Efforts Toward Synthesis of Novel Analogs of the Bacterial Second-Messenger, c-di-GMP
dc.contributor.advisor | Sintim, Herman O | en_US |
dc.contributor.author | Shurer, Andrew Joseph | en_US |
dc.contributor.department | Chemistry | en_US |
dc.contributor.publisher | Digital Repository at the University of Maryland | en_US |
dc.contributor.publisher | University of Maryland (College Park, Md.) | en_US |
dc.date.accessioned | 2009-07-03T05:47:49Z | |
dc.date.available | 2009-07-03T05:47:49Z | |
dc.date.issued | 2009 | en_US |
dc.description.abstract | The formation of bacterial biofilms is a common mechanism for antibiotic resistance. It has been shown that bis-(3'-5')-cyclic dimeric guanosine monophosphate, c-di-GMP, plays a key role in bacterial biofilm formation; therefore, the proteins that regulate the metabolism or adaptive response of c-di-GMP are favorable targets for novel antimicrobials. We herein describe a solid-support methodology developed in the Sintim Laboratory and efforts toward its application to the synthesis of novel c-di-GMP analogs. Our selected targets are a series of analogs bearing various substitutions at the 2'-position of the ribose backbone. Syntheses of 2'-deoxy and 2'-methoxy analogs were achieved as well as that of key intermediates toward the 2'-fluoro and conformationally flexible analogs. | en_US |
dc.format.extent | 1932773 bytes | |
dc.format.mimetype | application/pdf | |
dc.identifier.uri | http://hdl.handle.net/1903/9370 | |
dc.language.iso | en_US | |
dc.subject.pqcontrolled | Chemistry, Organic | en_US |
dc.subject.pquncontrolled | antibiotics | en_US |
dc.subject.pquncontrolled | bacteria | en_US |
dc.subject.pquncontrolled | biofilm | en_US |
dc.subject.pquncontrolled | cyclic diguanylic acid | en_US |
dc.subject.pquncontrolled | diguanylate cyclase | en_US |
dc.subject.pquncontrolled | phosphodiesterase | en_US |
dc.title | Efforts Toward Synthesis of Novel Analogs of the Bacterial Second-Messenger, c-di-GMP | en_US |
dc.type | Thesis | en_US |
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