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1.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 626-640, 2016.
Article in English | WPRIM | ID: wpr-812583

ABSTRACT

More than 80 aristolochic acids (AAs) and aristololactams (ALs) have been found in plants of the Aristolochiaceae family, but relatively few have been fully studied. The present study aimed at developing and validating a liquid chromatography tandem mass spectrometry (LC/MS(n)) for the analysis of these compounds. We characterized the fragmentation behaviors of 31 AAs, ALs, and their analogues via high performance liquid chromatography coupled with electrospray ionization mass spectrometry. We summarized their fragmentation rules and used these rules to identify the constituents contained in Aristolochia contorta, Ar. debilis, Ar. manshurensis, Ar. fangchi, Ar. cinnabarina, and Ar. mollissima. The AAs and ALs showed very different MS behaviors. In MS(1) of AAs, the characteristic pseudomolecular ions were [M + NH4](+), [M + H](+), and [M + H - H2O](+). However, only [M + H](+) was found in the MS(1) of ALs, which was simpler than that of AAs. Distinct MS(n)fragmentation patterns were found for AAs and ALs, showing the same skeleton among the different substituent groups. The distribution of the 31 constituents in the 6 species of Aristolochia genus was reported for the first time. 25 Analogues of AAs and ALs were detected in this genus. A hierarchical schemes and a calculating formula of the molecular formula of these nitrophenanthrene carboxylic acids and their lactams were proposed. In conclusion, this method could be applied to identification of similar unknown constituents in other plants.


Subject(s)
Aristolochiaceae , Chemistry , Aristolochic Acids , Chemistry , Chromatography, High Pressure Liquid , Methods , Drugs, Chinese Herbal , Chemistry , Molecular Structure , Tandem Mass Spectrometry , Methods
2.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 873-880, 2015.
Article in English | WPRIM | ID: wpr-812469

ABSTRACT

The present study was designed to investigate the bioactive constituents of Xanthoceras sorbifolia in terms of amounts and their antioxidant, DNA scission protection, and α-glucosidase inhibitory activities. Simultaneous quantification of 10 X. sorbifolia constituents was carried out by a newly established ultra-high performance liquid chromatography-quadrupole mass spectrometry method (UHPLC-MS). The antioxidant activities were evaluated by measuring DPPH radical scavenging and DNA scission protective activities. The α-glucosidase inhibitory activities were investigated by using an assay with α-glucosidase from Bacillus Stearothermophilus and disaccharidases from mouse intestine. We found that the wood of X. sorbifolia was rich in phenolic compounds with the contents of catechin, epicatechin, myricetin, and dihydromyricetin being 0.12-0.19, 1.94-2.16, 0.77-0.91, and 6.76-7.89 mg·g(-1), respectively. The four constituents strongly scavenged DPPH radicals (with EC50 being 4.2, 3.8 and 5.7 μg·mL(-1), respectively) and remarkably protected peroxyl radical-induced DNA strand scission (92.10%, 94.66%, 75.44% and 89.95% of protection, respectively, at a concentration of 10 μmol·L(-1)). A dimeric flavan 3-ol, epigallocatechin-(4β→8, 2β→O-7)-epicatechin potently inhibited α-glucosidase with an IC50 value being as low as 1.2 μg·mL(-1). The established UHPLC-MS method could serve as a quality control tool for X. sorbifolia. In conclusion, the high contents of antioxidant and α-glucosidase inhibitory constituents in X. sorbifolia support its use as complementation of other therapeutic agents for metabolic disorders, such as diabetes and hypertension.


Subject(s)
Antioxidants , Pharmacology , Biphenyl Compounds , Metabolism , Catechin , Pharmacology , Chromatography, High Pressure Liquid , DNA , DNA Damage , Flavonoids , Pharmacology , Glycoside Hydrolase Inhibitors , Pharmacology , Mass Spectrometry , Picrates , Metabolism , Plant Extracts , Chemistry , Pharmacology , Sapindaceae , Chemistry , Triterpenes , Pharmacology , Wood , Chemistry , alpha-Glucosidases , Metabolism
3.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 321-329, 2013.
Article in English | WPRIM | ID: wpr-812672

ABSTRACT

The stem of Cynomorium songaricum is a traditional Chinese medicine reputed to have tonic effects. C. coccineum growing in northern Africa and the Mediterranean region is regarded in Arabian medical practice as the "treasure of drugs". The major constituents of Cynomorium plants have been revealed to be phenolic compounds, steroids, triterpenes, etc. Pharmacologic studies showed that the Cynomorium plants had antioxidant, immunity-improving, anti-diabetic, neuroprotective, and other bioactivities. Some chemical constituents in Cynomorium plants are unstable, implying that the chemical components of the herbal medicines produced under different conditions may be variable. This review covers the literature published until December, 2011 and describes the pharmacologic effects and secondary metabolites of Cynomorium species.


Subject(s)
Animals , Humans , Cynomorium , Chemistry , Classification , Metabolism , Drugs, Chinese Herbal , Chemistry , Metabolism , Pharmacology
4.
China Journal of Chinese Materia Medica ; (24): 533-535, 2003.
Article in Chinese | WPRIM | ID: wpr-282274

ABSTRACT

<p><b>OBJECTIVE</b>To analyze and identify fatty acids in the seeds of Sterculia lychnophora.</p><p><b>METHOD</b>The compositions was isolated and determined by GC-MS technique, and area normalization method was used to make quantitative analyze of the content of compositions.</p><p><b>RESULTS</b>21 Fatty acids and 5 other compositions were isolated and determined.</p><p><b>CONCLUSION</b>The major fatty acids are 9,12(Z,Z)-octadecadienoic acid(37.96%), hexadecanoic acid(24.77%), 9-(Z)-octadecenoic acid(19.77%) and octadecanoic acid(5.01%).</p>


Subject(s)
Fatty Acids, Nonesterified , Chemistry , Fatty Acids, Unsaturated , Gas Chromatography-Mass Spectrometry , Palmitic Acid , Plants, Medicinal , Chemistry , Seeds , Chemistry , Sterculia , Chemistry
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