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[ANSA analysis. II. Aminonaphthalenesulfonamides–detecting groups for polysubstrate analysis of proteases]статья
Дата последнего поиска статьи во внешних источниках: 29 мая 2015 г.
- Авторы: Trushkin A.M., Kazantsev A.G., Kuznetsov N.V., Iakhimovich A.D., Moguchaia G.I.u, Rodina E.V., Gridneva N.A., Sharina I.G., Nedospasov A.A.
- Журнал: Biochemistry (Moscow)
- Том: 59
- Номер: 10
- Год издания: 1994
- Издательство: Pleiades Publishing, Ltd
- Местоположение издательства: Road Town, United Kingdom
- Первая страница: 1521
- Последняя страница: 1534
- Аннотация: The properties and synthetic methods of aminonaphthalenesulfonamides (ANSA) used as detectable groups of protease substrates are described. A list of chemical and physical properties of seventeen 5.1-ANSA with simple substituents is presented. A comparison of condition for the introduction and removal of acyl protecting groups (acetyl, trifluoroacetyl, phthaloyl, carbobenzoxy) used in ANSA synthesis is given. Examples of applicability of nitronaphthalenesulfonamides as intermediate compounds are given. The possibility of ANSA alkylation at both N(C) and N(S) is demonstrated. Substituted ANSA--sulfonylaziridenes--are used for the production of water-soluble derivatives containing the alcoxy group in the sulfonamide fragment. Criteria for the selection of detectable groups for polysubstrate analysis are discussed. Eighteen typical procedures for ANSA synthesis according to the schemes discussed are presented.
- Добавил в систему: Родина Елена Валерьевна