Ergoline and derivatives
Ergoline and its derivatives are a class of alkaloids characterized by their unique chemical structure, featuring an indole ring fused to a piperidine ring. These compounds have been widely studied for their diverse biological activities and therapeutic potentials. Ergoline itself is derived from the ergot fungus (Claviceps purpurea) and has historically been used in traditional medicine. Modern research has expanded its applications, particularly in the treatment of migraines due to its ability to constrict blood vessels.
Ergolines exhibit a wide range of pharmacological properties, including serotonin receptor agonism and modulation. They are known for their effects on the central nervous system, cardiovascular system, and gastrointestinal tract. Notable ergoline derivatives include lisuride, used in the treatment of Parkinson's disease; methylergonovine, an effective uterotonic agent; and ergotamine, commonly prescribed for migraine headaches.
Given their potential as therapeutic agents, ergolines continue to be of significant interest in both academic research and pharmaceutical development. However, due to their psychoactive properties, caution must be exercised when handling these compounds.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Agroclavine; (-)-form, 18-Hydroxy, O-β-D-fructofuranoside | 28986-92-7 | C22H28N2O6 |
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Elymoclavine-O-beta-fructofuranoside | 121844-72-2 | C22H28N2O6 |
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Agroclavine; (-)-form, 18-Hydroxy, O-[β-D-fructofuranosyl-(2→1)-β-D-fructofuranoside] | 121864-94-6 | C28H38N2O11 |
Related Literature
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
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