2011
DOI: 10.1016/j.phytol.2011.04.008
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Chemical constituents from Xylosma longifolia and their anti-tubercular activity

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Cited by 12 publications
(16 citation statements)
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“…In the 1 H NMR spectrum, two groups of aromatic protons signals at δ 7.49 (1H, dd, J = 1.9, 8.3 Hz), δ 7.45 (1H, d, J = 1.9 Hz), δ 6.90 (1H, d, J = 8.3 Hz), and δ 6.78 (1H, dd, J = 1.6, 8.2 Hz), δ 6.74 (1H, d, J = 8.2 Hz) and δ 6.91 (1H, d, J = 1.6 Hz) appeared as two ABX coupling systems, which belonged to two 1, 3, 4-tri-substituted aromatic rings. The 13 C NMR data of 2 were most close to those of 3-methoxy-4-hydroxyphenylpropane-7, 8-(6′-benzoyl-2′, 1′-O-β-glucopyranosyl)-7, 8, 9-triol (Truong et al, 2011), except the signals of C-3′′ and C-4′′ of 2, which are down-field by 18 and 17 ppm, respectively, indicating an ortho-dioxide substitution at 3′′ and 4′′ in 2. Their substitution position were further confirmed by the long-range correlations between δ 3.83(-OCH3) and δ 147.3(C-3′′), δ 9.03(-OH) and δ 151.7(C-4′′), and δ 7.49(H-6′′) and δ 151.7(C-4′′) in the HMBC experiment.…”
Section: Structural Elucidation Of Compoundsmentioning
confidence: 68%
“…In the 1 H NMR spectrum, two groups of aromatic protons signals at δ 7.49 (1H, dd, J = 1.9, 8.3 Hz), δ 7.45 (1H, d, J = 1.9 Hz), δ 6.90 (1H, d, J = 8.3 Hz), and δ 6.78 (1H, dd, J = 1.6, 8.2 Hz), δ 6.74 (1H, d, J = 8.2 Hz) and δ 6.91 (1H, d, J = 1.6 Hz) appeared as two ABX coupling systems, which belonged to two 1, 3, 4-tri-substituted aromatic rings. The 13 C NMR data of 2 were most close to those of 3-methoxy-4-hydroxyphenylpropane-7, 8-(6′-benzoyl-2′, 1′-O-β-glucopyranosyl)-7, 8, 9-triol (Truong et al, 2011), except the signals of C-3′′ and C-4′′ of 2, which are down-field by 18 and 17 ppm, respectively, indicating an ortho-dioxide substitution at 3′′ and 4′′ in 2. Their substitution position were further confirmed by the long-range correlations between δ 3.83(-OCH3) and δ 147.3(C-3′′), δ 9.03(-OH) and δ 151.7(C-4′′), and δ 7.49(H-6′′) and δ 151.7(C-4′′) in the HMBC experiment.…”
Section: Structural Elucidation Of Compoundsmentioning
confidence: 68%
“…and Trichophyton sp. where the pathogens have developed resistance against the specific fungicides [24,26,83,84]. The development of natural antifungal agents would also help to decrease the negative impact of synthetic agents such as residues, resistance and environmental pollution.…”
Section: Discussionmentioning
confidence: 99%
“…The root extract of X. terrae-reginae , the fractions of the leaves and barks of the roots of X. ciliatifolium and methanol leaf extract X. congestum result antibacterial activity [20-23]. Two new glucosides, 3-methoxy-4-hydroxyphenylpropane-7, 8-(6′-benzoyl-2′, 1′-O-β-glucopyranosyl)-7, 8, 9-trio, and 2-hydroxyphenyl-4-caffeoyl-β-d-glucoside, together with seven known compounds are isolated from the stem bark of X. longifolia and 8-hydroxy-6-methoxy-pentylisocoumarin exhibits against Mycobacterium tuberculosis [24]. The methanolic extract of the leaves of X. longifolium isolate β-sitosterol, β-amyrin, friedelin, olean-12-en-3α-ol-28-oic acid 3α-D-glucopyranoside [25], flavonoid kaempferol-3-β-xylopyranoside-4’-α-rhamnoside [26].…”
Section: Introductionmentioning
confidence: 99%
“…The MIC is defined as the lowest concentration effecting a reduction in fluorescence or luminescence of 90% with respect to untreated controls. Accordingly, five of the most active plants selected from the evaluated 2066 plant extracts were carried out for bioassay-guided fractionation, which led to the isolation of 11 active compounds (Table 3 and Figure 3) including six new molecules [35,36,37,38].…”
Section: Active Agentsmentioning
confidence: 99%