发明名称 Prostaglandin analogs as chloride channel opener
摘要 The use of a composition for opening Chloride (ClC) channels in a mammalian subject, which comprises an effective amount of a prostaglandin compound represented by the formula (II); with the proviso that the use does not include a method of medical treatment of humans, and with the proviso that the mammalian subject is not suffering from asthma and/or constipation, is disclosed. The use of this composition for treating a condition associated with reduced permeability in a mammalian subject by opening ClC channels is also disclosed. The condition associated with reduced chloride ion permeability may be cystic fibrosis. A composition for opening ClC channels in a mammalian subject, which comprises an effective amount of a prostaglandin compound, wherein the prostaglandin compound is represented by the formula (IV), is also disclosed. The use of a prostaglandin compound as shown by general formula (I), for manufacturing a pharmaceutical composition for opening ClC channels in a mammalian subject; with the proviso that the mammalian subject is not suffering from asthma and/or constipation, is also disclosed.
申请公布号 NZ531503(A) 申请公布日期 2006.01.27
申请号 NZ20020531503 申请日期 2002.08.29
申请人 SUCAMPO AG 发明人 UENO, RYUJI;CUPPOLETTI, JOHN
分类号 A61K31/5575;A61K31/557;A61P3/14;A61P11/06;A61P11/08;A61P13/12;A61P21/02;A61P25/00;A61P25/08;A61P25/20;A61P25/22;A61P25/28;A61P43/00;C07C405/00;(IPC1-7):A61K31/557 主分类号 A61K31/5575
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