Synthesis of Phosphoisosteres of Amyloid Dipeptide Components

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Abstract

A simple and effective method was proposed for the synthesis of new phosphinic peptides in free form, structural isosteres of the dipeptide components of beta-amyloid (Aβ42), potential inhibitors of zinc-metalloproteinases.

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About the authors

S. R. Golovash

Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences

Email: rvalery@dio.ru
Russian Federation, Chernogolovka

D. E. Ivanov

Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences

Email: rvalery@dio.ru
Russian Federation, Chernogolovka

A. V. Borodachev

Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences

Email: rvalery@dio.ru
ORCID iD: 0000-0002-3458-5129
Russian Federation, Chernogolovka

V. I. Shestov

Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences

Email: rvalery@dio.ru
Russian Federation, Chernogolovka

M. E. Dmitriev

Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences

Email: rvalery@dio.ru
ORCID iD: 0000-0001-8870-195X
Russian Federation, Chernogolovka

V. V. Ragulin

Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences

Author for correspondence.
Email: rvalery@dio.ru
ORCID iD: 0000-0002-3967-1034
Russian Federation, Chernogolovka

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