Tropane: Difference between revisions
CSV import |
No edit summary |
||
| (One intermediate revision by the same user not shown) | |||
| Line 38: | Line 38: | ||
{{Chemistry-stub}} | {{Chemistry-stub}} | ||
{{No image}} | {{No image}} | ||
Latest revision as of 18:48, 18 March 2025
Tropane is a bicyclic organic compound and a tertiary amine. It is the structural parent of many natural products collectively known as tropane alkaloids, which include compounds like atropine, cocaine, and scopolamine. Tropane is a key building block in the biosynthesis of these important alkaloids.
Structure and Properties[edit]
Tropane is composed of a seven-membered ring with a nitrogen atom and a three-membered ring fused together. The nitrogen atom, being a tertiary amine, carries a lone pair of electrons, which contributes to the compound's basicity. The bicyclic structure of tropane is rigid, which influences the biological activity of its derivatives.
Tropane Alkaloids[edit]
Tropane alkaloids are a class of alkaloids that contain a tropane ring in their structure. They are found in a variety of plants, particularly in the Solanaceae family, which includes species like deadly nightshade (Atropa belladonna), henbane (Hyoscyamus niger), and jimson weed (Datura stramonium).
Atropine[edit]
Atropine is a tropane alkaloid derived from the deadly nightshade plant. It is used in medicine to dilate the pupils and as an antidote for certain types of poisonings.
Cocaine[edit]
Cocaine is a tropane alkaloid derived from the coca plant. It is a powerful stimulant and is used medically as a topical anesthetic.
Scopolamine[edit]
Scopolamine is a tropane alkaloid derived from plants like henbane and jimson weed. It is used in medicine to treat motion sickness and postoperative nausea and vomiting.
Biosynthesis[edit]
The biosynthesis of tropane alkaloids involves the condensation of ornithine and acetoacetic acid to form hygrine, which is then cyclized to form tropinone. Tropinone is then reduced to form tropane.
