Protopine: Difference between revisions
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'''Protopine''' is | {{short description|An alkaloid found in several plant species}} | ||
==Protopine== | |||
[[File:Protopine_structure.svg|thumb|right|Chemical structure of protopine]] | |||
'''Protopine''' is a naturally occurring [[alkaloid]] found in several plant species, particularly within the [[Papaveraceae]] family. It is known for its potential pharmacological properties and has been the subject of various studies in the field of [[pharmacology]]. | |||
==Chemical Structure== | ==Chemical Structure== | ||
Protopine is a | Protopine is classified as a benzylisoquinoline alkaloid. Its chemical structure is characterized by a complex arrangement of carbon, hydrogen, nitrogen, and oxygen atoms, forming a distinctive ring system. The molecular formula of protopine is C20H19NO5. | ||
== | ==Occurrence== | ||
Protopine is found in several plant species, | Protopine is found in several plant species, including those in the [[Fumariaceae]] and [[Papaveraceae]] families. Notable plants containing protopine include [[Fumaria officinalis]] (common fumitory) and [[Chelidonium majus]] (greater celandine). | ||
==Pharmacological Properties== | ==Pharmacological Properties== | ||
Protopine has been studied for its potential | Protopine has been studied for its potential effects on the [[central nervous system]], as well as its [[analgesic]], [[anti-inflammatory]], and [[antispasmodic]] properties. It is believed to interact with various [[neurotransmitter]] systems, although the exact mechanisms of action are not fully understood. | ||
==Biosynthesis== | |||
The biosynthesis of protopine in plants involves several enzymatic steps, starting from the amino acid [[tyrosine]]. The process includes the formation of the intermediate compound [[norcoclaurine]], which undergoes further modifications to produce protopine. | |||
==Uses== | |||
While protopine itself is not widely used in clinical practice, its presence in medicinal plants contributes to the therapeutic effects of herbal preparations. These preparations are often used in traditional medicine for their purported benefits in treating various ailments. | |||
==Safety and Toxicity== | ==Safety and Toxicity== | ||
The safety profile of protopine is not well-documented, and its toxicity can vary depending on the dose and the form in which it is consumed. As with many alkaloids, caution is advised when using plant extracts containing protopine. | |||
== | ==Related pages== | ||
* [[Alkaloid]] | * [[Alkaloid]] | ||
* [[Papaveraceae]] | |||
* [[Fumariaceae]] | |||
* [[Benzylisoquinoline]] | * [[Benzylisoquinoline]] | ||
[[Category:Alkaloids]] | [[Category:Alkaloids]] | ||
[[Category:Pharmacology]] | [[Category:Pharmacology]] | ||
[[Category:Plant compounds]] | |||
Latest revision as of 11:54, 15 February 2025
An alkaloid found in several plant species
Protopine[edit]
Protopine is a naturally occurring alkaloid found in several plant species, particularly within the Papaveraceae family. It is known for its potential pharmacological properties and has been the subject of various studies in the field of pharmacology.
Chemical Structure[edit]
Protopine is classified as a benzylisoquinoline alkaloid. Its chemical structure is characterized by a complex arrangement of carbon, hydrogen, nitrogen, and oxygen atoms, forming a distinctive ring system. The molecular formula of protopine is C20H19NO5.
Occurrence[edit]
Protopine is found in several plant species, including those in the Fumariaceae and Papaveraceae families. Notable plants containing protopine include Fumaria officinalis (common fumitory) and Chelidonium majus (greater celandine).
Pharmacological Properties[edit]
Protopine has been studied for its potential effects on the central nervous system, as well as its analgesic, anti-inflammatory, and antispasmodic properties. It is believed to interact with various neurotransmitter systems, although the exact mechanisms of action are not fully understood.
Biosynthesis[edit]
The biosynthesis of protopine in plants involves several enzymatic steps, starting from the amino acid tyrosine. The process includes the formation of the intermediate compound norcoclaurine, which undergoes further modifications to produce protopine.
Uses[edit]
While protopine itself is not widely used in clinical practice, its presence in medicinal plants contributes to the therapeutic effects of herbal preparations. These preparations are often used in traditional medicine for their purported benefits in treating various ailments.
Safety and Toxicity[edit]
The safety profile of protopine is not well-documented, and its toxicity can vary depending on the dose and the form in which it is consumed. As with many alkaloids, caution is advised when using plant extracts containing protopine.
