Literature DB >> 27153932

Twelve-membered macrolactones: privileged scaffolds for the development of new therapeutics.

Richard S Brzozowski1, William M Wuest1.   

Abstract

Natural products commonly produced as secondary metabolites of various plants and micro-organisms represent a diverse chemical space of compounds. The diversity of natural products makes them an attractive target for interrogation by both chemists and biologists alike. Indeed, the study of 12-membered macrolactones has already led to the discovery of lead drug compounds and new biological targets, which has motivated the development of diverted total synthetic routes to libraries of analogs. This review explores the discovery, biological characterization, and synthesis of several 12-membered macrolactones, exploiting examples that underscore their importance in the drug discovery field. It is our hope that this review will motivate further interest in this class of natural products, a group of molecules that we think merit the classification of 'privileged scaffolds' within the medicinal chemistry community, to further investigate and develop novel compounds with promising bioactivity.
© 2017 John Wiley & Sons A/S.

Keywords:  antibiotic; biosynthesis; diverted total synthesis; macrolactone; natural product

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Year:  2017        PMID: 27153932     DOI: 10.1111/cbdd.12783

Source DB:  PubMed          Journal:  Chem Biol Drug Des        ISSN: 1747-0277            Impact factor:   2.817


  2 in total

1.  Diverted Total Synthesis of Carolacton-Inspired Analogs Yields Three Distinct Phenotypes in Streptococcus mutans Biofilms.

Authors:  Amy E Solinski; Alexander B Koval; Richard S Brzozowski; Kelly R Morrison; Americo J Fraboni; Carrie E Carson; Anisa R Eshraghi; Guangfeng Zhou; Robert G Quivey; Vincent A Voelz; Bettina A Buttaro; William M Wuest
Journal:  J Am Chem Soc       Date:  2017-05-17       Impact factor: 15.419

2.  Ring Expansion Leads to a More Potent Analogue of Ipomoeassin F.

Authors:  Guanghui Zong; Zhijian Hu; Kwabena Baffour Duah; Lauren E Andrews; Jianhong Zhou; Sarah O'Keefe; Lucas Whisenhunt; Joong Sup Shim; Yuchun Du; Stephen High; Wei Q Shi
Journal:  J Org Chem       Date:  2020-12-02       Impact factor: 4.354

  2 in total

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