Lanostane-type triterpenoids from the sclerotia of Inonotus obliquus possessing anti-tumor promoting activity

European Journal of Medicinal Chemistry

Volumn 43, Issue 11, 2008, Pages 2373-2379

  Taji, Sayaka ^a   Yamada, Takeshi ^a   Wada, Shun ichi ^a   Tokuda, Harukuni ^b   Sakuma, Kazuo ^c   Tanaka, Reiko ^a  

^a OSAKA MEDICAL COLLEGE   (Japan)

^b KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^c Salad Melon Company Limited   (Japan)

Author keywords

3 Hydroxylanosta 8,24 dien 21 al: EBV EA activation; Lanosta 7:9(11),23E triene 3 ,22R,25 triol; Lanosta 8,23E diene 3 ,22R,25 triol; Mouse skin carcinogenesis assay

Indexed keywords

3BETA HYDROXYLANOSTA 8,24 DIEN 21 AL; EPSTEIN BARR VIRUS ANTIGEN; INONOTUS OBLIQUUS EXTRACT; LANOSTA 7:9(11),23 TRIENE 3BETA,22,25 TRIOL; LANOSTA 8,23 DIENE 3BETA,22,25 TRIOL; LANOSTA 8,24 DIEN 3BETA,21 DIOL; LANOSTEROL; TRITERPENOID; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANTINEOPLASTIC ACTIVITY; ARTICLE; CARCINOGEN TESTING; CHEMICAL STRUCTURE; CONTROLLED STUDY; DRUG EFFECT; EPSTEIN BARR VIRUS; FUNGAL SCLEROTIUM; MOUSE; NONHUMAN; SENSITIVE TO CARCINOGENESIS MOUSE;

ANIMALS; ANTIGENS, VIRAL; ANTINEOPLASTIC AGENTS; BASIDIOMYCOTA; HERPESVIRUS 4, HUMAN; MAGNETIC RESONANCE SPECTROSCOPY; MICE; MODELS, MOLECULAR; MOLECULAR STRUCTURE; SKIN NEOPLASMS; TRITERPENES;

EID: 54049086979     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2008.01.037     Document Type: Article

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