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Structure and oxidation capacity of amino acid chloramine derivatives and their effects on platelet aggregation
Authors:M.?A.?Murina  author-information"  >  author-information__contact u-icon-before"  >  mailto:marina_murina@mail.ru"   title="  marina_murina@mail.ru"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,N.?A.?Chudina,D.?I.?Roshchupkin,N.?S.?Belakina,V.?I.?Sergienko
Affiliation:(1) Research Institute of Physicochemical Medicine, Ministry of Health of Russia, Moscow
Abstract:Comparison of antiaggregation capacity of N-chloramine acids with different position of the chloramine group in the molecule showed that in the most efficient compounds the distance between the chloramine and carboxyl groups was 3–5 carbon atoms. This feature of antiaggregation activity was not related to the difference in oxidation capacity of N-chloramine acids. It was hypothesized that the revealed structural dependence of antiaggregation activity of N-chloramine acids is determined by the structure of platelet membrane, in particular, the presence of a negatively charged group near the site of interaction between N-chloramine acids and platelet membrane.Translated from Byulletenrsquo Eksperimentalrsquonoi Biologii i Meditsiny, Vol. 138, No. 12, pp. 632–634, December, 2004This revised version was published online in April 2005 with a corrected cover date.
Keywords:chloramine derivatives of amino acids  platelets  aggregation  chemiluminescence  luminol
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