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coniine

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Definitions of coniine in various dictionaries:

noun - a poisonous alkaloid

CONIINE - Coniine refers to a poisonous chemical compound, an alkaloid present in and isolable from poison hemlock (Conium maculatum), where its presence has b...

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A poisonous colorless liquid alkaloid, C5H10NC3H7, found in the poison hemlock.
A volatile poisonous compound found in hemlock and other plants. It affects the motor nerves, causing paralysis and asphyxia.

Coniine description
Coniine refers to a poisonous chemical compound, an alkaloid present in and isolable from poison hemlock (Conium maculatum), where its presence has been a source of significant economic, medical, and historico-cultural interest; coniine is also produced by the yellow pitcher plant (Sarracenia flava), and fool's parsley (Aethusa cynapium). Its ingestion and extended exposure are toxic to humans and all classes of livestock; its mechanism of poisoning involves disruption of the peripheral nervous system, with death caused by respiratory paralysis. The biosynthesis of coniine contains as its penultimate step the non-enzymatic cyclisation of 5-oxooctylamine to -coniceine, a Schiff base differing from coniiine only by its carbon-nitrogen double bond in the ring. This pathway results in natural coniine that is a mixturea racematecomposed of two enantiomers, the stereoisomers (S)-(+)-coniine, and (R)-()-coniine, depending on the direction taken by the chain that branches from the ring. Both

Coniine description

Coniine refers to a poisonous chemical compound, an alkaloid present in and isolable from poison hemlock (Conium maculatum), where its presence has been a source of significant economic, medical, and historico-cultural interest; coniine is also produced by the yellow pitcher plant (Sarracenia flava), and fool's parsley (Aethusa cynapium). Its ingestion and extended exposure are toxic to humans and all classes of livestock; its mechanism of poisoning involves disruption of the peripheral nervous system, with death caused by respiratory paralysis. The biosynthesis of coniine contains as its penultimate step the non-enzymatic cyclisation of 5-oxooctylamine to -coniceine, a Schiff base differing from coniiine only by its carbon-nitrogen double bond in the ring. This pathway results in natural coniine that is a mixturea racematecomposed of two enantiomers, the stereoisomers (S)-(+)-coniine, and (R)-()-coniine, depending on the direction taken by the chain that branches from the ring. Both

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