Titlebook: Chemistry and Biological Actions of 4-Nitroquinoline 1-Oxide; Hideya Endo,Tetsuo Ono,Takashi Sugimura Book 1971 Springer-Verlag Berlin · H

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Microbiology,In 1955, . applied the chemical to a fungus, ., in the hope of inducing mutants. This served as trigger to start a new road of microbiology with 4-nitroquinoline 1-oxide.

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Open Gauge Algebra and Ghost Unification,ctron-withdrawing effect of the ring nitrogen, and that a representative electrophile of the nitronium cation attacks the 5- and 8-positions of the molecule to produce 5- and 8-nitroquinolines under rather drastic nitration conditions. In 1943, . speculated on the basis of his brilliant work on arom

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Anomalous Jacobians and the Vector Anomaly,ical structure: thus, it has two strong polar groups, i. e. the N-oxide and nitro groups in the molecule, and for this reason 4-nitroquinoline 1-oxide is susceptible to nucleophilic attack in chemical reaction. The or-electronic energy obtained by means of the molecular orbital method reflects this

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Quick-Turnaround ASIC Design in VHDLs metabolism, identification of the active principle and its target in carcinogenesis. However, because of the difficulty of analyzing animal cells, the natural tendency was to confine the initial work to the study of the drug’s effects on microorganisms. It was these bacterial and phage studies whi

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Book 1971nitroquinoline i-oxide. Original papers on this subject are numerous and widely scattered over many branches of science; it was felt that these papers should be reviewed and the knowledge brought together in one volume before it became too unwieldy. This we have attempted to do in this monograph. Ou

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Molecular Aspects of the Action,ate, which interacts with DNA resulting in DNA inactivation, gene mutations and the impairment of transcriptional and translational processes. This chapter deals with the molecular aspects of the effects of 4-nitroquinoline 1-oxide and its derivatives, mainly focussing on their actions on macromolecules and their synthesis.