Spontaneous rearrangement of aminoalkylisothioureas into mercaptoalkylguanidines, a novel class of nitric oxide synthase inhibitors with selectivity towards the inducible isoform-Reference-Cited by-同舟云学术

Spontaneous rearrangement of aminoalkylisothioureas into mercaptoalkylguanidines, a novel class of nitric oxide synthase inhibitors with selectivity towards the inducible isoform

Published:1996-02 Issue:4 Volume:117 Page:619-632
ISSN:0007-1188
Container-title:British Journal of Pharmacology
language:en
Short-container-title:

Author:

Southan Garry J.,Zingarelli Basilia,O'Connor Michael,Salzman Andrew L.,Szabó Csaba

Publisher

Wiley

Subject

Pharmacology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1476-5381.1996.tb15236.x/fullpdf

Reference45 articles.

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3. Aminoguanidine, a novel inhibitor of nitric oxide formation, prevents diabetic vascular dysfunction;CORBETT;Diabetes,1992

4. Nitric oxide mediates glutamate neuro-toxicity in primary cortical cultures;DAWSON;Proc. Natl. Acad. Sci. U.S.A.,1991

5. Synthesis of aminoalkylisothiouronium salts and their conversion to mercap-toalkylguanidines and thiazolines;DOHERTY;J. Am. Chem. Soc.,1957

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