Open Access
Life Sciences, volume 69, issue 2, pages 229-237
Cytotoxic activities of acetoxyscirpenediol and ergosterol peroxide from Paecilomyces tenuipes
KYONG NYON NAM
1
,
Young Joon Jo
2
,
Young A. Kim
2
,
Jin Hai Hyun
3
,
Ha Young Kim
1
1
Department of Life Science, University of Seoul, Seoul 130-743, South Korea.
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Publication type: Journal Article
Publication date: 2001-06-01
Journal:
Life Sciences
scimago Q1
wos Q1
SJR: 1.257
CiteScore: 12.2
Impact factor: 5.2
ISSN: 00243205, 18790631
PubMed ID:
11441913
General Biochemistry, Genetics and Molecular Biology
General Medicine
General Pharmacology, Toxicology and Pharmaceutics
Abstract
Paecilomyces tenuipes is one of the famous Chinese medicinal entomopathogenic fungi that parasites in the lavae of silkworm. Two cytotoxic components were isolated from methanolic extract of the carpophores of this fungus that was cultivated artificially. Spectral analyses of the cytotoxic components showed that they were known ergosterol peroxide (5alpha,8alpha-epidioxy-24(R)-methylcholesta-6,22-dien-3beta-ol) and acetoxyscirpenediol (4beta-acetoxyscirpene-3alpha,15-diol) that were isolated for the first time from this fungus. The 50% inhibitory concentrations (IC50) of ergosterol peroxide against human gastric tumor cell line (SNU-1), human hepatoma cell line (SNU-354), human colorectal tumor cell line (SNU-C4) and murine sarcoma-180 were 18.7, 158.2, 84.6 and 74.1 microM, respectively. The IC50 values of acetoxyscirpenediol against SNU-1, SNU-C4, SNU-354 and sarcoma-180 were 1.2,4.0, 2.2 and 1.9 microM, respectively. Cytotoxic activities of acetoxyscirpenediol were about 4.0-6.6 times stronger than those of cisplatin which is currently used clinically for cancer patients.
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