210354-22-6 Usage
General Description
(S)-2-amino-(1-iminoethylamino)-5-thioheptanoic acid is a chemical compound that consists of an amino acid and a thiol group. It is a derivative of the amino acid cysteine and contains a sulfur atom within its molecular structure. (S)-2-AMINO-(1-IMINOETHYLAMINO)-5-THIOHEPTANOIC ACID has potential biological and pharmaceutical applications due to its ability to form disulfide bonds and contribute to protein structure and function. Additionally, its thiol group can participate in redox reactions and has been studied for its potential antioxidant and anti-inflammatory properties. The (S) configuration in its name indicates that it is a stereoisomer with a specific spatial arrangement of its atoms, which may have implications for its biological activity and interactions with other molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 210354-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,3,5 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 210354-22:
(8*2)+(7*1)+(6*0)+(5*3)+(4*5)+(3*4)+(2*2)+(1*2)=76
76 % 10 = 6
So 210354-22-6 is a valid CAS Registry Number.
210354-22-6Relevant articles and documents
Inhibition of inducible nitric oxide synthase by acetamidine derivatives of hetero-substituted lysine and homolysine
Young, Robert J.,Beams, Richard M.,Carter, Keith,Clark, Helen A.R.,Coe, Diane M.,Chambers, C. Lynn,Davies, P. Ifeyinwa,Dawson, John,Drysdale, Martin J.,Franzman, Karl W.,French, Colin,Hodgson, Simon T.,Hodson, Harold F.,Kleanthous, Savvas,Rider, Peter,Sanders, Daniela,Sawyer, David A.,Scott, Keith J.,Shearer, Barry G.,Stocker, Richard,Smith, Steven,Tackley, Miriam C.,Knowles, Richard G.
, p. 597 - 600 (2007/10/03)
The synthesis and in vitro evaluation of the acetamidine derivatives of hetero-substituted lysine and homolysine analogues have identified potent inhibitors of human nitric oxide synthase enzymes, including examples with marked selectivity for the inducible isoform. (C) 2000 Elsevier Science Ltd. All rights reserved.
