Literature DB >> 30133094

Synthesis, Structural Reassignment, and Antibacterial Evaluation of 2,18-Seco-Lankacidinol B.

Yanmin Yao1, Lingchao Cai1, Ian B Seiple1.   

Abstract

Lankacidins are a group of polyketide natural products with activity against several strains of Gram-positive bacteria. We developed a route to stereochemically diverse variants of 2,18-seco-lankacidinol B and found that the stereochemical assignment at C4 requires revision. This has interesting implications for the biosynthesis of natural products of the lankacidin class, all of which possessed uniform stereochemistry prior to this finding. We have evaluated 2,18-seco-lankacidinolB and three stereochemical derivatives against a panel of pathogenic Gram-positive and Gram-negative bacteria.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  antibiotics; biosynthesis; natural products; structural reassignment; total synthesis

Mesh:

Substances:

Year:  2018        PMID: 30133094      PMCID: PMC6494672          DOI: 10.1002/anie.201808612

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  18 in total

1.  Total synthesis of (+)-ambruticin.

Authors:  P Liu; E N Jacobsen
Journal:  J Am Chem Soc       Date:  2001-10-31       Impact factor: 15.419

2.  Extensive mutational analysis of modular-iterative mixed polyketide biosynthesis of lankacidin in Streptomyces rochei.

Authors:  Satoshi Tatsuno; Kenji Arakawa; Haruyasu Kinashi
Journal:  Biosci Biotechnol Biochem       Date:  2009-12-07       Impact factor: 2.043

3.  Synthesis of the macrocyclic core of leiodermatolide.

Authors:  Ian Paterson; Tanya Paquet; Stephen M Dalby
Journal:  Org Lett       Date:  2011-07-14       Impact factor: 6.005

4.  Synthetic Studies toward the C14-C29 Fragment of Mirabalin.

Authors:  Johan Cornil; Pierre-Georges Echeverria; Sébastien Reymond; Phannarath Phansavath; Virginie Ratovelomanana-Vidal; Amandine Guérinot; Janine Cossy
Journal:  Org Lett       Date:  2016-09-07       Impact factor: 6.005

5.  Studies on T-2636 antibiotics. II. Isolation and chemical properties of T-2636 antibiotics.

Authors:  S Harada; T Kishi; K Mizuno
Journal:  J Antibiot (Tokyo)       Date:  1971-01       Impact factor: 2.649

6.  Cyclization mechanism for the synthesis of macrocyclic antibiotic lankacidin in Streptomyces rochei.

Authors:  Kenji Arakawa; Fuminori Sugino; Kazuya Kodama; Tatsuya Ishii; Haruyasu Kinashi
Journal:  Chem Biol       Date:  2005-02

7.  Gram-scale synthesis of iejimalide B.

Authors:  Julien Gagnepain; Emilie Moulin; Alois Fürstner
Journal:  Chemistry       Date:  2011-05-09       Impact factor: 5.236

8.  Side chain modifications in lankacidin group antibiotics.

Authors:  J W McFarland; D K Pirie; J A Retsema; A R English
Journal:  Antimicrob Agents Chemother       Date:  1984-02       Impact factor: 5.191

9.  Biomimetic Synthesis of Lankacidin Antibiotics.

Authors:  Kuan Zheng; Defeng Shen; Ran Hong
Journal:  J Am Chem Soc       Date:  2017-09-06       Impact factor: 15.419

10.  Analysis of modular-iterative mixed biosynthesis of lankacidin by heterologous expression and gene fusion.

Authors:  Satoshi Tatsuno; Kenji Arakawa; Haruyasu Kinashi
Journal:  J Antibiot (Tokyo)       Date:  2007-11       Impact factor: 2.649

View more
  1 in total

1.  Modular Chemical Synthesis of Streptogramin and Lankacidin Antibiotics.

Authors:  Lingchao Cai; Ian B Seiple; Qi Li
Journal:  Acc Chem Res       Date:  2021-04-01       Impact factor: 22.384

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.