| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 有关电润湿元件的改进 | CN200980136451.5 | 2009-09-18 | CN102159651B | 2015-02-11 | 梅拉妮·玛丽亚·范德魏耶尔-瓦格曼斯; 罗马里克·马萨德; 罗伯特·A·海斯 |
| 一种用于电润湿元件的流体的染料，该染料具有选自式I、II和III构成的组中的通式，其中，Q具有通式：-Het1R1或-Het1R1R2；V具有通式：-Het2R3或-Het2R3R4；Het1和Het2是杂原子；R1和R3是H；R2和R4是任何官能团；T和U是任何官能团；W、X、Y和Z是H或烷基；且F、G、L和M是H或烷基，且条件是染料不具有通式：(IV)。本发明还涉及包含本发明染料的流体，包含该流体的电润湿元件和光学显示器件，以及染料在降低光致漂白中的用途。 | ||||||
| 2 | 染料化合物、流体载体和电润湿设备 | CN201580033383.5 | 2015-06-19 | CN106471003A | 2017-03-01 | 罗宾·勒吉伊特; 于里安·曼斯; 苏克迪普·桑胡 |
| 用于电润湿设备的流体包括至少一种选自由A和B组成的组的化合物，其中R1、R2、R3和R4每一者独立地为烷基。在实例中，流体包括选自(式1)、(式2)、(式3)、(式4)的染料化合物。 | ||||||
| 3 | 有关电润湿元件的改进 | CN200980136451.5 | 2009-09-18 | CN102159651A | 2011-08-17 | 梅拉妮·玛丽亚·范德魏耶尔-瓦格曼斯; 罗马里克·马萨德; 罗伯特·A·海斯 |
| 一种用于电润湿元件的流体的染料，该染料具有选自式Ⅰ、Ⅱ和Ⅲ构成的组中的通式，其中，Q具有通式：-Het1R1或-Het1R1R2；V具有通式：-Het2R3或-Het2R3R4；Het1和Het2是杂原子；R1和R3是H；R2和R4是任何官能团；T和U是任何官能团；W、X、Y和Z是H或烷基；且F、G、L和M是H或烷基，且条件是染料不具有通式：(IV)。本发明还涉及包含本发明染料的流体，包含该流体的电润湿元件和光学显示器件，以及染料在降低光致漂白中的用途。 | ||||||
| 4 | 생체 내 산성 소포체 영상용 이광자 염료 및 이를 이용한생체 내 산성 소포체의 영상화 방법 | KR1020070133747 | 2007-12-18 | KR100924999B1 | 2009-11-04 | 조봉래 |
| 생체 내 산성 소포체 영상용 이광자 염료 및 이를 이용한 이를 이용한 생체 내 산성 소포체의 영상화 방법이 제공된다. 본 발명에 따른 산성 소포체 영상용 이광자 염료는 하기의 구조를 가지며, 시토졸에 존재하는 산성 소포체와 선택적으로 결합하여 높은 강도의 이광자 여기 형광을 발광할 수 있으므로, 산성 소포체의 효과적인 영상화가 가능하다. | ||||||
| 5 | Electrowetting device | US14228776 | 2014-03-28 | US09447282B2 | 2016-09-20 | Robin Leguijt; Romaric Mathieu Massard; Jurriën Mans; Muhammad Arief Adityaputra |
| Electrowetting apparatus including a compound comprising a plurality of colorant moieties and a linker. The plurality of colorant moieties includes a first colorant moiety having a first net dipole and a second colorant moiety having a second net dipole, wherein the plurality of colorant moieties are linked by and disposed around the linker so that the first net dipole and the second net dipole at least partially cancel each other. | ||||||
| 6 | Reducible compounds which provide leuco dyes for analytical compositions, elements and methods of using same | US215140 | 1988-07-05 | US5108903A | 1992-04-28 | Jared B. Mooberry |
| Certain reducible compounds are useful in analytical compositions, elements and methods, for example for the detection of bacterial cells. These compounds comprise a moiety which provides a leuco dye upon reduction. This lecuo dye can then be oxidized with additional molecules of reducible compound in order to provide a detectable dye. Thus, these reducible compounds are considered bioamplifiers from which a multiplicity of dye molecules can be provided from a single reducible compound molecule. Structurally, the reducible compounds are quinones having suitable substituents which promote varying amounts of leuco dye release at physiological pH. | ||||||
| 7 | Thioether naphthoxidine derivatives | US36483964 | 1964-05-04 | US3362967A | 1968-01-09 | HANS BOSSHARD; WERNER BOSSARD |
| 8 | Dyeing or printing synthetic polyamide textile material | US41890764 | 1964-12-16 | US3311444A | 1967-03-28 | REINHOLD KRALLMANN |
| 9 | Process for the preparation of naphthazarin intermediate | US27515639 | 1939-05-23 | US2238959A | 1941-04-22 | WHELEN MYRON S |
| 10 | Dyestuffs of the naphthalene series | US19328838 | 1938-03-01 | US2183870A | 1939-12-19 | RUDOLF ROBL |
| 11 | Dyestuffs of the naphthoquinone series | US37987429 | 1929-07-20 | US1991885A | 1935-02-19 | HOLLAND ELLIS GEORGE; CHARLES OLPIN HENRY; WILLIAM KIRK ERNEST |
| 12 | Green dyestuff and process of making same | US39518220 | 1920-07-09 | US1396483A | 1921-11-08 | VICTOR VILLIGER; VON KRANNICHFELDT HEINRICH |
| 13 | Dyestuffs and process of making same | US26598818 | 1918-12-09 | US1327260A | 1920-01-06 | WHEELER ALVIN S |
| 14 | CDC7 KINASE INHIBITORS AND USES THEREOF | US17330957 | 2021-05-26 | US20210283099A1 | 2021-09-16 | Mark G. Frattini; Hakim Djaballah; Thomas J. Kelly |
| The invention provides compounds, methods, pharmaceutical compositions, and kits for the treatment of proliferative disorders such as cancer. In one aspect, the methods comprise compounds that inhibit the activity of protein kinases, such as cell division cycle (Cdc) kinase. In another aspect, the methods comprise compounds that inhibit Cdc7 and/or Dbf4 activity. In another aspect, the methods comprise compounds that exhibit anti-proliferative properties useful in treating diseases such as cancer. Compounds useful for any of the methods include compounds of the Formula (A) or (B): or pharmaceutically acceptable salts thereof. Exemplary compounds of Formula (A) or (B) include granaticin A, granaticin B, dihydrogranaticin A, dihydrogranaticin B, medermycin, and actinorhodin. | ||||||
| 15 | Carrier fluid compounds and dye compounds for electrowetting apparatus | US14310484 | 2014-06-20 | US10338372B2 | 2019-07-02 | Robin Leguijt; Jurriën Mans; Sukhdip Sandhu |
| Electrowetting apparatus including at least one compound selected from the group consisting of: wherein each of R1, R2, R3 and R4 is independently an alkyl group. In examples a fluid includes a dye compound selected from: | ||||||
| 16 | Process for production of black coloring material and cosmetics containing said black coloring material and use thereof | US838305 | 1992-03-10 | US5358538A | 1994-10-25 | Susumu Shimoyama; Ujo Maeda; Keiko Maeda; Yasuko Noda; Kunio Kataoka; Eiichi Eto; Satoru Shimoyama; Tasuku Shimoyama |
| A process for the production of a black coloring material characterised by treating a compound selected from finely powdered sugar, protein and a polyamide polymer, having amino groups with a naphthoquinone derivative represented by the general formula (1): ##STR1## wherein R.sub.1 represents a hydrogen atom, a hydroxyl group, a halogen atom, or a group represented by the following formula: ##STR2## wherein R.sub.2 represents a hydrogen atom or a hydroxyl group, R.sub.3 represents an alkyl group, an alkenyl group or a hydroxylalkyl group, and n represents 1 or 2; cosmetics comprising a black coloring material produced by the above process; and a process for staining a substrate using the obtained black coloring material. | ||||||
| 17 | Water-soluble cationic naphthoquinoneimine dyestuffs containing a quaternary ammonium group | US3649654D | 1968-12-12 | US3649654A | 1972-03-14 | KELLER HEINZ; GROSSMANN HANS |
| CONDENSATION PRODUCTS OF A PRIMARY PHENYLAMINE WHICH CONTAINS A QUATERNARY AMMONIUM GROUP, AND A COMPOUND OF THE FORMULA
1-(H2N-),2,3,6,7-TETRA(Y-),4-(HO-),5-(X=),8-(O=) NAPHTHALENE 1-(NH=),2,3,6,7-TETRA(Y-),4-(O=),5-(H-X-),8-(HO-) NAPHTHALENE IN WHICH X IS AN OXYGEN ATOM OR THE NH GROUP, AND Y S A HYDROGEN ATOM, A CHLORINE ATOM, ABROMINE ATOM OR A LOWER ALKYL GROUP, ARE SUITABLE FOR DYEING ANIMAL AND HUMAN HAIR, AND PARTICULARLY FOR DYEING LIVING HUMAN HAIR. |
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| 18 | Dyeing composition and method | US1451760 | 1960-03-14 | US3147288A | 1964-09-01 | MAX FROHNSDORFF RAYMOND STANLE |
| 19 | Process for the manufacture of halogenated naphthoquinone-imine | US44743754 | 1954-08-02 | US2764600A | 1956-09-25 | ERNST MERIAN |
| 20 | Condensation products of the naphthoquinone-imine series | US14404250 | 1950-02-13 | US2553050A | 1951-05-15 | VALENTIN KARTASCHOFF; ERNEST MERIAN |
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