Synthesis of 20‐Membered Macrocyclic Pseudo‐Natural Products Yields Inducers of LC3 Lipidation-Reference-Cited by-同舟云学术

Synthesis of 20‐Membered Macrocyclic Pseudo‐Natural Products Yields Inducers of LC3 Lipidation

Published:2022-01-25 Issue:11 Volume:134 Page:
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angewandte Chemie

Author:

Niggemeyer Georg¹²,Knyazeva Anastasia³⁴,Gasper Raphael⁵,Corkery Dale³⁴,Bodenbinder Pia¹²,Holstein Julian J.²⁶,Sievers Sonja⁷,Wu Yao‐Wen³⁴,Waldmann Herbert¹²^ORCID

Affiliation:

1. Max Planck Institute of Molecular Physiology Department of Chemical Biology Otto-Hahn-Strasse 11 44227 Dortmund Germany

2. Technical University Dortmund Faculty of Chemistry, Chemical Biology Otto-Hahn-Strasse 6 44221 Dortmund Germany

3. Umeå University Department of Chemistry 90187 Umeå Sweden

4. Umeå University Umeå Center for Microbial Research 90187 Umeå Sweden

5. Max Planck Institute of Molecular Physiology Crystallography and Biophysics Unit Otto-Hahn-Strasse 11 44227 Dortmund Germany

6. Technical University Dortmund Faculty of Chemistry, Inorganic Chemistry Otto-Hahn-Strasse 6 44221 Dortmund Germany

7. Compound Management and Screening Center (COMAS) Otto-Hahn-Strasse 11 44221 Dortmund Germany

Funder

European Research Council

Vetenskapsrådet

Knut och Alice Wallenbergs Stiftelse

Göran Gustafssons Stiftelse för Naturvetenskaplig och Medicinsk Forskning

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202114328

Reference53 articles.

1. Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019

2. Guided by evolution: from biology oriented synthesis to pseudo natural products

3. Pseudo-natural products and natural product-inspired methods in chemical biology and drug discovery

4. Pseudo Natural Products—Chemical Evolution of Natural Product Structure

5. Pseudo Natural Products—Chemical Evolution of Natural Product Structure

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