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Narcissus and Daffodil

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MeO<br />

MeO<br />

HO<br />

O<br />

O<br />

O<br />

NMe<br />

Galanthamine<br />

HO<br />

HO<br />

H<br />

H<br />

Lycorine<br />

Fortucine<br />

OH<br />

OH<br />

N<br />

H<br />

N<br />

OH<br />

Figure 8.1 Formulae of galanthamine, lycorine <strong>and</strong> fortucine.<br />

Sources of galanthamine 243<br />

the case of surgical interventions (Klyuev <strong>and</strong> Babayan, 1979; Kovanev et al.,<br />

1967; Krylov, 1999; Mashkovsky <strong>and</strong> Kruglova-L’vova, 1951; Mashkovsky, 1955,<br />

1984; Saev <strong>and</strong> Tenev, 1963; Sokolov <strong>and</strong> Zamotaev, 1989; Turova <strong>and</strong> Sapozhnikova,<br />

1982). It counteracts the sedative, hypnotic or respiratory effects of<br />

benzazepines <strong>and</strong> is used for treatment of schizophrenia (Snorrason, 1996).<br />

Galanthamine is a selective acetylcholinesterase inhibitor which was recently clinically<br />

trialled for the treatment of Alzheimer’s disease (Fulton <strong>and</strong> Benfield, 1996;<br />

Selles et al., 1997b). The biogenetic precursor of galanthamine, (±)-narwedine, has<br />

been studied as a respiratory stimulator (Bazhenova et al., 1972). Narwedine was<br />

shown to inhibit the action of narcotics <strong>and</strong> hypnotics, <strong>and</strong> to increase the effect of<br />

analgesics.<br />

Lycorine (Figure 8.1), also known as Narcissin <strong>and</strong> Galanthidin (Negwer, 1978),<br />

<strong>and</strong> dihydrolycorine have antiarrhythmic action (Aliev, 1972), <strong>and</strong> lycorine hydrochloride<br />

is used in medicine in Russia as a strong broncholytic (Klyuev <strong>and</strong><br />

Babayan, 1979). Some alkaloids of this group possess an inhibitory activity on<br />

herpes simplex virus (Renard-Nozaki et al., 1989). The pharmacological activity<br />

of Amaryllidaceae alkaloids has been reviewed by Ruan (1988) <strong>and</strong> Evidente et al.<br />

(1986).

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