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991.
992.
Abstract— Radiation-induced covalent binding of labelled carcinogens to DNA has been investigated under a variety of conditions using ultrafiltration or millipore filtration of TCA precipitable complexes. High yields of carcinogen binding at high DNA concentrations are also observed for a variety of small molecules and are not carcinogen-specific. At high carcinogen concentrations, radiation-induced unstable electrophilic carcinogenic species are produced, and undergo free-radical reactions which simulate cellular redox reactions involved in metabolic carcinogen activation, leading to the formation of covalently bound carcinogen adducts to DNA as a potential target macromolecule. The yields of carcinogen-DNA adducts increase linearly with dose and depend upon carcinogen concentration. The results of scavenger studies indicate that the oxidising species O2 - and OH are the principal activating species. Rate constants for the selective radiation-induced oxidation reactions of various chemical carcinogens with superoxide have been measured by a competition kinetic method using pulse radiolysis. The relatively long-lived superoxide radical reacts with carcinogens at a rate which is two orders of magnitude slower than the diffusion-controlled rate for the hydroxyl radical, thus allowing a measure of O2 - specificity in the presence of competing reactants within the cell. 相似文献
993.
The rates and products of addition of benzeneselenenyl chloride to ethylene and its six Me substituted derivatives have been determined in methylene chloride at 25°. Unlike the addition of 4-chlorobenzenesulfenyl chloride to this same series of compounds, the effect of Me groups on the rates of addition is not cumulative. Also the regiochemistry of the product is different. For arenesulfenyl chloride additions, products of anti-Markownikoff orientation are formed preferentially under conditions of kinetic control. Under similar conditions regiospecific formation of the Markownikoff adduct is observed for the addition of benzeneselenenyl chloride to methylpropene and 2-methyl-2-butene. These data indicate a difference in both rate and product determining transition states between additions of arenesulfenyl and selenenyl chlorides to alkenes. 相似文献
994.
995.
996.
The symplectic groupSp(2N
fNc) is proposed as the internal symmetry group of quark bound states; hereN
f andN
c designate respectively the number of quark flavors and that of color degrees of freedom of the quark. The effective Lagrangian of quark bound states in a quark—gluon system is constructed in the infinitely strong coupling limit. Several consequences of theSp(2N
fNc)-symmetry in the caseN
f=3 are examined.Translated from Zapiski Nauchnykh Seminarov Leningradskogo Otdeleniya Matematicheskogo Instituta im. V. A. Steklova AN SSSR, Vol. 131, pp. 47–71, 1983.The authors are grateful to I. Ya. Aref'eva, M. K. Volkov, G. V. Efimov, L. N. Lipatov, A. A. Migdal, V. N. Pervushin, and V. N. Popov for discussions and critical remarks. 相似文献
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