Postsynthetic generation of a major acrolein adduct of 2′-deoxyguanosine in oligomeric DNA

被引:47
作者
Khullar, S
Varaprasad, CV
Johnson, F [1 ]
机构
[1] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Dept Pharmacol Sci, Stony Brook, NY 11794 USA
关键词
D O I
10.1021/jm980605u
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
引用
收藏
页码:947 / 950
页数:4
相关论文
共 18 条
  • [1] A high-yield synthesis of deoxy-2-fluoroinosine and its incorporation into oligonucleotides.
    Adib, A
    Potier, PF
    Doronina, S
    Huc, I
    Behr, JP
    [J]. TETRAHEDRON LETTERS, 1997, 38 (17) : 2989 - 2992
  • [2] IDENTIFICATION OF ADDUCTS FORMED BY REACTION OF GUANINE NUCLEOSIDES WITH MALONDIALDEHYDE AND STRUCTURALLY RELATED ALDEHYDES
    BASU, AK
    OHARA, SM
    VALLADIER, P
    STONE, K
    MOLS, O
    MARNETT, LJ
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1988, 1 (01) : 53 - 59
  • [3] BEAUCAGE SL, 1993, METHODS MOL BIOL
  • [4] BENAMIRA M, 1992, J BIOL CHEM, V267, P22392
  • [5] CHARACTERIZATION OF THYMIDINE ADDUCTS FORMED BY ACROLEIN AND 2-BROMOACROLEIN
    CHENNA, A
    RIEGER, RA
    IDEN, CR
    [J]. CARCINOGENESIS, 1992, 13 (12) : 2361 - 2365
  • [6] A STUDY OF CHEMICAL CARCINOGENESIS .104. A STUDY OF REACTIONS OF ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS WITH DEOXYGUANOSINE
    CHUNG, FL
    ROY, KR
    HECHT, SS
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (01) : 14 - 17
  • [7] CHUNG FL, 1984, CANCER RES, V44, P990
  • [8] Improved strategies for postoligomerization synthesis of oligodeoxynucleotides bearing structurally defined adducts at the N-2 position of deoxyguanosine
    DeCorte, BL
    Tsarouhtsis, D
    Kuchimanchi, S
    Cooper, MD
    Horton, P
    Harris, CM
    Harris, TM
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1996, 9 (03) : 630 - 637
  • [9] *DIV MED CHEM, 1998, 216 NAT ACS M BOST M
  • [10] AN HPLC-EC ASSAY FOR 1,N-2-PROPANO ADDUCTS OF 2'-DEOXYGUANOSINE WITH 4-HYDROXYNONENAL AND OTHER ALPHA,BETA-UNSATURATED ALDEHYDES
    DOUKI, T
    AMES, BN
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1994, 7 (04) : 511 - 518