Properties of Configurationally Stable Atropoenantiomers in Macrocyclic Natural Products and the Chrysophaentin Family-Reference-Cited by-同舟云学术

Properties of Configurationally Stable Atropoenantiomers in Macrocyclic Natural Products and the Chrysophaentin Family

Published:2023-02-02 Issue:4 Volume:56 Page:414-424
ISSN:0001-4842
Container-title:Accounts of Chemical Research
language:en
Short-container-title:Acc. Chem. Res.

Author:

Bewley Carole A.¹^ORCID,Sulikowski Gary A.²³^ORCID,Yang Zhongyue J.²³^ORCID,Bifulco Giuseppe⁴^ORCID,Cho Hyo-Moon¹,Fullenkamp Christopher R.²^ORCID

Affiliation:

1. Laboratory of Bioorganic Chemistry, 8 Center Drive, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, United States

2. Department of Chemistry, Vanderbilt University, 2213 Garland Avenue, Nashville, Tennessee 37235, United States

3. Vanderbilt Institute of Chemical Biology, Vanderbilt University, 7330 Stevenson Center, Nashville, Tennessee 37235, United States

4. Dipartimento di Farmacia, Università di Salerno, via Giovanni Paolo II 132, 84084 Fisciano (SA), Italy

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Vanderbilt Institute of Chemical Biology, Vanderbilt University

Publisher

American Chemical Society (ACS)

Subject

General Medicine,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.2c00648

Reference37 articles.

1. Chrysophaentins A−H, Antibacterial Bisdiarylbutene Macrocycles That Inhibit the Bacterial Cell Division Protein FtsZ

2. Chrysophaentins are competitive inhibitors of FtsZ and inhibit Z-ring formation in live bacteria

3. Antimicrobial Chrysophaentin Analogs Identified from Laboratory Cultures of the Marine Microalga Chrysophaeum taylorii

4. Synthesis of 9-Dechlorochrysophaentin A Enables Studies Revealing Bacterial Cell Wall Biosynthesis Inhibition Phenotype in B. subtilis

5. Retrospective analysis of natural products provides insights for future discovery trends

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