Antidiabetic profiling of veramycins, polyketides accessible by biosynthesis, chemical synthesis and precursor-directed modification

Author:

Dardić Denis1,Böhringer Nils23,Plaza Alberto1,Zubeil Florian1,Pohl Juliane12,Sommer Svenja12,Padva Leo12,Becker Jonathan2,Patras Maria A.1,Bill Mona-Katharina1,Kurz Michael4,Toti Luigi5,Görgens Sven W.4,Schuler Sören M. M.1,Billion André1,Schwengers Oliver2ORCID,Wohlfart Paulus5,Goesmann Alexander2,Tennagels Norbert5,Vilcinskas Andreas12,Hammann Peter E.5,Schäberle Till F.123ORCID,Bauer Armin4ORCID

Affiliation:

1. Fraunhofer Institute for Molecular Biology and Applied Ecology (IME), Branch for Bioresources, 35392 Gießen, Germany

2. Justus-Liebig-University Gießen, 35392 Gießen, Germany

3. German Center of Infection Research (DZIF), Partner Site Gießen-Marburg-Langen, 35392 Gießen, Germany

4. Sanofi-Aventis Deutschland GmbH, R&D Integrated Drug Discovery, 65926 Frankfurt am Main, Germany

5. Sanofi-Aventis Deutschland GmbH, R&D German Hub, 65926 Frankfurt am Main, Germany

Abstract

New polyketides, termed veramycins, were isolated along with their known congeners NFAT-133 and TM-123. Total synthesis from a central building block was accomplished, the BGC identified and a biosynthetic pathway for this molecule class proposed.

Funder

Hessisches Ministerium für Wissenschaft und Kunst

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

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