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Synthesis of 'clickable' acylhomoserine lactone quorum sensing probes: unanticipated effects on mammalian cell activation.


ABSTRACT: Alkynyl- and azido-tagged 3-oxo-C(12)-acylhomoserine lactone probes have been synthesized to examine their potential utility as probes for discovering the mammalian protein target of the Pseudomonas aeruginosa autoinducer, 3-oxo-C(12)-acylhomoserine lactone. Although such substitutions are commonly believed to be quite conservative, from these studies, we have uncovered a drastic difference in activity between the alkynyl- and azido-modified compounds, and provide an example where such structural modification has proved to be much less than conservative.

SUBMITTER: Garner AL 

PROVIDER: S-EPMC3081916 | biostudies-literature | 2011 May

REPOSITORIES: biostudies-literature

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Synthesis of 'clickable' acylhomoserine lactone quorum sensing probes: unanticipated effects on mammalian cell activation.

Garner Amanda L AL   Yu Jing J   Struss Anjali Kumari AK   Lowery Colin A CA   Zhu Jie J   Kim Sook Kyung SK   Park Junguk J   Mayorov Alexander V AV   Kaufmann Gunnar F GF   Kravchenko Vladimir V VV   Janda Kim D KD  

Bioorganic & medicinal chemistry letters 20101204 9


Alkynyl- and azido-tagged 3-oxo-C(12)-acylhomoserine lactone probes have been synthesized to examine their potential utility as probes for discovering the mammalian protein target of the Pseudomonas aeruginosa autoinducer, 3-oxo-C(12)-acylhomoserine lactone. Although such substitutions are commonly believed to be quite conservative, from these studies, we have uncovered a drastic difference in activity between the alkynyl- and azido-modified compounds, and provide an example where such structura  ...[more]

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