1984
DOI: 10.1055/s-2007-969674
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3β-Hydroxy-lanosta-8,24-dien-21-al, a New Triterpene fromInontus obliquus

Abstract: A new triterpene, 3beta-hydroxy-lanosta-8,24-dien-21-al, was identified from INONOTUS OBLIQUUS. The structure was determined by IR, MS, (1)-NMR and (13)C-NMR spectroscopy and by comparing its (13)C-NMR spectra with the spectra obtained for lanosterol, inotodiol, trametenolic acid and methyl trametenolate.

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Cited by 42 publications
(29 citation statements)
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“…Inotodiol has an OH group at position 22 (C-22) of lanosterol [9]. The chemical structure of the compound in subfraction 3 was determined by comparing the MS, 1 H-NMR, and 13 C-NMR spectra (data not shown) to published library spectra and spectra in the literature [7,9,15,16]. These analyses revealed that subfraction 3 is lanosterol.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Inotodiol has an OH group at position 22 (C-22) of lanosterol [9]. The chemical structure of the compound in subfraction 3 was determined by comparing the MS, 1 H-NMR, and 13 C-NMR spectra (data not shown) to published library spectra and spectra in the literature [7,9,15,16]. These analyses revealed that subfraction 3 is lanosterol.…”
Section: Resultsmentioning
confidence: 99%
“…3β-Hydroxy-lanosta-8,24-dien-21-al has been identified from I. obliquus [7], and a high-molecular-weight, water-soluble, lignin-like substance from edible mushrooms of I. obliquus has been reported to inhibit the protease of type-1 human immunodeficiency virus [8]. Inotodiol isolated from the sclerotia of I. obliquus has been reported to have an inhibitory effect in a two-stage carcinogenesis test on mouse skin using 7,12-dimethyl-benz[α]anthracene [9].…”
Section: Introductionmentioning
confidence: 99%
“…Partial Based on the spectral data and the literature on trametenolic acid, the isolated compound was identified as trametenolic acid [2]. …”
Section: Resultsmentioning
confidence: 99%
“…The antitumor activity of extracts and preparations of Chaga against Sarcoma 180 and Carcinoma 755 is due mainly to the presence of lanostane-type tetracyclic triterpenes such as lanosterol, inotodiol, and trametenolic acid [2,3]. According to the literature [3], inotodiol is the dominant tetracyclic triterpene of Chaga [3].…”
mentioning
confidence: 99%
“…Data in the literature available to us indicate that the biological activity of chaga extracts is associated with triterpenes: inonotic acid, obliquic acid, inotodiol, and lanosterol. Inotodiol and lanosterol have antiblastic (antitumor) activity [1,8,9].…”
mentioning
confidence: 99%