2004
DOI: 10.1016/j.phytochem.2003.10.024
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Lanostanes and friedolanostanes from the bark of Garcinia speciosa

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Cited by 24 publications
(25 citation statements)
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“…The crude methanol extract from the leaves of G. hombroniana was separated by chromatographic methods to yield five new triterpenes, garcihombronanes F-J (1)(2)(3)(4)(5), together with nine known compounds: five triterpenes [garcihombronanes B-E (6-9) 1 and methyl (25R)-3 -hydroxy-23-oxo-9,15-lanostadien-26-oate (10) 2 ], two flavonoid glucosides (vitexin 4 and isovitexin 5 ), and two ionone glycosides (blumenol C 9-O--D-apiofuranosyl-(1f6)--Dglucopyranoside 6 and vomifoliol 9-O--D-apiofuranosyl-(1f6)--D-glucopyranoside 7 ). The structures of the new compounds were elucidated by analysis of 1D and 2D NMR spectroscopic data, while the known compounds were identified by comparison of their spectroscopic data, especially 1 H and 13 C NMR data, with those of known compounds.…”
Section: Resultsmentioning
confidence: 99%
“…The crude methanol extract from the leaves of G. hombroniana was separated by chromatographic methods to yield five new triterpenes, garcihombronanes F-J (1)(2)(3)(4)(5), together with nine known compounds: five triterpenes [garcihombronanes B-E (6-9) 1 and methyl (25R)-3 -hydroxy-23-oxo-9,15-lanostadien-26-oate (10) 2 ], two flavonoid glucosides (vitexin 4 and isovitexin 5 ), and two ionone glycosides (blumenol C 9-O--D-apiofuranosyl-(1f6)--Dglucopyranoside 6 and vomifoliol 9-O--D-apiofuranosyl-(1f6)--D-glucopyranoside 7 ). The structures of the new compounds were elucidated by analysis of 1D and 2D NMR spectroscopic data, while the known compounds were identified by comparison of their spectroscopic data, especially 1 H and 13 C NMR data, with those of known compounds.…”
Section: Resultsmentioning
confidence: 99%
“…The obvious correlations between H-3 and H-5 indicated that the stereochemistry at C-3 was proved to be b-OH. The clear correlation between H-24 and H-26 confirmed that the configuration of the double bond (D 24 ) is E [18]. On the basis of evidences mentioned above, the structure of 1 was determined as 24(E)-3b -hydroxylanosta-8,24-dien-26-al-21-oic acid.…”
Section: Resultsmentioning
confidence: 72%
“…The 1 H and 13 C NMR assignments of compound 7 are added as Supplementary Data (Table S1). The absolute configuration at C-25 of the same compound isolated from Garcinia speciosa was established as R by X-ray diffraction (Vieira et al, 2004).…”
Section: Resultsmentioning
confidence: 99%