Characterization of thirty-nine polymethoxylated flavonoids (PMFs) in the branches of Murraya paniculata by HPLC-DAD-ESI-MS/MS

Chinese Journal of Natural Medicines

Volumn 11, Issue 1, 2013, Pages 63-70

  Zhang, Jia Yu ^a   Lu, Jian Qiu ^a   Gao, Xiao Yan ^a   Zhang, Qian ^a   Li, Ning ^b   Tu, Peng Fei ^a,b   Qiao, Yan Jiang ^a  

^a BEIJING UNIVERSITY OF CHINESE MEDICINE   (China)

^b PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

Author keywords

Characterization; HPLC DAD ESI MS MS; Murraya paniculata; Polymethoxylated flavonoids (PMFs)

Indexed keywords

3,5,6,7,3',4',5' HEPTAMETHOXYFLAVONE; CHALCONE DERIVATIVE; DIHYDROXY DIMETHOXYFLAVONE; FLAVANONE DERIVATIVE; FLAVONOID; GLYCOSIDE; HEXAMETHOXYCHALCONE; HEXAMETHOXYFLAVANONE; HEXAMETHOXYFLAVONE; MONOHYDROXY DIMETHOXYFLAVONE GLYCOSIDE; MONOHYDROXY PENTAMETHOXYFLAVONE; MONOHYDROXY TETRAMETHOXYFLAVONE GLYCOSIDE; MONOHYDROXY TRIMETHOXYCHALCONE; MONOHYDROXY TRIMETHOXYFLAVANONE; MONOHYDROXY TRIMETHOXYFLAVONE; MONOHYDROXY TRIMETHOXYFLAVONE GLYCOSIDE; PENTAMETHOXYCHALCONE; PENTAMETHOXYFLAVANONE; PENTAMETHOXYFLAVONE; TETRAHYDROXY DIHYDROXYFLAVONE GLYCOSIDE; TETRAMETHOXYCHALCONE; TETRAMETHOXYFLAVANONE; TETRAMETHOXYFLAVONE; TRIHYDROXY DIMETHOXYFLAVONE GLYCOSIDE; UNCLASSIFIED DRUG;

ARTICLE; ELECTROSPRAY MASS SPECTROMETRY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MURRAYA EXOTICA;

EID: 84872394823     PISSN: 20956975     EISSN: 18755364     Source Type: Journal    
DOI: 10.1016/S1875-5364(13)60009-6     Document Type: Article

References (24)

1. The Pharmacopoeia Commission of PRC Pharmacopoeia of the People's Republic of China [S] 2010, 10. Chemical Industry Publishing House, Beijing. 2010 ed.
2. Perry LM Medicinal Plants of East and Southeast Asia: Attributed Properties and Uses [M] 1980, 367. MIT Press, England.
3. Zheng HZ, Dong ZH, Yu J Modern Study of Traditional Chinese Medicine [M] 1997, 5493. Xueyuan Press, Beijing.
4. Moraes VRD, Tomazela DM, Ferracin RJ Enzymatic inhibition studies of selected flavonoids and chemosystematic significance of polymethoxylated flavonoids and quinoline alkaloids in Neoraputia (Rutaceae) [J]. J Brazil Chem Soc 2003, 14(3):380-387.
5. Kawaii S, Tomono Y, Katase E, et al. Antiproliferative activity of flavonoids on several cancer cell lines [J]. Biosci Biotechnol Biochem 1999, 63(5):896-899.
6. Anagnostopoulou MA, Kefalas P, Kokkalou E, et al. Analysis of antioxidant compounds in sweet orange peel by HPLC-diode array detection-electrospray ionization mass spectrometry [J]. Biomed Chromatogr 2005, 19(2):138-148.
7. Jayaprakasha GK, Negi PS, Sikder S, et al. Antibacterial activity of Citrus reticulata peel extracts, Hoppe-Seyler's Z [J]. Physiol Chem 2000, 55(11-12):1030-1034.
8. Yanez J, Vicente V, Alcaraz M, et al. Cytotoxicity and antiproliferative activities of several phenolic compounds against three melanocytes cell lines: Relationship between structure and activity [J]. Nutr Cancer 2004, 49(2):191-199.
9. Li RW, Theriault AG, Au K, et al. Citrus polymethoxylated flavones improve lipid and glucose homeostasis and modulate adipocylokines in fructose-induced insulin resistant hamsters [J]. Life Sci 2006, 79(4):365-373.
10. Wu YQ, Zhou CH, Tao J, et al. Antagonistic effects of nobiletin, a polymethoxyflavonoid, on eosinophilic airway inflammation of asthmatic rats and relevant mechanisms [J]. Life Sci 2006, 78(23):2689-2696.
11. Zhang JY, Li N, Che YY, et al. Characterization of seventy polymethoxylated flavonoids (PMFs) in the leaves of M. paniculata by on-line high-performance liquid chromatography coupled to photodiode array detection and electrospray tandem mass spectrometry [J]. J Pharm Biomed Anal 2011, 56(5):950-961.
12. He XG On-line identification of phytochemical constituents in botanical extracts by combined high-performance liquid chromatographic-diode array detection-mass spectrometric techniques [J]. J Chromatogr A 2000, 880(1-2):203-232.
13. Robards K Strategies for the determination of bioactive phenols in plants, fruit and vegetables [J]. J. Chromatogr A 2003, 1000(1-2):657-691.
14. Man SL, Gao WY, Zhang YJ, et al. Qualitative and quantitative determination of major saponins in Paris and Trillium by HPLC-ELSD and HPLC-MS/MS [J]. J Chromatogr B 2010, 878(29):2943-2948.
15. Wang YH, Qiu C, Wang DW, et al. Identification of multiple constituents in the traditional Chinese medicine formula Sheng-Mai San and rat plasma after oral administration by HPLC-DAD-MS/MS [J]. J Pharm Biomed Anal 2011, 54(5):1110-1127.
16. Chen LL, Wang YH, Dong TX, et al. Identification and determination of dbsorbed components of Danggui-Shaoyao-San in rat plasma [J]. Chin J Nat Prod 2011, 9(5):363-368.
17. Zhang Y, Li J, Zhou SX, et al. Polymethoxylated flavonoids from the leaves of M. paniculata [J]. Chin Pharm J 2010, 45(15):1139-1141.
18. Shan J, Wang XZ, Ma YD, et al. Studies on flavonoids from leaves of Murraya panaculata L. [J]. Chin Pharm J 2010, 45(24):1910-1912.
19. Le Quesne PW, Pastore MP, Raffauf RF The cytotoxic flavonoids of Lychnophora affinis [J]. Lloydia 1976, 39(6):391-394.
20. Domon B, Costello CE A systematic nomenclature for carbohydrate fragmentations in FAB-MS/MS spectra of glycoconjugates [J]. Glycoconj J 1988, 5(4):397-409.
21. Zhou DY, Chen DL, Xu Q, et al. Characterization of polymethoxylated flavones in Fructus aurantii by liquid chromatography with atmospheric pressure chemical ionization combined with tandem mass spectrometry [J]. J Pharm Biomed Anal 2007, 43(5):1692-1699.
22. Fabre N, Rustan I, de Hoffmann E, et al. Determination of flavone, flavonol, and flavanone aglycones by negative ion liquid chromatography electrospray ion trap mass spectrometry [J]. J Am Soc Mass 2001, 12(6):707-715.
23. Zhang JM, Brodbelt JS Structural characterization and isomer differentiation of chalcones by electrospray ionization tandem mass spectrometry [J]. J Mass Spectrom 2003, 38(5):555-572.
24. + ions from chalcone [J]. Rapid Commun Mass Spectrom 1991, 5(1):5-10.