Studies on the base pair binding specificity of CC-1065 to oligomer duplexes

This publication has 16 references indexed in Scilit:

• The binding of CC-1065 to thymidine and deoxyadenosine oligonucleotides and to poly(dA) · poly(dT)
  Chemico-Biological Interactions, 1986
• Reaction of the antitumor antibiotic CC-1065 with DNA. Location of the site of thermally induced strand breakage and analysis of DNA sequence specificity
  Biochemistry, 1985
• Binding of CC‐1065 to poly‐ and oligonucleotides
  Biopolymers, 1985
• Reaction of the Antitumor Antibiotic CC-1065 with DNA: Structure of a DNA Adduct with DNA Sequence Specificity
  Science, 1984
• Characterization of an adduct between CC-1065 and a defined oligodeoxynucleotide duplex
  Nucleic Acids Research, 1984
• The structure of CC-1065, a potent antitumor agent and its binding to DNA
  Journal of the American Chemical Society, 1981
• Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis
  Tetrahedron Letters, 1981
• Structure of CC-1065 (NSC-298223), a new antitumor antibiotic.
  The Journal of Antibiotics, 1980
• CC-1065 (NSC-298223), a new antitumor antibiotic. Production, in vitro biological activity, microbiological assays and taxonomy of the producing microorganism.
  The Journal of Antibiotics, 1978
• Studies on Polynucleotides. XXIV.¹ The Stepwise Synthesis of Specific Deoxyribopolynucleotides (4).² Protected Derivatives of Deoxyribonucleosides and New Syntheses of Deoxyribonucleoside-3″ Phosphates³
  Journal of the American Chemical Society, 1963