The Stereochemistry of trans-4-Hydroxynonenal-Derived Exocyclic 1,N(2)-2′-Deoxyguanosine Adducts Modulates Formation of Interstrand Cross-Links in the 5′-CpG-3′ Sequence

Eitemau Tebyg

• Rearrangement of the (6S,8R,11S) and (6R,8S,11R) Exocyclic 1,N(2)-Deoxyguanosine Adducts of trans-4-Hydroxynonenal to N(2)-Deoxyguanosine Cyclic Hemiacetal Adducts When Placed Complementary to Cytosine in Duplex DNA
  gan: Huang, Hai, et al.
  Cyhoeddwyd: (2008)
• Conformational Interconversion of the trans-4-Hydroxynonenal-Derived (6S,8R,11S) 1,N(2)-Deoxyguanosine Adduct When Mismatched with Deoxyadenosine in DNA
  gan: Huang, Hai, et al.
  Cyhoeddwyd: (2009)
• Spectroscopic Characterization of Interstrand Carbinolamine Crosslinks Formed in the 5'-CpG-3' Sequence by the Acrolein-Derived γ-OH-1,N(2)-Propano-2'-deoxyguanosine DNA Adduct
  gan: Cho, Young-Jin, et al.
  Cyhoeddwyd: (2005)
• Simplified synthesis of individual stereoisomers of the 4-hydroxynonenal adducts of deoxyguanosine
  gan: Christov, Plamen P, et al.
  Cyhoeddwyd: (2013)
• Stereospecific Formation of Interstrand Carbinolamine DNA Crosslinks by Crotonaldehyde- and Acetaldehyde-Derived α-CH(3)-γ-OH-1,N(2)-Propano-2’-deoxyguanosine Adducts in the 5′-CpG-3′ Sequence
  gan: Cho, Young-Jin, et al.
  Cyhoeddwyd: (2006)