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Guanidinoethyl sulfonate, also known as taurocyamine, is a natural guanidine-taurine analog derived from taurine. It is an intermediate of taurine and hypotaurine metabolism and is phosphorylated by taurocyamine kinase.1 Guanidinoethyl sulfonate competitively inhibits taurine uptake by sodium-dependent taurine transporters in rat hepatocytes (Ki = 1.75 mM).2 It also acts as a competitive glycine receptor antagonist in mouse striatal neurons.3 Plasma levels of guanidinoethyl sulfonate are significantly increased in patients with chronic renal failure.4
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1. Origin and properties of cytoplasmic and mitochondrial isoforms of taurocyamine kinase. FEBS J. 272(14), 3521-3530 (2005).
2. Characteristics of taurine transport in freshly isolated rat hepatocytes. Jpn. J. Pharmacol. 31(6), 1061-1070 (1981).
3. Guanidinoethyl sulphonate is a glycine receptor antagonist in striatum. Br. J. Pharmacol. 137(6), 855-860 (2002).
4. Plasma, urinary, and erythrocyte concentrations of guanidino compounds in patients with chronic renal failure. Ren Fail. 21(5), 499-514 (1999).