-6555626-B2 | Controlled amount of sulfonic acid groups; copolymer of an aromatic compound having a main chain containing electron withdrawing groups and aromatic compounds with no electron withdrawing groups; durability, strength, conductivity | JSR CORPORATION (JP) | 2003-04-29 | — | — | US | disclosed |
| US-20020188097-A1 | Polyether ketone polymers provide stable mechanical and thermal properties (durability) when sulfonated; for use in batteries/fuel cells | JSR CORPORATION (JP) | 2002-12-12 | — | — | US | disclosed |
| EP-0808335-B1 | AMORPHOUS TETRAFLUOROETHYLENE-HEXAFLUOROPROPYLENE COPOLYMERS | DU PONT (US) | 2002-12-11 | — | — | EP | disclosed |
| US-20020177656-A1 | Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same | JSR CORPORATION (JP) | 2002-11-28 | — | — | US | disclosed |
| US-6486280-B1 | Amorphous tetrafluoroethylene-hexafluoropropylene copolymers | E. I. DU PONT DE NEMOURS AND COMPANY | 2002-11-26 | — | — | US | disclosed |
| US-20020172850-A1 | Polymer electrolyte membrane and solid polymer electrolyte fuel cell using same | HONDA GIKEN KOGYO KABUSHIKI KAISHA, JSR CORPORATION | 2002-11-21 | — | — | US | disclosed |
| EP-1245555-A1 | Halogenated aromatic compound, polymer thereof, and proton-conductive membrane comprising same | JSR Corporation (JP) | 2002-10-02 | — | — | EP | disclosed |
| EP-1245554-A1 | Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same | JSR Corporation (JP) | 2002-10-02 | — | — | EP | disclosed |
| CN-1326996-A | amorphous tetrafluoroethylene-hexafluoropropylene copolymer | DU PONT (US) | 2001-12-19 | — | — | CN | disclosed |
| US-20010037000-A1 | Polyarylene copolymers and proton-conductive membrane | JSR CORPORATION (JP) | 2001-11-01 | — | — | US | disclosed |
| EP-0956312-B1 | PROCESS FOR PRODUCING PHENYLENE-CONTAINING POLYMER AND FILM-FORMING MATERIAL | JSR CORP (JP) | 2001-10-10 | — | — | EP | disclosed |
| US-6300465-B1 | Process for producing phenylene-containing polymer and film-forming material | JSR CORPORATION (JP) | 2001-10-09 | — | — | US | disclosed |
| EP-1138712-A2 | Polyarylene copolymers and proton-conductive membrane | JSR Corporation (JP) | 2001-10-04 | — | — | EP | disclosed |
| EP-0956312-A1 | PROCESS FOR PRODUCING PHENYLENE-CONTAINING POLYMER AND FILM-FORMING MATERIAL | JSR Corporation (JP) | 1999-11-17 | — | — | EP | disclosed |
| WO-1998033836-A1 | PROCESS FOR PRODUCING PHENYLENE-CONTAINING POLYMER AND FILM-FORMING MATERIAL | JSR CORPORATION (JP) | 1998-08-06 | — | — | WO | disclosed |
| CN-1173882-A | amorphous tetrafluoroethylene-hexafluoropropylene copolymer | DU PONT (US) | 1998-02-18 | — | — | CN | disclosed |
| US-5637663-A | RADICAL INITIATING A CONTINUOUS COPOLYMERIZATION | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1997-06-10 | — | — | US | disclosed |
| WO-1996024622-A1 | PRODUCTION OF FLUOROPOLYMERS, FLUOROPOLYMER SUSPENSION AND POLYMER FORMED THEREFROM | ALLIEDSIGNAL INC. (US) | 1996-08-15 | — | — | WO | disclosed |
| EP-0632825-B1 | METHOD OF CLEANING EPOXY ARTICLES | OCCIDENTAL CHEM CO (US) | 1996-07-10 | — | — | EP | disclosed |
| US-5453477-A | Formation of stable suspension without surfactant, improved processing properties, emulsifier-free | ALLIEDSIGNAL INC. (US) | 1995-09-26 | — | — | US | disclosed |
| EP-0605558-A1 | BARRIER FILM | AlliedSignal Inc. (US) | 1994-07-13 | — | — | EP | disclosed |
| EP-0605610-A1 | HIGH BARRIER PCTFE FILM | AlliedSignal Inc. (US) | 1994-07-13 | — | — | EP | disclosed |
| US-5328948-A | Chlorotrifluoroethylene-ethylene copolymer blend with ionomers for extrusion moldings | AUSIMONT, U.S.A., INC. (US) | 1994-07-12 | — | — | US | disclosed |
| US-5266674-A | Copolymers | PHILLIPS PETROLEUM COMPANY (US) | 1993-11-30 | — | — | US | disclosed |
| US-5244507-A | Chlorobenzotrifluorides, printed circuits | OCCIDENTAL CHEMICAL CORPORATION (US) | 1993-09-14 | — | — | US | disclosed |
| WO-1993006158-A1 | HIGH BARRIER PCTFE FILM | ALLIED-SIGNAL INC. (US) | 1993-04-01 | — | — | WO | disclosed |
| WO-1993006159-A1 | BARRIER FILM | ALLIED-SIGNAL INC. (US) | 1993-04-01 | — | — | WO | disclosed |
| EP-0069195-B1 | STABILIZED ETHYLENE/CHLOROTRIFLUOROETHYLENE COPOLYMER COMPOSITION | Ausimont, U.S.A., Inc. (US) | 1988-08-24 | — | — | EP | disclosed |
| US-4659370-A | Substituted phenoxypropionates and herbicidal compositions containing same and their herbicidal use | NIHON TOKUSHU NOYAKU SEIZO K.K. (JP) | 1987-04-21 | — | — | US | disclosed |
| US-4614536-A | Certain pyridyloxy-phenoxy-propionate derivatives, herbicidal compositions containing same and their herbicidal method of use | NIHON TOKUSHU NOYAKU SEIZO, K.K. (JP) | 1986-09-30 | — | — | US | disclosed |
| US-4584396-A | Substituted phenoxypropionates and herbicidal compositions | NIHON TOKUSHU NOYAKU SEIZO K.K. (JP) | 1986-04-22 | — | — | US | disclosed |
| EP-0068260-B1 | SUBSTITUTED PHENOXYPROPIONATES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS HERBICIDES | NIHON TOKUSHU NOYAKU SEIZO K.K. (JP) | 1986-03-05 | — | — | EP | disclosed |
| EP-0097357-B1 | PROCESS FOR PREPARING TRIFLUOROMETHYLBENZENE DERIVATIVES | Daikin Kogyo Co., Ltd. (JP) | 1986-01-08 | — | — | EP | disclosed |
| US-4539354-A | PHOSPHITE DERIVATIVE OF A PHENOL, A GROUP II METAL CARBOXYLATE ANDAN ESTER OF A POLYOL | ALLIED CORPORATION (US) | 1985-09-03 | — | — | US | disclosed |
| EP-0151763-A2 | Stabilized fluoropolymer composition | ALLIED CORPORATION (US) | 1985-08-21 | — | — | EP | disclosed |
| EP-0092112-B1 | SUBSTITUTED PHENOXY PROPIONATES | NIHON TOKUSHU NOYAKU SEIZO K.K. (JP) | 1985-03-06 | — | — | EP | disclosed |
| US-4500346-A | Substituted phenoxypropionates and herbicidal compositions containing same and their herbicidal use | NIHON TOKUSHU NOYAKU SEIZO K.K. (JP) | 1985-02-19 | — | — | US | disclosed |
| US-4496677-A | A HINDERED PHENOL PENTAERYTHRIOL DIPHOSPHITE AND A GROUP 22 SALT OF CARBOXYLIC ACID | ALLIED CORPORATION (US) | 1985-01-29 | — | — | US | disclosed |
| US-4493800-A | REACTING A TRIFLUOROMETHYLHALOGENOBENZENE WITH COPPER CYANIDE | DAIKIN KOGYO CO., LTD. (JP) | 1985-01-15 | — | — | US | disclosed |
| US-4441913-A | PRE- AND POST-EMERGENCE | NIHON TOKUSHU NOYAKU SEIZO K.K. (JP) | 1984-04-10 | — | — | US | disclosed |
| EP-0097357-A1 | Process for preparing trifluoromethylbenzene derivatives | Daikin Kogyo Co., Ltd. (JP) | 1984-01-04 | — | — | EP | disclosed |
| EP-0095117-A1 | Phenoxypropionic-acid derivatives, processes for their preparation and their use as herbicides | BAYER AG (DE) | 1983-11-30 | — | — | EP | disclosed |
| EP-0092112-A1 | Substituted phenoxy propionates | NIHON TOKUSHU NOYAKU SEIZO K.K. (JP) | 1983-10-26 | — | — | EP | disclosed |
| EP-0019388-B1 | PREPARATION OF TRIFLUOROMETHYL-SUBSTITUTED PHENOLS AND PHENATES AND THE PREPARATION, FROM THESE PHENOLS AND PHENATES, OF NITRO- AND TRIFLUOROMETHYL-SUBSTITUTED DIPHENYL ETHERS | ROHM AND HAAS COMPANY (US) | 1983-03-23 | — | — | EP | disclosed |
| EP-0069195-A2 | Stabilized ethylene/chlorotrifluoroethylene copolymer composition | Ausimont, U.S.A., Inc. (US) | 1983-01-12 | — | — | EP | disclosed |
| EP-0068260-A2 | Substituted phenoxypropionates, process for their preparation and their use as herbicides | NIHON TOKUSHU NOYAKU SEIZO K.K. (JP) | 1983-01-05 | — | — | EP | disclosed |
| US-4289909-A | Process for preparing 1-dichloroacyl-4-substituted phenoxy benzene and intermediates therefor | CHEVRON RESEARCH (US) | 1981-09-15 | — | — | US | disclosed |
| US-4287213-A | Dichloroacyl diphenyl ether mite ovacides | CHEVRON RESEARCH COMPANY (US) | 1981-09-01 | — | — | US | disclosed |
| US-4262152-A | REACTION OF TRIFLUOROMETHYLHALOBENZENE WITH A BASE IN A COSOLVENT SYSTEM TO YIELD A TRIFLUOROMETHYL PHENOLATE | ROHM AND HAAS COMPANY (US) | 1981-04-14 | — | — | US | disclosed |
| US-4259510-A | TREATING A TRIFLUOROMETHYLHALOBENZENE WITH A HYDROXIDE FOLLOWED BY ETHERIFICATION WITH A HALONITROBENZENE | ROHM AND HAAS COMPANY | 1981-03-31 | — | — | US | disclosed |
| EP-0019388-A1 | Preparation of trifluoromethyl-substituted phenols and phenates and the preparation, from these phenols and phenates, of nitro- and trifluoromethyl-substituted diphenyl ethers | ROHM AND HAAS COMPANY (US) | 1980-11-26 | — | — | EP | disclosed |
| US-4207266-A | CARBON TETRALIDE, HYDROGEN FLUORIDE, LEWIS ACID AD AROMATIC HYDROCARBON | ROHM AND HAAS COMPANY (US) | 1980-06-10 | — | — | US | disclosed |
| US-4155940-A | M-Bromo-benzotrifluorides | BAYER AKTIENGESELLSCHAFT (DE) | 1979-05-22 | — | — | US | disclosed |
| US-4155940-A | M-Bromo-benzotrifluorides | BAYER AKTIENGESELLSCHAFT (DE) | 1979-05-22 | — | — | US | 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 (10 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-20100256142-A1 | SYNTHESIS OF FUNCTIONALIZED OCTAHYDRO-ISOQUINOLIN-1-ONE-8- CARBOXAMIDES, OCTAHYDRO-ISOQUINOLIN-1-ONE-8-CARBOXYLIC ESTERS AND ANALOGS, AND THERAPEUTIC METHODS | OPRM1, OPRK1, OPRL1 | IDO1 167/4885HTR3E 1696/4885HTR3B 553/4885 |
| US-20190127337-A1 | HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE | AOC1, AOC2, AOC3 | IDO1 2681/4885HTR3E 4533/4885HTR3B 4017/4885 |
| US-20140128560-A1 | PROCESS TO PREPARE CROSSLINKABLE TRIFLUOROSTYRENE POLYMERS AND MEMBRANES | STOM, PXMP4, TMSB4X | IDO1 4883/4885HTR3E 4604/4885HTR3B 4496/4885 |
| US-10759765-B2 | Heterocyclic carboxylic acid amide ligand and applications thereof in copper catalyzed coupling reaction of aryl halogeno substitute | AOC1, AOC2, AOC3 | IDO1 2681/4885HTR3E 4533/4885HTR3B 4017/4885 |
| US-20100113834-A1 | chlorinating 3,3,3-trifluoropropionaldehyde with a radical initiator; also producing 3,3,3-trifluoropropionic acid by hydrolysis; useful as an intermediate of medicines and agricultural chemicals and a fluoropolymer | HACL2, CBR3, PFAS | IDO1 2725/4885HTR3E 773/4885HTR3B 1434/4885 |
| US-20060135715-A1 | Trifluorostyrene containing compounds, and their use in polymer electrolyte membranes | PEF1, PHOSPHO1, NHERF1 | IDO1 4878/4885HTR3E 3803/4885HTR3B 4308/4885 |
| US-20180207628-A1 | OXALIC ACID MONOAMIDE LIGAND, AND USES THEREOF IN COUPLING REACTION OF COPPER-CATALYZED ARYL HALOGEN SUBSTITUTE | AOC2, AOC1, AOC3 | IDO1 1005/4885HTR3E 4787/4885HTR3B 4608/4885 |
| US-20090139401-A1 | Single-crystalline organic carboxylic acid metal complex, process for producing the same, and use thereof | CA1, CA3, CA12 | IDO1 2837/4885HTR3E 4308/4885HTR3B 3907/4885 |
| US-20110046247-A1 | CROSSLINKABLE MONOMER | MFAP1, FGB, PFDN6 | IDO1 4862/4885HTR3E 3987/4885HTR3B 3618/4885 |
| US-20080032184-A1 | Stable Trifluorostyrene Containing Compounds, And Their Use In Polymer Electroyte Membranes | NHERF1, AFF1, SLCO2A1 | IDO1 4693/4885HTR3E 2213/4885HTR3B 2353/4885 |
“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.