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Biological and Pharmaceutical Bulletin, 1996/10/15, Vol.19(10), pp.1261-1265
1996
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Autor(en) / Beteiligte
Titel
Dihydropyrazine Derivatives as a New Type of DNA Strand Breaking Agent
Ist Teil von
  • Biological and Pharmaceutical Bulletin, 1996/10/15, Vol.19(10), pp.1261-1265
Ort / Verlag
Tokyo: The Pharmaceutical Society of Japan
Erscheinungsjahr
1996
Quelle
MEDLINE
Beschreibungen/Notizen
  • The DNA strand-breaking activity of some dihydropyrazine derivatives, 2, 3-dihydro-5, 6-dimethylpyrazine (3), 2, 3-dihydro-2, 5, 6-trimethylpyrazine (4), 2, 3-dihydro-2, 2, 5, 6-tetramethylpyrazine (5), trans-2, 3-dimethyl-5, 6, 7, 8, 9, 10-hexahydroquinoxaline (6), its cis-compound (7) and the mixture of 6 and 7 (8) was tested by agarose gel electrophoresis using plasmide pBR322 ccc-DNA as a substrate. The order of DNA strand-breaking activity in the presence of Cu2+ was (7)>(8)≥(5)>(2)>(6)>(4)≥(1)≥(3). 2, 5-Bis(D-arabino-tetrahydroxybutyl)-2, 5-dihydropyrazine (1) and 2, 5-dihydro-3, 6-dimethylpyrazine (2) have already been described in terms of DNA breaking activity in a previous paper.The activity was suggested to be due to the dihydropyrazine skeleton, in addition to active oxygen radicals formed in an aqueous solutoin. The introduction of a methyl group to the dihydropyrazine skeleton enhanced the activities of dihydropyrazine derivatives. The possible chemical basis for DNA strand breakage by dihydropyrazine derivatives, especially in the presence of Cu2+, was discussed.

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