Efforts Toward Synthesis of Novel Analogs of the Bacterial Second-Messenger, c-di-GMP

dc.contributor.advisorSintim, Herman Oen_US
dc.contributor.authorShurer, Andrew Josephen_US
dc.contributor.departmentChemistryen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2009-07-03T05:47:49Z
dc.date.available2009-07-03T05:47:49Z
dc.date.issued2009en_US
dc.description.abstractThe 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.extent1932773 bytes
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/1903/9370
dc.language.isoen_US
dc.subject.pqcontrolledChemistry, Organicen_US
dc.subject.pquncontrolledantibioticsen_US
dc.subject.pquncontrolledbacteriaen_US
dc.subject.pquncontrolledbiofilmen_US
dc.subject.pquncontrolledcyclic diguanylic aciden_US
dc.subject.pquncontrolleddiguanylate cyclaseen_US
dc.subject.pquncontrolledphosphodiesteraseen_US
dc.titleEfforts Toward Synthesis of Novel Analogs of the Bacterial Second-Messenger, c-di-GMPen_US
dc.typeThesisen_US

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Shurer_umd_0117N_10427.pdf
Size:
1.84 MB
Format:
Adobe Portable Document Format