Ontology highlight
ABSTRACT:
SUBMITTER: Nagasawa HT
PROVIDER: S-EPMC2274902 | biostudies-literature | 2007 Dec
REPOSITORIES: biostudies-literature
Nagasawa Herbert T HT Goon David J W DJ Crankshaw Daune L DL Vince Robert R Patterson Steven E SE
Journal of medicinal chemistry 20071127 26
A series of prodrugs of 3-mercaptopyruvate (3-MP), the substrate for the enzyme 3-mercaptopyruvate/cyanide sulfurtransferase (3-MPST) that converts cyanide to the nontoxic thiocyanate, which are highly effective cyanide antidotes, have been developed. These prodrugs of 3-MP are unique in being not only orally bioavailable, but may be administered up to an hour prior to cyanide as a prophylactic agent and are both rapid- or slow-acting when given parenterally. ...[more]