发明名称 P62-ZZ CHEMICAL INHIBITOR
摘要 A method for treating a p62-mediated disease (e.g., multiple myeloma) in a subject, the method comprising administering to the subject a therapeutically effective amount of at least one p62-ZZ inhibitor compound.
申请公布号 US2016031799(A1) 申请公布日期 2016.02.04
申请号 US201514727710 申请日期 2015.06.01
申请人 ID4PHARMA, LLC 发明人 Xie Xiang-Qun;Roodman Garson David;Myint Kyaw-Zeyar;Kurihara Noriyoshi
分类号 C07C229/36;A61K31/216;A61K45/06;C07C217/58;A61K31/137 主分类号 C07C229/36
代理机构 代理人
主权项 1. A method for treating a p62-mediated disease in a subject, the method comprising administering to the subject a therapeutically effective amount of at least one p62-ZZ inhibitor compound of structural Formula I: or a pharmaceutically acceptable salt or ester thereof, wherein Ar is an arylene or heteroarylene;R1 has a structure of: wherein W is an alkanediyl, alkenediyl, a carbonyl, or a combination thereof;X is —NR5—, wherein R5 is H or an alkyl, or —O—; andY is a hydroxyalkyl, an aminoalkyl, or a carboxylalkyl;each R2 is the same or different and has a structure of: wherein Z is —NR6—, wherein R6 is H or an alkyl, —O—, —S—, or —CH2—;Z1 is (—CH2—)m wherein m is 0 to 5, or an alkenediyl having 2 to 6 carbon atoms;Cy is a 3-8-membered cycloalkyl, heterocycloalkyl, aryl or heteroaryl ring; andeach R4 is the same or different and is selected from hydroxy, halogen, substituted or unsubstituted alkoxy, substituted or unsubstituted alkyl, or amino; and c is 0 to 5; andeach R3 is the same or different and is selected from hydrogen, hydroxy, halogen, —CN, substituted or unsubstituted alkoxy, substituted or unsubstituted alkyl, amino, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or a nitro, wherein a is 0 to 5, and b is 0 to 3.
地址 Pittsburgh PA US