A Study of the Alkylating Abilities of 1-(2-Hydroxyethyl)-1-Nitrosourea and 1-Ethyl-1-Nitrosourea

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Authors
Dowuona, David
Issue Date
1980
Type
Thesis
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en_US
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Abstract
In this thesis project, we studied two alkylating reagents with similar structural and chemical properties, 1-{2-hydroxyethyl)-1-nitrosourea (HNU) and l-ethyl-l-nitrosourea (ENU). Since they react via similar reactive intermediates, it is expected that they would both alkylate DNA to the same extents and at the same sites and have equal carcinogenic potency. It was also proposed that the HNU DNA phosphotriester product would be unstable: while the ENU phosphotriesters would be stable. Accordingly, if DNA reactions and tumourigenicity were identical for the 2 compounds, the importance of phosphotriesters in alkylation carcinogenesis would be further cast in doubt. The first part of the proposal, that HNU and ENU. are equicarcinogenic, has been previously shown. The purpose of this study was to provide background information to support or refute the proposal of equal alkylation by ENU and HNU.
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31 p.
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Kalamazoo College
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U.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder. All rights reserved.
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