CAS号36148-89-7 两性霉素B甲酯 | CAS号1112349-87-7 amphotericin B ...
合成工艺路线路线简述
两性霉素b甲酯置于lithium Hydroxide体系中,用 四氢呋喃,水 用作溶剂,化学反应 1.0H,以80%的收率获得两性霉素b 参考文献:Total Synthesis Of Amphotericin B 标题:Total Synthesis Of Amphotericin B 摘要: Doi:10.1021/ja00243A043
1: Azanza JR, Sádada B, Reis J. Liposomal formulations of amphotericin B: differences according to the scientific evidence. Rev Esp Quimioter. 2015 Dec;28(6):275-81. Review. doi: 10.1007/s40265-013-0069-4. Review. doi: 10.1016/j.arth.2015.06.002. Epub 2015 Jun 11. doi: 10.1016/j.mycmed.2014.04.003. Epub 2014 Oct 16. doi: 10.5414/CP202015. doi: 10.1016/j.ejmech.2015.03.022. Epub 2015 Mar 14. doi: 10.1093/mmy/myv111. Epub 2016 Jan 14. Review. doi: 10.1021/acs.bioconjchem.5b00463. Epub 2015 Sep 10. doi: 10.1128/AAC.02484-12. Epub 2013 May 28. 10: Tang X, Zhu H, Sun L, Hou W, Cai S, Zhang R, Liu F. Enhanced antifungal effects of amphotericin B-TPGS-b-(PCL-ran-PGA) nanoparticles in vitro and in vivo. Int J Nanomedicine. 2014 Nov 24;9:5403-13. doi: 10.2147/IJN.S71623. eCollection 2014. 11: Mishra J, Dey A, Singh N, Somvanshi R, Singh S. Evaluation of toxicity & therapeutic efficacy of a new liposomal formulation of amphotericin B in a mouse model. Indian J Med Res. 2013 Apr;137(4):767-76.
合成参考文献
摘要:Tested as SID 174520445 in AID 781330: https://pubchem.ncbi.nlm.nih.gov/bioassay/781330#sid=174520445