Magnificamide Is a New Effective Mammalian α-Amylase Inhibitor


Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Somente assinantes

Resumo

Recombinant analogue of the sea anemone Heteractismagnifica peptide was obtained, and the kinetic parameters of its interaction with mammalian α-amylases were determined. Magnificamide inhibits α-amylases significantly stronger than the medical drug acarbose (PrecoseTM or GlucobayTM). Magnificamide is assumed to find application as a drug for prevention and treatment of metabolic disorders and type 2 diabetes mellitus.

Sobre autores

O. Sintsova

Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Sciences

Autor responsável pela correspondência
Email: sintsova0@gmail.com
Rússia, Vladivostok, 690022

E. Leychenko

Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Sciences

Email: sintsova0@gmail.com
Rússia, Vladivostok, 690022

I. Gladkikh

Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Sciences

Email: sintsova0@gmail.com
Rússia, Vladivostok, 690022

A. Kalinovskii

Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Sciences; School of Natural Sciences, Far Eastern Federal University

Email: sintsova0@gmail.com
Rússia, Vladivostok, 690022; Vladivostok, 690091

M. Monastyrnaya

Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Sciences

Email: sintsova0@gmail.com
Rússia, Vladivostok, 690022

E. Kozlovskaya

Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Sciences

Email: sintsova0@gmail.com
Rússia, Vladivostok, 690022

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML

Declaração de direitos autorais © Pleiades Publishing, Inc., 2019