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  2. 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.

  3. 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]

  4. Angiotensin II receptor blocker - Wikipedia

    en.wikipedia.org/wiki/Angiotensin_II_receptor...

    In August 2020, the European Medicines Agency (EMA) provided guidance to marketing authorization holders on how to avoid the presence of nitrosamine impurities in human medicines and asked them to review all chemical and biological human medicines for the possible presence of nitrosamines and to test the products at risk. [73]

  5. 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]

  6. Rifampicin - Wikipedia

    en.wikipedia.org/wiki/Rifampicin

    In August 2020, the U.S. Food and Drug Administration (FDA) became aware of nitrosamine impurities in certain samples of rifampin. [61] The FDA and manufacturers are investigating the origin of these impurities in rifampin, and the agency is developing testing methods for regulators and industry to detect the 1-methyl-4-nitrosopiperazine (MNP ...

  7. 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 ...

  8. N-Nitrosonornicotine - Wikipedia

    en.wikipedia.org/wiki/N-Nitrosonornicotine

    In cigarette smoke, NNN has been found in levels between 2.2 and 6.6 parts per million (ppm). The FDA has put limits of nitrosamines in other consumable products (such as cured meats) at levels below 10 parts per billion (ppb). [14]

  9. N-Nitrosodiethylamine - Wikipedia

    en.wikipedia.org/wiki/N-Nitrosodiethylamine

    N-Nitrosodiethylamine (NDEA) is an organic compound with the formula Et 2 NNO (Et = C 2 H 5).A member of the nitrosamines, it is a light-sensitive, volatile, clear yellow oil that is soluble in water, lipids, and other organic solvents.