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  2. Nitrosamine formation during digestion - Wikipedia

    en.wikipedia.org/wiki/Nitrosamine_formation...

    The effects of nitroso compounds vary dramatically across the gastrointestinal tract, and with diet. Nitroso compounds present in stool do not induce nitrosamine formation, because stool has neutral pH. [7] [8] Stomach acid catalyzes nitrosamine compound formation and is the main location of the reaction during digestion. [9]

  3. Tobacco-specific nitrosamines - Wikipedia

    en.wikipedia.org/wiki/Tobacco-specific_nitrosamines

    Among the tobacco-specific nitrosamines, nicotine-derived nitrosamine ketone (NNK) and N-nitrosonornicotine (NNN) are the most carcinogenic. [1] Others include N ′-nitrosoanatabine (NAT) and N-nitrosoanabasine (NAB). NNK and its metabolite 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) are potent systemic lung carcinogens in rats ...

  4. Nitrosamine - Wikipedia

    en.wikipedia.org/wiki/Nitrosamine

    With regards to structure, the C 2 N 2 O core of nitrosamines is planar, as established by X-ray crystallography. The N-N and N-O distances are 132 and 126 pm, respectively in dimethylnitrosamine, [13] one of the simplest members of a large class of N-nitrosamines. Nitrosamines are not directly carcinogenic.

  5. FDA Has Recalled Thousands of Bottles of Antidepressant ... - AOL

    www.aol.com/lifestyle/fda-recalled-thousands...

    FDA found the source of nitrosamines can be related to the drug's manufacturing process or its chemical structure or even the conditions in which they are stored or packaged," the FDA said in a ...

  6. N-Nitrosodimethylamine - Wikipedia

    en.wikipedia.org/wiki/N-Nitrosodimethylamine

    Generally, people should not be exposed to a lifetime risk of cancer exceeding 1 in 100,000 from nitrosamines in their medicines. [12] EU regulators first became aware of nitrosamines in medicines in mid-2018, and took regulatory actions, including recalling medicines and stopping the use of active substances from certain manufacturers. [12]

  7. N-Nitrosonornicotine - Wikipedia

    en.wikipedia.org/wiki/N-Nitrosonornicotine

    N-Nitrosonornicotine (NNN) is a tobacco-specific nitrosamine produced during the curing and processing of tobacco. NNN from synthesis of nicotine and nitrous acid. Toxicity

  8. NNK - Wikipedia

    en.wikipedia.org/wiki/NNK

    Nicotine-derived nitrosamine ketone (NNK) is one of the key tobacco-specific nitrosamines derived from nicotine. It plays an important role in carcinogenesis . [ 1 ] The conversion of nicotine to NNK entails opening of the pyrrolidine ring.

  9. Why that ‘raw water' trend is actually dangerous - AOL

    www.aol.com/article/lifestyle/2018/01/28/why...

    The article argues that advantages in dental technology, including fluoride toothpaste, are the real cause of our perfect smiles. Nowadays, the fluoride in the water might be unnecessary.