Tham khảo Baicalein

  1. ↑ Matsumoto, Takumi (2008). Phytochemistry Research Progress. ISBN 9781604562323. 
  2. ↑ Wang H, Hui KM, Xu S, Chen Y, Wong JT, Xue H (2002). “Two flavones from Scutellaria baicalensis Georgi and their binding affinities to the benzodiazepine site of the GABAA receptor complex”. Pharmazie 57 (12): 857–8. PMID 12561253. 
  3. ↑ Hui KM, Wang XH, Xue H (2000). “Interaction of flavones from the roots of Scutellaria baicalensis with the benzodiazepine site”. Planta Med. 66 (1): 91–3. PMID 10705749. doi:10.1055/s-0029-1243121. 
  4. ↑ Zhang SQ, Obregon D, Ehrhart J, Deng J, Tian J, Hou H, Giunta B, Sawmiller D, Tan J (2013). “Baicalein reduces β-amyloid and promotes nonamyloidogenic amyloid precursor protein processing in an Alzheimer's disease transgenic mouse model”. J. Neurosci. Res. 91 (9): 1239–46. PMC 3810722. PMID 23686791. doi:10.1002/jnr.23244. 
  5. ↑ Liao JF, Wang HH, Chen MC, Chen CC, Chen CF (1998). “Benzodiazepine binding site-interactive flavones from Scutellaria baicalensis root”. Planta Med. 64 (6): 571–2. PMID 9776664. doi:10.1055/s-2006-957517. 
  6. ↑ Edwin Lowell Cooper; Nobuo Yamaguchi (ngày 1 tháng 1 năm 2004). Complementary and Alternative Approaches to Biomedicine. Springer Science & Business Media. tr. 188–. ISBN 978-0-306-48288-5. 
  7. 1 2 de Carvalho RS, Duarte FS, de Lima TC (2011). “Involvement of GABAergic non-benzodiazepine sites in the anxiolytic-like and sedative effects of the flavonoid baicalein in mice”. Behav. Brain Res. 221 (1): 75–82. PMID 21377498. doi:10.1016/j.bbr.2011.02.038. 
  8. 1 2 Wang F, Xu Z, Ren L, Tsang SY, Xue H (2008). “GABA A receptor subtype selectivity underlying selective anxiolytic effect of baicalin”. Neuropharmacology 55 (7): 1231–7. PMID 18723037. doi:10.1016/j.neuropharm.2008.07.040. 
  9. ↑ Liao JF, Hung WY, Chen CF (2003). “Anxiolytic-like effects of baicalein and baicalin in the Vogel conflict test in mice”. Eur. J. Pharmacol. 464 (2–3): 141–6. PMID 12620506. doi:10.1016/s0014-2999(03)01422-5. 
  10. ↑ Awad R, Arnason JT, Trudeau V, Bergeron C, Budzinski JW, Foster BC, Merali Z (2003). “Phytochemical and biological analysis of skullcap (Scutellaria lateriflora L.): a medicinal plant with anxiolytic properties”. Phytomedicine 10 (8): 640–9. PMID 14692724. doi:10.1078/0944-7113-00374. 
  11. 1 2 Stefanie Schwartz (ngày 9 tháng 1 năm 2008). Psychoactive Herbs in Veterinary Behavior Medicine. John Wiley & Sons. tr. 139–. ISBN 978-0-470-34434-7. 
  12. ↑ Deschamps JD, Kenyon VA, Holman TR (tháng 6 năm 2006). “Baicalein is a potent in vitro inhibitor against both reticulocyte 15-human and platelet 12-human lipoxygenases”. Bioorg. Med. Chem. 14 (12): 4295–301. PMID 16500106. doi:10.1016/j.bmc.2006.01.057. 
  13. ↑ Hsieh CJ, Hall K, Ha T, Li C, Krishnaswamy G, Chi DS (2007). “Baicalein inhibits IL-1β- and TNF-α-induced inflammatory cytokine production from human mast cells via regulation of the NF-κB pathway”. Clin Mol Allergy 5 (1): 5. PMC 2206049. PMID 18039391. doi:10.1186/1476-7961-5-5. 
  14. ↑ Lin Y-L, Lin R-J, Shen K-P, Dai Z-K, Chen I-J, Wu J-R, Wu B-N (2011). “Baicalein, isolated from Scutellaria baicalensis, protects against endothelin-1-induced pulmonary artery smooth muscle cell proliferation via inhibition of TRPC1 channel expression”. Journal of Ethnopharmacology 138 (2): 373–381. PMID 21963569. doi:10.1016/j.jep.2011.09.014. 
  15. ↑ Xiong Z, Jiang B, Wu PF và đồng nghiệp (2011). “Antidepressant effects of a plant-derived flavonoid baicalein involving extracellular signal-regulated kinases cascade”. Biol. Pharm. Bull. 34 (2): 253–9. PMID 21415537. doi:10.1248/bpb.34.253. 
  16. ↑ Si D, Wang Y, Zhou Y-H, Guo Y, Wang J, Zhou H, Li Z-S, Fawcett JP (tháng 3 năm 2009). “Mechanism of CYP2C9 inhibition by flavones and flavonols” (PDF). Drug Metabolism and Disposition 37 (3): 629–34. PMID 19074529. doi:10.1124/dmd.108.023416. 
  17. ↑ Tarragó T, Kichik N, Claasen B, Prades R, Teixidó M, Giralt E (tháng 8 năm 2008). “Baicalin, a prodrug able to reach the CNS, is a prolyl oligopeptidase inhibitor”. Bioorganic and Medicinal Chemistry 16 (15): 7516–24. PMID 18650094. doi:10.1016/j.bmc.2008.04.067. 
  18. ↑ Chen Y, Liu T, Wang K, Hou C, Cai S, Huang Y, Du Z, Huang H, Kong J, Chen Y (tháng 4 năm 2016). “Baicalein Inhibits Staphylococcus aureus Biofilm Formation and the Quorum Sensing System In Vitro.”. PLOS ONE 11 (4): e0153468. PMC 4851419. PMID 27128436. doi:10.1371/journal.pone.0153468. 

Tài liệu tham khảo

WikiPedia: Baicalein http://www.chemspider.com/Chemical-Structure.44449... http://www.clinicalmolecularallergy.com/content/5/... http://linkinghub.elsevier.com/retrieve/pii/S00142... http://linkinghub.elsevier.com/retrieve/pii/S0028-... http://linkinghub.elsevier.com/retrieve/pii/S0166-... http://linkinghub.elsevier.com/retrieve/pii/S0944-... http://linkinghub.elsevier.com/retrieve/pii/S0968-... http://p4502c.googlepages.com/dmd2.pdf //www.ncbi.nlm.nih.gov/pmc/articles/PMC2206049 //www.ncbi.nlm.nih.gov/pmc/articles/PMC3810722