ID Name Structure References (top 5) Molecular Target(s)


in 1 ingredients:

  • 63
  • in 5 recipes:

  • 146
  • 174
  • 285
  • 317
  • 430

  • Properties
    C10H13N5O5    283.24

    1:  Fuhrman FA, Fuhrman GJ, Nachman RJ, Mosher HS.
    Isoguanosine: isolation from an animal.
    Science.    impact factor:   24.595
    1981;  212(4494): 557-8

    2:  Kamiya H, Kasai H.
    Formation of 2-hydroxydeoxyadenosine triphosphate, an oxidatively damaged nucleotide, and its incorporation by DNA polymerases. Steady-state kinetics of the incorporation.
    J Biol Chem.    impact factor:   7.666
    1995;  270(33): 19446-50

    3:  Roberts C, Chaput JC, Switzer C.
    Beyond guanine quartets: cation-induced formation of homogenous and chimeric DNA tetraplexes incorporating iso-guanine and guanine.
    Chem Biol.    impact factor:   6.242
    1997;  4(12): 899-908

    4:  Kawakami J, Kamiya H, Yasuda K, Fujiki H, Kasai H, Sugimoto N.
    Thermodynamic stability of base pairs between 2-hydroxyadenine and incoming nucleotides as a determinant of nucleotide incorporation specificity during replication.
    Nucleic Acids Res.    impact factor:   5.748
    2001;  29(16): 3289-96

    5:  Ohtsubo T, Nishioka K, Imaiso Y, Iwai S, Shimokawa H, Oda H, Fujiwara T, Nakabeppu Y.
    Identification of human MutY homolog (hMYH) as a repair enzyme for 2-hydroxyadenine in DNA and detection of multiple forms of hMYH located in nuclei and mitochondria.
    Nucleic Acids Res.    impact factor:   5.748
    2000;  28(6): 1355-64

    Time used: 437 milliseconds.

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