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Functionalised bicyclic tetramates derived from cysteine as antibacterial agents.


ABSTRACT: Routes to bicyclic tetramates derived from cysteine permitting ready incorporation of functionality at two different points around the periphery of a heterocyclic skeleton are reported. This has enabled the identification of systems active against Gram-positive bacteria, some of which show gyrase and RNA polymerase inhibitory activity. In particular, tetramates substituted with glycosyl side chains, chosen to impart polarity and aqueous solubility, show high antibacterial activity coupled with modest gyrase/polymerase activity in two cases. An analysis of physicochemical properties indicates that the antibacterially active tetramates generally occupy physicochemical space with MW of 300-600, clog?D7.4 of -2.5 to 4 and rel. PSA of 11-22%. This work demonstrates that biologically active 3D libraries are readily available by manipulation of a tetramate skeleton.

SUBMITTER: Panduwawala TD 

PROVIDER: S-EPMC6686852 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Functionalised bicyclic tetramates derived from cysteine as antibacterial agents.

Panduwawala Tharindi D TD   Iqbal Sarosh S   Thompson Amber L AL   Genov Miroslav M   Pretsch Alexander A   Pretsch Dagmar D   Liu Shuang S   Ebright Richard H RH   Howells Alison A   Maxwell Anthony A   Moloney Mark G MG  

Organic & biomolecular chemistry 20190601 22


Routes to bicyclic tetramates derived from cysteine permitting ready incorporation of functionality at two different points around the periphery of a heterocyclic skeleton are reported. This has enabled the identification of systems active against Gram-positive bacteria, some of which show gyrase and RNA polymerase inhibitory activity. In particular, tetramates substituted with glycosyl side chains, chosen to impart polarity and aqueous solubility, show high antibacterial activity coupled with m  ...[more]

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