𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Aromatic amine carcinogenesis: Activation and interaction with nucleic acid bases

✍ Scribed by Gilda Loew; B. S. Sudhindra; S. Burt; G. R. Pack; R. Macelroy

Book ID
104579680
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
1022 KB
Volume
16
Category
Article
ISSN
0020-7608

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Theoretical studies on protein–nucleic a
Theoretical studies on protein–nucleic acid interactions. III. Stacking of aromatic amino acids with bases and base pairs of nucleic acids
✍ N. Vasant Kumar; Girjesh Govil πŸ“‚ Article πŸ“… 1984 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 658 KB

Stacking of aromatic amino acids tryptophan (Trp), tyrosine (Tyr), phenylalanine (Phe), and histidine (His) with bases and base pairs of nucleic acids has been studied. Stacking energies of the amino acid-base (or base pair) complexes have been calculated by second-order perturbation theory. Our res

Metabolic activation of chemical carcino
Metabolic activation of chemical carcinogens and binding of metabolites with nucleic acid bases
✍ Chikayoshi Nagata; Masahiko Kodama; Teruyuki Kimura; TamiΓ© Yamaguchi πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 English βš– 585 KB

## Abstract A free radical was produced enzymatically by incubating benzo(a)pyrene with liver microsomes. This radical, identified as the 6‐oxybenzo(a) pyrene radical, was sufficiently reactive to bind covalently with nucleic acid bases. Similar reactive free radicals were produced enzymatically fr

Conformer equilibria of triostin A and i
Conformer equilibria of triostin A and its conformer-specific interaction with nucleic acid bases
✍ Yoshimasa Kyogoku; Naoki Higuchi; Mayumi Watanabe; Keiichi Kawano πŸ“‚ Article πŸ“… 1981 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 587 KB

## Abstract A quinoxaline antibiotic triostin A has a bicyclic octadepsipeptide structure. Proton and carbon‐13 nmr spectra showed the presence of two symmetrical conformations favoring polar and nonpolar solvents, respectively. They interconvert slowly on the nmr time scale, and this slow intercon