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  2. Pyrrolizidine alkaloid - Wikipedia

    en.wikipedia.org/wiki/Pyrrolizidine_alkaloid

    It has been estimated that 3% of the world's flowering plants contain pyrrolizidine alkaloids. [4] Honey can contain pyrrolizidine alkaloids, [5] [6] as can grains, milk, offal and eggs. [7] To date (2011), there is no international regulation of PAs in food, unlike those for herbs and medicines. [8]

  3. Pyrrolizidine - Wikipedia

    en.wikipedia.org/wiki/Pyrrolizidine

    Pyrrolizidine is a heterocyclic organic compound. Formally, it is a saturated derivative of pyrrolizine . Pyrrolizidine forms the central chemical structure of a variety of alkaloids known collectively as pyrrolizidine alkaloids . [ 1 ]

  4. Pyrrolizidine alkaloidosis - Wikipedia

    en.wikipedia.org/wiki/Pyrrolizidine_Alkaloidosis

    Pyrrolizidine alkaloidosis poisoning in the United States has remained moderately rare among humans. The most common reports are the outcome of the misuse of medicinal home remedies, or the alkaloids are present in food and drink substances such as milk and honey when the animal carriers were exposed to the toxins.

  5. Amabiline - Wikipedia

    en.wikipedia.org/wiki/Amabiline

    Amabiline is a pyrrolizidine alkaloid first isolated in 1967 from Cynoglossum amabile. [1] It is also found in the seeds and flowers of borage (Borago officinalis) [2] and in borage seed oil. [3] [4] Chemically, it is the ester derived from viridifloric acid and supinidine. [5]

  6. Category:Pyrrolizidine alkaloids - Wikipedia

    en.wikipedia.org/wiki/Category:Pyrrolizidine...

    Pages in category "Pyrrolizidine alkaloids" The following 12 pages are in this category, out of 12 total. This list may not reflect recent changes. ...

  7. Riddelliine - Wikipedia

    en.wikipedia.org/wiki/Riddelliine

    Riddelliine is a naturally occurring pyrrolizidine alkaloid, a class of compounds occurring in rangeland plants of the genera Crotalaria, Amsinckia, and Senecio. [5] It consists of a macrocyclic diester of retronecine (an unsaturated alcohol) and riddelliic acid (an oxygenated, branched, dicarboxylic acid). [5]

  8. Senecionine - Wikipedia

    en.wikipedia.org/wiki/Senecionine

    Like other pyrrolizidine alkaloids, senecionine is toxic when ingested. The ingested molecule is a protoxin that is metabolized to its active form. [3] In large quantities, ingestion can lead to critical illness, including convulsions and death. Studies in rodents have shown an LD 50 of 65 mg/kg. [4]

  9. Retronecine - Wikipedia

    en.wikipedia.org/wiki/Retronecine

    Retronecine is a pyrrolizidine alkaloid found in a variety of plants in the genera Senecio and Crotalaria, and the family Boraginaceae. It is the most common central core for other pyrrolizidine alkaloids. [1]