TY - JOUR
T1 - Structure elucidation of the adducts formed by fjord-region dibenzo[a,l]pyrene 11,12-dihydrodiol 13,14-epoxides and deoxyadenosine
AU - Li, Kai Ming
AU - George, Mathai
AU - Gross, Michael L.
AU - Seidel, Albrecht
AU - Luch, Andreas
AU - Rogan, Eleanor G.
AU - Cavalieri, Ercole L.
PY - 1999
Y1 - 1999
N2 - Model adducts to be used in the identification of biologically formed adducts were synthesized by reaction of fjord-region dibenzo[a,l]pyrene 11,12-dihydrodiol 13,14-epoxides (DB[a,l]PDE) and deoxyadenosine (dA). The (±)-anti-DB[a,l]PDE was reacted with dA in dimethylformamide at 100 °C for 30 min to give four DB[a,l]PDE-14-N6dA adducts: (-)-anti-trans (26%), (+)anti-trans (26%), (-)-anti-cis (17%), and (+)-anti-cis (17%). The (±)- syn-DB[a,l]PDE was reacted with dA under the same conditions to yield four DB[a,l]PDE-14-N6dA adducts and one N7Ade adduct: (+)-syn-cis (19%), (+)-syn- trans (13%), (-)-syn-cis (19%), (-)-syn-trans (13%), and (±)syn-DB[a,l]PDE- 14-N7Ade (22%). The structures of the eight stereoisomers of DB[a,l]PDE14- N6dA were unequivocally assigned by reacting optically pure (-)-anti- DB[a,l]PDE and (+)syn-DB[a,l]PDE with dA and by a combination of NMR, circular dichroism, and fast atom bombardment mass spectrometry. Reactions at 100 °C yielded mainly the trans-opened adducts at the benzylic C-14 position for both (±)-anti-DB[a,l]PDE and (-)-anti-DB[a,l]PDE, whereas (±)-syn- DB[a,l]PDE and (+)-syn-DB[a,l]PDE afforded mainly cis-opened adducts. At room temperature, however, only trans-opened adducts were obtained from (±)-anti- DB[a,l]PDE and only cis-opened adducts from (±)-syn-DB[a,l]PDE. Steric hindrance created by the fjord region may be an important factor for the stereoselectivity observed at room temperature.
AB - Model adducts to be used in the identification of biologically formed adducts were synthesized by reaction of fjord-region dibenzo[a,l]pyrene 11,12-dihydrodiol 13,14-epoxides (DB[a,l]PDE) and deoxyadenosine (dA). The (±)-anti-DB[a,l]PDE was reacted with dA in dimethylformamide at 100 °C for 30 min to give four DB[a,l]PDE-14-N6dA adducts: (-)-anti-trans (26%), (+)anti-trans (26%), (-)-anti-cis (17%), and (+)-anti-cis (17%). The (±)- syn-DB[a,l]PDE was reacted with dA under the same conditions to yield four DB[a,l]PDE-14-N6dA adducts and one N7Ade adduct: (+)-syn-cis (19%), (+)-syn- trans (13%), (-)-syn-cis (19%), (-)-syn-trans (13%), and (±)syn-DB[a,l]PDE- 14-N7Ade (22%). The structures of the eight stereoisomers of DB[a,l]PDE14- N6dA were unequivocally assigned by reacting optically pure (-)-anti- DB[a,l]PDE and (+)syn-DB[a,l]PDE with dA and by a combination of NMR, circular dichroism, and fast atom bombardment mass spectrometry. Reactions at 100 °C yielded mainly the trans-opened adducts at the benzylic C-14 position for both (±)-anti-DB[a,l]PDE and (-)-anti-DB[a,l]PDE, whereas (±)-syn- DB[a,l]PDE and (+)-syn-DB[a,l]PDE afforded mainly cis-opened adducts. At room temperature, however, only trans-opened adducts were obtained from (±)-anti- DB[a,l]PDE and only cis-opened adducts from (±)-syn-DB[a,l]PDE. Steric hindrance created by the fjord region may be an important factor for the stereoselectivity observed at room temperature.
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U2 - 10.1021/tx980197x
DO - 10.1021/tx980197x
M3 - Article
C2 - 10490496
AN - SCOPUS:0032871769
SN - 0893-228X
VL - 12
SP - 758
EP - 767
JO - Chemical Research in Toxicology
JF - Chemical Research in Toxicology
IS - 9
ER -