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Chemical structure of benzo[a]pyrene Chemical structure of benzo[e]pyrene. A benzopyrene is an organic compound with the formula C 20 H 12.Structurally speaking, the colorless isomers of benzopyrene are pentacyclic hydrocarbons and are fusion products of pyrene and a phenylene group.
Benzo[a]pyrene (BaP or B[a]P) is a polycyclic aromatic hydrocarbon and the result of incomplete combustion of organic matter at temperatures between 300 °C (572 °F) and 600 °C (1,112 °F). The ubiquitous compound can be found in coal tar, tobacco smoke and many foods, especially grilled meats.
Benzo[e]pyrene is a polycyclic aromatic hydrocarbon with the chemical formula C 20 H 12. It is listed as a Group 3 carcinogen by the IARC. [1] See also. Benzopyrene;
(like numbers place letters first are omitted while indexing compounds, later on they are added again if necessary) the proper name for this compound is Benzo[a]anthracene. Pyrene: Benzo[a]pyrene, by adding 4 carbon atoms to pyrene the left most ring is the extra one. Benzo[e]pyrene, by adding 4 carbon atoms to the pyrene along its short axis.
This test showed that myricetin was more effective in preventing mutagenesis initiated by certain carcinogenic polycyclic aromatic hydrocarbons (benzo(a)pyrene, dibenzo(a,h)pyrene, and dibenzo(a,i)pyrene) as compared to others in which it was less effective in preventing against mutagenesis (benzo(a)pyrene 4, 5-oxide and the bay-region diol ...
One significant compound the bacteria can biodegrade is benzo(a)pyrene (BaP). [13] BaP is a polycyclic aromatic hydrocarbon (PAH), well-known organic pollutant associated with properties of teratogenicity, mutagenicity, and carcinogenicity. BaP is a degradation-resistant compound; thus, it is more inclined to accumulate in the environment. [14]
Benzo[a]pyrene-7,8-dihydrodiol-9,10-epoxide is a metabolite of benzo[a]pyrene formed by the introduction of vicinal hydroxyl and epoxide functional groups to the fifth benzene ring. [7] These oxidations are stereoselective , producing the pair of enantiomers with the hydroxyl groups on opposite sides of the pyrene plane and with the epoxide on ...
Benzo[a]pyrene now has been well characterized in toxicology reports and is a known potent carcinogen. [10] Benzo[ a ]pyrene requires metabolic activation to become, ultimately, BPDE ((±)- anti -7β,8α-dihydroxy-9α,10α-epoxy-7,8,9,10-tetrahydrobenzo[ a ]pyrene) which binds to the DNA to form a covalent trans adducts at the N2 position of ...