Cinchona alkaloids
Cinchona alkaloids are a group of bioactive compounds derived from the bark of Cinchona trees, primarily found in South America. These alkaloids have long been recognized for their significant medicinal properties and were among the first effective treatments for malaria. The most well-known member is quinine, which has potent antimalarial activity. Other important cinchona alkaloids include cinchonine, cinchophen, and emetine, each with its own unique pharmacological profile. These compounds exert their effects through various mechanisms, including modulating ion channels and affecting neurotransmission. Despite the availability of synthetic alternatives, cinchona alkaloids remain crucial in the treatment of specific types of malaria due to their unique efficacy and lower toxicity profiles compared to some synthetic drugs. Their study continues to contribute to the understanding of complex biological interactions and the development of novel therapeutic strategies.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Cinchonan-3,9-diol,10,11-dihydro-6'- methoxy-,(9S)-,sulfate (1:1) (salt) | 130061-81-3 | C20H28N2O7S |
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Quininium, 1-mercapto-,hydroxide, hydrogen sulfate, inner salt (8CI) | 26075-98-9 | C20H25N2O5S2 |
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Quinine 1’-Oxide | 54821-44-2 | C20H24N2O3 |
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Cinchonidine Dihydrochloride | 524-54-9 | C19H24Cl2N2O |
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199588-72-2 | C34H33ClN2O | |
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910879-22-0 | C20H26N2O2 | |
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2-Hydroxy-3-mercaptopropanoic acid; (S)-form, S-Benzyl, quinine salt | 30134-74-8 | C30H36N2O5S |
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9-Hydroxy-6'-methoxy-11-norcinchonan-10-oic acid; (8R,9S)-form | 78609-50-4 | C19H22N2O4 |
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9-Hydroxy-6'-methoxy-11-norcinchonan-10-oic acid; (8S,9R)-form, Et ester | 157253-79-7 | C21H26N2O4 |
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35064-63-2 | C20H25N2O2 |
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