Methanolysis of the K-region epoxide of 7,12-dimethylbenz (a) anthracene (DMBA) gave rise to two hydroxy-methoxy derivatives which were dehydrated to S-methoxy-DMBA and 6-methoxy-DMBA at a ratio of 5: 1. The data indicate that methanol attacks preferentially at the 5-position of the arene oxide. The
Oncogenicity of k-region epoxides of benzo(a)pyrene and 7,12-dimethylbenz(a)anthracene
✍ Scribed by James W. Flesher; Ronald G. Harvey; Katherine L. Sydnor
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- French
- Weight
- 252 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Female Sprague‐Dawley rats were given a subcutaneous injection of the parent hydrocarbon or its K‐region epoxide in 0.1 ml sesame oil on alternate days to a total of 30 doses and observed for sarcoma at the site of injection for 275 days. The parent compounds, benzo(a)pyrene (0.2 μmole/dose) and 7,12‐dimethylbenz(a)anthracene (0.2 μmole/dose), induced sarcoma in 100% of the animals with an average latent period of 101 and 95 days, respectively, whereas five of 12 rats (42%) injected with the K‐region epoxide of B(a)P (1.0 μmole/dose), developed sarcoma in 151±22 days, and the K‐region epoxide of DMBA (0.4 μmole/dose) failed to elicit tumors. Under these experimental conditions, these K‐region epoxides are, at best, only weak carcinogens.
📜 SIMILAR VOLUMES
## Abstract Structural information about the products formed when 7,12‐dimethylbenz(__a__)anthracene (DMBA) is bound to DNA in mammalian cell cultures has been sought through studies of the photosensitivities of these products and of various model compounds. Under conditions of light exposure in wh
## Abstract One of the most potent carcinogens is 7,12‐dimethylbenz(a)anthracene (7,12‐DMBA), which is used routinely to conduct studies to evaluate carcinogen inhibitors. Its pharmacokinetics have not been reported in the literature. In view of its significant effects on drug metabolizing enzymes
T r i t i u m l a b e l l e d K-region oxides o f pyrene, benzoCalpyrene and d i b e n z [ G ] a n t h r a c e n e have been prepared by c y c l i z a t i o n o f the corresponding t r a n s -d i h y d r o d i o l s which were obtained by r e d u c t i o n o f K-region quinones w i t h sodium b o r