𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of the phenolic esters of 1-hydroxy- and 3-hydroxy-7,8-diol-9,10-epoxides of benzo[a]pyrene

✍ Scribed by Panna L. Kole; Subodh Kumar


Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
291 KB
Volume
31
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ 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


πŸ“œ SIMILAR VOLUMES


Role of glutathione conjugate efflux in
✍ Sanjay K. Srivastava; Simon C. Watkins; Erin Schuetz; Shivendra V. Singh πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 277 KB

## Abstract Glutathione (GSH) conjugation of (+)‐anti‐benzo[__a__]pyrene‐7,8‐diol‐9,10‐epoxide [(+)‐anti‐BPDE], 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

Novel trifluoroethanol mediated synthesi
✍ Andagar R Ramesha; Heiko Kroth; Donald M Jerina πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 74 KB

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