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1.
公开(公告)号:EP1382591A4
公开(公告)日:2006-01-18
申请号:EP02720602
申请日:2002-04-25
申请人: EISAI CO LTD
发明人: AKAIKE AKINORI , SUGIMOTO HACHIRO , NISHIZAWA YUKIO , YONAGA MASAHIRO , ASAKAWA NAOKI , ASAI NAOKI , MANO NARIYASU , TERAUCHI TARO , DOKO TAKASHI
IPC分类号: A61P17/00 , C07C43/13 , C07C43/315 , C07C47/36 , C07C47/37 , C07C47/46 , C07C62/06 , C07C62/14 , C07C69/00 , C07C229/46 , C07C235/26 , C07C247/12 , C07C255/31 , C07C271/22 , C07C309/66 , C07C309/73 , C07C317/18 , C07C317/24 , C07C317/28 , C07C317/44 , C07C317/46 , C07C317/48 , C07C317/50 , C07C323/13 , C07C323/22 , C07C323/26 , C07C323/43 , C07C323/53 , C07C323/55 , C07C323/58 , C07C323/60 , C07C327/32 , C07C35/44
CPC分类号: C07C69/757 , C07C43/13 , C07C43/315 , C07C47/36 , C07C47/37 , C07C47/46 , C07C62/06 , C07C62/14 , C07C229/46 , C07C235/26 , C07C247/12 , C07C255/31 , C07C271/22 , C07C309/66 , C07C309/73 , C07C317/18 , C07C317/24 , C07C317/28 , C07C317/44 , C07C317/46 , C07C317/48 , C07C317/50 , C07C323/13 , C07C323/22 , C07C323/26 , C07C323/43 , C07C323/53 , C07C323/55 , C07C323/58 , C07C323/60 , C07C327/32 , C07C2603/90 , C07C2603/95
摘要: A novel compound which is highly effective in ameliorating the cellular disorders caused by radicals and in inhibiting the neurotoxicity induced by excitatory neurotransmitters such as glutamic acid. It is a compound represented by the following formula, a salt thereof, or a hydrate of either. (I) In the formula, Z means an optionally substituted, divalent, C2-3 organic group, etc., and R3 represents carboxyl, etc.
摘要翻译: 本发明提供一种新兴化合物,其表现出对自由基引起的细胞损伤的抑制作用以及由兴奋性输尿管如谷氨酸诱导的神经毒性。 具体地,它提供由下式表示的化合物,其盐或它们的水合物。 其中Z表示2〜3个可具有取代基的碳原子的二价有机基团等; R 3表示羧基等。
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公开(公告)号:EP1510516A4
公开(公告)日:2005-11-02
申请号:EP03733170
申请日:2003-05-29
申请人: EISAI CO LTD
发明人: OHI NORIHITO , SATO NOBUAKI , SOEJIMA MOTOHIRO , DOKO TAKASHI , TERAUCHI TARO , NAOE YOSHIMITSU , MOTOKI TAKAFUMI
IPC分类号: A61K31/407 , A61K31/416 , A61K31/4162 , A61K31/4178 , A61K31/4184 , A61K31/4196 , A61K31/42 , A61K31/422 , A61K31/4245 , A61K31/427 , A61K31/43 , A61K31/437 , A61K31/4439 , A61K31/444 , A61K31/454 , A61K31/496 , A61K31/497 , A61K31/4985 , A61K31/506 , A61K31/5377 , A61K31/55 , A61P21/00 , A61P25/00 , A61P25/14 , A61P25/16 , A61P25/28 , A61P29/00 , A61P37/06 , A61P43/00 , C07D231/56 , C07D401/06 , C07D403/04 , C07D403/06 , C07D405/06 , C07D409/04 , C07D409/06 , C07D413/04 , C07D413/14 , C07D471/04 , C07D487/04 , C07D495/04 , A61K31/415 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D471/08 , C07D519/00
CPC分类号: A61K31/506 , A61K31/407 , A61K31/416 , A61K31/4162 , A61K31/4178 , A61K31/4184 , A61K31/4196 , A61K31/42 , A61K31/422 , A61K31/4245 , A61K31/427 , A61K31/43 , A61K31/437 , A61K31/4439 , A61K31/444 , A61K31/454 , A61K31/496 , A61K31/497 , A61K31/4985 , A61K31/5377 , A61K31/55 , C07D231/56 , C07D401/06 , C07D403/04 , C07D403/06 , C07D405/06 , C07D409/04 , C07D409/06 , C07D413/04 , C07D413/14 , C07D471/04 , C07D487/04 , C07D495/04
摘要: A novel compound having excellent JNK inhibitory activity. It is a compound represented by the following general formula or a salt thereof. (I) In the formula, R1 represents -(CO)h-(NRa)j-(CRb=CRc)k-Ar (wherein Ra, Rb, and Rc each independently represents hydrogen, halogeno, hydroxy, optionally substituted C1-6 alkyl, etc.); Cy means a 5- or 6-membered aromatic heterocycle; and V's each independently means -L-X-Y [wherein L means a single bond, optionally substituted C1-6 alkylene, etc.; X means a single bond, -A- (wherein A represents NR2, O, CO, S, SO, or SO2), etc.; and Y means hydrogen, halogeno, nitro, etc.].
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公开(公告)号:EP1380576A4
公开(公告)日:2005-02-16
申请号:EP02724612
申请日:2002-04-15
申请人: EISAI CO LTD
发明人: OINUMA HITOSHI , OHI NORIHITO , SATO NOBUAKI , SOEJIMA MOTOHIRO , SESHIMO HIDENORI , TERAUCHI TARO , DOKO TAKASHI , KOHMURA NAOHIRO
IPC分类号: A61P21/00 , A61P25/00 , A61P25/08 , A61P25/14 , A61P25/16 , A61P25/28 , A61P29/00 , A61P37/00 , A61P43/00 , C07D231/56 , A61K31/416 , C07D401/04 , C07D401/06 , C07D401/12 , C07D401/14 , C07D403/04 , C07D403/12 , C07D405/04 , C07D405/12 , C07D405/14 , C07D409/04
CPC分类号: C07D231/56
摘要: A novel 1H-indazole compound having excellent JNK inhibitory activity. It is a compound represented by the following general formula (I), a salt thereof, or a hydrate of either: (I) wherein R means C6-14 aromatic cyclic hydrocarbon group; R , R , and R each independently means hydrogen, halogeno, cyano, etc.; L means a single bond, C1-6 alkylene, etc.; X means a single bond, a group represented by -CO-NH- or -NH-CO-, etc.; and Y means C3-8 cycloalkyl, a C6-14 aromatic cyclic hydrocarbon group, a 5- to 14-membered aromatic heterocyclic group, etc.
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