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EA200601252A1 - Новый класс веществ, вызывающих дифференцировку клеток и являющихся ингибиторами гистондеацетилазы, и способы их применения - Google Patents

Новый класс веществ, вызывающих дифференцировку клеток и являющихся ингибиторами гистондеацетилазы, и способы их применения

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Publication number
EA200601252A1
EA200601252A1 EA200601252A EA200601252A EA200601252A1 EA 200601252 A1 EA200601252 A1 EA 200601252A1 EA 200601252 A EA200601252 A EA 200601252A EA 200601252 A EA200601252 A EA 200601252A EA 200601252 A1 EA200601252 A1 EA 200601252A1
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EA
Eurasian Patent Office
Prior art keywords
group
alkyl
cells
compound
radical
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EA200601252A
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English (en)
Inventor
Виктория М. Ришон
Пол А. Маркс
Ричард А. Рифкинд
Рональд Бреслоу
Сандро Бельведер
Лиланд Гершелл
Томас А. Миллер
Original Assignee
Слоан-Кеттеринг Инститьют Фор Кэнсер Рисёч
Дзе Трастиз Оф Коламбиа Юниверсити Ин Дзе Сити Оф Нью-Йорк
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Application filed by Слоан-Кеттеринг Инститьют Фор Кэнсер Рисёч, Дзе Трастиз Оф Коламбиа Юниверсити Ин Дзе Сити Оф Нью-Йорк filed Critical Слоан-Кеттеринг Инститьют Фор Кэнсер Рисёч
Publication of EA200601252A1 publication Critical patent/EA200601252A1/ru

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    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72Nitrogen atoms
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    • C07C235/72Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atoms of the carboxamide groups bound to acyclic carbon atoms
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • C07C259/06Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
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    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
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    • C07C311/39Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C07C311/42Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
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Abstract

Настоящее изобретение предусматривает соединение, имеющее формулукаждый из радикалов Rи Rявляется фенильной, циклогексильной, циклогексиламино-, нафтильной, пиридинамино-, пиперидиновой, 9-пурин-6-амино-, тиазоламино-, гидроксильной, разветвленной или неразветвленной алкильной, алкенильной, алкилокси-, бензилокси-, фенилалкилокси-, пиридинильной, хинолильной или тиеногруппой, в которых алкил представляет собой метил, этил или t-бутил; где радикал Rявляется гидроксиламино-, гидроксильной, амино-, алкиламино- или алкилоксигруппой, в которых алкил представляет собой метил, этил или t-бутил; где радикал Rявляется атомом водорода, галогеном, фенильной группой или циклогексильной группой; где А могут быть одинаковыми или различными и представлять собой амидную группу или группы -О-, -S-, -NR- или -СН-, где радикал Rявляется C-Cалкилом; в котором n является целым числом от 3 до 10; и где фенильная, нафтильная, хинолильная, алкильная или циклогексильная группы могут быть замещены диметиламиногруппой, или фармацевтически приемлемую соль этого соединения. Настоящее изобретение также предусматривает применение указанного соединения для избирательного индуцирования конечной дифференцировки неопластических клеток и обусловленного этим ингибирования пролиферации этих клеток, а также для лечения опухоли, характеризующейся пролиферацией неопластических клеток, для дифференцировки опухолевых клеток в опухоли и для ингибирования активности гистондеацетилазы. Наконец, настоящее изобретение предусматривает фармацевтическую композицию, включающую фармацевтически приемлемый носитель и терапевтически приемлемое количество вышеуказанного соединения.
EA200601252A 1999-09-08 2000-08-24 Новый класс веществ, вызывающих дифференцировку клеток и являющихся ингибиторами гистондеацетилазы, и способы их применения EA200601252A1 (ru)

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