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Xiang-Hai Cai

Publications and source records attributed to Xiang-Hai Cai.

3 recordsLinked to original sources

New antioxidant phenolic glycosides from Walsura yunnanensis.

Four new polyphenolic glycosides (1-4) were isolated from the BuOH extract of the bark of Walsura yunnanenis C. Y. Wu. These compounds comprise two lignans, i.e., the 9-O-alpha-L-arabinopyranosides 1 and 2 of (-)-isolariciresinol and of (+)-5-methoxyisolariciresinol, respectively, and the two phenolic glycosides 3,4,5-trimethoxyphenyl 2-O-(alpha-L-fucopyranosyl)-beta-D-glucopyranoside (3) and 3,5-dihydroxyphenyl 6-O-(4-hydroxy-3,5-dimethoxybenzoyl)-beta-D-glucopyranoside (walsuraside; 4). In addition, three known compounds, 3,4,5-trimethoxyphenyl beta-D-glucopyranoside, asperglaucide, and butyl alpha-D-fructofuranoside were identified. Their structures were elucidated spectroscopically and by chemical transformation (hydrolysis). The new compounds 1, 2, and 4 displayed significant antioxidant activities, with IC(50) values in the range of ca. 42 to 49 microg/ml.

Antioxidants↗

Compound representatives of a new type of triterpenoid from Aglaia odorata.

[structure: see text] A novel triterpenoid, 21,25-cyclodammar-20(22)-ene-3beta,24alpha-diol, has been isolated from Aglaia odorata. Its structure was elucidated on the basis of 1D- and 2D-NMR and MS spectra and then confirmed by X-ray diffraction. It represents a new type of natural five-membered-ring triterpenoid, named cyclodammarane. Its possible biopathway was that squalene-2,3;22,23-diepioxide was directly cyclized to form 24,25-epoxydammar-20(21)-en-3-ol, followed by protonation of the remaining 24,25-epoxide and the cation attacking 21(20) methylene to generate the E ring.

Aglaia↗

Quinones from Chirita eburnea.

Five new quinone derivatives, (R)-7-hydroxy-alpha-dunnione (1), (R)-8-hydroxy-alpha-dunnione (2), (R)-7,8-dihydroxy-alpha-dunnione (3), (R)-7-methoxy-6,8-dihydroxy-alpha-dunnione (4), and 1,7-dihydroxy-2-hydroxymethylanthraquinone (5), along with seven known compounds, were isolated from Chirita eburnea. All structures were elucidated by spectroscopic techniques (NMR, MS, UV, and IR). The EtOAc fraction of the EtOH extract and compounds 3 and 4 showed free radical (DPPH) scavenging activity, with IC50 values of 101.7 +/- 5.2 microg/mL, 124.82 +/- 8.4 microM, and 45.72 +/- 3.6 microM, respectively, compared with 86.91 +/-6.8 microM for ascorbate.

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