Dissertation/Thesis Abstract

Total Synthesis of Apratoxin A Analogues
by Jackel, Matthew David, Ph.D., The Ohio State University, 2012, 349; 10631017
Abstract (Summary)

Apratoxin A is a potent cytotoxic compound that was isolated from the marine cyanobacterium Lygbya majuscula by Moore, Paul, and co-workers and reported in 2001. Structurally, this natural product is a macrocyclic depsipeptide that contains an unprecedented polyketide domain and a heavily methylated polypeptide domain. The biological mode of action of apratoxin A, to date, has not been fully elucidated. In addition, the mode of action cannot be correlated with any of the standard anti-cancer agents in the National Cancer Institute's library, which suggests a unique mode of action.

Herein are reported our efforts towards discovering an apratoxin A analogue that retains its anti-cancer activity, but eliminates its action against normal cells. We have developed an efficient synthetic route towards the oxazoline analogue of apratoxin A that relies upon a late stage installation of the oxazoline moiety. The convergent nature of the synthetic route has provided us with access to several oxazoline analogues that will be assayed for anti-cancer activity. Also, a second generation synthesis of oxazoline analogues has been developed, which shortens the overall synthetic route and eliminates late stage epimerization problems seen in the original synthesis of oxazoline apratoxin A. In addition, we have developed a reliable synthetic route to an oxazoline analogue that contains a polyethylene glycol domain, which terminates with an azide. The azide has been successfully used in a 1,3-dipolar cycloaddition with a biotinylated alkyne, which will be assayed to help determine the molecular targets of apratoxin A. Furthermore, the polyethylene glycol azide provides us with a handle to install additional biological tags.

Indexing (document details)
Advisor: Forsyth, Craig J.
Commitee: Parquette, Jon, Stambuli, James
School: The Ohio State University
Department: Chemistry
School Location: United States -- Ohio
Source: DAI-B 78/11(E), Dissertation Abstracts International
Source Type: DISSERTATION
Subjects: Chemistry, Organic chemistry
Keywords: Apratoxin A analogues, Total synthesis
Publication Number: 10631017
ISBN: 9780355013238
Copyright © 2019 ProQuest LLC. All rights reserved. Terms and Conditions Privacy Policy Cookie Policy
ProQuest