Progress in Drug Research / Fortschritte Der Arzneimittelforschung / Progrès Des Recherches Pharmaceutiques 1978
DOI: 10.1007/978-3-0348-7102-0_6
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Antiviral agents

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1985
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Cited by 6 publications
(14 citation statements)
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“…Lycorine, one of the principal alkaloids of the Amaryllidacea, exerts an antiviral effect on several RNA and DNA viruses; isolated from Clivia miniata (Amaryllidacea) (Leven et al, 1983). Is a secondary metabolite of Streptomyces species S-885 and is toxic to HeLa cells; has anti-polio activity at 0.02 mg/ml (Swallow et al, 1975).…”
Section: Lycorinementioning
confidence: 99%
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“…Lycorine, one of the principal alkaloids of the Amaryllidacea, exerts an antiviral effect on several RNA and DNA viruses; isolated from Clivia miniata (Amaryllidacea) (Leven et al, 1983). Is a secondary metabolite of Streptomyces species S-885 and is toxic to HeLa cells; has anti-polio activity at 0.02 mg/ml (Swallow et al, 1975).…”
Section: Lycorinementioning
confidence: 99%
“…Found in Olea europaea L. (Oleaceae); exhibit in vitro antiviral activiy against viruses (Swallow et al, 1975). Castelanone is a nortriterpenoid with a quassinoid skeletal type occurs in the root bark of Castela tweediei (Simaroubaceae); exhibits in vitro antiviral activiy against the oncogenic Rous sarcoma virus (Rembold, 1989).…”
Section: Miscellaneous Compoundsmentioning
confidence: 99%
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“…During the last two decades, nucleoside analogues have been explored extensively as antiviral agents [3,6,20,23,24], A nov el approach which evolved from this earli er work was the use of an aliphatic or acyclic side chain to replace the cyclic carbohydrate moiety of the nucleoside. The earliest successful attempts at devel oping antiviral nucleosides with aliphatic side chains are represented by two pu rines; 9-(2' -hydroxyethoxymethyl)-guanine (acyclovir) [7,17] and S-9-(2',3'-dihydroxypropyl)-adenine (DHPA) [4].…”
Section: Introductionmentioning
confidence: 99%
“…Little or no antiherpesvirus activity has been found for several l-(2'-hydroxyethoxymethyl) derivatives of cytosine, or uracil [2,8,9,18] or for l-(2'-aminoethoxymethyl)-uracils [10], We have explored the activity of a number of uracil and cytosine derivatives with one of the following acyclic side chains: 2-hydroxyethoxymethyl, 2-aminoethoxymethyl, or 1,3-dihydroxypropoxymethyl. We primarily concentrated on 5-substitutions as have other investigators [2,9,24], Therefore, a number of ana logues of pyrimidine acyclic nucleosides have been synthesized and analyzed for cell growth inhibitor potency and for anti herpes activity.…”
Section: Introductionmentioning
confidence: 99%