Synthesis of the phenolic esters of 1-hydroxy- and 3-hydroxy-7,8-diol-9,10-epoxides of benzo[a]pyrene
β Scribed by Panna L. Kole; Subodh Kumar
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 291 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A chemical synthesis of the phenolic ester of the trio1 epoxide derivatives of carcinogenic benzo[alpyrene is described.
The chemical synthesis of the various reactive metabolites has been an essential factor in elucidating the molecular mechanism that is responsible for QOlycyClic aromatic hydrocarbon
π SIMILAR VOLUMES
## Abstract Glutathione (GSH) conjugation of (+)βantiβbenzo[__a__]pyreneβ7,8βdiolβ9,10βepoxide [(+)βantiβBPDE], the activated metabolite of benzo[__a__]pyrene, is believed to be an important mechanism in detoxification of this environmental and dietary carcinogen. Here, we demonstrate that the intr
The exocyclic amino groups of deoxyadenosine and deoxyguanosine readily add to C-10 of the benzo[a]pyrene 7,8-diol 9,10-epoxides at room temperature overnight in trifluoroethanol. Whereas the dG adducts are obtained as a mixture of cis-and trans-opened diastereomers, the dA adducts arise exclusively