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  2. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    As a result, while anthracene reacts with maleic acid, phenanthrene does not, and triphenylene is the most stable species of these three. [ 1 ] Three Clar structures with an increasing number of π-sextets: anthracene (on the left), phenanthrene (in the middle), and triphenylene (on the right).

  3. Phenanthrene - Wikipedia

    en.wikipedia.org/wiki/Phenanthrene

    Phenanthrene is used to make dyes, plastics, pesticides, explosives, and drugs. It has also been used to make bile acids, cholesterol and steroids. [3] Phenanthrene occurs naturally and also is a man-made chemical. Commonly, humans are exposed to phenanthrene through inhalation of cigarette smoke, but there are many routes of exposure.

  4. Polycyclic aromatic hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Polycyclic_aromatic...

    A Polycyclic aromatic hydrocarbon (PAH) is a class of organic compounds that is composed of multiple aromatic rings.Most are produced by the incomplete combustion of organic matter— by engine exhaust fumes, tobacco, incinerators, in roasted meats and cereals, [1] or when biomass burns at lower temperatures as in forest fires.

  5. Anthracene - Wikipedia

    en.wikipedia.org/wiki/Anthracene

    Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C 14 H 10, consisting of three fused benzene rings. It is a component of coal tar. Anthracene is used in the production of the red dye alizarin and other dyes. Anthracene is colorless but exhibits a blue (400–500 nm peak) fluorescence under ultraviolet radiation. [13]

  6. DNA adduct - Wikipedia

    en.wikipedia.org/wiki/DNA_adduct

    A metabolite of benzopyrene forms an intercalated DNA adduct, at center. In molecular genetics, a DNA adduct is a segment of DNA bound to a cancer-causing chemical. This process could lead to the development of cancerous cells, or carcinogenesis. DNA adducts in scientific experiments are used as biomarkers of exposure.

  7. Diboraanthracene - Wikipedia

    en.wikipedia.org/wiki/Diboraanthracene

    The most widely used synthetic route to DBA utilizes electrophilic borylation chemistry as the key transformation, [6] [7] which dates to 1969 from Seibert et al. [8] and 1998 from Eisch et al. [9] Starting with the commercially available chemical 1,2-dibromobenzene, lithium-halogen exchange [10] followed by silylation yields 1,2-bis(trimethylsilyl) benzene as the intermediate.

  8. The 5 Best Proteins to Eat If You’re Taking a Weight-Loss ...

    www.aol.com/5-best-proteins-eat-youre-001354105.html

    Protein is an essential macronutrient for everyone, and if you’re taking a weight loss drug, such as GLP-1 medications, you should be extra mindful about your intake.This is because muscle loss ...

  9. Genotoxicity - Wikipedia

    en.wikipedia.org/wiki/Genotoxicity

    The alteration can have direct or indirect effects on the DNA: the induction of mutations, mistimed event activation, and direct DNA damage leading to mutations. The permanent, heritable changes can affect either somatic cells of the organism or germ cells to be passed on to future generations. [ 1 ]