1988
DOI: 10.1021/np50056a004
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Betulin-3-Caffeate from Quercus suber, 13C-nmr Spectra of Some Lupenes

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Cited by 60 publications
(43 citation statements)
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“…Betulinic acid was isolated from n-hexane fraction using silica gel column chromatography. The chemical structure of the compound was determined by means of 1 H-NMR (600 MHz) and EI-MS and identifi ed to betulinc acid by comparison with spectral data from the literature (Patra et al, 1988;Do et al, 1991). The compound was dissolved in ethanol and added to the cell culture at the desired concentrations.…”
Section: Reagents and Cell Culturementioning
confidence: 99%
“…Betulinic acid was isolated from n-hexane fraction using silica gel column chromatography. The chemical structure of the compound was determined by means of 1 H-NMR (600 MHz) and EI-MS and identifi ed to betulinc acid by comparison with spectral data from the literature (Patra et al, 1988;Do et al, 1991). The compound was dissolved in ethanol and added to the cell culture at the desired concentrations.…”
Section: Reagents and Cell Culturementioning
confidence: 99%
“…for corresponding formulas) were identified as henryoside (8) [9], O-hydroxybenzyl salicylate [12], salicyloylsalicin [12], (þ)-licarin A [13], 3,22-dihydroxyolean-12-en-25-al [14], (2a,3b)-olean-12-ene-2,3-diol [15], 6-hydroxy-3-oxoolean-12-en-28-oic acid [16], ovalifoliogenin [17], ursomyricerone [18], olean-12-ene-2,3,22-triol [19], maniladiol [20], crategolic acid [21], camaldulensic acid [22], masticadienic acid [23], betulinic acid [24], alismoxide [8], 3,3',4',7-tetrahydroxyflavone [25], apigenin [26], 3,4-dimethylbenzoic acid [27], 4-hydroxybenzoic acid [28], 2H-1-benzopyran-2-one [29], umbelliferone [30], aesculetin [31], gallic acid [32], 3,5-dihydroxybenzoic acid methyl ester [33], and 3,5-dihydroxybenzoic acid [32] on the basis of their NMR data and by comparison with the literature data. To the Table 3.…”
Section: H 24 O 15 As Elucidated By Its Hr-esi-ms ([M à H]mentioning
confidence: 99%
“…PMR and 13 C NMR spectra of 2a-n, 3, and 4 agreed completely with their structures. Resonances of H and C atoms in NMR spectra of 2a-n, 3, and 4 were assigned based on two-dimensional NMR spectra of 2d, f, g, i, m, and 4 using literature data for betulonic acid and its amino-acid derivatives [9,10]. We verified the resonances for H-2′ (8.23 ppm) and H-4′ (7.00 ppm) (protons of the imidazole ring) of 2m, for which chemical shifts at 7.01 and 8.25 ppm, respectively, were assigned [11].…”
Section: Synthesis Of Betulonic Acid Amidesmentioning
confidence: 99%