子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 101 | Stabilized adducts of menadione bisulfite with p-aminobenzoic acid or adenine | US518769 | 1983-08-02 | US4577019A | 1986-03-18 | Enrico Bruschi |
| Stabilized adducts of K vitaminic compounds, as menadione bisulfite or a derivative thereof and stabilizing vitamins as, particularly, nicotine amide or nicotinic acid. Feed compositions containing the same. Process for their preparation. | ||||||
| 102 | Binucleating ligand-metal complexes as oxidation catalysts | US659396 | 1984-10-10 | US4545937A | 1985-10-08 | John E. Bulkowski |
| There is taught a class of homogeneous oxidation catalysts characterized by the presence therein of two chelated cations of Cu(I) in each molecule. | ||||||
| 103 | Oxidation process of reactive aromatics with reactivation of the catalyst using potassium permanganate | US403615 | 1982-07-23 | US4477380A | 1984-10-16 | Ulrich Knips; Bertram Bohmer; Roland Herzberg |
| In the oxidation of reactive aromatics with molecular oxygen in carboxylic acid solution in the presence of a catalyst consisting of a cobalt compound and possibly with addition of a manganese and a bromine compound suitable as Co-catalyst, an inactivation of the catalyst system readily occurs. This is prevented in that after each reaction cycle the catalyst is reactivated by treatment with a strong oxidant and the water formed in the reaction is removed by distillation. | ||||||
| 104 | Quinone compounds and their use in suppressing the production of SRS-A in mammals | US248042 | 1981-03-26 | US4393075A | 1983-07-12 | Shinji Terao; Mitsuru Shiraishi; Yoshitaka Maki |
| New quinone compounds of the formula: ##STR1## wherein R.sup.1 is methyl or methoxy, or the two R.sup.1 groups jointly represent --CH.dbd.CH--CH.dbd.CH--; X is --CH.dbd.CH-- or --C.dbd.C--; Y.sup.1 is hydrogen, hydroxyl, carboxyl, cyano, acyloxy or --COZ in which Z is amino which may be substituted; m is zero or an integer of 1 to 3; n is zero or an integer of 1 to 10; n' is an integer of 1 to 5; k is an integer of 1 to 3; and when k is 2 or 3, n' is optionally variable within the range of 1 to 5 in each occurrence of the --X--(CH.sub.2).sub.n' group; and their hydroquinone forms and salts, have useful physiological activities such as antiasthmatic, antiallergic and bloodpressure decreasing activities. | ||||||
| 105 | Substituted ortho-quinone dimer | US62333 | 1979-07-31 | US4362668A | 1982-12-07 | Richard J. Lee |
| Ortho-quinones with alkyl, olefin polymer, or halogen substituents and a process for the preparation of these compounds comprising a base catalyzed halogen oxidation of alkylated phenol. | ||||||
| 106 | Manufacture of pyranthrones | US3673220D | 1970-10-09 | US3673220A | 1972-06-27 | BOCK GUSTAV |
| A new process for the manufacture of pyranthrones (I) from 2,2'' -dialkyl-1,1''-dianthraquinonyls (II) by heating (II) at from 150* to 210* C. in polar organic solvents in the presence of alkali metal acetates.
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| 107 | METHOD FOR MINIMIZING FOULING, CORROSION, AND SOLVENT DEGRADATION IN LOW-TEMPERATURE REFINERY AND NATURAL GAS PROCESSES | PCT/US2020/065184 | 2020-12-16 | WO2021126892A1 | 2021-06-24 | SORIA, John |
A method of oxygen scavenging, the method (i) providing an oxygen scavenger composition; and (ii) adding the oxygen scavenger composition to an aqueous feed and/or a hydrocarbon feed of a hydrocarbon processing system. |
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| 108 | MITOCHONDRIA-TARGETED ATOVAQUONE: A MORE POTENT AND MORE EFFECTIVE ANTITUMOR, ANTIMICROBIAL, AND ANTIMALARIAL DRUG | PCT/US2020/057363 | 2020-10-26 | WO2021081500A1 | 2021-04-29 | KALYANARAMAN, Balaraman; CHENG, Gang; HARDY, Micael Joël |
The present invention provides novel mitochondria-targeted Atovaquone compounds (Mito-ATO), a mitochondria-targeted derivative of Atovaquone, and methods of using such compounds. Methods of treating cancer using mito-ATO are also provided. Methods of enhancing an anti-tumor immune response by administering mito-ATO are further provided. |
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| 109 | 氨基亚甲基环己烷1,3-二酮化合物的用途 | PCT/CN2018/087452 | 2018-05-18 | WO2018214814A1 | 2018-11-29 | 罗成; 乐立艳; 万伟; 张元元; 蒋华良; 陈凯先 |
氨基亚甲基环己烷1,3-二酮化合物的用途，具体涉及下式(I)所示化合物或其药学上可接受的盐单独或者与其他药物联合在制备调节细胞自噬及治疗细胞自噬，特别是哺乳动物ATG8同源蛋白，相关的疾病的药物中的用途。 |
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| 110 | INHIBITORS OF APURINIC/APYRIMIDINIC ENDONUCLEASE 1 (APE1) AND THEIR USE | PCT/GB2011/052386 | 2011-12-02 | WO2012073041A3 | 2012-06-07 | MADHUSUDAN, Srinivasan; FISCHER, Peter; LAUGHTON, Charles |
The invention provides a compound with the structural formula of any one of Formula 1 to Formula 18 or a pharmaceutically acceptable salt thereof, and uses thereof. |
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| 111 | METHODS FOR PREPARING HYPERICIN | PCT/US2010/048937 | 2010-09-15 | WO2011034922A1 | 2011-03-24 | TOBIA, Alfonso, J.; CABANA, Bernard, E.; VADLAPATLA, Venkata; CONNOLLY, Ronald, H. |
The present invention provides a method for making hypericin comprising the steps of converting a protohypericin to a protohypericin salt, and irradiating the protohypericin salt with visible light to form hypericin. The present invention also provides an apparatus comprising a transparent column having a top end and a bottom end, an inlet attached to the column at the top end to flow reactants into the column, a container attached to the column at the bottom end; and a visible light source positioned to cast light on to the column. The present invention further provides a method for making hypericin using said apparatus. |
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| 112 | Vitamin E acetate intermediates 2,3,5-trimethylbenzoquinone synthesis method | IES20180121 | 2018-04-04 | IES20180121A2 | 2019-06-12 | FEI PENG |
| The present invention discloses vitamin E acetate intermediates 2,3,5-trimethylbenzoquinone synthesis method by 2-methyl-4-hydroxy-3,6-dimethylol toluene, 2,5-hexanediol solution were added to the reaction vessel, controlled the stirring speed, raising the solution temperature, added molybdenum disulfide powder, raised the temperature of the solution, kept for 90-140 min; extracted with N-methylaniline solution for several times, washed with 2-methylpyridine solution for several times, standing for stratification, recrystallized in 3-methyl-2-butanol solution, dehydrated with dehydrating agent, finally got finished product 2, 3,5 -trimethyl benzoquinone. | ||||||
| 113 | ПРОИЗВОДНЫЕ 2-ГИДРОКСИ-3-ФЕНИЛЭТИНИЛТИО (СЕЛЕНО)-1,4-ХИНОНОВ В КАЧЕСТВЕ ПОВЕРХНОСТНО-АКТИВНЫХ ВЕЩЕСТВ И МОЮЩЕЕ СРЕДСТВО ИХ СОДЕРЖАЩЕЕ | RU2013152521 | 2013-11-26 | RU2547823C1 | 2015-04-10 | ZACHINJAEV JAROSLAV VASIL EVICH; KHARITONENKO ALEKSANDR LEONIDOVICH; SERGIENKO JURIJ VLADIMIROVICH; TITOVA TAMILA SEMENOVNA; ZACHINJAEVA ANNA VLADIMIROVNA; KOVALEVA LJUDMILA IVANOVNA |
| Предложеныпроизводные 2-гидрокси-3-фенилэтинилтио(селено)-1,4-хиноновв качествеповерхностно-активныхвеществв составемоющегосредствадляочисткинефтеналивногооборудованияотзагрязненийорганическойи неорганическойприроды. Такжепредложеномоющеесредстводляочисткинефтеналивногооборудованияотзагрязненийорганическойи неорганическойприроды, включающеесиликатнатрия, карбонатнатрия, смачивательОП-10, поверхностно-активноевеществои воду, причемв качествеповерхностно-активноговеществаоносодержитприследующемсодержанииперечисленныхкомпонентов, мас.%: силикатнатрия - 0,70-0,75, карбонатнатрия - 3,5-3,75, смачивательОП-10 - 0,23-0,25, производное 2-гидрокси-3-фенилэтинилтио(селено)-1,4-хинонов - 0,23-0,25, вода - остальное. Техническийрезультат - полнаяочисткаочищаемыхповерхностейприминимальномрасходемоющегосредстваи сокращениевремениееобработки. 2 н.п. ф-лы, 1 табл. | ||||||
| 114 | ПРИМЕНЕНИЕ АЛЮМИНИЯ АЗОТНОКИСЛОГО В КАЧЕСТВЕ УСИЛИТЕЛЯ ДЕЙСТВИЯ АЗОТА И КАК СИСТЕМНОГО АКТИВАТОРА МОРФОГЕНЕТИЧЕСКИХ ПРОЦЕССОВ РАСТЕНИЙ И УДОБРЕНИЕ НА ЕГО ОСНОВЕ | UAA201001780 | 2010-02-19 | UA96494C2 | 2011-11-10 | MAZILNIKOV HENNADII VASYLIOVYCH; SHYMANSKYI ARKADII PETROVYCH; LYKHODID YURII ANATOLIIOVYCH; MELNYK STEFANIIA STEFANIVNA |
| Применениеалюминияазотнокислогов качествеусилителядействияазотаи каксистемногоактиватораморфогенетическихпроцессоврастенийи удобрение, содержащееалюминийазотнокислый, гидрохинон, ортованадатнатрияи гидроксидкалия. | ||||||
| 115 | Sposób wytwarzania 2-hydroksy-3-(3-metylobuten-2-yl)naftochinonu-1,4 | PL38139506 | 2006-12-27 | PL207841B1 | 2011-02-28 | BORUSZCZAK ZYGMUNT |
| 116 | Perylenequinone derivatives and uses thereof | GB0802753 | 2006-07-28 | GB2442915B | 2009-12-16 | SHARMA SANJAY K; WOO THOMAS; NAICKER SELVARAJ |
| The present invention relates to compounds which are perylenequinone derivatives, their stereoisomers and atropisomers. These compounds can be particularly useful as photosensitizers or sononsensitizers in photodynamic or sonodynamic therapy. The invention also relates to various methods for using these compounds in photodynamic and/or sonodynamic therapy. The compounds also are useful as therapeutic agents for treating various hyperproliferative disorders. | ||||||
| 117 | DERIVATIVES OF 3-ARYL-2,5-DIHYDROXY-1,4-BENZOQUINONE, METHOD FOR SYNTHESIS AND PHARMACEUTICAL COMPOSITION | UA20040907252 | 2003-02-04 | UA79448C2 | 2007-06-25 | DASSONVILLE ALEXANDRA; BRETECHE ANNE; DUFLOS MURIEL; LE BAUT GUILLAUME; PFEIFFER BRUNO; RENARD PIERRE; LEVENS NIGEL; HUSSON-ROBERT BERNADETTE |
| The invention concerns a compound of formula (I), wherein: R1 and R2, identical or different, represent each a hydrogen atom or an acyl or alkyl group; Ar represents an aryl or heteroaryl group; A represents a group selected from formula (II); R4 represents a hydrogen atom or an alkyl group; R5 represents a hydrogen atom or a group selected among alkyl, aryl and heteroaryl; R3 represents an aryl, heteroaryl, dicyclopropylmethyl or benzhydryl group, or A-R3 represents an optionally substituted naphthyl group, excluding 2,5-dihydioxy-3-(4-methoxyphenyl)-6-(2-phenylethenyl)-1,4-benzoquinone, 2,5-dihydroxy-3-(4-methoxyphenyl)-6-(2-naphthyl)-1,4-benzoquinone, and 2,5-dihydroxy-3 (2-naphthyl)-6-phenyl-1,4-benzoquinone. The inventive compound is useful for preparing medicines. | ||||||
| 118 | BRPI0502766 | 2005-06-20 | BRPI0502766A | 2007-02-21 | VARGAS MARIA DOMINGUES; PINTO ANGELO DA CUNHA; CAMARA CELSO AMORIM; CARVALHO JOAO ERNESTO DE; KOHN LUCIANA KONECNY | |
| 119 | Perylenequinone derivatives and uses thereof | AU2006279189 | 2006-07-28 | AU2006279189A1 | 2007-02-15 | SHARMA SANJAY K; WOO THOMAS; NAICKER SELVARAJ |
| 120 | OA9800080 | 1998-06-12 | OA10696A | 2002-11-26 | BOUTHERIN-FALSON ODILE; DESQUAND-BILLIALD STEPHANIE; FAVROU ANITA; FINET MICHEL; TEMBO OLIVIER; TORREGROSA JEAN LUC; YANNIC-ARNOULT SYLVIE; DOMAGALA-LE MARQUER FLORENCE | |
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