Synthesis of hydroxyl containing N-imides of 4-substituted naphthalic acid

1999 ◽  
Vol 35 (5) ◽  
pp. 621-624 ◽  
Author(s):  
R. A. Minakova ◽  
A. I. Bedrik ◽  
V. M. Shershukov ◽  
Yu. N. Surov ◽  
N. S. Pivnenko
Keyword(s):  
Naphthalic Acid

Mechanism of DNA strand breaks by mitonafide, an imide derivative of 3-nitro-1,8-naphthalic acid

1985 ◽  
Vol 34 (21) ◽  
pp. 3845-3852 ◽  
Author(s):  
Birandra K. Sinha ◽  
John Strong ◽  
Neil W. Gibson ◽  
Balaraman Kalyanaraman
Keyword(s):  
Dna Strand Breaks ◽  
Strand Breaks ◽  
Dna Strand ◽  
Naphthalic Acid

ChemInform Abstract: Formation and Cleavage of the Quinazolinium Ring in Vilsmeier-Haack Formylation of 4-Dialkylamino-Substituted Naphthalic Acid Derivatives.

ChemInform ◽  
2010 ◽  
Vol 32 (30) ◽  
pp. no-no
Author(s):  
L. D. Patsenker ◽  
I. G. Ermolenko ◽  
E. E. Artyukhova ◽  
B. M. Krasovitskii
Keyword(s):  
Naphthalic Acid

Synthesis and mode(s) of action of a new series of imide derivatives of 3-nitro-1,8 naphthalic acid

1980 ◽  
Vol 4 (1) ◽  
Author(s):  
M.F. Bra�a ◽  
J.M. Castellano ◽  
C.M. Rold�n ◽  
A. Santos ◽  
D. V�zquez ◽  
...  
Keyword(s):  
Derivatives Of ◽  
Naphthalic Acid

Formation and cleavage of the quinazolinium ring in Vilsmeier-Haack formylation of 4-dialkylamino-substituted naphthalic acid derivatives

2000 ◽  
Vol 36 (5) ◽  
pp. 611-612 ◽  
Author(s):  
L. D. Patsenker ◽  
I. G. Ermolenko ◽  
E. E. Artyukhova ◽  
B. M. Krasovitskii
Keyword(s):  
Naphthalic Acid

Mode of Action of Naphthalic Acid as a Safener for Imazethapyr

1991 ◽  
Vol 46 (9-10) ◽  
pp. 893-896 ◽  
Author(s):  
Dale L. Shaner
Keyword(s):  
Root System ◽  
Mode Of Action ◽  
Potassium Salt ◽  
Oxidase Inhibitor ◽  
Mixed Function Oxidase ◽  
Meristematic Tissue ◽  
Naphthalic Acid

Abstract The tolerance of maize to root-applied imazethapyr can be increased by pretreating plants with the potassium salt of naphthalic acid (NAK). This safening effect appears to be the result of NAK stimulating the ability of maize to rapidly metabolize imazethapyr to 5′-hydroxyethyl-imazethapyr, possibly through a mixed function oxidase. The safening effect of NAK can be antagonized by 1-aminobenzotriazole (ABT), a mixed function oxidase inhibitor. The increased rate of hydroxylation of imazethapyr to 5′-hydroxyethyl-imazethapyr immobilizes the herbicide in the root system which decreases the accumulation of herbicide in the meristematic tissue. This decreased accumulation, in turn, lowers the phytotoxicity of imazethapyr on maize.

scholarly journals Intercalative binding to DNA of antitumour drugs derived from 3-nitro-1,8-naphthalic acid

1979 ◽  
Vol 7 (1) ◽  
pp. 217-230 ◽  
Author(s):  
M.J. Waring ◽  
A. González ◽  
A. Jiménez ◽  
D. Vázquez
Keyword(s):  
Antitumour Drugs ◽  
Intercalative Binding ◽  
Naphthalic Acid
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