Covalent modification and single-strand scission of DNA by a new antitumor antibiotic kapurimycin A3

Biochemistry ◽  
1990 ◽  
Vol 29 (46) ◽  
pp. 10449-10455 ◽  
Author(s):  
Mitsunobu Hara ◽  
Mayumi Yoshida ◽  
Hirofumi Nakano
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.


FEBS Letters ◽  
1979 ◽  
Vol 107 (2) ◽  
pp. 355-358 ◽  
Author(s):  
Hiroyoshi Ariga ◽  
Hiroto Shimojo ◽  
So Hidaka ◽  
Kin-ichiro Miura

1974 ◽  
Vol 15 (3) ◽  
pp. 148-155
Author(s):  
K. IGARASHI ◽  
F. YATAGAI ◽  
T. TAKAHASHI ◽  
A. MATSUYAMA

Biochemistry ◽  
1990 ◽  
Vol 29 (24) ◽  
pp. 5676-5681 ◽  
Author(s):  
Mitsunobu Hara ◽  
Yutaka Saitoh ◽  
Hirofumi Nakano

Sign in / Sign up

Export Citation Format

Share Document