Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | GAA | P10253 | 1/20 | 0.56 |
| ▸ | ALDH1A1 | P00352 | 6/20 | 0.52 |
| ▸ | KMT2A | Q03164 | 5/20 | 0.52 |
| ▸ | MAPT | P10636 | 4/20 | 0.52 |
| ▸ | KDM4E | B2RXH2 | 3/20 | 0.52 |
| ▸ | HPGD | P15428 | 3/20 | 0.52 |
| ▸ | CYP1A2 | P05177 | 3/20 | 0.48 |
| ▸ | MEN1 | O00255 | 4/20 | 0.47 |
| ▸ | VDR | P11473 | 1/20 | 0.47 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.47 |
| ▸ | POLB | P06746 | 1/20 | 0.46 |
| ▸ | CASP3 | P42574 | 1/20 | 0.44 |
| ▸ | HTT | P42858 | 2/20 | 0.43 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.43 |
| ▸ | XBP1 | P17861 | 1/20 | 0.43 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.43 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.43 |
| ▸ | EHMT2 | Q96KQ7 | 1/20 | 0.43 |
| ▸ | EHMT1 | Q9H9B1 | 1/20 | 0.43 |
| ▸ | F2 | P00734 | 1/20 | 0.43 |
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 | |
|---|---|---|---|---|
| SCHEMBL20768726 | 0.83 | GAA (0.56) | GAAALDH1A1KMT2AMAPTKDM4E | |
| SCHEMBL28985297 | 0.83 | ALDH1A1 (0.45) | GAAALDH1A1KMT2AMAPTKDM4E | |
| SCHEMBL3359433 | 0.81 | GAA (0.54) | GAAALDH1A1KMT2AMAPTKDM4E | |
| SCHEMBL798345 | 0.79 | GAA (0.52) | GAAALDH1A1KMT2AMAPTKDM4E | |
| SCHEMBL17516239 | 0.79 | GAA (0.52) | GAAALDH1A1KMT2AMAPTKDM4E | |
| SCHEMBL3863655 | 0.79 | GAA (0.52) | GAAALDH1A1KMT2AMAPTKDM4E | |
| SCHEMBL19341881 | 0.79 | GAA (0.52) | GAAALDH1A1KMT2AMAPTKDM4E | |
| SCHEMBL14159314 | 0.79 | GAA (0.52) | GAAALDH1A1KMT2AMAPTKDM4E | |
| SCHEMBL12963641 | 0.79 | GAA (0.52) | GAAALDH1A1KMT2AMAPTKDM4E | |
| SCHEMBL13286163 | 0.79 | GAA (0.52) | GAAALDH1A1KMT2AMAPTKDM4E |
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 164 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-10815390-B2 | Polyimide resin composition and varnish produced from terminal-modified imide oligomer prepared using 2-phenyl-4,4′-diaminodiphenyl ether and thermoplastic aromatic polyimide prepared using oxydiphthalic acid, polyimide resin composition molded article and prepreg having excellent heat resistance and mechanical characteristic, and fiber-reinforced composite material thereof | KANEKA CORPORATION (JP) | 2020-10-27 | — | — | US | claimed |
| US-20180273798-A1 | POLYIMIDE RESIN COMPOSITION AND VARNISH PRODUCED FROM TERMINAL-MODIFIED IMIDE OLIGOMER PREPARED USING 2-PHENYL-4,4'-DIAMINODIPHENYL ETHER AND THERMOPLASTIC AROMATIC POLYIMIDE PREPARED USING OXYDIPHTHALIC ACID, POLYIMIDE RESIN COMPOSITION MOLDED ARTICLE AND PREPREG HAVING EXCELLENT HEAT RESISTANCE AND MECHANICAL CHARACTERISTIC, AND FIBER-REINFORCED COMPOSITE MATERIAL THEREOF | KANEKA CORPORATION (JP) | 2018-09-27 | — | — | US | claimed |
| US-10017666-B2 | Polyimide resin composition and varnish produced from terminal-modified imide oligomer prepared using 2-phenyl-4,4′-diaminodiphenyl ether and thermoplastic aromatic polyimide prepared using oxydiphthalic acid, polyimide resin composition molded article and prepreg having excellent heat resistance and mechanical characteristic, and fiber-reinforced composite material thereof | KANEKA CORPORATION (JP) | 2018-07-10 | — | — | US | claimed |
| EP-2025387-B1 | METHOD FOR PRODUCING MONODISPERSE CHELATE RESIN | LANXESS DEUTSCHLAND GMBH (DE) | 2018-04-18 | — | — | EP | claimed |
| EP-2995649-B1 | POLYIMIDE RESIN COMPOSITION COMPRISING TERMINAL-MODIFIED IMIDE OLIGOMER PREPARED USING 2-PHENYL-4,4'-DIAMINODIPHENYL ETHER AND AROMATIC THERMOPLASTIC POLYIMIDE PREPARED USING OXYDIPHTHALIC ACID, VARNISH, POLYIMIDE RESIN COMPOSITION MOLDED ARTICLE HAVING EXCELLENT HEAT RESISTANCE AND MECHANICAL PROPERTIES, PREPREG, AND FIBER-REINFORCED COMPOSITE MATERIAL CONTAINING SAID PREPREG | KANEKA CORP (JP) | 2017-11-08 | — | — | EP | claimed |
| US-20160083618-A1 | POLYIMIDE RESIN COMPOSITION AND VARNISH PRODUCED FROM TERMINAL-MODIFIED IMIDE OLIGOMER PREPARED USING 2-PHENYL-4,4'-DIAMINODIPHENYL ETHER AND THERMOPLASTIC AROMATIC POLYIMIDE PREPARED USING OXYDIPHTHALIC ACID, POLYIMIDE RESIN COMPOSITION MOLDED ARTICLE AND PREPREG HAVING EXCELLENT HEAT RESISTANCE AND MECHANICAL CHARACTERISTIC, AND FIBER-REINFORCED COMPOSITE MATERIAL THEREOF | KANEKA CORPORATION (JP) | 2016-03-24 | — | — | US | claimed |
| EP-2995649-A1 | POLYIMIDE RESIN COMPOSITION COMPRISING TERMINAL-MODIFIED IMIDE OLIGOMER PREPARED USING 2-PHENYL-4,4'-DIAMINODIPHENYL ETHER AND AROMATIC THERMOPLASTIC POLYIMIDE PREPARED USING OXYDIPHTHALIC ACID, VARNISH, POLYIMIDE RESIN COMPOSITION MOLDED ARTICLE HAVING EXCELLENT HEAT RESISTANCE AND MECHANICAL PROPERTIES, PREPREG, AND FIBER-REINFORCED COMPOSITE MATERIAL CONTAINING SAID PREPREG | Kaneka Corporation (JP) | 2016-03-16 | — | — | EP | claimed |
| EP-2097375-B1 | METHOD FOR PURIFYING BISIMIDES | SABIC INNOVATIVE PLASTICS IP (NL) | 2013-04-24 | — | — | EP | claimed |
| US-8177982-B2 | Method of producing monodisperse chelate resins | LANXESS DEUTSCHLAND GMBH (DE) | 2012-05-15 | — | — | US | claimed |
| EP-1078688-B1 | Method for producing monodisperse anion exchangers | LANXESS DEUTSCHLAND GMBH (DE) | 2012-05-09 | — | — | EP | claimed |
| EP-1078690-B1 | Method for producing monodisperse ion exchangers with chelating groups | LANXESS DEUTSCHLAND GMBH (DE) | 2011-10-12 | — | — | EP | claimed |
| EP-2097375-A1 | METHOD FOR PURIFYING BISIMIDES | Sabic Innovative Plastics IP B.V. (NL) | 2009-09-09 | — | — | EP | claimed |
| US-20090045137-A1 | Method of producing monodisperse chelate resins | LANXESS DEUTSCHLAND GMBH (DE) | 2009-02-19 | — | — | US | claimed |
| US-7408070-B2 | Method for purifying bisimides | SABIC INNOVATIVE PLASTICS IP B.V. (US) | 2008-08-05 | — | — | US | claimed |
| WO-2008063208-A1 | METHOD FOR PURIFYING BISIMIDES | SABIC INNOVATIVE PLASTICS IP B.V. (NL) | 2008-05-29 | — | — | WO | claimed |
| EP-1078937-B1 | Process for the preparation of monodisperse crosslinked bead polymers containing thiourea groups and their use for adsorbing metal compounds | LANXESS DEUTSCHLAND GMBH (DE) | 2007-08-15 | — | — | EP | claimed |
| US-20070073063-A1 | Method for purifying bisimides | GENERAL ELECTRIC COMPANY (US) | 2007-03-29 | — | — | US | claimed |
| US-4933469-A | Method for preparing oxybisphthalimides | GENERAL ELECTRIC COMPANY (US) | 1990-06-12 | — | — | US | claimed |
| US-4780544-A | HEATING N-ORGANONITROPHTHALIMIDE IN PRESENCE OF APROTIC SOLVENT IN ALKALI METAL CARBOXYLATE | GENERAL ELECTRIC COMPANY (US) | 1988-10-25 | — | — | US | claimed |
| US-20230374180-A1 | Novel Chelate Resins | LANXESS DEUTSCHLAND GMBH (DE) | 2023-11-23 | — | — | US | disclosed |
| EP-4222182-A1 | NOVEL CHELATE RESINS | LANXESS Deutschland GmbH (DE) | 2023-08-09 | — | — | EP | disclosed |
| CN-116323693-A | Novel chelating resins | 朗盛德国有限责任公司 | 2023-06-23 | — | — | CN | disclosed |
| EP-3898517-B1 | PRODUCTION OF LITHIUM CARBONATE FROM BRINE | LANXESS DEUTSCHLAND GMBH (DE) | 2023-06-14 | — | — | EP | disclosed |
| CN-115175951-A | Resin composition, cured product, prepreg, metal foil-clad laminate, resin sheet, and printed wiring board | 三菱瓦斯化学株式会社 | 2022-10-11 | — | — | CN | disclosed |
| WO-2022069389-A1 | NOVEL CHELATE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2022-04-07 | — | — | WO | disclosed |
| CN-111978240-B | Preparation method of 4,4' -oxo-bis-phthalimide | 南京康德祥医药科技有限公司 | 2022-03-11 | — | — | CN | disclosed |
| US-20220048783-A1 | Production of High Purity Lithium Carbonate from Brines | LANXESS DEUTSCHLAND GMBH (DE) | 2022-02-17 | — | — | US | disclosed |
| EP-3898517-A1 | PRODUCTION OF HIGH PURITY LITHIUM CARBONATE FROM BRINES | LANXESS Deutschland GmbH (DE) | 2021-10-27 | — | — | EP | disclosed |
| US-10882038-B2 | Aluminum-doped, iminoacetic acid group-containing chelate resins | LANXESS DEUTSCHLAND GMBH (DE) | 2021-01-05 | — | — | US | disclosed |
| CN-111978240-A | Preparation method of 4,4' -oxo-bis-phthalimide | 南京康德祥医药科技有限公司 | 2020-11-24 | — | — | CN | disclosed |
| US-10815390-B2 | Polyimide resin composition and varnish produced from terminal-modified imide oligomer prepared using 2-phenyl-4,4′-diaminodiphenyl ether and thermoplastic aromatic polyimide prepared using oxydiphthalic acid, polyimide resin composition molded article and prepreg having excellent heat resistance and mechanical characteristic, and fiber-reinforced composite material thereof | KANEKA CORPORATION (JP) | 2020-10-27 | — | — | US | disclosed |
| WO-2020126974-A1 | PRODUCTION OF HIGH PURITY LITHIUM CARBONATE FROM BRINES | LANXESS DEUTSCHLAND GMBH (DE) | 2020-06-25 | — | — | WO | disclosed |
| EP-3102328-B1 | NOVEL ALUMINIUM DOPED CHELATE RESINS CONTAINING IMINODIACETIC ACID GROUPS | LANXESS DEUTSCHLAND GMBH (DE) | 2020-06-17 | — | — | EP | disclosed |
| US-10478814-B2 | Caesium selective resin | LANXESS DEUTSCHLAND GMBH (DE) | 2019-11-19 | — | — | US | disclosed |
| EP-3319726-B1 | CESIUM-SELECTIVE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2019-09-11 | — | — | EP | disclosed |
| US-20180273798-A1 | POLYIMIDE RESIN COMPOSITION AND VARNISH PRODUCED FROM TERMINAL-MODIFIED IMIDE OLIGOMER PREPARED USING 2-PHENYL-4,4'-DIAMINODIPHENYL ETHER AND THERMOPLASTIC AROMATIC POLYIMIDE PREPARED USING OXYDIPHTHALIC ACID, POLYIMIDE RESIN COMPOSITION MOLDED ARTICLE AND PREPREG HAVING EXCELLENT HEAT RESISTANCE AND MECHANICAL CHARACTERISTIC, AND FIBER-REINFORCED COMPOSITE MATERIAL THEREOF | KANEKA CORPORATION (JP) | 2018-09-27 | — | — | US | disclosed |
| US-20180200709-A1 | NOVEL ALUMINUM-DOPED, IMINOACETIC ACID GROUP-CONTAINING CHELATE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2018-07-19 | — | — | US | disclosed |
| US-20180193828-A1 | CAESIUM SELECTIVE RESIN | LANXESS DEUTSCHLAND GMBH (DE) | 2018-07-12 | — | — | US | disclosed |
| US-10017666-B2 | Polyimide resin composition and varnish produced from terminal-modified imide oligomer prepared using 2-phenyl-4,4′-diaminodiphenyl ether and thermoplastic aromatic polyimide prepared using oxydiphthalic acid, polyimide resin composition molded article and prepreg having excellent heat resistance and mechanical characteristic, and fiber-reinforced composite material thereof | KANEKA CORPORATION (JP) | 2018-07-10 | — | — | US | disclosed |
| US-10017401-B2 | Aluminum-doped, iminodiacetic acid group-containing chelate resins | LANXESS DEUTSCHLAND GMBH (DE) | 2018-07-10 | — | — | US | disclosed |
| EP-3325524-A1 | NOVEL ALUMINUM-DOPED, IMINOACETIC ACID GROUP-CONTAINING CHELATE RESINS | Lanxess Deutschland GmbH (DE) | 2018-05-30 | — | — | EP | disclosed |
| EP-3183275-B1 | SULPHONATED, AMINOMETHYLATED CHELATE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2018-05-23 | — | — | EP | disclosed |
| EP-3319726-A1 | CAESIUM SELECTIVE RESIN | LANXESS Deutschland GmbH (DE) | 2018-05-16 | — | — | EP | disclosed |
| US-9950320-B2 | Sulfonated aminomethylated chelate resins | LANXESS DEUTSCHLAND GMBH (DE) | 2018-04-24 | — | — | US | disclosed |
| EP-2025387-B1 | METHOD FOR PRODUCING MONODISPERSE CHELATE RESIN | LANXESS DEUTSCHLAND GMBH (DE) | 2018-04-18 | — | — | EP | disclosed |
| EP-2995649-B1 | POLYIMIDE RESIN COMPOSITION COMPRISING TERMINAL-MODIFIED IMIDE OLIGOMER PREPARED USING 2-PHENYL-4,4'-DIAMINODIPHENYL ETHER AND AROMATIC THERMOPLASTIC POLYIMIDE PREPARED USING OXYDIPHTHALIC ACID, VARNISH, POLYIMIDE RESIN COMPOSITION MOLDED ARTICLE HAVING EXCELLENT HEAT RESISTANCE AND MECHANICAL PROPERTIES, PREPREG, AND FIBER-REINFORCED COMPOSITE MATERIAL CONTAINING SAID PREPREG | KANEKA CORP (JP) | 2017-11-08 | — | — | EP | disclosed |
| US-20170216833-A1 | SULFONATED AMINOMETHYLATED CHELATE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2017-08-03 | — | — | US | disclosed |
| EP-3183275-A1 | SULFONATED AMINOMETHYLATED CHELATE RESINS | Lanxess Deutschland GmbH (DE) | 2017-06-28 | — | — | EP | disclosed |
| WO-2017013110-A1 | NOVEL ALUMINUM-DOPED, IMINOACETIC ACID GROUP-CONTAINING CHELATE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2017-01-26 | — | — | WO | disclosed |
| EP-3102328-A1 | NOVEL ALUMINUM-DOPED, IMINODIACETIC ACID GROUP-CONTAINING CHELATE RESINS | Lanxess Deutschland GmbH (DE) | 2016-12-14 | — | — | EP | disclosed |
| US-20160347632-A1 | NOVEL ALUMINUM-DOPED, IMINODIACETIC ACID GROUP-CONTAINING CHELATE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2016-12-01 | — | — | US | disclosed |
| US-20160083618-A1 | POLYIMIDE RESIN COMPOSITION AND VARNISH PRODUCED FROM TERMINAL-MODIFIED IMIDE OLIGOMER PREPARED USING 2-PHENYL-4,4'-DIAMINODIPHENYL ETHER AND THERMOPLASTIC AROMATIC POLYIMIDE PREPARED USING OXYDIPHTHALIC ACID, POLYIMIDE RESIN COMPOSITION MOLDED ARTICLE AND PREPREG HAVING EXCELLENT HEAT RESISTANCE AND MECHANICAL CHARACTERISTIC, AND FIBER-REINFORCED COMPOSITE MATERIAL THEREOF | KANEKA CORPORATION (JP) | 2016-03-24 | — | — | US | disclosed |
| EP-2995649-A1 | POLYIMIDE RESIN COMPOSITION COMPRISING TERMINAL-MODIFIED IMIDE OLIGOMER PREPARED USING 2-PHENYL-4,4'-DIAMINODIPHENYL ETHER AND AROMATIC THERMOPLASTIC POLYIMIDE PREPARED USING OXYDIPHTHALIC ACID, VARNISH, POLYIMIDE RESIN COMPOSITION MOLDED ARTICLE HAVING EXCELLENT HEAT RESISTANCE AND MECHANICAL PROPERTIES, PREPREG, AND FIBER-REINFORCED COMPOSITE MATERIAL CONTAINING SAID PREPREG | Kaneka Corporation (JP) | 2016-03-16 | — | — | EP | disclosed |
| WO-2016026804-A1 | SULFONATED AMINOMETHYLATED CHELATE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2016-02-25 | — | — | WO | disclosed |
| EP-2259875-B1 | PICOLYLAMINE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2014-09-24 | — | — | EP | disclosed |
| EP-2630115-B1 | Crosslinking monomers for aliphatic polyamides | NEXAM CHEMICAL AB (SE) | 2014-05-14 | — | — | EP | disclosed |
| CN-103539931-A | Preparation method of catalyst for synthesizing medium and low-molecular weight polyethylene oxide | SHANGHAI LIAN SHENG CHEMICAL CO LTD | 2014-01-29 | — | — | CN | disclosed |
| US-8563622-B2 | Picolylamine resins | LANXESS DEUTSCHLAND GMBH (DE) | 2013-10-22 | — | — | US | disclosed |
| US-8562922-B2 | Picolylamine resins | LANXESS DEUTSCHLAND GMBH (US) | 2013-10-22 | — | — | US | disclosed |
| EP-2259874-B1 | PICOLYLAMINE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2013-10-09 | — | — | EP | disclosed |
| US-20130245140-A1 | CHELATE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2013-09-19 | — | — | US | disclosed |
| US-8440730-B2 | Method for improved removal of cations by means of chelating resins | LANXESS DEUTSCHLAND GMBH (DE) | 2013-05-14 | — | — | US | disclosed |
| EP-2097375-B1 | METHOD FOR PURIFYING BISIMIDES | SABIC INNOVATIVE PLASTICS IP (NL) | 2013-04-24 | — | — | EP | disclosed |
| US-8399528-B2 | Method for improved removal of cations by means of chelating resins | LANXESS DEUTSCHLAND GMBH (DE) | 2013-03-19 | — | — | US | disclosed |
| EP-2089348-B1 | METHOD FOR MAKING POLYETHERIMIDES | SABIC INNOVATIVE PLASTICS IP (NL) | 2013-02-20 | — | — | EP | disclosed |
| CN-101352670-B | Method for producing monodisperse chelate resin | LANXESS DEUTSCHLAND GMBH | 2012-09-12 | — | — | CN | disclosed |
| US-8177982-B2 | Method of producing monodisperse chelate resins | LANXESS DEUTSCHLAND GMBH (DE) | 2012-05-15 | — | — | US | disclosed |
| EP-1078688-B1 | Method for producing monodisperse anion exchangers | LANXESS DEUTSCHLAND GMBH (DE) | 2012-05-09 | — | — | EP | disclosed |
| US-8134016-B2 | Method for purifying dianhydrides | SABIC INNOVATIVE PLASTICS IP B.V. (NL) | 2012-03-13 | — | — | US | disclosed |
| EP-1078690-B1 | Method for producing monodisperse ion exchangers with chelating groups | LANXESS DEUTSCHLAND GMBH (DE) | 2011-10-12 | — | — | EP | disclosed |
| US-20110132844-A1 | METHOD FOR IMPROVED REMOVAL OF CATIONS BY MEANS OF CHELATING RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2011-06-09 | — | — | US | disclosed |
| EP-2094691-B1 | METHOD FOR PURIFYING DIANHYDRIDES | SABIC INNOVATIVE PLASTICS IP (NL) | 2011-05-25 | — | — | EP | disclosed |
| US-20110091365-A1 | PICOLYLAMINE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2011-04-21 | — | — | US | disclosed |
| US-20110089116-A1 | METHOD FOR IMPROVED REMOVAL OF CATIONS BY MEANS OF CHELATING RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2011-04-21 | — | — | US | disclosed |
| US-20110086935-A1 | PICOLYLAMINE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2011-04-14 | — | — | US | disclosed |
| EP-2305382-A1 | Method for improved removal of cations using chelate resins | LANXESS Deutschland GmbH (DE) | 2011-04-06 | — | — | EP | disclosed |
| EP-2305381-A2 | Method for improved removal of cations using chelate resins | Lanxess Deutschland GmbH (DE) | 2011-04-06 | — | — | EP | disclosed |
| EP-2259874-A1 | PICOLYLAMINE RESINS | LANXESS Deutschland GmbH (DE) | 2010-12-15 | — | — | EP | disclosed |
| EP-2259875-A1 | PICOLYLAMINE RESINS | LANXESS Deutschland GmbH (DE) | 2010-12-15 | — | — | EP | disclosed |
| US-20100307979-A1 | CHELATE RESIN | LANXESS DEUTSCHLAND GMBH (DE) | 2010-12-09 | — | — | US | disclosed |
| CN-101778671-A | Chelate resin | LANXESS DEUTSCHLAND GMBH | 2010-07-14 | — | — | CN | disclosed |
| EP-2175994-A2 | CHELATE RESIN | Lanxess Deutschland GmbH (DE) | 2010-04-21 | — | — | EP | disclosed |
| WO-2009109522-A1 | PICOLYLAMINE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2009-09-11 | — | — | WO | disclosed |
| WO-2009109520-A1 | PICOLYLAMINE RESINS | LANXESS DEUTSCHLAND GMBH (DE) | 2009-09-11 | — | — | WO | disclosed |
| EP-2097375-A1 | METHOD FOR PURIFYING BISIMIDES | Sabic Innovative Plastics IP B.V. (NL) | 2009-09-09 | — | — | EP | disclosed |
| EP-2097375-A1 | METHOD FOR PURIFYING BISIMIDES | Sabic Innovative Plastics IP B.V. (NL) | 2009-09-09 | — | — | EP | disclosed |
| EP-2094691-A1 | METHOD FOR PURIFYING DIANHYDRIDES | Sabic Innovative Plastics IP B.V. (NL) | 2009-09-02 | — | — | EP | disclosed |
| EP-2089348-A1 | METHOD FOR MAKING POLYETHERIMIDES | Sabic Innovative Plastics IP B.V. (NL) | 2009-08-19 | — | — | EP | disclosed |
| US-20090045137-A1 | Method of producing monodisperse chelate resins | LANXESS DEUTSCHLAND GMBH (DE) | 2009-02-19 | — | — | US | disclosed |
| EP-2025387-A1 | Method for producing monodisperse chelate resin | LANXESS Deutschland GmbH (DE) | 2009-02-18 | — | — | EP | disclosed |
| WO-2009013142-A2 | CHELATE RESIN | LANXESS DEUTSCHLAND GMBH (DE) | 2009-01-29 | — | — | WO | disclosed |
| CN-101352670-A | Method for producing monodisperse chelate resin | LANXESS DEUTSCHLAND GMBH (DE) | 2009-01-28 | — | — | CN | disclosed |
| US-20080319210-A1 | METHOD FOR PURIFYING DIANHYDRIDES | SHPP GLOBAL TECHNOLOGIES B.V. (NL) | 2008-12-25 | — | — | US | disclosed |
| US-7446214-B2 | Method for purifying oxybisphthalic anhydrides | SABIC INNOVATIVE PLASTICS IP B.V. (US) | 2008-11-04 | — | — | US | disclosed |
| US-20080229882-A1 | Process for Purifying Sulphuric Acids | LANXESS DEUTSCHLAND GMBH (DE) | 2008-09-25 | — | — | US | disclosed |
| US-7411032-B2 | Method for making polyetherimides | SABIC INNOVATIVE PLASTICS IP B.V. (US) | 2008-08-12 | — | — | US | disclosed |
| US-7408070-B2 | Method for purifying bisimides | SABIC INNOVATIVE PLASTICS IP B.V. (US) | 2008-08-05 | — | — | US | disclosed |
| US-7408070-B2 | Method for purifying bisimides | SABIC INNOVATIVE PLASTICS IP B.V. (US) | 2008-08-05 | — | — | US | disclosed |
| WO-2008063208-A1 | METHOD FOR PURIFYING BISIMIDES | SABIC INNOVATIVE PLASTICS IP B.V. (NL) | 2008-05-29 | — | — | WO | disclosed |
| WO-2008063208-A1 | METHOD FOR PURIFYING BISIMIDES | SABIC INNOVATIVE PLASTICS IP B.V. (NL) | 2008-05-29 | — | — | WO | disclosed |
| WO-2008063206-A1 | METHOD FOR MAKING POLYETHERIMIDES | SABIC INNOVATIVE PLASTICS IP B.V. (NL) | 2008-05-29 | — | — | WO | disclosed |
| WO-2008063207-A1 | METHOD FOR PURIFYING DIANHYDRIDES | SABIC INNOVATIVE PLASTICS IP B.V. (NL) | 2008-05-29 | — | — | WO | disclosed |
| US-20080096987-A1 | Method for the Production of Monodispersed Ion Exchangers Containing Pores | LANXESS DEUTSCHLAND GMBH (DE) | 2008-04-24 | — | — | US | disclosed |
| US-20070259046-A1 | Process for removal of solvents from bead polymers | LANXESS DEUTSCHLAND GMBH (DE) | 2007-11-08 | — | — | US | disclosed |
| EP-1852445-A1 | Method for removing solvents from bead polymers | Lanxess Deutschland GmbH (DE) | 2007-11-07 | — | — | EP | disclosed |
| EP-1078937-B1 | Process for the preparation of monodisperse crosslinked bead polymers containing thiourea groups and their use for adsorbing metal compounds | LANXESS DEUTSCHLAND GMBH (DE) | 2007-08-15 | — | — | EP | disclosed |
| US-20070073063-A1 | Method for purifying bisimides | GENERAL ELECTRIC COMPANY (US) | 2007-03-29 | — | — | US | disclosed |
| US-20070073063-A1 | Method for purifying bisimides | GENERAL ELECTRIC COMPANY (US) | 2007-03-29 | — | — | US | disclosed |
| US-20070073035-A1 | Method for making polyetherimides | GENERAL ELECTRIC COMPANY (US) | 2007-03-29 | — | — | US | disclosed |
| US-20070073066-A1 | Method for purifying dianhydrides | GENERAL ELECTRIC COMPANY (US) | 2007-03-29 | — | — | US | disclosed |
| EP-1713845-A2 | METHOD FOR THE PRODUCTION OF MONODISPERSED ION EXCHANGERS CONTAINING PORES | Lanxess Deutschland GmbH (DE) | 2006-10-25 | — | — | EP | disclosed |
| US-7077964-B2 | Process for preparing monodisperse ion exchangers having chelating functional | BAYER AKTIENGESELLSCHAFT (DE) | 2006-07-18 | — | — | US | disclosed |
| EP-1663860-A2 | METHOD FOR THE PURIFICATION OF SULPHURIC ACIDS | Lanxess Deutschland GmbH (DE) | 2006-06-07 | — | — | EP | disclosed |
| US-7053129-B1 | Process for preparing monodisperse anion exchangers | BAYER AKTIENGESELLSCHAFT (DE) | 2006-05-30 | — | — | US | disclosed |
| WO-2005075530-A2 | METHOD FOR THE PRODUCTION OF MONODISPERSED ION EXCHANGERS CONTAINING PORES | LANXESS DEUTSCHLAND GMBH (DE) | 2005-08-18 | — | — | WO | disclosed |
| EP-1203777-B1 | Process for removal of catalyst residues | BAYER INC (CA) | 2005-07-06 | — | — | EP | disclosed |
| WO-2005028362-A2 | METHOD FOR THE PURIFICATION OF SULPHURIC ACIDS | LANXESS DEUTSCHLAND GMBH (DE) | 2005-03-31 | — | — | WO | disclosed |
| EP-1140887-B1 | PHASE TRANSFER CATALYZED METHOD FOR PREPARING OXYBISPHTHALIC COMPOUNDS | GEN ELECTRIC (US) | 2004-09-15 | — | — | EP | disclosed |
| EP-1140887-B1 | PHASE TRANSFER CATALYZED METHOD FOR PREPARING OXYBISPHTHALIC COMPOUNDS | GEN ELECTRIC (US) | 2004-09-15 | — | — | EP | disclosed |
| US-20040082744-A1 | Process for preparing monodisperse ion exchangers having chelating functional | LANXESS DEUTSCHLAND GMBH (DE) | 2004-04-29 | — | — | US | disclosed |
| US-6699913-B1 | REACTING DROPLETS MADE FROM MONOVINYLAROMATIC AND POLYVINYLAROMATIC COMPOUNDS TO GIVE CROSSLINKED BEAD; AMIDOMETHYLATION WITH PHTHALIMIDE DERIVATIVE;LEUCKART-WALLACH-ALKYLATION | BAYER AKTIENGESELLSCHAFT (DE) | 2004-03-02 | — | — | US | disclosed |
| US-6646059-B2 | Utilizing an ion-exchange resin having thiourea functional groups | BAYER INC. (CA) | 2003-11-11 | — | — | US | disclosed |
| US-20020120071-A1 | Process for removing iron-and rhodium-containing catalyst residues from hydrogenated nitrile rubber | LANXESS INC. (CA) | 2002-08-29 | — | — | US | disclosed |
| EP-1203777-A1 | Process for removal of catalyst residues | Bayer Inc. (CA) | 2002-05-08 | — | — | EP | disclosed |
| US-20020035216-A1 | Process for preparing monodisperse, crosslinked bead polymers having thiourea groups and their use for adsorbing metal compounds | KLIPPER REINHOLD (DE) | 2002-03-21 | — | — | US | disclosed |
| US-6329435-B1 | REACTING MONOMER DROPLETS OF MONOVINYLAROMATIC COMPOUND AND POLYVINYLAROMATIC COMPOUND TO GIVE BEAD POLYMER; AMIDOMETHYLATING, CONVERTING TO AMINOMETHYLATED BEAD POLYMER, REACTING WITH THIOUREA OR ITS DERIVATIVE | BAYER AKTIENGESELLSCHAFT (DE) | 2001-12-11 | — | — | US | disclosed |
| US-20010043881-A1 | Process for gas adsorption using aminomethylated bead polymers | BAYER AKTIENGESELLSCHAFT (DE) | 2001-11-22 | — | — | US | disclosed |
| EP-1155728-A1 | Method for gas adsorption using aminomethylated bead polymers | BAYER AG (DE) | 2001-11-21 | — | — | EP | disclosed |
| EP-1140887-A1 | PHASE TRANSFER CATALYZED METHOD FOR PREPARING OXYBISPHTHALIC COMPOUNDS | GENERAL ELECTRIC COMPANY (US) | 2001-10-10 | — | — | EP | disclosed |
| EP-1078937-A1 | Process for the preparation of monodisperse crosslinked bead polymers containing thiourea groups and their use for adsorbing metal compounds | BAYER AG (DE) | 2001-02-28 | — | — | EP | disclosed |
| EP-1078689-A2 | Method for producing monodispersed anion exchangers with strong basic functional groups | BAYER AG (DE) | 2001-02-28 | — | — | EP | disclosed |
| EP-1078690-A2 | Method for producing monodispersed ion exchangers with chelating groups and the use thereof | BAYER AG (DE) | 2001-02-28 | — | — | EP | disclosed |
| EP-1078688-A2 | Method for producing monodispersed anion exchangers | BAYER AG (DE) | 2001-02-28 | — | — | EP | disclosed |
| WO-2000035897-A1 | PHASE TRANSFER CATALYZED METHOD FOR PREPARING OXYBISPHTHALIC COMPOUNDS | GENERAL ELECTRIC COMPANY (US) | 2000-06-22 | — | — | WO | disclosed |
| US-6028203-A | REACTING WITH AN ALKANOATE OR CARBONATE SALT IN A NON-POLAR SOLVENT IN THE PRESENCE OF A HEXAALKYLGUANIDINIUM SALT AS PHASE TRANSFER CATALYST | GENERAL ELECTRIC COMPANY (US) | 2000-02-22 | — | — | US | disclosed |
| US-5574000-A | Cyclohexenone oxime ethers, their preparation and their use as herbicides | BASF AKTIENGESELLSCHAFT (DE) | 1996-11-12 | — | — | US | disclosed |
| US-5563114-A | Cyclohexenone oxime ethers, their preparation, intermediates for their preparation and their use as herbicides | BASF AKTIENGESELLSCHAFT (DE) | 1996-10-08 | — | — | US | disclosed |
| US-5491123-A | Herbicides containing 3-aminobenzo(B)thiophenes as antidotes | BASF AKTIENGESELLSCHAFT (DE) | 1996-02-13 | — | — | US | disclosed |
| US-5378677-A | Applying with cyclohexenone derivative | BASF AKTIENGESELLSCHAFT (DE) | 1995-01-03 | — | — | US | disclosed |
| US-5374609-A | Cyclohexenone oxime ethers and their use as herbicides | BASF AKTIENGESELLSCHAFT (DE) | 1994-12-20 | — | — | US | disclosed |
| EP-0398205-B1 | Polyimides and co-polyimides based on dioxydiphthalic anhydride | OCCIDENTAL CHEM CO (US) | 1994-12-14 | — | — | EP | disclosed |
| US-5364833-A | Controlling grasses in wheat and rice crops | BASF AKTIENGESELLSCHAFT (DE) | 1994-11-15 | — | — | US | disclosed |
| US-5330965-A | Effective against grasses, agricultural use | BASF AKTIENGESELLSCHAFT (DE) | 1994-07-19 | — | — | US | disclosed |
| EP-0330220-B1 | Process for the preparation and recovery of oxydiphthalic anhydrides | OCCIDENTAL CHEM CO (US) | 1994-06-01 | — | — | EP | disclosed |
| US-5250505-A | Particularly effective against grasses; low application rate; high selectivity; nonphytotoxic when used for broad-leaf crops and rice | BASF AKTIENGESELLSCHAFT (DE) | 1993-10-05 | — | — | US | disclosed |
| US-5228896-A | Pre- and postemergence herbicides | BASF AKTIENGESELLSCHAFT (DE) | 1993-07-20 | — | — | US | disclosed |
| US-5212261-A | LATENT, HEAT-CURABLE EPOXY RESIN COMPOSITIONS CONTAINING METAL CARBOXYLATE CURING SYSTEMS | HENKEL RESEARCH CORPORATION (US) | 1993-05-18 | — | — | US | disclosed |
| US-5190573-A | CYCLOHEXENONE OXIME ETHERS, THEIR PREPARATION AND THEIR USE AS HERBICIDES | BASF AKTIENGESELLSCHAFT (DE) | 1993-03-02 | — | — | US | disclosed |
| EP-0495425-A2 | Preparation of diphenyl ether | OCCIDENTAL CHEMICAL CORPORATION (US) | 1992-07-22 | — | — | EP | disclosed |
| WO-1992011307-A1 | LATENT, HEAT-CURABLE EPOXY RESIN COMPOSITIONS CONTAINING METAL CARBOXYLATE CURING SYSTEMS | HENKEL RESEARCH CORPORATION (US) | 1992-07-09 | — | — | WO | disclosed |
| US-5117002-A | PREPARATION OF DIPHENYL ETHER | OCCIDENTAL CHEMICAL CORPORATION (US) | 1992-05-26 | — | — | US | disclosed |
| US-5076831-A | Herbicides | BASF AKTIENGESELLSCHAFT (DE) | 1991-12-31 | — | — | US | disclosed |
| US-5022914-A | Pre- and post-emergence; broad leaf plants; rice | BASF AKTIENGESELLSCHAFT (DE) | 1991-06-11 | — | — | US | disclosed |
| US-5021168-A | Reacting halophthalic anhydride with potassium carbonate | OCCIDENTAL CHEMICAL CORPORATION (US) | 1991-06-04 | — | — | US | disclosed |
| US-5003031-A | Polyimides and co-polyimides based on dioxydiphthalic anhydride | OCCIDENTAL CHEMICAL CORPORATION (US) | 1991-03-26 | — | — | US | disclosed |
| US-4948904-A | REACTING HYDROXYPHTHALIC ANHYDRIDE WITH BROMOPHTHALIC OR FLUOROPHTHALIC ANHYDRIDE IN PRESENCE OF COPPER CATALYST | OCCIDENTAL CHEMICAL CORPORATION (US) | 1990-08-14 | — | — | US | disclosed |
| US-4946985-A | REACTING A HALOPHTHALIC ANHYDRIDE WITH WATER AND ALKALI METAL COMPOUND; COPPER CATALYST | OCCIDENTAL CHEMICAL CORPORATION (US) | 1990-08-07 | — | — | US | disclosed |
| US-4933469-A | Method for preparing oxybisphthalimides | GENERAL ELECTRIC COMPANY (US) | 1990-06-12 | — | — | US | disclosed |
| US-4933469-A | Method for preparing oxybisphthalimides | GENERAL ELECTRIC COMPANY (US) | 1990-06-12 | — | — | US | disclosed |
| US-4933469-A | Method for preparing oxybisphthalimides | GENERAL ELECTRIC COMPANY (US) | 1990-06-12 | — | — | US | disclosed |
| US-4870194-A | HALOPHTHALIC ANHYDRIDE AND POTASSIUM CARBONATE | OCCIDENTAL CHEMICAL CORPORATION (US) | 1989-09-26 | — | — | US | disclosed |
| EP-0330220-A2 | Process for the preparation and recovery of oxydiphthalic anhydrides | OCCIDENTAL CHEMICAL CORPORATION (US) | 1989-08-30 | — | — | EP | disclosed |
| US-4780544-A | HEATING N-ORGANONITROPHTHALIMIDE IN PRESENCE OF APROTIC SOLVENT IN ALKALI METAL CARBOXYLATE | GENERAL ELECTRIC COMPANY (US) | 1988-10-25 | — | — | US | disclosed |
| US-4780544-A | HEATING N-ORGANONITROPHTHALIMIDE IN PRESENCE OF APROTIC SOLVENT IN ALKALI METAL CARBOXYLATE | GENERAL ELECTRIC COMPANY (US) | 1988-10-25 | — | — | US | disclosed |
| US-4780544-A | HEATING N-ORGANONITROPHTHALIMIDE IN PRESENCE OF APROTIC SOLVENT IN ALKALI METAL CARBOXYLATE | GENERAL ELECTRIC COMPANY (US) | 1988-10-25 | — | — | 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 (3 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-20070073063-A1 | Method for purifying bisimides | FHIT, PBRM1, TNS4 | GAA 3931/4885ALDH1A1 4754/4885KMT2A 363/4885 |
| US-20080319210-A1 | METHOD FOR PURIFYING DIANHYDRIDES | AQP4, TRRAP, GYPA | GAA 2045/4885ALDH1A1 2726/4885KMT2A 266/4885 |
| US-20070073066-A1 | Method for purifying dianhydrides | AQP4, TRRAP, GYPA | GAA 2045/4885ALDH1A1 2726/4885KMT2A 266/4885 |
“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.