Unveiling the active isomer of cycloalanopine, a cyclic opine from Lactobacillus rhamnosus LS8, through synthesis and analog production-Reference-Cited by-同舟云学术

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Unveiling the active isomer of cycloalanopine, a cyclic opine from Lactobacillus rhamnosus LS8, through synthesis and analog production

Published:2020 Issue:4 Volume:11 Page:528-531
ISSN:2632-8682
Container-title:RSC Medicinal Chemistry
language:en
Short-container-title:RSC Med. Chem.

Author:

Antwi Isaac¹²³⁴,Chiorean Sorina¹²³⁴^ORCID,van Belkum Marco J.¹²³⁴,Vederas John C.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. University of Alberta

3. Edmonton

4. Canada

Abstract

Stereochemistry of the antimicrobial isomer of a cyclic opine was determined by synthesis using oxidative cyclisation of a bis-hydrazide.

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/MD/D0MD00033G

Reference28 articles.

1. Novel bacteriocins from lactic acid bacteria (LAB): various structures and applications

2. The expanding structural variety among bacteriocins from Gram-positive bacteria

3. Lipopeptides from Bacillus and Paenibacillus spp.: A Gold Mine of Antibiotic Candidates

4. Antimicrobial Peptides: An Emerging Category of Therapeutic Agents

5. A novel antimicrobial substance produced by Lactobacillus rhamnous LS8

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