Synthesis and preliminary cytotoxicity study of a cephalosporin-CC-1065 analogue prodrug
AUTOR(ES)
Wang, Yuqiang
FONTE
BioMed Central
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=59845Documentos Relacionados
- Synthesis and cytotoxicity of a biotinylated CC-1065 analogue
- Characterization of an adduct between CC-1065 and a defined oligodeoxynucleotide duplex.
- Theoretical study of the sequence specificity in the covalent binding of the antitumor drug CC-1065 to DNA.
- CC-1065 and the duocarmycins: unraveling the keys to a new class of naturally derived DNA alkylating agents.
- (+)-CC-1065 as a structural probe of Mu transposase-induced bending of DNA: overcoming limitations of hydroxyl-radical footprinting