Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TYMS | P04818 | 9/20 | 0.63 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.41 |
| ▸ | CYP1A2 | P05177 | 3/20 | 0.41 |
| ▸ | HPGD | P15428 | 2/20 | 0.41 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.41 |
| ▸ | THRB | P10828 | 1/20 | 0.41 |
| ▸ | MEN1 | O00255 | 1/20 | 0.41 |
| ▸ | POLB | P06746 | 1/20 | 0.41 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.41 |
| ▸ | MCL1 | Q07820 | 2/20 | 0.40 |
| ▸ | CES2 | O00748 | 1/20 | 0.40 |
| ▸ | BCHE | P06276 | 1/20 | 0.40 |
| ▸ | CES1 | P23141 | 1/20 | 0.40 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.39 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.39 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.39 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.39 |
| ▸ | ERBB2 | P04626 | 1/20 | 0.38 |
| ▸ | FYN | P06241 | 1/20 | 0.38 |
| ▸ | MAOA | P21397 | 1/20 | 0.38 |
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 | |
|---|---|---|---|---|
| SCHEMBL13009292 | 1.00 | TYMS (0.63) | TYMSALDH1A1CYP1A2HPGDHSD17B10 | |
| SCHEMBL30904850 | 1.00 | TYMS (0.63) | TYMSALDH1A1CYP1A2HPGDHSD17B10 | |
| SCHEMBL30606666 | 0.87 | TYMS (0.52) | TYMSALDH1A1CYP1A2HSD17B10MEN1 | |
| SCHEMBL36626 | 0.87 | TYMS (0.52) | TYMSALDH1A1CYP1A2HSD17B10MEN1 | |
| SCHEMBL31185814 | 0.87 | TYMS (0.52) | TYMSALDH1A1CYP1A2HSD17B10MEN1 | |
| SCHEMBL29349446 | 0.87 | TYMS (0.52) | TYMSALDH1A1CYP1A2HSD17B10MEN1 | |
| SCHEMBL13009255 | 0.87 | TYMS (0.52) | TYMSALDH1A1CYP1A2HSD17B10MEN1 | |
| SCHEMBL12683613 | 0.83 | ALDH1A1 (0.60) | TYMSALDH1A1CYP1A2HPGDHSD17B10 | |
| SCHEMBL1977388 | 0.81 | TYMS (0.67) | TYMSALDH1A1CYP1A2HPGDHSD17B10 | |
| SCHEMBL27948308 | 0.80 | TYMS (0.56) | TYMSALDH1A1CYP1A2HPGDHSD17B10 |
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 134 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118005811-A | Responsive room-temperature phosphorescent polymer material, and preparation method and application thereof | 中国科学院化学研究所 | 2024-05-10 | — | — | CN | claimed |
| CN-105566127-A | Triamine monomer and preparation method and application thereof | UNIV JILIN | 2016-05-11 | — | — | CN | claimed |
| EP-1542975-B1 | 9-CYANO-SUBSTITUTED PERYLENE-3,4-DICARBOXYLIC ACID MONOIMIDES | BASF SE (DE) | 2016-03-09 | — | — | EP | claimed |
| US-7550606-B2 | 9-cyano-substituted perylene-3,4-dicarboxylic acid monoimides | BASF AKTIENGESELLSCHAFT (DE) | 2009-06-23 | — | — | US | claimed |
| US-20090023937-A1 | 9-CYANO-SUBSTITUTED PERYLENE-3,4-DICARBOXYLIC ACID MONOIMIDES | BASF AKTIENGESELLSCHAFT (DE) | 2009-01-22 | — | — | US | claimed |
| US-7446198-B2 | 9-Cyano-substituted perylene-3, 4-dicarboxylic monoimides | BASF AKTIENGESELLSCHAFT (DE) | 2008-11-04 | — | — | US | claimed |
| CN-100400514-C | 9-cyano-substituted perylene-3, 4-dicarboxylic monoimides | BASF AG (DE) | 2008-07-09 | — | — | CN | claimed |
| EP-1019388-B1 | PREPARATION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDES | CIBA SC HOLDING AG (CH) | 2007-03-14 | — | — | EP | claimed |
| US-20060229385-A1 | 9-Cyano-Substituted Perylene-3, 4-Dicarboxylic Monoimides | BASF AKTIENGESELLSCHAFT (DE) | 2006-10-12 | — | — | US | claimed |
| CN-1681792-A | 9-cyano-substituted perylene-3,4-dicarboxylic acid monoimides | BASF AG (DE) | 2005-10-12 | — | — | CN | claimed |
| EP-0854144-B1 | Preparation of perylen-3,4-dicarboxylic acid anhydrides | CIBA SC HOLDING AG (CH) | 2002-07-17 | — | — | EP | claimed |
| EP-0657436-B1 | Process for the preparation of perylene-3,4-dicarboxylic acid derivatives | CIBA SC HOLDING AG (CH) | 2001-12-12 | — | — | EP | claimed |
| EP-1053228-A1 | PERYLENE IMIDE MONOCARBOXYLIC ACIDS AS COLORANTS | Ciba SC Holding AG (CH) | 2000-11-22 | — | — | EP | claimed |
| US-6093834-A | Preparation of perylene-3,4-dicarboxylic acid anhydrides | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2000-07-25 | — | — | US | claimed |
| EP-1019388-A1 | PREPARATION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDES | Ciba SC Holding AG (CH) | 2000-07-19 | — | — | EP | claimed |
| US-5981773-A | REACTING A CORRESPONDING PERYLENE-3,4:9,10-TETRACARBOXYLIC DIANHYDRIDE WITH A STERICALLY HINDERED AMINE, AS A BASE, AT AN ELEVATED TEMPERATURE | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 1999-11-09 | — | — | US | claimed |
| WO-1999031069-A1 | PERYLENE IMIDE MONOCARBOXYLIC ACIDS AS COLORANTS | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 1999-06-24 | — | — | WO | claimed |
| US-5900490-A | Preparation of perylene-3, 4-Dicarboxylic acid anhydrides | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 1999-05-04 | — | — | US | claimed |
| WO-1998031678-A1 | PREPARATION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDES | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 1998-07-23 | — | — | WO | claimed |
| JP-10204076-A | — | — | None | — | — | JP | disclosed |
| US-12018159-B2 | Ultra bright dimeric or polymeric dyes and methods for preparation of the same | Sony Group Corporation (JP) | 2024-06-25 | — | — | US | disclosed |
| US-12018159-B2 | Ultra bright dimeric or polymeric dyes and methods for preparation of the same | Sony Group Corporation (JP) | 2024-06-25 | — | — | US | disclosed |
| CN-118005811-A | Responsive room-temperature phosphorescent polymer material, and preparation method and application thereof | 中国科学院化学研究所 | 2024-05-10 | — | — | CN | disclosed |
| EP-3294811-B1 | ULTRA BRIGHT DIMERIC OR POLYMERIC DYES | SONY GROUP CORP (JP) | 2024-02-28 | — | — | EP | disclosed |
| WO-2023004855-A1 | HIGH-PERFORMANCE BLACK COLOR PASTE AND PREPARATION METHOD THEREFOR | 东莞市彩材科技有限公司 | 2023-02-02 | — | — | WO | disclosed |
| CN-109563106-B | Silver ion carboxylate alkyl primary amine complexes | 柯达公司 | 2021-07-27 | — | — | CN | disclosed |
| CN-109562628-B | Silver ion carboxylate N-heteroaromatic complex and use | 柯达公司 | 2021-07-27 | — | — | CN | disclosed |
| US-20210095130-A1 | ULTRA BRIGHT DIMERIC OR POLYMERIC DYES AND METHODS FOR PREPARATION OF THE SAME | Sony Group Corporation (JP) | 2021-04-01 | — | — | US | disclosed |
| US-10954391-B2 | Water soluble fluorescent or colored dyes and methods for their use | SONY CORPORATION (JP) | 2021-03-23 | — | — | US | disclosed |
| US-10865310-B2 | Ultra bright dimeric or polymeric dyes | SONY CORPORATION OF AMERICA (US) | 2020-12-15 | — | — | US | disclosed |
| US-20200172489-A1 | FLUORESCENT COMPOUND AND AUTOPHAGY DETECTION REAGENT USING SAME | DOJINDO LABORATORIES (JP) | 2020-06-04 | — | — | US | disclosed |
| US-20200172489-A1 | FLUORESCENT COMPOUND AND AUTOPHAGY DETECTION REAGENT USING SAME | DOJINDO LABORATORIES (JP) | 2020-06-04 | — | — | US | disclosed |
| US-20200109287-A1 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | Sony Group Corporation (JP) | 2020-04-09 | — | — | US | disclosed |
| CN-110650946-A | Fluorescent compound and autophagy detection reagent using same | 株式会社同仁化学研究所 | 2020-01-03 | — | — | CN | disclosed |
| US-10435563-B2 | Water soluble fluorescent or colored dyes and methods for their use | SONY CORPORATION (JP) | 2019-10-08 | — | — | US | disclosed |
| US-20190177549-A1 | ULTRA BRIGHT DIMERIC OR POLYMERIC DYES AND METHODS FOR PREPARATION OF THE SAME | Sony Group Corporation (JP) | 2019-06-13 | — | — | US | disclosed |
| US-20180163052-A1 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | Sony Group Corporation (JP) | 2018-06-14 | — | — | US | disclosed |
| US-20180163052-A1 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | Sony Group Corporation (JP) | 2018-06-14 | — | — | US | disclosed |
| US-9978517-B2 | Electro-polarizable compound and capacitor | CAPACITOR SCIENCES INCORPORATED (US) | 2018-05-22 | — | — | US | disclosed |
| US-9978517-B2 | Electro-polarizable compound and capacitor | CAPACITOR SCIENCES INCORPORATED (US) | 2018-05-22 | — | — | US | disclosed |
| US-20180079909-A1 | ULTRA BRIGHT DIMERIC OR POLYMERIC DYES | SONY CORPORATION (JP) | 2018-03-22 | — | — | US | disclosed |
| US-20180079909-A1 | ULTRA BRIGHT DIMERIC OR POLYMERIC DYES | SONY CORPORATION (JP) | 2018-03-22 | — | — | US | disclosed |
| EP-2732480-B1 | WAVELENGTH CONVERTING ELEMENT. | PHILIPS LIGHTING HOLDING BV (NL) | 2018-03-21 | — | — | EP | disclosed |
| WO-2018022925-A1 | ULTRA BRIGHT DIMERIC OR POLYMERIC DYES AND METHODS FOR PREPARATION OF THE SAME | SONY CORPORATION (JP) | 2018-02-01 | — | — | WO | disclosed |
| US-20170327465-A1 | 4-HYDROXYQUINOLINE COMPOUNDS | BASF SE (DE) | 2017-11-16 | — | — | US | disclosed |
| US-20170287637-A1 | ELECTRO-POLARIZABLE COMPOUND AND CAPACITOR | CAPACITOR SCIENCES INCORPORATED | 2017-10-05 | — | — | US | disclosed |
| US-20170287637-A1 | ELECTRO-POLARIZABLE COMPOUND AND CAPACITOR | CAPACITOR SCIENCES INCORPORATED | 2017-10-05 | — | — | US | disclosed |
| EP-3224247-A1 | 4-HYDROXYQUINOLINE COMPOUNDS | BASF SE (DE) | 2017-10-04 | — | — | EP | disclosed |
| US-9765220-B2 | Water soluble fluorescent or colored dyes and methods for their use | SONY CORPORATION (JP) | 2017-09-19 | — | — | US | disclosed |
| US-9765220-B2 | Water soluble fluorescent or colored dyes and methods for their use | SONY CORPORATION (JP) | 2017-09-19 | — | — | US | disclosed |
| EP-2714842-B1 | COLOR CONVERSION FILMS COMPRISING POLYMER-SUBSTITUTED ORGANIC FLUORESCENT DYES | ECOLE POLYTECHNIQUE FED LAUSANNE EPFL (CH) | 2017-02-22 | — | — | EP | disclosed |
| WO-2016183185-A1 | ULTRA BRIGHT DIMERIC OR POLYMERIC DYES | SONY CORPORATION (JP) | 2016-11-17 | — | — | WO | disclosed |
| US-20160208100-A1 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | Sony Group Corporation (JP) | 2016-07-21 | — | — | US | disclosed |
| US-20160208100-A1 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | Sony Group Corporation (JP) | 2016-07-21 | — | — | US | disclosed |
| WO-2016083915-A1 | 4-HYDROXYQUINOLINE COMPOUNDS | BASF SE (DE) | 2016-06-02 | — | — | WO | disclosed |
| CN-105566127-A | Triamine monomer and preparation method and application thereof | UNIV JILIN | 2016-05-11 | — | — | CN | disclosed |
| US-9115869-B2 | Wavelength converting element | KONINKLIJKE PHILIPS N.V. (NL) | 2015-08-25 | — | — | US | disclosed |
| US-8986842-B2 | Color conversion films comprising polymer-substituted organic fluorescent dyes | ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL) (CH) | 2015-03-24 | — | — | US | disclosed |
| WO-2015027176-A1 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | SONY CORPORATION (JP) | 2015-02-26 | — | — | WO | disclosed |
| EP-2617578-B1 | HEAT-SENSITIVE CHROMOGENIC COMPOSITION AND HEAT-SENSITIVE RECORDING MATERIAL FORMED USING SAID COMPOSITION | YAMAMOTO CHEMICALS INC (JP) | 2015-02-25 | — | — | EP | disclosed |
| CN-101351524-B | Use of rylene derivatives as photosensitizers in solar cells | BASF SE | 2015-01-21 | — | — | CN | disclosed |
| US-8888906-B2 | Heat-sensitive color-developing composition and heat-sensitive recording material comprising the composition | YAMAMOTO CHEMICALS, INC. (JP) | 2014-11-18 | — | — | US | disclosed |
| US-8888906-B2 | Heat-sensitive color-developing composition and heat-sensitive recording material comprising the composition | YAMAMOTO CHEMICALS, INC. (JP) | 2014-11-18 | — | — | US | disclosed |
| US-20140153247-A1 | WAVELENGTH CONVERTING ELEMENT | KONINKLIJKE PHILIPS N.V. (NL) | 2014-06-05 | — | — | US | disclosed |
| US-8501046-B2 | Use of rylene derivatives as photosensitizers in solar cells | BASF SE (DE) | 2013-08-06 | — | — | US | disclosed |
| US-20130180430-A1 | HEAT-SENSITIVE COLOR-DEVELOPING COMPOSITION AND HEAT-SENSITIVE RECORDING MATERIAL COMPRISING THE COMPOSITION | YAMAMOTO CHEMICALS, INC. (JP) | 2013-07-18 | — | — | US | disclosed |
| US-20130180430-A1 | HEAT-SENSITIVE COLOR-DEVELOPING COMPOSITION AND HEAT-SENSITIVE RECORDING MATERIAL COMPRISING THE COMPOSITION | YAMAMOTO CHEMICALS, INC. (JP) | 2013-07-18 | — | — | US | disclosed |
| US-8481736-B2 | Liquid crystalline rylene tetracarboxylic acid derivatives and use thereof | BASF SE (DE) | 2013-07-09 | — | — | US | disclosed |
| US-8481736-B2 | Liquid crystalline rylene tetracarboxylic acid derivatives and use thereof | BASF SE (DE) | 2013-07-09 | — | — | US | disclosed |
| US-8481736-B2 | Liquid crystalline rylene tetracarboxylic acid derivatives and use thereof | BASF SE (DE) | 2013-07-09 | — | — | US | disclosed |
| CN-102959660-A | Photoelectric conversion device comprising hydroxamic acid derivative or salt thereof as additive and process for producing same | BASF SE | 2013-03-06 | — | — | CN | disclosed |
| EP-2546901-A1 | Wavelength converting element | Koninklijke Philips Electronics N.V. (NL) | 2013-01-16 | — | — | EP | disclosed |
| US-20120301724-A1 | COLOR CONVERSION FILMS COMPRISING POLYMER-SUBSTITUTED ORGANIC FLUORESCENT DYES | ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL) (CH) | 2012-11-29 | — | — | US | disclosed |
| WO-2012160521-A1 | COLOR CONVERSION FILMS COMPRISING POLYMER-SUBSTITUTED ORGANIC FLUORESCENT DYES | ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL) (CH) | 2012-11-29 | — | — | WO | disclosed |
| US-20120283432-A1 | USE OF RYLENE DERIVATIVES AS PHOTOSENSITIZERS IN SOLAR CELLS | MAX-PLANCK-GESEL. ZUR FOERDERUNG DER WISSEN. E.V. (DE) | 2012-11-08 | — | — | US | disclosed |
| US-20120271003-A1 | Block Copolymers As Thermoplastic Elastomers Made Of Polyisobutene Blocks And Oligoamide Blocks | BASF SE (DE) | 2012-10-25 | — | — | US | disclosed |
| US-20120234380-A1 | TERRYLENE COMPOUNDS, PREPARATION THEREOF AND USE THEREOF IN ORGANIC SOLAR CELLS | BASF SE (DE) | 2012-09-20 | — | — | US | disclosed |
| WO-2012123888-A1 | TERRYLENE COMPOUNDS, PREPARATION THEREOF AND USE THEREOF IN ORGANIC SOLAR CELLS | BASF SE (DE) | 2012-09-20 | — | — | WO | disclosed |
| US-8231809-B2 | Solid p-semiconductors may also be used in the inventive dye-sensitized solar cells without increasing the cell resistance, since the rylene derivatives absorb strongly and therefore require only thin n-semiconductor layers | BASF AKTIENGESELLSCHAFT (DE) | 2012-07-31 | — | — | US | disclosed |
| US-20120138125-A1 | FLUORESCENT SOLAR CONVERSION CELLS BASED ON FLUORESCENT TERYLENE DYES | BASF SE (DE) | 2012-06-07 | — | — | US | disclosed |
| US-20110042651-A1 | LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF | BASF SE (DE) | 2011-02-24 | — | — | US | disclosed |
| US-20110042651-A1 | LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF | BASF SE (DE) | 2011-02-24 | — | — | US | disclosed |
| US-20110042651-A1 | LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF | BASF SE (DE) | 2011-02-24 | — | — | US | disclosed |
| CN-101467276-A | Liquid crystalline rylene tetracarboxylic acid derivatives and use thereof | MAX PLANCK GESELLSCHAFT (DE) | 2009-06-24 | — | — | CN | disclosed |
| US-7550606-B2 | 9-cyano-substituted perylene-3,4-dicarboxylic acid monoimides | BASF AKTIENGESELLSCHAFT (DE) | 2009-06-23 | — | — | US | disclosed |
| US-7550606-B2 | 9-cyano-substituted perylene-3,4-dicarboxylic acid monoimides | BASF AKTIENGESELLSCHAFT (DE) | 2009-06-23 | — | — | US | disclosed |
| US-20090078312-A1 | VERFAHREN ZUR HERSTELLUNG VON MIT RYLENTETRACARBONSAEUREDIIMIDEN BESCHICHTETEN SUBSTRATEN | BASF SE (DE) | 2009-03-26 | — | — | US | disclosed |
| WO-2009027952-A1 | BENZOTERRYLENE DERIVATIVES | SABIC INNOVATIVE PLASTICS IP B.V. (US) | 2009-03-05 | — | — | WO | disclosed |
| US-20090056793-A1 | BENZOTERRYLENE DERIVATIVES | SABIC INNOVATIVE PLASTICS IP BV (NL) | 2009-03-05 | — | — | US | disclosed |
| US-20090056793-A1 | BENZOTERRYLENE DERIVATIVES | SABIC INNOVATIVE PLASTICS IP BV (NL) | 2009-03-05 | — | — | US | disclosed |
| US-20090023937-A1 | 9-CYANO-SUBSTITUTED PERYLENE-3,4-DICARBOXYLIC ACID MONOIMIDES | BASF AKTIENGESELLSCHAFT (DE) | 2009-01-22 | — | — | US | disclosed |
| US-20090023937-A1 | 9-CYANO-SUBSTITUTED PERYLENE-3,4-DICARBOXYLIC ACID MONOIMIDES | BASF AKTIENGESELLSCHAFT (DE) | 2009-01-22 | — | — | US | disclosed |
| US-7446198-B2 | 9-Cyano-substituted perylene-3, 4-dicarboxylic monoimides | BASF AKTIENGESELLSCHAFT (DE) | 2008-11-04 | — | — | US | disclosed |
| US-20080269482-A1 | Use of Rylene Derivatives as Photosensitizers in Solar Cells | BASF SE (DE) | 2008-10-30 | — | — | US | disclosed |
| US-20080245411-A1 | Fluorescent Solar Conversion Cells Based on Fluorescent Terylene Dyes | BASF SE | 2008-10-09 | — | — | US | disclosed |
| CN-100400514-C | 9-cyano-substituted perylene-3, 4-dicarboxylic monoimides | BASF AG (DE) | 2008-07-09 | — | — | CN | 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 |
| EP-1019388-B1 | PREPARATION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDES | CIBA SC HOLDING AG (CH) | 2007-03-14 | — | — | EP | disclosed |
| EP-1019388-B1 | PREPARATION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDES | CIBA SC HOLDING AG (CH) | 2007-03-14 | — | — | EP | disclosed |
| US-7176255-B2 | Method for producing aqueous polymer dispersions containing colorants | BASF AKTIENGESELLSCHAFT (DE) | 2007-02-13 | — | — | US | disclosed |
| US-20060229385-A1 | 9-Cyano-Substituted Perylene-3, 4-Dicarboxylic Monoimides | BASF AKTIENGESELLSCHAFT (DE) | 2006-10-12 | — | — | US | disclosed |
| CN-1681792-A | 9-cyano-substituted perylene-3,4-dicarboxylic acid monoimides | BASF AG (DE) | 2005-10-12 | — | — | CN | disclosed |
| US-20050075453-A1 | Method for producing aqueous polymer dispersions containing colorants | BASF AKTIENGESELLSCHAF (DE) | 2005-04-07 | — | — | US | disclosed |
| US-6727318-B1 | EMULSION POLYMERIZATION OF ETHYLENICALLY UNSATURATED AND DYE-COMPRISING MONOMERS IN PRESENCE OF FREE-RADICAL INITIATORS | BASF AKTIENGESELLSCHAFT (DE) | 2004-04-27 | — | — | US | disclosed |
| EP-0854144-B1 | Preparation of perylen-3,4-dicarboxylic acid anhydrides | CIBA SC HOLDING AG (CH) | 2002-07-17 | — | — | EP | disclosed |
| CN-1281440-A | Perylene imide monocarboxylic acids as colorants | CIBA SC HOLDING AG (CH) | 2001-01-24 | — | — | CN | disclosed |
| US-6166210-A | Perylene imide monocarboxylic acids | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2000-12-26 | — | — | US | disclosed |
| EP-1053228-A1 | PERYLENE IMIDE MONOCARBOXYLIC ACIDS AS COLORANTS | Ciba SC Holding AG (CH) | 2000-11-22 | — | — | EP | disclosed |
| US-6136976-A | REACTING PERYLENE-3,4,9,10-TETRACARBOXYLIC ACID OR ITS ANHYDRIDE WITH AN AMIDE IN PRESENCE OF INTER DILUENT AND TRANSITION METAL CATALYST OR ZINC METAL OR SALT CATALYST UNDER SUPERATMOSPHERIC PRESSURE | BASF AKTIENGESELLSCHAFT (DE) | 2000-10-24 | — | — | US | disclosed |
| US-6093834-A | Preparation of perylene-3,4-dicarboxylic acid anhydrides | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2000-07-25 | — | — | US | disclosed |
| US-6093834-A | Preparation of perylene-3,4-dicarboxylic acid anhydrides | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2000-07-25 | — | — | US | disclosed |
| US-6093834-A | Preparation of perylene-3,4-dicarboxylic acid anhydrides | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2000-07-25 | — | — | US | disclosed |
| EP-1019388-A1 | PREPARATION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDES | Ciba SC Holding AG (CH) | 2000-07-19 | — | — | EP | disclosed |
| EP-1019388-A1 | PREPARATION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDES | Ciba SC Holding AG (CH) | 2000-07-19 | — | — | EP | disclosed |
| CN-1243511-A | Preparation of -3,4-dicarboxylic anhydrides | CIBA SC HOLDING AG (CH) | 2000-02-02 | — | — | CN | disclosed |
| CN-1243511-A | Preparation of -3,4-dicarboxylic anhydrides | CIBA SC HOLDING AG (CH) | 2000-02-02 | — | — | CN | disclosed |
| US-5981773-A | REACTING A CORRESPONDING PERYLENE-3,4:9,10-TETRACARBOXYLIC DIANHYDRIDE WITH A STERICALLY HINDERED AMINE, AS A BASE, AT AN ELEVATED TEMPERATURE | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 1999-11-09 | — | — | US | disclosed |
| US-5981773-A | REACTING A CORRESPONDING PERYLENE-3,4:9,10-TETRACARBOXYLIC DIANHYDRIDE WITH A STERICALLY HINDERED AMINE, AS A BASE, AT AN ELEVATED TEMPERATURE | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 1999-11-09 | — | — | US | disclosed |
| US-5981773-A | REACTING A CORRESPONDING PERYLENE-3,4:9,10-TETRACARBOXYLIC DIANHYDRIDE WITH A STERICALLY HINDERED AMINE, AS A BASE, AT AN ELEVATED TEMPERATURE | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 1999-11-09 | — | — | US | disclosed |
| WO-1999031069-A1 | PERYLENE IMIDE MONOCARBOXYLIC ACIDS AS COLORANTS | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 1999-06-24 | — | — | WO | disclosed |
| US-5900490-A | Preparation of perylene-3, 4-Dicarboxylic acid anhydrides | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 1999-05-04 | — | — | US | disclosed |
| US-5900490-A | Preparation of perylene-3, 4-Dicarboxylic acid anhydrides | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 1999-05-04 | — | — | US | disclosed |
| US-5900490-A | Preparation of perylene-3, 4-Dicarboxylic acid anhydrides | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 1999-05-04 | — | — | US | disclosed |
| CN-1194981-A | Preparation of perylene-3,4-dicarboxylic acid anhydrides | CIBA GEIGY AG (CH) | 1998-10-07 | — | — | CN | disclosed |
| CN-1194981-A | Preparation of perylene-3,4-dicarboxylic acid anhydrides | CIBA GEIGY AG (CH) | 1998-10-07 | — | — | CN | disclosed |
| CN-1194981-A | Preparation of perylene-3,4-dicarboxylic acid anhydrides | CIBA GEIGY AG (CH) | 1998-10-07 | — | — | CN | disclosed |
| JP-H10204076-A | PRODUCTION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDE | CIBA SPECIALTY CHEM HOLDING INC | 1998-08-04 | — | — | JP | disclosed |
| WO-1998031678-A1 | PREPARATION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDES | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 1998-07-23 | — | — | WO | disclosed |
| WO-1998031678-A1 | PREPARATION OF PERYLENE-3,4-DICARBOXYLIC ANHYDRIDES | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 1998-07-23 | — | — | WO | disclosed |
| EP-0854144-A1 | Preparation of perylen-3,4-dicarboxylacid anhydrides | Ciba SC Holding AG (CH) | 1998-07-22 | — | — | EP | disclosed |
| US-5650513-A | Process for preparing perylene-3,4-dicarboxylic acid derivatives, the derivatives thus prepared and their use | CIBA-GEIGY CORPORATION (US) | 1997-07-22 | — | — | US | disclosed |
| US-5650513-A | Process for preparing perylene-3,4-dicarboxylic acid derivatives, the derivatives thus prepared and their use | CIBA-GEIGY CORPORATION (US) | 1997-07-22 | — | — | US | disclosed |
| EP-0657436-A2 | Process for the preparation of perylene-3,4-dicarboxylic acid derivatives, the compounds prepared according to this process and their use | CIBA-GEIGY AG (CH) | 1995-06-14 | — | — | EP | disclosed |
| EP-0657436-A2 | Process for the preparation of perylene-3,4-dicarboxylic acid derivatives, the compounds prepared according to this process and their use | CIBA-GEIGY AG (CH) | 1995-06-14 | — | — | 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 (16 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-10435563-B2 | Water soluble fluorescent or colored dyes and methods for their use | CHRM1, CHRM2, IK | TYMS 947/4885ALDH1A1 357/4885CYP1A2 1000/4885 |
| US-10954391-B2 | Water soluble fluorescent or colored dyes and methods for their use | CHRM1, CHRM2, IK | TYMS 947/4885ALDH1A1 357/4885CYP1A2 1000/4885 |
| US-20180163052-A1 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | CHRM1, CHRM2, IK | TYMS 947/4885ALDH1A1 357/4885CYP1A2 1000/4885 |
| US-20110042651-A1 | LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF | TPR, ROR1, CA3 | TYMS 199/4885ALDH1A1 4792/4885CYP1A2 3691/4885 |
| US-20170287637-A1 | ELECTRO-POLARIZABLE COMPOUND AND CAPACITOR | KCNJ2, KCNE1, KCNN4 | TYMS 3185/4885ALDH1A1 4095/4885CYP1A2 1757/4885 |
| US-20090056793-A1 | BENZOTERRYLENE DERIVATIVES | NR2E3, NR1H3, NR1H2 | TYMS 4159/4885ALDH1A1 715/4885CYP1A2 82/4885 |
| US-20120283432-A1 | USE OF RYLENE DERIVATIVES AS PHOTOSENSITIZERS IN SOLAR CELLS | NR2E3, NR2E1, NR1D2 | TYMS 4147/4885ALDH1A1 4248/4885CYP1A2 168/4885 |
| US-20160208100-A1 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | CHRM1, CHRM2, IK | TYMS 947/4885ALDH1A1 357/4885CYP1A2 1000/4885 |
| US-20090023937-A1 | 9-CYANO-SUBSTITUTED PERYLENE-3,4-DICARBOXYLIC ACID MONOIMIDES | CA9, F9, CA13 | TYMS 3098/4885ALDH1A1 1588/4885CYP1A2 800/4885 |
| US-20060229385-A1 | 9-Cyano-Substituted Perylene-3, 4-Dicarboxylic Monoimides | CBR3, NR2C2, NR0B2 | TYMS 4000/4885ALDH1A1 3964/4885CYP1A2 607/4885 |
| US-20170327465-A1 | 4-HYDROXYQUINOLINE COMPOUNDS | DRD4, NQO2, DRD5 | TYMS 3922/4885ALDH1A1 610/4885CYP1A2 219/4885 |
| US-20200109287-A1 | WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE | CHRM1, CHRM2, IK | TYMS 947/4885ALDH1A1 357/4885CYP1A2 1000/4885 |
| US-20090078312-A1 | VERFAHREN ZUR HERSTELLUNG VON MIT RYLENTETRACARBONSAEUREDIIMIDEN BESCHICHTETEN SUBSTRATEN | AXIN2, NCSTN, NES | TYMS 221/4885ALDH1A1 3203/4885CYP1A2 1813/4885 |
| US-20080269482-A1 | Use of Rylene Derivatives as Photosensitizers in Solar Cells | NR2E3, NR2E1, NR1D2 | TYMS 4154/4885ALDH1A1 4269/4885CYP1A2 173/4885 |
| US-20120234380-A1 | TERRYLENE COMPOUNDS, PREPARATION THEREOF AND USE THEREOF IN ORGANIC SOLAR CELLS | TTI1, C1S, CD4 | TYMS 135/4885ALDH1A1 1813/4885CYP1A2 294/4885 |
| US-20200172489-A1 | FLUORESCENT COMPOUND AND AUTOPHAGY DETECTION REAGENT USING SAME | NR2E3, GPR6, ATG13 | TYMS 4876/4885ALDH1A1 4201/4885CYP1A2 2689/4885 |
“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.