1190-74-5Relevant articles and documents
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Khym et al.
, (1958)
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SYNTHESIS OF N-DERIVATIVES OF GUANIDINOETHANETHIOLS AND THEIR ANTIRADIATION ACTIVITZ ON THE YEAST Saccharomyces Cerevisiae
Rodyunin, A. A.,Zolotareva, L. T.,Mandrugin, A. A.,Fedoseev, V. M.
, p. 738 - 740 (1990)
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Synthesis and evaluation of alternative substrates for arginase
Han, Shoufa,Moore, Roger A.,Viola, Ronald E.
, p. 81 - 94 (2007/10/03)
Two novel carboxyl-containing arginase substrates, 4-guanidino-3-nitrobenzoic acid and 4-guanidino-2-nitrophenylacetic acid, have been synthesized and found to give enhanced catalysis and dramatically lower Km values relative to 1-nitro-3-guanidinobenzene, a substrate designed for use in a chromophoric arginase assay. To more efficiently mimic the natural substrate, a series of sulfur analogs of L-arginine were synthesized and kinetically characterized. The parent compound, L-thioarginine, with the bridging guanidinium nitrogen of L-arginine replaced with sulfur, functions as efficiently as the natural substrate. The desamino analog shows extremely low turnover, while the kcat of the descarboxy analog is only 75-fold lower than that of arginine. These results suggest that the bridging nitrogen of L-arginine is not important for either substrate binding or catalysis, while the α-carboxyl group facilitates substrate binding, and the α-amino group is necessary for efficient catalysis. Isothiourea homologs previously reported to be nitric oxide synthase inhibitors have been found to undergo a rapid non-enzymatic rearrangement to a species that is probably the true inhibitor.
