发明名称 Arachidonic acid analogs and methods for analgesic treatment using same
摘要 The present invention provides arachidonic acid (AA) analogs and compositions containing those analogs as active agents for use in analgesic treatments. Various methods of manufacturing the inventive compounds are provided and pharmaceutical formulations, including injectable and oral dosages, are described. Certain analogs are additionally useful as antipyretic compositions and in related fever reducing treatments.
申请公布号 US9096494(B2) 申请公布日期 2015.08.04
申请号 US201414158064 申请日期 2014.01.17
申请人 CYTOMETIX, INC. 发明人 Brostrom Lane;Falck John R.
分类号 C07C233/09;C07C237/22;C07C275/20 主分类号 C07C233/09
代理机构 Quarles & Brady, LLP 代理人 Quarles & Brady, LLP
主权项 1. A compound having the structure:wherein: R1 is H, or a C1-C6 alkyl, C3-C6 alkenyl, C3-C6 cycloalkyl or C3-C6 cycloalkenyl which is unsubstituted or substituted with a hydroxyl group or a C1-C6 alky; R2 is H, or a C1-C3 alkyl; or R1 and R2 form a C3-C6 heterocyclic ring with the nitrogen bonded to said R1 and R2; R3 is:in which: R4 is H, or a C1-C6 alkyl, C3-C6 alkenyl, C3-C6 cycloalkyl or C3-C6 cycloalkenyl; R5 is a C1-C6 alkyl, C1-C6 alkoxy, or C2-C6 alkyl ether which is unsubstituted or substituted with one or more of hydroxyl, phenyl, phenyloxy, or fluorine, or R5 is NR7R8, or C(O)NR7R8 in which R7 and R8 are independently selected from H, a C1-C6 alkyl, C3-C6 alkenyl, C3-C6 cycloalkyl or C3-C6 cycloalkenyl; R6 is H, or a C1-C6 alkyl, C3-C6 alkenyl, C3-C6 cycloalkyl or C3-C6 cycloalkenyl; n is 0, 1, 2, 3, or 4; position a is —CH2—, —C(CH3)—, —C(CH3)2—, O or NR9 where R9 is H, OH, or a C1-C6 alkyl; position b is —CH2—, —CH(CH3)—, —C(CH3)2—, O, S, or NR10 where R10 is H, OH, or a C1-C6 alkyl; wherein position a and b are not both heteroatoms; m is 0, 1, 2, 3, or 4; wherein when m is 0, then position b is a carbon; p is 1, 2, or 3; or a pharmaceutically acceptable salt thereof.
地址 Bayside WI US