543-18-0 Usage
Description
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. Guanidinoethyl sulfonate competitively inhibits taurine uptake by sodium-dependent taurine transporters in rat hepatocytes (Ki = 1.75 mM). It also acts as a competitive glycine receptor antagonist in mouse striatal neurons. Plasma levels of guanidinoethyl sulfonate are significantly increased in patients with chronic renal failure.
Chemical Properties
White Solid
Uses
Different sources of media describe the Uses of 543-18-0 differently. You can refer to the following data:
1. A potent inhibitor of taurine transport
2. A potent inhibitor of taurine transport.
Definition
ChEBI: Zwitterionic form of taurocyamine arising from transfer of a proton from the sulfo to the guanidino group; major species at pH 7.3.
in vitro
guanidinoethyl sulphonate was found to be an analogue of taurine and an inhibitor of taurine transport. guanidinoethyl sulphonate was also shown to be a weak agonist at gaba(a) receptors, and was able to antagonize gaba-evoked responses. guanidinoethyl sulphonate did not gate glyr. 3. but antagonized glycine responses in a concentration-dependent and surmountable manner. glycine receptor-mediated taurine responses were competitively antagonized by guanidinoethyl sulphonate. taurine dose-response curves, in contrast to the glycine dose-response curves were shifted by guanidinoethyl sulphonate to the right in a parallel manner [1].
in vivo
guanidinoethyl sulphonate delivered in the drinking water of rats for 1 month could effectively reduce taurine levels in brain structures and outside the brain by between 50 and 80 %, depending on the tissue. this partial taurine depletion could not affect either basal synaptic transmission or the late phase of long-term potentiation in hippocampal slices. in-vivo microdialysis studies in the hippocampus demonstrated that guanidinoethyl sulphonate was able to reduce extracellular taurine levels and the magnitude of taurine released in response to the application of either n-methyl-d-aspartate or a hypoosmotic solution [2].
references
[1] sergeeva, o. a.,chepkova, a.n., and hass, h.l. guanidinoethyl sulphonate is a glycine receptor antagonist in striatum. british journal of pharmacology 137, 855-860 (2002).[2] suárez lm, muoz md, gonzález jc, bustamante j, del río rm, solís jm. the taurine transporter substrate guanidinoethyl sulfonate mimics the action of taurine on long-term synaptic potentiation. amino acids. 2016 nov;48(11):2647-2656. epub 2016 jul 15.
Check Digit Verification of cas no
The CAS Registry Mumber 543-18-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 543-18:
(5*5)+(4*4)+(3*3)+(2*1)+(1*8)=60
60 % 10 = 0
So 543-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H9N3O3S/c4-3(5)6-1-2-10(7,8)9/h1-2H2,(H4,4,5,6)(H,7,8,9)
543-18-0Relevant articles and documents
ORGANIC DISULFIDES AND RELATED SUBSTANCES. IX. SYMMETRICAL
FIELD,FERRETTI,CRENSHAW,OWEN
, p. 39 - 44 (1964)
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ACIDES α ET β AMIDINO SULFONIQUES
Garrigues, Bernard,Lopez, Lucien,Mulliez, Michel
, p. 195 - 202 (2007/10/02)
The titel compounds (4 or 11, Table) are synthesized by coupling, in an aqueous basic medium, of the α or β amino sulfonic acids with thioiminoethers salts or cyanamide ( Fig. 4). Key words: thioiminoethers; cyclization in aqueous medium; sulfonopeptides;
