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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] It is one of five classes of iminosugars. These are often synthesized from a carbohydrate. [2]

  4. 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. ...

  5. 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.

  6. 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]

  7. Pyrrolidine alkaloids - Wikipedia

    en.wikipedia.org/wiki/Pyrrolidine_alkaloids

    Alkaloids with partial pyrrolidine structure are usually sub-categorized based on their occurrence and biogenetic origin. Hygrin and cuscohygrin were isolated from the leaves of the coca shrub , [ 2 ] while (-)-codonopsinine was isolated from the woodland vine tiger bell .

  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. Category:Pyrrolizidines - Wikipedia

    en.wikipedia.org/wiki/Category:Pyrrolizidines

    Pyrrolizidine alkaloids (12 P) Pages in category "Pyrrolizidines" The following 2 pages are in this category, out of 2 total. This list may not reflect recent changes