WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru WHO monographs on selected medicinal plants - travolekar.ru
Lichen Islandicus fumarprotocetraric acid, protolichestearic acid and cetraric acids (5, 13). A biologically active aliphatic -lactone, (+)-protolichesterinic acid has also been reported (14). The structures of fumarprotocetraric acid, cetraric acid and (+)-protolichesterinic acid are presented below. CHO H 3 C CHO H 3 C HO CO 2 H HO O O OH O O H 3 C H 3 C O O O Cetraric acid CH 3 Fumarprotocetraric acid CO 2 H OH O O CO 2 H H 3 C (+)-Protolichesterinic acid O H O H CO 2 H CH 2 Medicinal uses Uses supported by clinical data Used orally as a demulcent to treat inflammation and dryness of the pharyngeal mucosa (15, 16). Uses described in pharmacopoeias and well established documents Used orally for treatment of loss of appetite and nausea (3, 17). Uses described in traditional medicine Used to treat asthma, cramps, bronchitis, cough, diabetes, exhaustion, gastric disturbances, immune depletion, migraine, nausea in pregnancy and wounds. Also used as an emergency food source, an emollient and a galactagogue (4, 18–20). Pharmacology Experimental pharmacology Antimicrobial and antiviral activities An aqueous extract of the thalli and protolichesterinic acid were screened for in vitro activity against Mycobacterium aurum, a nonpathogenic organism with a similar sensitivity profile to M. tuberculosis. Protolichesterinic acid had a minimum inhibitory concentration (MIC) of 125.0 μg/ml (21). An aqueous extract of the thalli was screened for in vitro activity against Helicobacter pylori. (+)-Protolichesterinic acid was identified as 143
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Lichen Islandicus<br />
fumarprotocetraric acid, protolichestearic acid and cetraric acids (5, 13).<br />
A biologically active aliphatic -lact<strong>on</strong>e, (+)-protolichesterinic acid has<br />
also been reported (14). The st<strong>ru</strong>ctures of fumarprotocetraric acid, cetraric<br />
acid and (+)-protolichesterinic acid are presented below.<br />
CHO H 3 C<br />
CHO H 3 C<br />
HO<br />
CO 2 H<br />
HO<br />
O<br />
O<br />
OH<br />
O<br />
O<br />
H 3 C<br />
H 3 C<br />
O<br />
O<br />
O<br />
Cetraric acid CH 3 Fumarprotocetraric acid<br />
CO 2 H<br />
OH<br />
O<br />
O<br />
CO 2 H<br />
H 3 C<br />
(+)-Protolichesterinic acid<br />
O<br />
H<br />
O<br />
H<br />
CO 2 H<br />
CH 2<br />
Medicinal uses<br />
Uses supported by clinical data<br />
Used orally as a demulcent to treat inflammati<strong>on</strong> and dryness of the pharyngeal<br />
mucosa (15, 16).<br />
Uses described in pharmacopoeias and well established documents<br />
Used orally for treatment of loss of appetite and nausea (3, 17).<br />
Uses described in traditi<strong>on</strong>al medicine<br />
Used to treat asthma, cramps, br<strong>on</strong>chitis, cough, diabetes, exhausti<strong>on</strong>,<br />
gastric disturbances, immune depleti<strong>on</strong>, migraine, nausea in pregnancy<br />
and wounds. Also used as an emergency food source, an emollient and a<br />
galactagogue (4, 18–20).<br />
Pharmacology<br />
Experimental pharmacology<br />
Antimicrobial and antiviral activities<br />
An aqueous extract of the thalli and protolichesterinic acid were screened<br />
for in vitro activity against Mycobacterium au<strong>ru</strong>m, a n<strong>on</strong>pathogenic organism<br />
with a similar sensitivity profile to M. tuberculosis. Protolichesterinic<br />
acid had a minimum inhibitory c<strong>on</strong>centrati<strong>on</strong> (MIC) of 125.0 μg/ml<br />
(21). An aqueous extract of the thalli was screened for in vitro activity<br />
against Helicobacter pylori. (+)-Protolichesterinic acid was identified as<br />
143