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1.
Chinese Pharmaceutical Journal ; (24): 1702-1705, 2012.
Article in Chinese | WPRIM | ID: wpr-860573

ABSTRACT

OBJECTIVE: To study the chemical constituents of the leaves of Lindera aggregata. METHODS: Various column chromatographic techniques were used to separate and purify the chemical constituents and their structures were elucidated by spectral analysis. RESULTS: Twelve compounds were isolated and identified as hydroxylindestrenolide (I), linderalactone (II), pseudone-olinderane(III), quercetin-3-O-α-L-rhamnoside(IV), kaempferol-3-O-α-L-arabinofuranoside(V), kaempferol-3-O-β-D-galactopyrano-side(VI), kaempferol-3-O-β-D-xylopyranoside (VII), quercetin-3-O-(2″-O-β-D-glucopyranosyl) -α-L-arabinofuranoside (VII), querce-tin-3-O-(2″-O-β-Z)-glucx)pyranosyl) -β-D-xylopyranoside(IX), syringoside (X), acantrifoside E(XI), 2,6-dimethoxy-4-hydroxyphenol-1-O-β-D-glucopyranoside(XII). CONCLUSION: The compounds VI-XII were isolated from Lindera genus for the first time.

2.
Article in Chinese | WPRIM | ID: wpr-321002

ABSTRACT

Objective To investigate the prevalence of anti-hepatitis E virus (HEV) and genotypes of hepatitis E virus in 8 species of animals including swine, cattle, sheep, horse, donkey, dog, chicken and duck in the suburb of Beijing. Methods Serum samples were collected from the 8 species of animals, and fecal samples of younger swine were collected from 2 stock farms. Anti-HEV was detected by Double Antigen Sandwich Assay. HEV RNA from fecal samples was detected by a reverse transcription nested polymerase chain reaction (RT-nPCR). Parts of the PCR products were cloned and sequenced. The swine HEV sequences were analyzed genetically. Results The positive rates of anti-HEV in serum specimens of swine, cattle, horse, donkey, sheep, dog, duck and chicken were 80.43%(481/598), 15.02%(52/346), 14.29%(40/280) ,0(0/26) ,9.88%(33/334), 0(0/ 21) ,3.03% (7/231) and 2.53%(8/316), respectively. The anti-HEV prevalence of adult swine(≥6 months)and younger swine(≤3 months)were 87.86%(369/420)and 62.92%(112/178)respectively. 74 of 111 (66.67% ) pig faces were positive for HEV RNA. Sequence analysis on these positive samples showed that there were 6 groups of HEV designated as bjsw1, bjsw2, bjsw3, bjsw4, bjsw5 and bjsw6. The 6 strains of HEV shared 94.5%-99.6% sequence identity of partial HEV ORF2 nucleotide with each other. The identities of HEV ORF2 nucleotide sequences between the 6 strains and genotype 1, 2, 3 and 4 were 75.6%-78.6% , 75.6%-76.2%, 77.1%-80.7% and 83.7%-94.5%, respectively. The sequence identity between the 6 strains and human HEV genotype 4d was 90.0%-94.5% . Conclusion HEV infection was seen in swine, cattle, horse, sheep, duck and chicken in the suburbs of Beijing. The anti-HEV positive rate appeared the highest in swine and the lowest in dog and donkey. The six strains of HEV isolated from younger swine belonged to genotype 4d.

3.
Zhongguo Zhong Yao Za Zhi ; (24): 351-353, 2005.
Article in Chinese | WPRIM | ID: wpr-279165

ABSTRACT

<p><b>OBJECTIVE</b>To study the metabolites of marine fungus Alternalia sp.</p><p><b>METHOD</b>Compounds were separated by column chromatography and their structures were elucidated by means of chemical and spectral analysis.</p><p><b>RESULT</b>Six compounds were isolated from the ethyl acetate and n-butanol extracts of the fermentation of marine fungus Alternalia sp. Their structures were elucidated as p-benzyloxy-phenol ( I ), p-hydroxy phenyl ethylamine( II ), 3-hydroxymethyl-8-hydroxyl-pyrrolopiperazine-2, 5-dione ( III ), 3-isobutyl-6-secbutyl-piperazine-2, 5-dione (IV), 5alpha, 8alpha-epidioxy-ergosta-6, 22-diene-3beta-ol (V), 3beta-hydroxxy-cholesta-5-ene (VI).</p><p><b>CONCLUSION</b>Compounds I , II, III, IV have the activity of inducing morphological deformation of mycelia germinated from conidia of Pyricularia oryzae. Compounds I , II , III were isolated from the genus Alternalia for the first time.</p>


Subject(s)
Antifungal Agents , Pharmacology , Ascomycota , Fermentation , Fungi , Chemistry , Molecular Structure , Phenethylamines , Chemistry , Pharmacology , Phenols , Chemistry , Pharmacology
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