Synthesis of 13C4-labelled oxidized metabolites of the carcinogenic polycyclic aromatic hydrocarbon benzo[a]pyrene |
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Authors: | Anhui Wu Daiwang Xu Ding Lu Trevor M Penning Ian A Blair Ronald G Harvey |
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Institution: | 1. The Ben May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, United States;2. The Centers for Cancer Pharmacology and Excellence in Environmental Toxicology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States |
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Abstract: | Polycyclic aromatic hydrocarbons (PAHs), such as benzoa]pyrene (BaP), are ubiquitous environmental contaminants that are implicated in causing lung cancer. BaP is a component of tobacco smoke that is transformed enzymatically to active forms that interact with DNA. We reported previously development of a sensitive stable isotope dilution LC/MS method for analysis of BaP metabolites. We now report efficient syntheses of 13C4-BaP and the complete set of its 13C4-labelled oxidized metabolites needed as internal standards They include the metabolites not involved in carcinogenesis (Group A) and the metabolites implicated in initiation of cancer (Group B). The synthetic approach is novel, entailing use of Pd-catalyzed Suzuki, Sonogashira, and Hartwig cross-coupling reactions combined with PtCl2-catalyzed cyclization of acetylenic compounds. This synthetic method requires fewer steps, employs milder conditions, and product isolation is simpler than conventional methods of PAH synthesis. The syntheses of 13C4-BaP and 13C4-BaP-8-ol each require only four steps, and the 13C-atoms are all introduced in a single step. 13C4-BaP-8-ol serves as the synthetic precursor of all the oxidized metabolites of 13C-BaP implicated in initiation of cancer. The isotopic purities of the synthetic 13C4-BaP metabolites were estimated to be ≥99.9%. |
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Keywords: | Carcinogenic polycyclic aromatic hydrocarbons (PAHs) Enzymatic activation of PAH carcinogens Synthesis of PAHs via Pd-catalyzed cross-coupling reactions AKR1A1"} {"#name":"keyword" "$":{"id":"cekeyw80"} "$$":[{"#name":"text" "_":"aldo-keto reductase 1A1 enzyme BTI"} {"#name":"keyword" "$":{"id":"cekeyw200"} "$$":[{"#name":"text" "_":"bis-(trifluoroacetoxy)iodobenzene IBX"} {"#name":"keyword" "$":{"id":"cekeyw220"} "$$":[{"#name":"text" "$$":[{"#name":"italic" "_":"o"} {"#name":"__text__" "_":"-iodoxybenzoic acid 8′-hydroxy-2′-deoxyguanosine PAH"} {"#name":"keyword" "$":{"id":"cekeyw520"} "$$":[{"#name":"text" "_":"polycyclic aromatic hydrocarbon ROS"} {"#name":"keyword" "$":{"id":"cekeyw540"} "$$":[{"#name":"text" "_":"reactive oxygen species TMSA"} {"#name":"keyword" "$":{"id":"cekeyw560"} "$$":[{"#name":"text" "_":"(trimethylsilyl)acetylene |
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