发明名称 Pharmaceutical compounds for use in the therapy of <i>Clostridium difficile </i>infection
摘要 The invention relates to a compound described by a general formula (1), wherein each X independently can be OPO32−, OPSO22− or OSO3−; R1 comprises a solubility function such as a polyethylene glycol moiety and each X independently can be OPO32−, OPSO22−, − or OSO3−; and Z is an alkyl chain comprising 1 to 3 carbon and/or hetero atoms. The invention further relates to polysulfate derivatives or mixed polyphosphate/sulphate derivatives of six-membered cyclic polyols for use in the therapy of infection by Clostridium difficile.
申请公布号 US9358243(B2) 申请公布日期 2016.06.07
申请号 US201214347649 申请日期 2012.09.28
申请人 ETH ZURICH 发明人 Castagner Bastien;Leroux Jean-Christophe;Ivarsson Mattias;Schneider Gisbert;Pratsinis Anna
分类号 A61K31/6615;C07F9/117;C07C305/20;C07F9/09;A61K31/255;A61K45/06;A61K31/185;A61K31/4164;A61K31/7048;A61K38/14 主分类号 A61K31/6615
代理机构 JMB Davis Ben-David 代理人 JMB Davis Ben-David
主权项 1. A method for treating a C. difficile infection, comprising administering to a subject a composition comprising a compound described by general formula (16a) or (16b):wherein a) X2 is OSO3−, and X1, X3, X4, X5 and X6 are each independently selected from OPO32−, OPSO22− or OSO3−; b) X1, X3 and X5 are OPO32− and X2, X4 and X6 are OSO3− c) X1, X3 and X5 are OSO3− and X2, X4 and X6 are OPO32− d) X4, X5 and X6 are OSO3− and X1, X2 and X3 are OPO32−, e) X4, X5 and X6 are OPO32− and X1, X2 and X3 are OSO3− or f) X2 and X5 are OPO32− and X1, X3, X4, and X6 are OSO3−, g) X2 and X5 are OSO3− and X1, X3, X4, and X6 are OPO32−, h) X2 and X3 are OPO32− and X1, X4, X5, and X6 are OSO3−, or i) X2 and X3 are OSO3− and X1, X4, X5, and X6 are OPO32−.
地址 Zurich CH