Literature DB >> 17604170

Sulfenamides as prodrugs of NH-acidic compounds: a new prodrug option for the amide bond.

Victor R Guarino1, Veranja Karunaratne, Valentino J Stella.   

Abstract

The objective of this report is to introduce the novel concept of utilizing sulfenamides as prodrugs for compounds containing an NH-acidic functionality, particularly weakly acidic amide-type functionalities (amides, ureas, carbamates, etc.). Included are the syntheses and physicochemical characterizations of some model sulfenamides to illustrate the promise of this new prodrug technology.

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Year:  2007        PMID: 17604170     DOI: 10.1016/j.bmcl.2007.06.037

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Reversion of sulfenamide prodrugs in the presence of free thiol-containing proteins.

Authors:  Kwame W Nti-Addae; Jennifer S Laurence; Andria L Skinner; Valentino J Stella
Journal:  J Pharm Sci       Date:  2011-02-03       Impact factor: 3.534

2.  New class of biodegradable polymers formed from reactions of an inorganic functional group.

Authors:  Jun Yoo; Denison J Kuruvilla; Sheetal R D'Mello; Aliasger K Salem; Ned B Bowden
Journal:  Macromolecules       Date:  2012-02-21       Impact factor: 6.057

  2 in total

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