发明名称 Anti-inflammatory compounds
摘要 New clerodane compounds isolated from plant material from Dodonaea polyandra are disclosed. The compounds have anti-inflammatory activity. Pharmaceutical and cosmetic compositions containing the compounds, as well as methods of treating inflammation using the compounds, are also disclosed.
申请公布号 US9403786(B2) 申请公布日期 2016.08.02
申请号 US201013509194 申请日期 2010.11.10
申请人 University of South Australia;Chuulangun Aboriginal Corporation 发明人 Semple Susan J.;Simpson Bradley S.;McKinnon Ross Allan;Claudie David;Gerber Jacobus P.;Wang Jiping;Moreton, Sr. George
分类号 C07D307/42;C07D307/54 主分类号 C07D307/42
代理机构 Olson & Cepuritis, Ltd. 代理人 Olson & Cepuritis, Ltd.
主权项 1. A compound of formula (I)or a pharmaceutically acceptable salt or an ester prodrug thereof, wherein: T is a double bond; R1 is selected from the group consisting of: COOR7, CONR7R8, COSR7, COR7, SO3H, SO2NR7R8, SO2R7, SONR7R8, and SOR7; R2, R3, and R4 are each independently selected from the group consisting of: H, optionally substituted C1-C12 alkyl, and optionally substituted C2-C12 alkenyl; R5 and R6 are each independently selected from the group consisting of: H, OH, optionally substituted C1-C12 alkyl, ═O, (CH2)mOC(O)R9, C1-C12 oxyalkyl, C1-C12 alkyloxy, C2-C12 oxyalkenyl, and C2-C12 alkenyloxy, provided at least one of R5 and R6 is (CH2)mOC(O)R9; R7 and R8 are each independently selected from the group consisting of: H, optionally substituted C1-C12 alkyl, optionally substituted C2-C12 alkenyl, optionally substituted C2-C12 alkynyl, optionally substituted C1-C10 heteroalkyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted C1-C12 heterocycloalkyl, optionally substituted C1-C12 heterocycloalkenyl, optionally substituted C6-C18 aryl, and optionally substituted C1-C18 heteroaryl; R9 is phenyl; Ar is an optionally substituted aryl group; and m and n are integers each of which is selected from the group consisting of 0, 1, 2, 3, and 4.
地址 Adelaide, S.A. AU
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