2009
DOI: 10.1248/cpb.57.1076
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Anti-human Immunodeficiency Virus-1 Protease Activity of New Lanostane-Type Triterpenoids from Ganoderma sinense

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Cited by 91 publications
(53 citation statements)
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“…More interestingly, this fungus also produces many oxygenated triterpenoids (especially ganoderic acids) with a wide range of biological activities. These include differential effects on the thromboxane A2-signaling pathways in human platelets [3], inhibition of eukaryotic DNA polymerases [4], cytotoxicity to several cancer cells in vitro [1,5], inhibition of tumor invasion in vitro and in vivo [1,6,7], anti-human immunodeficiency virus-1 protease activity [8], and regulation of osteoclastogenesis [9].…”
Section: Introductionmentioning
confidence: 99%
“…More interestingly, this fungus also produces many oxygenated triterpenoids (especially ganoderic acids) with a wide range of biological activities. These include differential effects on the thromboxane A2-signaling pathways in human platelets [3], inhibition of eukaryotic DNA polymerases [4], cytotoxicity to several cancer cells in vitro [1,5], inhibition of tumor invasion in vitro and in vivo [1,6,7], anti-human immunodeficiency virus-1 protease activity [8], and regulation of osteoclastogenesis [9].…”
Section: Introductionmentioning
confidence: 99%
“…Colossolactone types of triterpenoids such as colossolactone V ( 10 ), colossolactone VII ( 8 ), colossolactone VIII ( 7 ), schisanlactone A ( 33 ), colossolactone G ( 5 ) and colossolactone A ( 9 ) were isolated from the chloroform extract from G. lucidium with and IC 50 value of 5–39 μ g/ml (El Dine et al 2008). Similarly in Sato et al (2009), isolated lanostane-type triterpenoids-ganoderiol F ( 22 ), ganoderic acid GS-2 ( 48 ) and 20-hydroxylucidenic acid N ( 74 ), 20(21)-dehydrolucidenic acid N ( 39 ) from CHCl 3 extract of the fruiting body of G. sinense and demonstrated the anti-HIV-1 protease activity with IC 50 values of 20–40 μ M (El Dine et al 2008; Sato et al 2009). Compounds from the CHCl 3 extract of the fruiting bodies of G. colossum , farnesyl hydroquinone, ganomycin I ( 29 ) and ganomycin B ( 28 ), competitively inhibit the active site of HIV-1 protease enzyme with IC 50 values of 7.5 and 1.0 μ g/ml, respectively (El Dine et al 2008).…”
Section: Antiviral Activities Of Compounds and Extracts From Ganodermmentioning
confidence: 63%
“…Our phytochemical analysis of G. sinense led to the isolation and structural determination of three new triterpene-farnesyl hydroquinone conjugates (35)(36)(37) and five new highly oxygenated lanostane-type triterpenoids (38)(39)(40)(41)(42) from the fruiting body of this medicinal mushroom. The structures of the new compounds were determined from spectroscopic data and they were named ganosinensins A−C (35−37), ganoderic acid GS-1 (38) (47), ganoderiol F (48), cerevisterol, 5,6-dihydroergosterol and ergosterol peroxide were also isolated [43][44].…”
Section: Ganoderma Triterpenes and Their Derivativesmentioning
confidence: 99%