Synthesis and resolution of putative diastereomeric N2-deoxyguanosine and N6-deoxyadenosine adducts of biologically active cyclopentaPAH
摘要:
Synthesis of the putative DNA adducts from 1,2-dihydroaceanthrylene-1,2-oxide and the exocyclic amino groups of deoxyguanosine and deoxyadenosine and from 3,4-dihydrocyclopenta[cd]pyrene and the exocyclic amino group of deoxyguanosine is reported.
Synthesis of cyclopenta[cd]pyrene-3,4-oxide, the suspected ultimate carcinogenic metabolite of cyclopenta[cd]pyrene
作者:Daniel J. McCaustland、Paul H. Ruehle、James C. Wiley
DOI:10.1039/c39800000093
日期:——
A synthesis of cyclopenta[cd]pyrene-3,4-oxide, the suspected ultimate carcinogenic metabolite of the widely distributed environmental carcinogen cyclopenta[cd]pyrene, is described.
描述了环戊五烯[ cd ] -3-3,4-氧化物的合成,这是广泛分布的环境致癌物环戊五烯[ cd ] ultimate的可能的最终致癌代谢产物。
Synthesis and resolution of putative diastereomeric N2-deoxyguanosine and N6-deoxyadenosine adducts of biologically active cyclopentaPAH
Synthesis of the putative DNA adducts from 1,2-dihydroaceanthrylene-1,2-oxide and the exocyclic amino groups of deoxyguanosine and deoxyadenosine and from 3,4-dihydrocyclopenta[cd]pyrene and the exocyclic amino group of deoxyguanosine is reported.