Discovery of a Small Molecule Insulin Mimetic with Antidiabetic Activity in Mice

Author:

Zhang Bei1,Salituro Gino2,Szalkowski Deborah1,Li Zhihua1,Zhang Yan2,Royo Inmaculada3,Vilella Dolores3,Dı́ez Maria Teresa3,Pelaez Fernando3,Ruby Caroline2,Kendall Richard L.4,Mao Xianzhi4,Griffin Patrick5,Calaycay Jimmy5,Zierath Juleen R.6,Heck James V.2,Smith Roy G.1,Moller David E.1

Affiliation:

1. Department of Molecular Endocrinology,

2. Department of Natural Product Drug Discovery,

3. Centro de Investigación Básica, Merck, Sharp & Dohme de España, S. A. Josefa Valcárcel 38, Madrid 28027, Spain.

4. Department of Cancer Research, Merck Research Laboratories, Post Office Box 4, West Point, PA 19486, USA.

5. Department of Molecular Diversity and Design, Merck Research Laboratories, R80W250, Post Office Box 2000, Rahway, NJ 07065, USA.

6. Department of Clinical Physiology, Karolinska Hospital, Karolinska Institute, S-171 76 Stockholm, Sweden.

Abstract

Insulin elicits a spectrum of biological responses by binding to its cell surface receptor. In a screen for small molecules that activate the human insulin receptor tyrosine kinase, a nonpeptidyl fungal metabolite (L-783,281) was identified that acted as an insulin mimetic in several biochemical and cellular assays. The compound was selective for insulin receptor versus insulin-like growth factor I (IGFI) receptor and other receptor tyrosine kinases. Oral administration of L-783,281 to two mouse models of diabetes resulted in significant lowering in blood glucose levels. These results demonstrate the feasibility of discovering novel insulin receptor activators that may lead to new therapies for diabetes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference28 articles.

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