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1.
China Journal of Chinese Materia Medica ; (24): 1020-1023, 2014.
Article in English | WPRIM | ID: wpr-321374

ABSTRACT

A new hasubanan alkaloid, hernsubanine E (1), as well as two known compounds p-hydroxybenzaldehyde (2) and (-)-syringaresinol (3) have been isolated from the whole plants of Stephania hernandifolia by various column chromatographic methods. Their structures were identified by physicochemical properties and spectral analyses. Compounds 2 and 3 were isolated from the genus of Stephania for the first time.


Subject(s)
Alkaloids , Chemistry , Heterocyclic Compounds, 4 or More Rings , Chemistry , Stephania , Chemistry
2.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 623-627, 2014.
Article in English | WPRIM | ID: wpr-812224

ABSTRACT

AIM@#To study the bufadienolides in the Chinese traditional drug "Ch'an Su" and their cytotoxic activity.@*METHOD@#Various chromatographic techniques were used to isolate the constituents, and their structures were elucidated through physical and spectroscopic data.@*RESULTS@#Twenty compounds were isolated, and eighteen were evaluated in vitro for their cytotoxic activity against A-549 and K-562 cells.@*CONCLUSION@#Compound 1 (bufalin 3β-acrylic ester) was a new bufadienolide and exhibited the most potent activity against the two tumor cell lines with IC50 values of 7.16 and 6.83 nmol · L(-1). The relationships between structure and activity are discussed.


Subject(s)
Humans , Amphibian Venoms , Chemistry , Pharmacology , Therapeutic Uses , Antineoplastic Agents , Chemistry , Pharmacology , Therapeutic Uses , Biological Products , Chemistry , Pharmacology , Therapeutic Uses , Bufanolides , Chemistry , Pharmacology , Therapeutic Uses , Inhibitory Concentration 50 , K562 Cells , Medicine, Chinese Traditional , Molecular Structure , Neoplasms , Drug Therapy , Structure-Activity Relationship
3.
China Journal of Chinese Materia Medica ; (24): 1247-1249, 2006.
Article in Chinese | WPRIM | ID: wpr-356733

ABSTRACT

<p><b>OBJECTIVE</b>To study the chemical constituents in the spikes of Schizonepeta tenuifolia.</p><p><b>METHOD</b>Compounds were isolated and purified with silica gel, ODS and Sephadex LH-20 gel column chromatography, and their structures were determined by using spectroscopic analysis including MS and NMR.</p><p><b>RESULT</b>Nine compounds were isolated and identified as 5, 7-dihydroxy-6, 4'-dimethoxyflavone (1), 5, 7-dihydroxy-6, 3', 4'-trimethoxyflavone (2), ursolic acid (3), 3-hydroxy-4(8)-ene-p-menthane-3(9)-lactone (4), 5, 7, 4'-trihydroxyflavone (5), 5, 4'-dihydroxy-7-methoxyflavone (6), hesperidin (7), luteolin (8) and daucesterol (9).</p><p><b>CONCLUSION</b>Compounds 1, 2, 6 were first obtained from the spikes of S. tenuifolia.</p>


Subject(s)
Flavones , Chemistry , Flowering Tops , Chemistry , Lamiaceae , Chemistry , Plants, Medicinal , Chemistry
4.
China Journal of Chinese Materia Medica ; (24): 1086-1088, 2005.
Article in Chinese | WPRIM | ID: wpr-239744

ABSTRACT

<p><b>OBJECTIVE</b>To study the chemical constituents of Mentha haplocalyx.</p><p><b>METHOD</b>The chemical constituents were isolated and purified with column chromatography and the structures were elucidated by spectral analysis.</p><p><b>RESULT</b>Nine compounds were obtained and identified as emodin (I), chrysophanol (II), physcione (II), benzoic acid (IV), trans-cinnamic acid (V), beta-sitosterol (VI), aloe-emodin (VII), ursolic acid (VIII) and daucosterol (IX).</p><p><b>CONCLUSION</b>Compounds I, II, III, V, VII were first isolated from M. haplocalyx.</p>


Subject(s)
Anthraquinones , Chemistry , Emodin , Chemistry , Mentha , Chemistry , Plant Components, Aerial , Chemistry , Plants, Medicinal , Chemistry
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