Синефрін (Ukrainian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Синефрін" in Ukrainian language version.

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archive.org

compendium.ch

  • SA, HCI Solutions. Neo-Synephrine HCl - compendium.ch. compendium.ch. Архів оригіналу за 25 липня 2020. Процитовано 6 березня 2016.

doi.org

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Wagner H., Ulrich-Merzenich G. (2009). Synergy research: approaching a new generation of phytopharmaceuticals. Phytomedicine. 16 (2–3): 97—110. doi:10.1016/j.phymed.2008.12.018. PMID 19211237.
  • Wheaton T. A., Stewart I. (1970). The distribution of tyramine, N-methyltyramine, hordenine, octopamine and synephrine in higher plants. Lloydia. 33 (2): 244—254. PMID 5495514.
  • Ko H. C., Chen K. T., Chen C. F., Su J. P., Chen C. M., Wang G. J. (2006). Chemical and biological comparisons on Evodia with two related species of different locations and conditions. Journal of Ethnopharmacology. 108 (2): 257—263. doi:10.1016/j.jep.2006.05.020. PMID 16824714.
  • Kim S. P., Moon E., Nam S. H., Friedman M. (2012). Composition of Herba Pogostemonis water extract and protection of infected mice against Salmonella typhimurium-induced liver damage and mortality by stimulation of innate immune cells. Journal of Agricultural and Food Chemistry. 60 (49): 12122—12130. doi:10.1021/jf304466t. PMID 23186318.
  • Pellati F., Benvenuti S., Melegari M. (2005). Enantioselective LC analysis of synephrine in natural products on a protein-based chiral stationary phase. Journal of Pharmaceutical and Biomedical Analysis. 37 (5): 839—849. doi:10.1016/j.jpba.2004.09.008. PMID 15862657.
  • Mattoli L., Cangi F., Maidecchi A., Ghiara C., Tubaro M., Traldi P. (2005). A rapid liquid chromatography electrospray ionization mass spectrometry method for evaluation of synephrine in Citrus aurantium L. samples. Journal of Agricultural and Food Chemistry. 53 (26): 9860—9866. doi:10.1021/jf051270+. PMID 16366666.
  • Avula B., Upparapalli S. K., Khan I. A. (2007). Simultaneous analysis of adrenergic amines and flavonoids in citrus peel jams and fruit juices by liquid chromatography: part 2. Journal of AOAC International. 90 (3): 633—40. doi:10.1093/jaoac/90.3.633. PMID 17580614.
  • Ibrahim K. E., Couch M. W., Williams C. M., Budd M. B., Yost R. A., Midgley J. M. (1984). Quantitative measurement of octopamines and synephrines in urine using capillary column gas chromatography negative ion chemical ionization mass spectrometry. Analytical Chemistry. 56 (9): 1695—1699. doi:10.1021/ac00273a037. PMID 6435479.
  • Wang R., Wan L., Li Q., Liu X., Huang Y. (2007). Chemiluminescence of synephrine based on the cerium(IV)–rhodamine B system. Luminescence. 22 (2): 140—146. doi:10.1002/bio.937. PMID 17089346.
  • Watson D.G., Midgley J.M., Chen R.N., Huang W., Bain G.M., McDonald N.M., Reid J.L., McGhee C.N.J. (1990). Analysis of biogenic amines and their metabolites in biological tissues and fluids by gas chromatography—negative ion chemical ionization mass spectrometry (GC-NICIMS). Journal of Pharmaceutical and Biomedical Analysis. 8 (8–12): 899—904. doi:10.1016/0731-7085(90)80139-g. PMID 2100639.
  • Ibrahim K. E., Couch M. W., Williams C. M., Fregly M. J., Midgley J. M. (1985). m-Octopamine: normal occurrence with p-octopamine in mammalian sympathetic nerves. Journal of Neurochemistry. 44 (6): 1862—1867. doi:10.1111/j.1471-4159.1985.tb07180.x. PMID 3921667.
  • Bartley A. P. Breksa III, Ishida B. K. (2010). PCR amplification and cloning of tyrosine decarboxylase involved in synephrine biosynthesis in Citrus. New Biotechnology. 27 (4): 308—316. doi:10.1016/j.nbt.2010.04.003. PMID 20403465.
  • D'Andrea G., Terrazzino S., Fortina D., Farruggioa A., Rinaldi L., Leon A. (2003). HPLC electrochemical detection of trace amines in human plasma and platelets and expression of mRNA transcripts of trace amine receptors in circulating leukocytes. Neuroscience Letters. 346 (1–2): 89—92. doi:10.1016/s0304-3940(03)00573-1. PMID 12850555.
  • Kappe T., Armstrong M. D. (1965). Ultraviolet absorption spectra and apparent acidic dissociation constants of some phenolic amines. Journal of Medicinal Chemistry. 8 (3): 368—374. doi:10.1021/jm00327a018. PMID 14323148.

web.archive.org

  • SA, HCI Solutions. Neo-Synephrine HCl - compendium.ch. compendium.ch. Архів оригіналу за 25 липня 2020. Процитовано 6 березня 2016.