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Novel FR-900493 Analogues That Inhibit the Outgrowth of Clostridium difficile Spores
[Image: see text] The spectrum of antibacterial activity for the nucleoside antibiotic FR-900493 (1) can be extended by chemical modifications. We have generated a small focused library based on the structure of 1 and identified UT-17415 (9), UT-17455 (10), UT-17460 (11), and UT-17465 (12), which ex...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830699/ https://www.ncbi.nlm.nih.gov/pubmed/29503973 http://dx.doi.org/10.1021/acsomega.7b01740 |
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author | Mitachi, Katsuhiko Yun, Hyun Gi Kurosu, Sara M. Eslamimehr, Shakiba Lemieux, Maddie R. Klaić, Lada Clemons, William M. Kurosu, Michio |
author_facet | Mitachi, Katsuhiko Yun, Hyun Gi Kurosu, Sara M. Eslamimehr, Shakiba Lemieux, Maddie R. Klaić, Lada Clemons, William M. Kurosu, Michio |
author_sort | Mitachi, Katsuhiko |
collection | PubMed |
description | [Image: see text] The spectrum of antibacterial activity for the nucleoside antibiotic FR-900493 (1) can be extended by chemical modifications. We have generated a small focused library based on the structure of 1 and identified UT-17415 (9), UT-17455 (10), UT-17460 (11), and UT-17465 (12), which exhibit anti-Clostridium difficile growth inhibitory activity. These analogues also inhibit the outgrowth of C. difficile spores at 2× minimum inhibitory concentration. One of these analogues, 11, relative to 1 exhibits over 180-fold and 15-fold greater activity against the enzymes, phospho-MurNAc-pentapeptide translocase (MraY) and polyprenyl phosphate-GlcNAc-1-phosphate transferase (WecA), respectively. The phosphotransferase inhibitor 11 displays antimicrobial activity against several tested bacteria including Bacillus subtilis, Clostridium spp., and Mycobacterium smegmatis, but no growth inhibitory activity is observed against the other Gram-positive and Gram-negative bacteria. The selectivity index (Vero cell cytotoxicity/C. difficileantimicrobial activity) of 11 is approximately 17, and 11 does not induce hemolysis even at a 100 μM concentration. |
format | Online Article Text |
id | pubmed-5830699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-58306992018-03-02 Novel FR-900493 Analogues That Inhibit the Outgrowth of Clostridium difficile Spores Mitachi, Katsuhiko Yun, Hyun Gi Kurosu, Sara M. Eslamimehr, Shakiba Lemieux, Maddie R. Klaić, Lada Clemons, William M. Kurosu, Michio ACS Omega [Image: see text] The spectrum of antibacterial activity for the nucleoside antibiotic FR-900493 (1) can be extended by chemical modifications. We have generated a small focused library based on the structure of 1 and identified UT-17415 (9), UT-17455 (10), UT-17460 (11), and UT-17465 (12), which exhibit anti-Clostridium difficile growth inhibitory activity. These analogues also inhibit the outgrowth of C. difficile spores at 2× minimum inhibitory concentration. One of these analogues, 11, relative to 1 exhibits over 180-fold and 15-fold greater activity against the enzymes, phospho-MurNAc-pentapeptide translocase (MraY) and polyprenyl phosphate-GlcNAc-1-phosphate transferase (WecA), respectively. The phosphotransferase inhibitor 11 displays antimicrobial activity against several tested bacteria including Bacillus subtilis, Clostridium spp., and Mycobacterium smegmatis, but no growth inhibitory activity is observed against the other Gram-positive and Gram-negative bacteria. The selectivity index (Vero cell cytotoxicity/C. difficileantimicrobial activity) of 11 is approximately 17, and 11 does not induce hemolysis even at a 100 μM concentration. American Chemical Society 2018-02-09 /pmc/articles/PMC5830699/ /pubmed/29503973 http://dx.doi.org/10.1021/acsomega.7b01740 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Mitachi, Katsuhiko Yun, Hyun Gi Kurosu, Sara M. Eslamimehr, Shakiba Lemieux, Maddie R. Klaić, Lada Clemons, William M. Kurosu, Michio Novel FR-900493 Analogues That Inhibit the Outgrowth of Clostridium difficile Spores |
title | Novel FR-900493 Analogues That Inhibit the Outgrowth
of Clostridium difficile Spores |
title_full | Novel FR-900493 Analogues That Inhibit the Outgrowth
of Clostridium difficile Spores |
title_fullStr | Novel FR-900493 Analogues That Inhibit the Outgrowth
of Clostridium difficile Spores |
title_full_unstemmed | Novel FR-900493 Analogues That Inhibit the Outgrowth
of Clostridium difficile Spores |
title_short | Novel FR-900493 Analogues That Inhibit the Outgrowth
of Clostridium difficile Spores |
title_sort | novel fr-900493 analogues that inhibit the outgrowth
of clostridium difficile spores |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830699/ https://www.ncbi.nlm.nih.gov/pubmed/29503973 http://dx.doi.org/10.1021/acsomega.7b01740 |
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