2003
DOI: 10.1016/s0367-326x(02)00305-2
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Antiviral lanostanoid triterpenes from the fungus Ganoderma pfeifferi

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Cited by 104 publications
(66 citation statements)
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“…Apart from Agaricus blazei, compounds from the basidiomycetes Ganoderma pfeifferi and Rozites caperata demonstrated antiviral activity for many viruses, such as herpes simplex (11,15). In this study, we evaluated the action of aqueous extract of A. blazei in the replication of HSV-1 and BoHV-1, in HEp-2 cell culture.…”
Section: Introductionmentioning
confidence: 99%
“…Apart from Agaricus blazei, compounds from the basidiomycetes Ganoderma pfeifferi and Rozites caperata demonstrated antiviral activity for many viruses, such as herpes simplex (11,15). In this study, we evaluated the action of aqueous extract of A. blazei in the replication of HSV-1 and BoHV-1, in HEp-2 cell culture.…”
Section: Introductionmentioning
confidence: 99%
“…Ganoderma pfeifferi triterpenes, ganodermadiol ( 20 ), lucidadiol ( 30 ) and applanoxidic acid G ( 4 ), were active against influenza virus type A with ED 50 of greater than 0.22 mM, 0.22 mM and 0.19 mM, respectively (MothanaRa et al 2003). Similarly others triterpenes such as ganoderone C ( 26 ) (IC 50 : 2.6  µ g/ml), lucialdehyde B ( 31 ) (IC 50 :3.0  µ g/ml) and ergosta-7, 22-dien-3 α -ol ( 14 ) (IC 50 : 0.78  µ g/ml) inhibited the growth of Madin-Darby canine kidney (MDCK) cells infected with influenza virus (Niedermeyer et al 2005).…”
Section: Antiviral Activities Of Compounds and Extracts From Ganodermmentioning
confidence: 99%
“…Similarly others triterpenes such as ganoderone C ( 26 ) (IC 50 : 2.6  µ g/ml), lucialdehyde B ( 31 ) (IC 50 :3.0  µ g/ml) and ergosta-7, 22-dien-3 α -ol ( 14 ) (IC 50 : 0.78  µ g/ml) inhibited the growth of Madin-Darby canine kidney (MDCK) cells infected with influenza virus (Niedermeyer et al 2005). Herpes simplex virus were inhibited by triterpenes such as compound ( 20 ) (ED 50 : 0.068 mM), ganoderone A ( 25 ) (IC 50 :0.075  µ g/ml), ( 31 ) (IC 50 :0.03  µ g/ml) and compound 14 (IC 50 : 0.03  µ g/ml), whereas compounds 21 and 51 were less effective in comparison (MothanaRa et al 2003; Niedermeyer et al 2005). G. lucidium triterpenes lanosta-7, 9 (11), 24-trien-3-one, 15; 26-dihydroxy (GLTA) ( 40 ) and ganoderic acid Y ( 19 ) possess inhibitory action towards enterovirus 71 with IC 50 value of 0.16–4 μ g/ml (Zhang et al 2015).…”
Section: Antiviral Activities Of Compounds and Extracts From Ganodermmentioning
confidence: 99%
“…4), Applanoxidic acid C, 5,, Ergosterol peroxide (5,6,8(14), 22-tetraen-3-one, Lucialdehyde B, Lucialdehyde D, Ganoderol A, Ganoderol B (Fig. 4), Ganoderone A and Ganoderone C. Niedermeyer et al 2005 Ganomycins A and B Mothana et al 2000 Ganodermadiol, Lucidadiol, and Applanoxidic acid G Mothana et al 2003 Lucialdehyde D, Ganoderone A, and Ganoderone C. Ganoderone A and Lucialdehyde B, (and ergosta-7,22-dien-3b- Sixteen compounds were isolated by 2, 5-dihydroxyacetophenone, methyl gentisate, (S)-dimethyl malate, muurola-4, 10 (14)-dien-11β-ol, dihydroepicub-enol, 5-hydroxymethylfuran carboxaldehyde, ergosta-7, 22E-dien-3β-ol, ergosta-7, 22E-dien-3-one, ergosta-7, 22E-diene-2β, 3α, 9α-triol, 6β-methoxyergo-sta-7, 22E-dien-3β, 5α-diol, ergosta-4, 6, 8(14), 22E-tetraen-3-one, ergosta4, 6, 8-(14), 22E-etetraen-3β-ol, 5α, 8α-epidioxy-ergosta-6, 22E-dien-3β-ol, 7α-methoxy-5α, 6α-epoxyergosta-8-(14), 22E-dien-3β-ol (14), ergosta-8, 22E-diene-3β, 5α, 6β, 7α-tetraol, and ergosta-5, 23-dien-3β-ol, acetate.…”
Section: G Concinnum Ryvarden 2000mentioning
confidence: 99%