Source:http://linkedlifedata.com/resource/pubmed/id/16178413
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2005-9-23
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pubmed:abstractText |
In order to isolate substances that inhibit the hemolytic activity of human serum against erythrocytes, we have evaluated whole plants of the Orostachys japonicus species with regard to its anti-complement activity, and have identified its active principles following activity-guided isolation. A methanol extract of the O. japonicus, as well as its n-hexane soluble fraction, exhibited significant anti-complement activity on the complement system, which was expressed as total hemolytic activity. A bioassay-guided chromatographic separation of the constituents resulted in the isolation of three known compounds 1-3 from the active n-hexane fraction. The structure of these compounds were analyzed, and they were identified as hydroxyhopanone (1), beta-sitosteryl-3-O-beta-D-glucopyranosyl-6'-O-palmitate (2), and beta-sitosteryl-3-O-beta-D-glucopyranoside (3), respectively. Of these compounds, compound 2 exhibited potent anti-complement activity (IC50= 1.0 +/- 0.1 microM) on the classical pathway of the complement, as compared to tiliroside (IC50= 76.5 +/- 1.1 microM), which was used as a positive control. However, compounds 1 and 3 exhibited no activity in this system.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Benzopyrans,
http://linkedlifedata.com/resource/pubmed/chemical/Complement Inactivating Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Flavonoids,
http://linkedlifedata.com/resource/pubmed/chemical/Glucosides,
http://linkedlifedata.com/resource/pubmed/chemical/Palmitates,
http://linkedlifedata.com/resource/pubmed/chemical/Plant Extracts,
http://linkedlifedata.com/resource/pubmed/chemical/Sitosterols,
http://linkedlifedata.com/resource/pubmed/chemical/sitosterol-3-O-glucopyranoside,
http://linkedlifedata.com/resource/pubmed/chemical/tiliroside
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0253-6269
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
892-6
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16178413-Benzopyrans,
pubmed-meshheading:16178413-Complement Inactivating Agents,
pubmed-meshheading:16178413-Complement Pathway, Classical,
pubmed-meshheading:16178413-Crassulaceae,
pubmed-meshheading:16178413-Dose-Response Relationship, Drug,
pubmed-meshheading:16178413-Flavonoids,
pubmed-meshheading:16178413-Glucosides,
pubmed-meshheading:16178413-Humans,
pubmed-meshheading:16178413-Inhibitory Concentration 50,
pubmed-meshheading:16178413-Korea,
pubmed-meshheading:16178413-Male,
pubmed-meshheading:16178413-Palmitates,
pubmed-meshheading:16178413-Plant Extracts,
pubmed-meshheading:16178413-Sitosterols
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pubmed:year |
2005
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pubmed:articleTitle |
A potent anti-complementary acylated sterol glucoside from Orostachys japonicus.
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pubmed:affiliation |
Faculty of Food Science and Biotechnology, Pukyong National University, Busan 608-737, Korea.
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pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro,
Research Support, Non-U.S. Gov't
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