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Nitrogen-bound diazeniumdiolated amidines.


ABSTRACT: In contrast to amidines bearing ionizable alpha-CH bonds, which react with nitric oxide (NO) to add diazeniumdiolate groups at their alpha-carbons, benzamidine forms an N-bound diazeniumdiolate that can be further derivatized at the other amidine nitrogen and/or the terminal oxygen to form caged NO compounds as potential NO prodrugs.

SUBMITTER: Biswas D 

PROVIDER: S-EPMC6959519 | biostudies-literature | 2010 Aug

REPOSITORIES: biostudies-literature

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Nitrogen-bound diazeniumdiolated amidines.

Biswas Debanjan D   Deschamps Jeffrey R JR   Keefer Larry K LK   Hrabie Joseph A JA  

Chemical communications (Cambridge, England) 20100630 31


In contrast to amidines bearing ionizable alpha-CH bonds, which react with nitric oxide (NO) to add diazeniumdiolate groups at their alpha-carbons, benzamidine forms an N-bound diazeniumdiolate that can be further derivatized at the other amidine nitrogen and/or the terminal oxygen to form caged NO compounds as potential NO prodrugs. ...[more]

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