Use of aminoguanidine (Pimagedine) to prevent the formation of advanced glycation endproducts.
By Paul J Thornalley. Archives of Biochemistry and Biophysics, 2003
663 citations recorded by the source corpus.
Subfields: Biochemistry, Clinical Biochemistry, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/85bc8542802ee5829fcaf686b4a9f95bf095d584
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In Biochemistry
In Clinical Biochemistry
In Molecular Biology
Citations in the corpus
- Diabetic neuropathy: mechanisms to management. (2008, background): “P A A uthor M anuscript Aminoguanidine: Aminoguanidine (also called pimagedine) is a nucleophilic hydrazine compound and has received the most attention as a potential anti-glycation drug (Thornalley, 2003).”
- Advanced lipid peroxidation end products in oxidative damage to proteins. Potential role in diseases and therapeutic prospects for the inhibitors (2008, background): “Aminoguanidine reacts in vitro and in vivo with the a-oxoaldehydes methylglyoxal and glyoxal and ALE precursors (MDA) to form 3-amino-1,2,4-triazine derivatives (Thornalley et al., 2000; Thornalley, 2003).”
- Aldehyde Sources, Metabolism, Molecular Toxicity Mechanisms, and Possible Effects on Human Health (2005, background): “Evidence for the hypothesis that α-oxoaldehydes were cytotoxic was the protection by α-oxoaldehyde reactive agents D-penicillamine, aminoguanidine, and semicarbazide against αoxoaldehyde cytotoxicity (Thornalley, 2003; Wondrak et al., 2002).”