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1.
China Journal of Chinese Materia Medica ; (24): 3049-3054, 2016.
Article in Chinese | WPRIM | ID: wpr-258420

ABSTRACT

The dried stems of Schisandra henryi var. henryi were extracted with 95% ethanol and the extracts were further subjected to partition, affording the ethyl acetate extracts(EtOAc Extrs.).The EtOAc Extrs.were separated and purified with silica gel and octadecyl-silylated silica gel column chromatography, preparative HPLC and preparative TLC. Thirteen known compounds were obtained and identified by spectral methods including MS and NMR, all of which were elucidated as t-cadinol(1), cadinane-4β,5α,10β-triol(2), cadinane-5α, 10α-diol-2-ene(3), oxyphyllenodiols A(4), 1β, 4β-dihydroxyeudesman-11-ene(5), cyperusol C(6), (7R)-opposit-4(15)-ene-1β,7-diol(7), dysodensiol E(8), epi-guaidiol A(9), aromadendrane-4β,10β-diol(10), tricyclohumuladiol(11), caryolane-1,9β-diol(12), and guaidiol A(13). Compounds 3, 5-10, and 13 were separated from the genus for the first time, while compounds 1-13 were separated from this species for the first time.

2.
China Journal of Chinese Materia Medica ; (24): 2357-2362, 2015.
Article in Chinese | WPRIM | ID: wpr-337929

ABSTRACT

Hedyotis hedyotidea has been traditionally used for the treatment of arthritis, cold, cough, gastro-enteritis, headstroke, etc. But few studies have screened the active compounds from extracts of H. hedyotidea. In this study, the structure of the chemical constituents from stems of H. hedyotidea were determined and the immunosuppressive activity of the compounds was evaluated. The compounds were separated and purified with silica gel, gel column chromatographies and preparative HPLC, and their structures were identified by spectral methods such as MS and NMR. Eleven compounds were obtained and identified as(6S,9S) -vomifoliol (1), betulonic acid (2), betulinic acid (3), betulin(4), 3-epi-betulinic acid (5), ursolic acid (6), β-sitosterol (7), stigmast-4-en-3-one (8), 7β-hydroxysitosterol (9), (3β,7β) -7-methoxystigmast-5-en-3-ol (10) and morindacin (11). This is the first report of compounds 1, 2, 4, 8, 9, 10 and 11 from H. hedyotidea. Compounds 1, 2 and 8-11 were firstly isolated from the genus Hedyotis, and compounds 9 and 10 were isolated from the family Rubiaceae for the first time. The immunosuppressive activity of these compounds was tested using the lymphocyte transsormationtest. Compounds 4, 6 and 9 showed significant immunosuppressive activity.


Subject(s)
Animals , Male , Mice , Drugs, Chinese Herbal , Chemistry , Pharmacology , Hedyotis , Chemistry , Immunosuppressive Agents , Chemistry , Pharmacology , Lymphocytes , Allergy and Immunology , Mass Spectrometry , Mice, Inbred C57BL , Molecular Structure , Plant Stems , Chemistry
3.
China Journal of Chinese Materia Medica ; (24): 3426-3429, 2012.
Article in Chinese | WPRIM | ID: wpr-308641

ABSTRACT

<p><b>OBJECTIVE</b>To study the chemical constituents from Schisandra glaucescens.</p><p><b>METHOD</b>The chemical constituents were separated and purifed with silica gel, gel column chromatography preparative HPLC, and their structures were identified by such spectral methods as MS and NMR.</p><p><b>RESULT</b>Twelve compounds were separated from petroleum ether fractions, and identified as t-cadinol (1), alpha-cadinol (2), torreyol (3), (+)-ent-epicubenol (4), ent-T-muurolol (5), (-)-15-hydroxycalamenene (6), (-)-cubebol (7), 4-epi-cubebol (8), caryophyllenol-I (9), caryophyllenol-II (10), oxyphyllenodiols A (11), caryolane-1,9/3-diol (12).</p><p><b>CONCLUSION</b>Compounds 4, 6-12 were separated from the genus for the first time, while compounds 1-12 were separated from this plant for the first time.</p>


Subject(s)
Chromatography, High Pressure Liquid , Drugs, Chinese Herbal , Chemistry , Magnetic Resonance Spectroscopy , Molecular Structure , Plant Stems , Chemistry , Schisandra , Chemistry , Sesquiterpenes , Chemistry
4.
China Journal of Chinese Materia Medica ; (24): 94-97, 2002.
Article in Chinese | WPRIM | ID: wpr-275004

ABSTRACT

<p><b>OBJECTIVE</b>To offer evidences for quality control of medicinal Asteropyrum plants.</p><p><b>METHOD</b>Pharmacognostic studies were made through field collection, market investigation, document utilization, comparative morphology and histology.</p><p><b>RESULT</b>The shape and properties, microscopic characteristics in root, rhizome, leaves were worked out.</p><p><b>CONCLUSION</b>Asteropyrum can be distinguished from close relative Coptis plants by microscopic and histology characteristics. Two species in Asteropyrum can also be identified by microscopic and histology characteristics, and the morphological and histology characteristics can be used as evidences for quality control of medicinal Asteropyrum plants.</p>


Subject(s)
Coptis , Pharmacognosy , Plant Leaves , Chemistry , Plant Roots , Chemistry , Plants, Medicinal , Quality Control , Ranunculaceae , Species Specificity
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