Chemical Profiling of Lobelia chinensis with High-Performance Liquid Chromatography/Quadrupole Time-of-Flight Mass Spectrometry (HPLC/Q-TOF MS) Reveals Absence of Lobeline in the Herb
暂无分享,去创建一个
[1] Hui Sun,et al. Mass spectrometry-driven drug discovery for development of herbal medicine. , 2018, Mass spectrometry reviews.
[2] Meihua Yang,et al. Simultaneous Analysis of Iridoid Glycosides and Anthraquinones in Morinda officinalis Using UPLC-QqQ-MS/MS and UPLC-Q/TOF-MSE , 2018, Molecules.
[3] H. Aisa,et al. Rapid Quantification and Quantitation of Alkaloids in Xinjiang Fritillaria by Ultra Performance Liquid Chromatography-Quadrupole Time-of-Flight Mass Spectrometry , 2017, Molecules.
[4] Roberto Larcher,et al. Targeted and untargeted profiling of alkaloids in herbal extracts using online solid-phase extraction and high-resolution mass spectrometry (Q-Orbitrap). , 2016, Journal of mass spectrometry : JMS.
[5] C. Leung,et al. Chemical Structure and Immunomodulating Activities of an α-Glucan Purified from Lobelia chinensis Lour , 2016, Molecules.
[6] L. Kursinszki,et al. HPLC-ESI-MS/MS of brain neurotransmitter modulator lobeline and related piperidine alkaloids in Lobelia inflata L. , 2015, Journal of mass spectrometry : JMS.
[7] Mei-wan Chen,et al. Lobelia chinensis: chemical constituents and anticancer activity perspective. , 2014, Chinese journal of natural medicines.
[8] T. Su,et al. UHPLC UHD Q-TOF MS/MS analysis of the impact of sulfur fumigation on the chemical profile of Codonopsis Radix (Dangshen). , 2014, The Analyst.
[9] C. Li,et al. Chiral separation of two diastereomeric pairs of enantiomers of novel alkaloid-lignan hybrids from Lobelia chinensis and determination of the tentative absolute configuration. , 2013, Journal of chromatography. A.
[10] Ying-Ting Lin,et al. Chemical constituents from Lobelia chinensis and their anti-virus and anti-inflammatory bioactivities , 2011, Archives of pharmacal research.
[11] C. Li,et al. Chemical constituents of Lobelia chinensis. , 2009, Fitoterapia.
[12] Chao Yan,et al. Two-dimensional liquid chromatography coupled with mass spectrometry for the analysis of Lobelia chinensis Lour. using an ESI/APCI multimode ion source. , 2008, Journal of separation science.
[13] L. Kursinszki,et al. LC-DAD and LC–MS–MS Analysis of Piperidine Alkaloids of Lobelia inflata L. (In Vitro and In Vivo) , 2008 .
[14] François-Xavier Felpin,et al. History, chemistry and biology of alkaloids from Lobelia inflata , 2004 .
[15] G. Kusano,et al. Two New Pyrrolidine Alkaloids, Radicamines A and B, as Inhibitors of α‐Glucosidase from Lobelia chinensis Lour. , 2002 .
[16] G. Kusano,et al. Two new pyrrolidine alkaloids, radicamines A and B, as inhibitors of alpha-glucosidase from Lobelia chinensis Lour. , 2001, Chemical & pharmaceutical bulletin.
[17] H. Ciolino,et al. Diosmin and diosmetin are agonists of the aryl hydrocarbon receptor that differentially affect cytochrome P450 1A1 activity. , 1998, Cancer research.
[18] P. Denkova,et al. Phytochemical Study and Antiinflammatory Properties of Lobelia laxiflora L , 1998, Zeitschrift fur Naturforschung. C, Journal of biosciences.
[19] R. Bye,et al. A comparative study of the analgesic and anti-inflammatory activities of pectolinarin isolated from Cirsium subcoriaceum and linarin isolated from Buddleia cordata. , 1998, Planta medica.
[20] M. Damaj,et al. Pharmacology of lobeline, a nicotinic receptor ligand. , 1997, The Journal of pharmacology and experimental therapeutics.
[21] K. Shimomura,et al. Polyacetylenes in Hairy Root Cultures of Lobelia chinensis Lour. , 1995 .
[22] G. Snatzke,et al. Über die Alkaloide aus Lobelia syphilitica L., I , 1961 .
[23] Dai Ying. Studies on chemical constituents of flavones from Lobelia chinensis Lour , 2009 .
[24] Yang Jun. Extraction of Alkaloids from Lobelia chinensis Lour and Their Inhibitory Effects on Growth of Stomach Cancer Cells , 2007 .
[25] 임록재,et al. 수염가래 Lobelia chinensis Lour. , 2001 .
[26] M. Tripathi,et al. Flavonoids of Abies pindrow leaves , 1996 .
[27] D. O'donovan,et al. The biosynthesis of lobelia alkaloids. Part III. Intermediates in the biosynthesis of lobeline; biosynthesis of 8, 10-diethyl-lobelidione. , 1975, Journal of the Chemical Society. Perkin transactions 1.