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Synthesis and antibiotic activity of oxazolidinone-catechol conjugates against
Pseudomonas aeruginosa is a Gram-negative pathogenic bacterium responsible for severe infections in which resistance to most of the approved families of antibiotics is increasing. Oxazolidinone antibiotics are active against many Gram-positive bacteria, but are only weakly active against Gram-negati...
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Published in: | Organic & biomolecular chemistry 2015-11, Vol.13 (47), p.11567-11579 |
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container_issue | 47 |
container_start_page | 11567 |
container_title | Organic & biomolecular chemistry |
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creator | Paulen, Aurélie Gasser, Véronique Hoegy, Françoise Perraud, Quentin Pesset, Bénédicte Schalk, Isabelle J Mislin, Gaëtan L. A |
description | Pseudomonas aeruginosa
is a Gram-negative pathogenic bacterium responsible for severe infections in which resistance to most of the approved families of antibiotics is increasing. Oxazolidinone antibiotics are active against many Gram-positive bacteria, but are only weakly active against Gram-negative pathogens. We describe the synthesis of conjugates between a catechol moiety and oxazolidinone antibiotics. These conjugates were significantly more active against
P. aeruginosa
(218-1024 μM) than linezolid (MIC > 1024 μM), the reference molecule from the oxazolidinone family. Antibiotic activity was slightly higher in medium depleted of iron, suggesting the involvement of a bacterial iron uptake system in this biological activity. The bacterial iron uptake pathway involved in the transport is still to be addressed, but the present data excluded a contribution of the enterobactin transporter PfeA.
An oxazolidinone antibiotic, conjugated to a catechol moiety, was shown to be at least eight times more active against
P. aeruginosa
, when compared to the linezolid, used as a reference compound. |
doi_str_mv | 10.1039/c5ob01859e |
format | article |
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is a Gram-negative pathogenic bacterium responsible for severe infections in which resistance to most of the approved families of antibiotics is increasing. Oxazolidinone antibiotics are active against many Gram-positive bacteria, but are only weakly active against Gram-negative pathogens. We describe the synthesis of conjugates between a catechol moiety and oxazolidinone antibiotics. These conjugates were significantly more active against
P. aeruginosa
(218-1024 μM) than linezolid (MIC > 1024 μM), the reference molecule from the oxazolidinone family. Antibiotic activity was slightly higher in medium depleted of iron, suggesting the involvement of a bacterial iron uptake system in this biological activity. The bacterial iron uptake pathway involved in the transport is still to be addressed, but the present data excluded a contribution of the enterobactin transporter PfeA.
An oxazolidinone antibiotic, conjugated to a catechol moiety, was shown to be at least eight times more active against
P. aeruginosa
, when compared to the linezolid, used as a reference compound.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/c5ob01859e</identifier><ispartof>Organic & biomolecular chemistry, 2015-11, Vol.13 (47), p.11567-11579</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Paulen, Aurélie</creatorcontrib><creatorcontrib>Gasser, Véronique</creatorcontrib><creatorcontrib>Hoegy, Françoise</creatorcontrib><creatorcontrib>Perraud, Quentin</creatorcontrib><creatorcontrib>Pesset, Bénédicte</creatorcontrib><creatorcontrib>Schalk, Isabelle J</creatorcontrib><creatorcontrib>Mislin, Gaëtan L. A</creatorcontrib><title>Synthesis and antibiotic activity of oxazolidinone-catechol conjugates against</title><title>Organic & biomolecular chemistry</title><description>Pseudomonas aeruginosa
is a Gram-negative pathogenic bacterium responsible for severe infections in which resistance to most of the approved families of antibiotics is increasing. Oxazolidinone antibiotics are active against many Gram-positive bacteria, but are only weakly active against Gram-negative pathogens. We describe the synthesis of conjugates between a catechol moiety and oxazolidinone antibiotics. These conjugates were significantly more active against
P. aeruginosa
(218-1024 μM) than linezolid (MIC > 1024 μM), the reference molecule from the oxazolidinone family. Antibiotic activity was slightly higher in medium depleted of iron, suggesting the involvement of a bacterial iron uptake system in this biological activity. The bacterial iron uptake pathway involved in the transport is still to be addressed, but the present data excluded a contribution of the enterobactin transporter PfeA.
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P. aeruginosa
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is a Gram-negative pathogenic bacterium responsible for severe infections in which resistance to most of the approved families of antibiotics is increasing. Oxazolidinone antibiotics are active against many Gram-positive bacteria, but are only weakly active against Gram-negative pathogens. We describe the synthesis of conjugates between a catechol moiety and oxazolidinone antibiotics. These conjugates were significantly more active against
P. aeruginosa
(218-1024 μM) than linezolid (MIC > 1024 μM), the reference molecule from the oxazolidinone family. Antibiotic activity was slightly higher in medium depleted of iron, suggesting the involvement of a bacterial iron uptake system in this biological activity. The bacterial iron uptake pathway involved in the transport is still to be addressed, but the present data excluded a contribution of the enterobactin transporter PfeA.
An oxazolidinone antibiotic, conjugated to a catechol moiety, was shown to be at least eight times more active against
P. aeruginosa
, when compared to the linezolid, used as a reference compound.</abstract><doi>10.1039/c5ob01859e</doi><tpages>13</tpages></addata></record> |
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title | Synthesis and antibiotic activity of oxazolidinone-catechol conjugates against |
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