Helenalin
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Names | |
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IUPAC name
(3aS,4S,4aR,7aR,8R,9aR)-4-Hydroxy-4a,8-dimethyl-3-methylidene-3,3a,4,4a,7a,8,9,9a-octahydroazuleno[6,5-b]furan-2,5-dione
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Identifiers | |
6754-13-8 ![]() |
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ChEMBL | ChEMBL338474 ![]() |
ChemSpider | 21713 ![]() |
Jmol 3D model | Interactive image |
KEGG | C09473 ![]() |
PubChem | 23205 |
UNII | 4GUY9L896T ![]() |
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Properties | |
C15H18O4 | |
Molar mass | 262.31 g·mol−1 |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Helenalin is a sesquiterpene lactone found in Arnica montana and Arnica chamissonis foliosa. Helenalin is a highly toxic compound, with hepatic and lymphatic tissues particularly vulnerable to its effects.[1] It is believed to be responsible for the toxicity and skin irritation associated with Arnica.[2][3] If enough of the plant is ingested, the helenalin produces severe gastroenteritis and internal bleeding of the digestive tract.[4]
Pharmacology
Helenalin has a variety of observed effects in vitro including anti-inflammatory and antitumor activities.[5]
Helenalin has been shown to selectively inhibit the transcription factor NF-κB, which plays a key role in regulating immune response, through a unique mechanism.[6] In vitro, it is also a potent, selective inhibitor of human telomerase[7]—which may partially account for its antitumor effects—has anti-trypanosomal activity,[8][9] and is toxic to Plasmodium falciparum.[10]
Animal and in vitro studies have also suggested that helenalin can reduce the growth of Staphylococcus aureus and reduce the severity of S. aureus infection.[11]
References
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