Magnificamide Is a New Effective Mammalian α-Amylase Inhibitor


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Abstract

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.

About the authors

O. V. Sintsova

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

Author for correspondence.
Email: sintsova0@gmail.com
Russian Federation, Vladivostok, 690022

E. V. Leychenko

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

Email: sintsova0@gmail.com
Russian Federation, Vladivostok, 690022

I. N. Gladkikh

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

Email: sintsova0@gmail.com
Russian Federation, Vladivostok, 690022

A. P. 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
Russian Federation, Vladivostok, 690022; Vladivostok, 690091

M. M. Monastyrnaya

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

Email: sintsova0@gmail.com
Russian Federation, Vladivostok, 690022

E. P. Kozlovskaya

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

Email: sintsova0@gmail.com
Russian Federation, Vladivostok, 690022

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