Tham khảo Avermectin

  1. ↑ Ōmura, Satoshi; Shiomi, Kazuro (2007). “Discovery, chemistry, and chemical biology of microbial products”. Pure and Applied Chemistry 79 (4): 581–591. doi:10.1351/pac200779040581. 
  2. 1 2 Pitterna, Thomas; Cassayre, Jérôme; Hüter, Ottmar Franz; Jung, Pierre M.J.; Maienfisch, Peter; Kessabi, Fiona Murphy; Quaranta, Laura; Tobler, Hans (2009). “New ventures in the chemistry of avermectins”. Bioorganic & Medicinal Chemistry 17 (12): 4085–4095. doi:10.1016/j.bmc.2008.12.069. 
  3. ↑ “The Nobel Prize in Physiology or Medicine 2015” (PDF). Nobel Foundation. Truy cập ngày 7 tháng 10 năm 2015. 
  4. ↑ Burg, R. W.; Miller, B. M.; Baker, E. E.; Birnbaum, J.; Currie, S. A.; Hartman, R.; Kong, Y.-L.; Monaghan, R. L.; Olson, G. (1979). “Avermectins, New Family of Potent Anthelmintic Agents: Producing Organism and Fermentation”. Antimicrobial Agents and Chemotherapy 15 (3): 361–7. PMC 352666. PMID 464561. doi:10.1128/AAC.15.3.361. 
  5. ↑ Takahashi, Y. (2002). “Streptomyces avermectinius sp. nov., an avermectin-producing strain”. International Journal of Systematic and Evolutionary Microbiology 52 (6): 2163–8. PMID 12508884. doi:10.1099/ijs.0.02237-0. 
  6. ↑ Hotson, I. K. (1982). “The avermectins: A new family of antiparasitic agents”. Journal of the South African Veterinary Association 53 (2): 87–90. PMID 6750121. 
  7. ↑ Cully, Doris F.; Vassilatis, Demetrios K.; Liu, Ken K.; Paress, Philip S.; Van Der Ploeg, Lex H. T.; Schaeffer, James M.; Arena, Joseph P. (1994). “Cloning of an avermectin-sensitive glutamate-gated chloride channel from Caenorhabditis elegans”. Nature 371 (6499): 707–11. Bibcode:1994Natur.371..707C. PMID 7935817. doi:10.1038/371707a0. 
  8. ↑ Bloomquist, Jeffrey R. (1996). “Ion Channels as Targets for Insecticides”. Annual Review of Entomology 41: 163–90. PMID 8546445. doi:10.1146/annurev.en.41.010196.001115. 
  9. ↑ Bloomquist, Jeffrey R. (2003). “Chloride channels as tools for developing selective insecticides”. Archives of Insect Biochemistry and Physiology 54 (4): 145–56. PMID 14635176. doi:10.1002/arch.10112. 
  10. ↑ Bloomquist, Jeffrey R. (1993). “Toxicology, mode of action and target site-mediated resistance to insecticides acting on chloride channels”. Comparative Biochemistry and Physiology C 106 (2): 301–314. doi:10.1016/0742-8413(93)90138-b. 
  11. ↑ Clark, J K; Scott, J G; Campos, F; Bloomquist, J R (1995). “Resistance to Avermectins: Extent, Mechanisms, and Management Implications”. Annual Review of Entomology 40: 1–30. PMID 7810984. doi:10.1146/annurev.en.40.010195.000245. 
  12. ↑ Toth, L. A.; Oberbeck, C; Straign, C. M.; Frazier, S; Rehg, J. E. (2000). “Toxicity evaluation of prophylactic treatments for mites and pinworms in mice”. Contemporary Topics in Laboratory Animal Science / American Association for Laboratory Animal Science 39 (2): 18–21. PMID 11487234. 
  13. ↑ Viktorov, A. V.; Yurkiv, V. A. (2003). “Effect of ivermectin on function of liver macrophages”. Bulletin of Experimental Biology and Medicine 136 (6): 569–71. PMID 15500074. doi:10.1023/b:bebm.0000020206.23474.e9. 
  14. ↑ Yang, Chen-Chang (2012). “Acute Human Toxicity of Macrocyclic Lactones”. Current Pharmaceutical Biotechnology 13 (6): 999–1003. PMID 22039794. doi:10.2174/138920112800399059. 
  15. 1 2 Ikeda, H.; Nonomiya, T.; Usami, M.; Ohta, T.; Omura, S. (1999). “Organization of the biosynthetic gene cluster for the polyketide anthelmintic macrolide avermectin in Streptomyces avermitilis”. Proceedings of the National Academy of Sciences 96 (17): 9509–9514. Bibcode:1999PNAS...96.9509I. PMC 22239. PMID 10449723. doi:10.1073/pnas.96.17.9509. 
  16. 1 2 3 4 5 6 7 8 9 10 Yoon, Y. J.; Kim, E.-S.; Hwang, Y.-S.; Choi, C.-Y. (2004). “Avermectin: Biochemical and molecular basis of its biosynthesis and regulation”. Applied Microbiology and Biotechnology 63 (6): 626–34. PMID 14689246. doi:10.1007/s00253-003-1491-4. 
  17. ↑ Zhang, Changsheng; Albermann, Christoph; Fu, Xun; Thorson, Jon S. (2006). “The in Vitro Characterization of the Iterative Avermectin Glycosyltransferase AveBI Reveals Reaction Reversibility and Sugar Nucleotide Flexibility”. Journal of the American Chemical Society 128 (51): 16420–1. PMID 17177349. doi:10.1021/ja065950k.