BIOMAT Database Logo BIOMAT Database Logo

[Electronic properties of N-heteroaromatics. 38. Chemical carcinogens. (12). The interaction of 4-nitroquinoline 1-oxide with phenol and its derivatives. Charge transfer and hydrogen bonding]. 1969

T Okano, and Y Sato, and S Takenaka

UI MeSH Term Description Entries
D007259 Infrared Rays That portion of the electromagnetic spectrum usually sensed as heat. Infrared wavelengths are longer than those of visible light, extending into the microwave frequencies. They are used therapeutically as heat, and also to warm food in restaurants. Heat Waves,Heat Wave,Infrared Ray,Ray, Infrared,Rays, Infrared,Wave, Heat,Waves, Heat
D010636 Phenols Benzene derivatives that include one or more hydroxyl groups attached to the ring structure.
D011804 Quinolines
D002273 Carcinogens Substances that increase the risk of NEOPLASMS in humans or animals. Both genotoxic chemicals, which affect DNA directly, and nongenotoxic chemicals, which induce neoplasms by other mechanism, are included. Carcinogen,Oncogen,Oncogens,Tumor Initiator,Tumor Initiators,Tumor Promoter,Tumor Promoters,Initiator, Tumor,Initiators, Tumor,Promoter, Tumor,Promoters, Tumor
D002626 Chemistry, Pharmaceutical Chemistry dealing with the composition and preparation of agents having PHARMACOLOGIC ACTIONS or diagnostic use. Medicinal Chemistry,Chemistry, Pharmaceutic,Pharmaceutic Chemistry,Pharmaceutical Chemistry,Chemistry, Medicinal
D006859 Hydrogen The first chemical element in the periodic table with atomic symbol H, and atomic number 1. Protium (atomic weight 1) is by far the most common hydrogen isotope. Hydrogen also exists as the stable isotope DEUTERIUM (atomic weight 2) and the radioactive isotope TRITIUM (atomic weight 3). Hydrogen forms into a diatomic molecule at room temperature and appears as a highly flammable colorless and odorless gas. Protium,Hydrogen-1
D013057 Spectrum Analysis The measurement of the amplitude of the components of a complex waveform throughout the frequency range of the waveform. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed) Spectroscopy,Analysis, Spectrum,Spectrometry

Related Publications

T Okano, and Y Sato, and S Takenaka
[Electronic properties of N-heteroaromatics. XLI. Charge-transfer interactions of the carcinogen 4-nitroquinoline 1-oxide with methylsubstituted benzenes and methylsubstituted aniline derivatives].
October 1969, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
T Okano, and Y Sato, and S Takenaka
[Electronic properties of N-heteroaromatics. 31. Interaction of the carcinogen 4-nitroquinoline 1-oxide with nicotinamide].
March 1969, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
T Okano, and Y Sato, and S Takenaka
[Electronic properties of N-heteroaromatics. XXX. Chemical carcinogens. Conversion of 4-nitroquinoline 1-oxide into 4-hydroxyaminoquinoline 1-oxide in the presence of ascorbic acid].
January 1969, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
T Okano, and Y Sato, and S Takenaka
[Electronic properties of N-heteroaromatics. XIV. Charge-transfer interactions between 4-nitropyridine 1-oxide and aniline derivatives].
November 1967, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
T Okano, and Y Sato, and S Takenaka
Electronic properties of N-heteroaromatics. XXXV. Further observations on the charge transfer interaction of the carcinogen, 4-nitroquinoline 1-oxide, with DNA and deoxyribonucleosides: analysis of the visible difference bands.
June 1969, Gan,
T Okano, and Y Sato, and S Takenaka
Electronic properties of N-heteroaromatics. XL. A nuclear magnetic resonance study of the interaction of 4-nitroquinoline 1-oxide with deoxyribonucleosides.
October 1969, Gan,
T Okano, and Y Sato, and S Takenaka
Charge transfer in the molecular interaction of 4-nitroquinoline 1-oxide and related carcinogens with DNA and deoxyribonucleosides.
February 1969, Gan,
T Okano, and Y Sato, and S Takenaka
[Electronic properties of N-heteroaromatics. XXIV. Interactions of the carcinogen 4-nitroquinoline 1-oxide with thiamine. Complex formation and substitution reaction].
September 1968, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
T Okano, and Y Sato, and S Takenaka
In vivo interaction of 4-nitroquinoline-1-oxide and its derivatives with DNA.
November 1967, Nature,
T Okano, and Y Sato, and S Takenaka
The in vitro interaction of the carcinogens, 4-nitroquinoline-N-oxide and its metabolite 4-hydroxylaminoquinoline-N-oxide, with intact rat liver mitochondria.
February 1978, Chemico-biological interactions,
Copied contents to your clipboard!