Gelsemium alkaloids
Gelsemium alkaloids are a group of secondary metabolites found primarily in the flowering plant Gelsemium elegans, commonly known as yellow jessamine or woodbine. These alkaloids exhibit significant pharmacological activity and have been the subject of extensive research due to their potential therapeutic benefits. The most notable members include gelsemine and gelsemiol, which possess diverse biological activities.
Gelsemium alkaloids are known for their analgesic, sedative, and anti-inflammatory properties. They also demonstrate antimicrobial and neuroprotective effects, making them promising candidates for developing new treatments against various diseases. However, caution is advised due to their toxic nature, particularly when consumed in large quantities or improperly.
In the pharmaceutical industry, gelsemium alkaloids are of interest as potential components in pain management formulations and anti-inflammatory medications. Their study continues to shed light on their molecular mechanisms and therapeutic potentials, though further research is necessary for safe and effective application in clinical settings.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Gelsemine,monohydrochloride (9CI) | 35306-33-3 | C20H23ClN2O2 |
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Gelsemicine | 6887-28-1 | C20H26N2O4 |
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Gelsevirine | 38990-03-3 | C21H24N2O3 |
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Rankinidine | 106466-66-4 | C20H24N2O3 |
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Voachalotine oxindole | 26126-84-1 | C22H26N2O4 |
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Gelseganine A; 7'β-Hydroxy, 4',11'-didehydro | 1095492-41-3 | C31H38N2O8 |
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Gelselegine; 14R-Hydroxy | 1620516-60-0 | C20H26N2O5 |
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Gelselegine; 19ξ-Hydroxy, N-Me | 1169463-43-7 | C21H28N2O5 |
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Humantenirine; 11-Demethoxy, 19,20-dihydro, 14β,20S-dihydroxy | 1798328-46-7 | C20H26N2O5 |
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Humantenirine; 11-Demethoxy, N4-Me, 19,20-dihydro | 1620516-61-1 | C21H28N2O3 |
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