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  2. Pyrrolizidine alkaloid - Wikipedia

    en.wikipedia.org/wiki/Pyrrolizidine_alkaloid

    Pyrrolizidine alkaloids (PAs), sometimes referred to as necine bases, are a group of naturally occurring alkaloids based on the structure of pyrrolizidine. Their use dates back centuries and is intertwined with the discovery, understanding, and eventual recognition of their toxicity on humans and animals.

  3. Loline alkaloid - Wikipedia

    en.wikipedia.org/wiki/Loline_alkaloid

    Another group of alkaloids, the senecio-type alkaloids, are produced by various plants and like the lolines, the senecio alkaloids possess a pyrrolizidine ring structure. Unlike the lolines, however, the senecio alkaloids exhibit strong hepatotoxicity , [ 13 ] owing to a double bond between C-1 and C-2 in their ring structure. [ 13 ]

  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. ...

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  6. Pyrrolizidine alkaloidosis - Wikipedia

    en.wikipedia.org/wiki/Pyrrolizidine_Alkaloidosis

    Pyrrolizidine alkaloidosis can result in damage to the liver, kidneys, heart, brain, smooth muscles, lungs, DNA, lesions all over the body, and could be a potential cause of cancer. [ 1 ] [ 2 ] Pyrrolizidine alkaloidosis is known by many other names such as "Pictou Disease" in Canada [ 3 ] and "Winton Disease" in New Zealand. [ 4 ]

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  9. 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]

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