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1.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 168-173, 2020.
Article in Chinese | WPRIM | ID: wpr-873201

ABSTRACT

Objective:Aphanamixis grandifolia,a perennial herb of genus Aphanamixis (Meliaceae),has effects in soothing activating collaterals,dredging paisy,expelling wind-evil and removing wetness. This paper aimed to investigate terpenoids from the stems and leaves of A. grandifolia and reveal the effective substances. Method:Totally 22 kg leaves and twigs of A. grandifolia were extracted with 90% EtOH for three times by heating reflux. These extracts were decompressed and concentrated,and then dissolved in water. The solvent was successively extracted with petroleum ether and ethyl acetate. The chemical constituents from petroleum ether and ethyl acetate fractions were isolated by macroporous,silica gel,Sephadex LH-20 and ODS columns,and their chemical structures were determined through MS,NMR analysis(1H and 13C-NMR)and spectroscopic data from literatures,respectively. Result:Twelve compounds were obtained and identified as 16α-hydroxy-3-oxo-24-methyllanosta-7,9(11),24(31)-triene-21-oic acid (1),23(E)-cycloart-en-25-ethoxy-3-ol(2),23(Z)-9,19-cycloart-ene-3β,25-diol(3),23(E)-cycloart-en-3β,25-diol(4),labda-8,13-(E)-dien-15-ol(5),labda-7,13-(E)-dien-15-ol(6),vulgarol(7),(S,E)-6-[6-(5,5-dimethyl-4-oxo-4,5-dihydrofuran-3-yl]-2-methylhepta-1,6-dien-1-yl]-4-methyl-5,6-dihydro-2H-pyran-one(8),nemoralisin(9),nemoralisin C(10),1S,4R,5S,6R,7S,10S-1(5),6(7)-diepoxy-4-guaiol(11) and 1S,4S,5S,10R-4,10-guaianediol(12),respectively. Conclusion:The structures involves triterpenoids,diterpenoids and sesquiterpennoids,and eight of them (1-3,5-8 and 12) are obtained from A. grandifolia for the first time. Those compounds are also isolated from the geneus Aphanamixis for the first time.

2.
China Medical Equipment ; (12): 21-24, 2018.
Article in Chinese | WPRIM | ID: wpr-706534

ABSTRACT

Objective: To observe and analyze the clinical effect, satisfaction and life quality of an exhaust device that was applied in patients with pneumothorax in emergency internal medicine. Methods: The clinical data of 90 patients with pneumothorax were analyzed, and all of them were divided into observation group (45 cases) and control group (45 cases) according to the different clinical treatment plan. The patients of observation group received pneumothorax treatment by using exhaust device and that of control group received pneumothorax treatment by using conventional exhaust device. The clinical effect, satisfaction degree and situation of life quality post-treatment between the two groups were analyzed and compared. Results: The total effective rate and satisfaction of observation group (97.78% and 97.78%) were significantly higher than that of control group (80.00% and 77.78%) (x2=7.200, x2=8.389, P<0.05). And the result of follow-up of half a year showed that the difference of total score of life quality between observation group (83.50±14.48) and control group (65.34±13.15) was significant (t=6.228, P<0.05). Conclusion: In the treatment of patients with pneumothorax in emergency internal medicine, the application of an exhaust device of pneumothorax can make the gas was wholly absorbed, and significantly enhance the satisfaction and life quality of patients.

3.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 406-410, 2013.
Article in English | WPRIM | ID: wpr-812661

ABSTRACT

AIM@#To study the Amaryllidaceae alkaloids of the bulbs of Lycoris radiata.@*METHODS@#The chemical constituents were isolated and purified by various chromatographic techniques, and the chemical structures were elucidated on the basis of spectroscopic methods. In addition, the antiviral activities of alkaloids 1-10 were evaluated using flu virus A.@*RESULTS@#One new homolycorine-type alkaloid 2α-methoxy-6-O-ethyloduline (1), together with nine known alkaloids 2α-methoxy-6-O-methyloduline (2), trispherine (3), 8-O-demethylhomolycorine (4), homolycorine (5), 9-O-demethylhomolycorine (6), oduline (7), lycorenine (8), 6α-O-methyllycorenine (9) and O-ethyllycorenine (10) were obtained.@*CONCLUSION@#Alkaloid 1 is a new compound, and 1-3 were major alkaloids in this plant. Alkaloids 1-3 showed weak antiviral activities against flu virus A with IC50 values of 2.06, 0.69, and 2.71 μg·mL-1 and CC50 values of 14.37, 4.79, and 80.12 μg·mL-1, respectively.


Subject(s)
Alkaloids , Chemistry , Pharmacology , Antiviral Agents , Chemistry , Pharmacology , Flowers , Chemistry , Influenza A virus , Lycoris , Chemistry , Molecular Structure , Plant Extracts , Chemistry , Pharmacology
4.
Acta Pharmaceutica Sinica ; (12): 924-926, 2003.
Article in Chinese | WPRIM | ID: wpr-301174

ABSTRACT

<p><b>AIM</b>To study the chemical constituents of Ligularia dictyoneura.</p><p><b>METHODS</b>Various chromatographic techniques were used to separate and purify the compounds. Their spectral data (MS, IR, NMR) were measured for structure elucidation.</p><p><b>RESULTS</b>Four sesquiterpenes were isolated from Ligularia dictyoneura and their structures were identified as ligudicin A (1), ligudicin C (2), ligudicin D (3) and isopetasin (4).</p><p><b>CONCLUSION</b>Compound 1 is a new compound, compound 2 is a new natural product, and compounds 3 and 4 are obtained from Ligularia dictyoneura for the first time.</p>


Subject(s)
Asteraceae , Chemistry , Molecular Conformation , Molecular Structure , Plants, Medicinal , Chemistry , Sesquiterpenes , Chemistry
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