Synthetic studies on antitumor antibiotic, bleomycin. 27. Man-designed bleomycin with altered sequence specificity in DNA cleavage

1990 ◽  
Vol 112 (2) ◽  
pp. 838-845 ◽  
Author(s):  
Masami Otsuka ◽  
Takeshi Masuda ◽  
Andreas Haupt ◽  
Masaji Ohno ◽  
Takashi Shiraki ◽  
...  
Science ◽  
1984 ◽  
Vol 226 (4676) ◽  
pp. 843-844 ◽  
Author(s):  
L. Hurley ◽  
V. Reynolds ◽  
D. Swenson ◽  
G. Petzold ◽  
T. Scahill

1985 ◽  
Vol 16 (31) ◽  
Author(s):  
M. OTSUKA ◽  
M. NARITA ◽  
M. YOSHIDA ◽  
S. KOBAYASHI ◽  
M. OHNO ◽  
...  

1994 ◽  
Vol 7 (3) ◽  
pp. 227-231 ◽  
Author(s):  
M. Palumbo ◽  
M. Mabilia ◽  
A. Pozzan ◽  
G. Capranico ◽  
S. Tinelli ◽  
...  

1976 ◽  
Vol 54 (16) ◽  
pp. 2563-2572 ◽  
Author(s):  
J. William Lown ◽  
Soo-Khoon Sim

The syntheses of a group of 2-(o-nitrophenyl)- and 2-(o-aminophenyl)-5,8-quinolinediones which are structurally related to the antitumor antibiotic streptonigrin are described. Ambiguities in the position of required nucleophilic displacements are resolved by independent synthesis. The rates of single strand cleavage of PM2 ccc-DNA (covalently-closed circular-DNA) induced by these compounds are compared, which correlates with antitumor activity. The 2-(o-nitrophenyl) derivatives give consistently more rapid DNA cleavage than the 2-(o-aminophenyl) compounds. The autoxidations of the dihydroxyquinolines are subject to selective catalysis by Cu2+ on. 2-(o-Aminophenyl)-7-amino-6-methoxy-5,6-quinolinedione which has a substitution pattern most closely resembling streptonigrin also closely parallels the rate of scission of DNA of the latter in the presence of NADPH.


ChemInform ◽  
2010 ◽  
Vol 26 (11) ◽  
pp. no-no
Author(s):  
N. FUJII ◽  
Y. YAMASHITA ◽  
K. ANDO ◽  
T. AGATSUMA ◽  
Y. SAITOH ◽  
...  

1993 ◽  
Vol 46 (7) ◽  
pp. 1173-1174 ◽  
Author(s):  
NOBORU FUJII ◽  
YOSHINORI YAMASHITA ◽  
SHIGERU CHIBA ◽  
YOUICHI UOSAKI ◽  
YUTAKA SAITOH ◽  
...  

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