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Quoted phrases not found in phrase index: "aceto-b-naphthylamine", "acetyl-b-naphthylamine"
Page 1
Metabolism of 2-naphthylamine and benzidine by rat and human bladder organ cultures.
Moore BP, Potter PM, Hicks RM. Moore BP, et al. Carcinogenesis. 1984 Jul;5(7):949-54. doi: 10.1093/carcin/5.7.949. Carcinogenesis. 1984. PMID: 6733857
In contrast, large amounts of the acetylated metabolites, N-acetylbenzidine, N,N-diacetylbenzidine and N-acetyl-2-naphthylamine were formed both in rat and human bladder cultures. The results suggest that metabolism of these carcinogens in situ in the …
In contrast, large amounts of the acetylated metabolites, N-acetylbenzidine, N,N-diacetylbenzidine and N-acetyl-2-na
The biochemistry of aromatic amines. The metabolism of 2-naphthylamine and 2-naphthylhydroxylamine derivatives.
Boyland E, Manson D. Boyland E, et al. Biochem J. 1966 Oct;101(1):84-102. doi: 10.1042/bj1010084. Biochem J. 1966. PMID: 5971797 Free PMC article.
1. 2-Naphthylhydroxylamine and 2-nitrosonaphthalene were present in urine of dogs but not of guinea pigs, hamsters, rabbits or rats dosed with 2-naphthylamine. N-Acetyl-2-naphthylhydroxylamine and its O-sulphonic acid and O-glucosiduronic acid w …
1. 2-Naphthylhydroxylamine and 2-nitrosonaphthalene were present in urine of dogs but not of guinea pigs, hamsters, rabbits or rats dosed wi …
The metabolic activation of 2-naphthylamine to mutagens in the Ames test.
Tong S, Smith J, Manson D, Gorrod JW, Ioannides C. Tong S, et al. Anticancer Res. 1986 Sep-Oct;6(5):1107-12. Anticancer Res. 1986. PMID: 3800318
In the presence of activation systems derived from control and 3-methylcholanthrene-treated hamsters and Arochlor 1254-treated rats only 2-naphthylamine exhibited a mutagenic response while its hydroxy-derivatives and 2-acetamidonaphthalene were devoid of mutagenici …
In the presence of activation systems derived from control and 3-methylcholanthrene-treated hamsters and Arochlor 1254-treated rats only 2-n …
Acylation of carcinogenic hydroxamic acids by carbamoyl phosphate to form reactive esters.
Lotlikar PD, Luha L. Lotlikar PD, et al. Biochem J. 1971 Aug;124(1):69-74. doi: 10.1042/bj1240069. Biochem J. 1971. PMID: 5126476 Free PMC article.
On the other hand the less reactive N-hydroxy derivatives of 2-acetamidonaphthalene, 2-acetamidophenanthrene and 4-acetamidostilbene reacted severalfold more with carbamoyl phosphate than with acetyl-CoA. 5. ...
On the other hand the less reactive N-hydroxy derivatives of 2-acetamidonaphthalene, 2-acetamidophenanthrene and 4-acet …