Journal of Medicinal Chemistry 2007-12-27

Novel, orally effective cyanide antidotes.

Herbert T Nagasawa, David J W Goon, Daune L Crankshaw, Robert Vince, Steven E Patterson

Index: J. Med. Chem. 50(26) , 6462-4, (2007)

Full Text: HTML

Abstract

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.


Related Compounds

Related Articles:

Structure and kinetic analysis of H2S production by human mercaptopyruvate sulfurtransferase.

2013-07-05

[J. Biol. Chem. 288(27) , 20002-13, (2013)]

Identification of putative sulfurtransferase genes in the extremophilic Acidithiobacillus ferrooxidans ATCC 23270 genome: structural and functional characterization of the proteins.

2005-04-01

[OMICS 9(1) , 13-29, (2005)]

Properties of the Escherichia coli rhodanese-like protein SseA: contribution of the active-site residue Ser240 to sulfur donor recognition.

2001-07-06

[FEBS Lett. 500(3) , 153-6, (2001)]

Alternative sulphur donors for detoxification of cyanide in the chicken.

1991-01-01

[Comp. Biochem. Physiol. C, Comp. Pharmacol. Toxicol. 99(3) , 309-15, (1991)]

Electron paramagnetic resonance evidence for a cysteine-based radical in pyruvate formate-lyase inactivated with mercaptopyruvate.

1995-05-02

[Biochemistry 34(17) , 5712-7, (1995)]

More Articles...