ABSTRACT
Four new polyhydroxylated steroids plaksterols A-D (1-4), together with two known related steroids ergost-7,9(11),22-trien-3ß,5α,6α-triol (5) and ergosta-6ß-methoxy-7,22-diene-3ß,5α-diol (6), were isolated from methanol extract of the South China Sea marine sponge Plakortis sp. Their structures were identified by spectroscopic analysis, including NMR, MS, and IR. The cytotoxicity of the polyhydroxylated steroids were evaluated, and compound 6 showed moderate inhibitory activities against K562, HL-60 and BEL-7402 cells.
Subject(s)
Plakortis/chemistry , Steroids/chemistry , Animals , Cell Line, Tumor , China , Humans , Molecular Structure , Pacific Ocean , Steroids/isolation & purification , Steroids/pharmacologyABSTRACT
A chemical investigation was conducted on the aerial parts of the mangrove plant Sonneratia paracaseolaris, yielding five new triterpenoid paracaseolins A-E (1-4, and 11) together with twelve known analogues (5-10, 12-17). Their structures were established by extensive spectroscopic methods and comparisons their spectroscopic data with those of the known related compounds. The cytotoxicities against P388, HeLa, A549, and K562 tumor cell lines and anti-H1N1 (Influenza A virus) activities for the isolates were evaluated. Compound 4 showed potent cytotoxicity against the A549 cell line with an IC50 value of 1.89 µM, and compound 1 exhibited significant anti-H1N1 virus activity with an IC50 value of 28.4 µg/mL. A preliminary structure activity relationship was discussed.
Subject(s)
Antiviral Agents/pharmacology , Embryophyta/chemistry , Plant Extracts/chemistry , Triterpenes/chemistry , Triterpenes/pharmacology , Animals , Antineoplastic Agents, Phytogenic/pharmacology , Cell Line, Tumor , Cell Survival , Drug Discovery , Humans , Influenza A Virus, H1N1 Subtype/drug effects , Mice , Molecular Structure , Structure-Activity Relationship , Triterpenes/toxicityABSTRACT
A phytochemical study on the rhizomes of Cimicifuga foetida resulted in the isolation of two new cycloartane triterpenoids (1 and 2), eight new cycloartane glycosides (3-10), and six known cycloartane glycoside analogues (11-16). The structures of 1-10 were determined by application of spectroscopic methods, with the absolute configuration of 1 determined by X-ray crystallography. Compounds 1-6, as three pairs of epimers at C-10 and C-24, belong to a seven-membered-ring variant of 9,10-seco-9,19-cycloartane triterpenoids, and glycosides 3-10 were found to be 3-O-ß-D-xylopyranosides. The cytotoxicity of the isolates was evaluated against five selected human tumor cell lines, and the known compounds 15 and 16 showed cytotoxicity against the hepatocellular carcinoma SMMC-7721 cell line with IC50 values of 5.5 and 6.3 µM, respectively.
Subject(s)
Cimicifuga/chemistry , Drugs, Chinese Herbal/isolation & purification , Glycosides/isolation & purification , Triterpenes/isolation & purification , Crystallography, X-Ray , Drugs, Chinese Herbal/chemistry , Drugs, Chinese Herbal/pharmacology , Glycosides/chemistry , Glycosides/pharmacology , Humans , Molecular Conformation , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Rhizome/chemistry , Triterpenes/chemistry , Triterpenes/pharmacologyABSTRACT
The 15 parent PAHs in surface seawater from Qingdao coastal areas have been quantified by solid phase extraction-high performance liquid chromatography with fluorescent detection. The results showed that the concentration of total PAHs ranged from 8.23 ng x L(-1) to 272.02 ng x L(-1), with highest concentration near estuary and lowest at rural location. As for PAHs composition, 2, 3 ring PAHs were dominant, with percentage ranged from 52.2% to 93.8%, while the remaining were 4 to 6 ring PAHs which were ranged from 6.2% to 47.8%. The concentration of total PAHs correlates strongly with dissolved organic carbon (R = 0.944 7) in surface seawater. There was no significant fluctuation in the concentration and composition of PAHs in surface seawater from Qingdao bay area in a one-month period. The two ratios of paired PAH isomeric compounds, fluoranthene to fluoranthene plus pyrene[ Fl/(Fl + Py)] and anthracene to phenanthrene plus anthracene [An/(An + Ph)], for source apportionment suggested that various petroleum related sources, such as oil spill and petroleum combustion, were the major origin at most sampling sites, except in clean areas where PAHs were predominantly derived from coal and wood combustion.
Subject(s)
Environmental Monitoring , Polycyclic Aromatic Hydrocarbons/analysis , Seawater/analysis , Water Pollutants, Chemical/analysis , China , Environmental Monitoring/methods , Oceans and Seas , Petroleum/analysisABSTRACT
OBJECTIVE: To establish the HPLC-fingerprint of the water-soluble constituents of Carthamus tinctorius. METHODS: 18 samples of Carthamus tinctorius from different producing areas were determined by Agilent 1100 DAD-HPLC under the chromatographic conditions: column by SinoChrom ODS-BP (250 mm x 4.6 mm, 5 microm), methanol-0.7% H3PO4 water with gradient elution, column temperature 30 degrees C, flow rate by 1 ml/min, wavelength 280 nm, and inject volume 20 microl. RESULTS: The HPLC-fingerprint of the water-soluble constituents of Cartharnus tinctorius was established on the basis of 10 bitch of drugs from Xinjiang according to SPSS analysis. CONCLUSION: A reliable method is provided for the quality identification of Carthamus tinctorius.