发明名称 O-SUBSTITUTED HYDROXYARYL DERIVATIVES
摘要 A medicament having inhibitory activity against NF-.KAPPA.B activation which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I-1) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: (see formula I-1) wherein "A1" represents an acyl group which may be substituted, (provided that unsubstituted acetyl group and unsubstituted acryloyl group are excluded,) or a C1 to C6 alkyl group which may be substituted, "E1" represents an aryl group which may be substituted or a heteroaryl group which may be substituted, ring Z represents an arene which may have one or more substituents in addition to the group represented by formula -O-A1 wherein A1 has the same meaning as that defined above and the group represented by formula -CONHE1 wherein E1 has the same meaning as that defined above, or a heteroarene which may have one or more substituents in addition to the group represented by formula -O-A1 wherein A1 has the same meaning as that defined above and the group represented by formula -CONHE1 wherein E1 has the same meaning as that defined above.
申请公布号 CA2488363(C) 申请公布日期 2011.01.04
申请号 CA20032488363 申请日期 2003.06.05
申请人 INSTITUTE OF MEDICINAL MOLECULAR DESIGN, INC. 发明人 MUTO, SUSUMU;ITAI, AKIKO
分类号 C07C235/64;A61K31/265;A61K31/27;A61K31/335;A61K31/395;A61K31/661;A61P29/00;A61P37/06;A61P43/00;C07C271/22;C07C271/42;C07C301/02;C07D209/48;C07D211/62;C07D213/79;C07D213/803;C07D265/22;C07D265/26;C07D269/00;C07D273/00;C07D277/46;C07D295/185;C07D295/205;C07D309/10;C07D317/48;C07D317/60;C07F9/12;C07K5/06;C07K5/065;C07K5/068;C07K5/072 主分类号 C07C235/64
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