发明名称 Aminopyrazole derivatives
摘要 <CHEM> Aminopyrazole derivatives represented by formula (I), or salts thereof, wherein X<1> and X<2> are each a hydrogen atom or a halogen atom, or X<1> and X<2> may be united together to form a lower alkylenedioxy group, Q is a pyridyl group or a quinolyl group, R<1> is a hydrogen atom, a substituted or unsubstituted lower alkyl or aryl group, R<2> is a hydrogen atom, a lower alkyl group, or an aralkyl group, and R<3> represents a hydrogen atom, an organic sulfonyl group, or -C(=Y)-R<4> in which R<4> is a hydrogen atom or an organic residue and Y is an oxygen or sulfur atom, provided that, when R<3> is a hydrogen atom, R<1> is a group other than a hydrogen atom and R<2> is a hydrogen atom. These aminopyrazole derivatives or their salts have excellent p38MAP kinase inhibiting activities and are hence useful in the prevention or treatment of diseases associated with tumor necrosis factor alpha , interleukin 1, interleukin 6 or cyclooxygenase II.
申请公布号 AU1691100(A) 申请公布日期 2000.07.31
申请号 AU20000016911 申请日期 1999.12.21
申请人 TEIKOKU HORMONE MFG. CO., LTD. 发明人 NOBUYOSHI MINAMI;MICHITAKA SATO;KOICHI HASUMI;NORIO YAMAMOTO;KATSUYUKI KEINO;TERUAKI MATSUI;ARIHIRO KANADA;SHUJI OHTA;TAKAHISA SAITO;SHUICHIRO SATO;AKIRA ASAGARASU;SATOSHI DOI;MOTOHIRO KOBAYASHI;JUN SATO;HAJIME ASANO
分类号 A61P1/00;A61P3/00;A61P7/00;A61P9/00;A61P11/00;A61P17/00;A61P19/00;A61P21/00;A61P25/00;A61P27/00;A61P29/00;A61P31/00;A61P37/00;A61P43/00;C07D401/04;C07D405/14 主分类号 A61P1/00
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