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1.HYDROXAMATE DERIVATIVES FOR HDAC INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THEREOF 审中-公开
标题翻译: HYDROXAMATDERIVATE FOR HDAC抑制剂和药物组合物,以公开(公告)号:EP2771321A4
公开(公告)日:2015-04-08
申请号:EP12843187
申请日:2012-10-26
发明人: KIM YUNTAE , LEE CHANGSIK , YANG HYUN-MO , CHOI HOJIN , MIN JAEKI , KIM SOYOUNG , KIM DAL-HYUN , HA NINA , KIM JUNG-MIN , LIM HYOJIN , KO EUNHEE
IPC分类号: C07D209/08 , A61K31/403 , A61P19/02 , A61P25/00 , A61P29/00 , C07D209/86 , C07D209/88 , C07D231/56 , C07D401/04 , C07D403/04 , C07D403/06 , C07D405/12 , C07D471/04 , C07D487/04
CPC分类号: C07D209/08 , C07D209/86 , C07D209/88 , C07D231/56 , C07D401/04 , C07D403/04 , C07D403/06 , C07D405/12 , C07D471/04 , C07D487/04
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2.
公开(公告)号:EP2066632A4
公开(公告)日:2011-04-27
申请号:EP07808403
申请日:2007-09-21
发明人: CHOI NAM-SONG , KIM YOUNG-MI , KIM YOUNG-HOON , LEE JAE-KWANG , LIM IN-TAEK , CHOI HO-JIN , YANG HYUN-MO , KONG SUN-JU , MOON SEUNG-KEE , KIM SOO-JIN , YU HYUN-JUNG , SHIN JAE-SU , KWON YOUNG-MIN , LEE SUNG-SOOK , AHN SOON-KIL
IPC分类号: C07D213/69 , A61K31/12 , A61P35/00 , C07C49/786 , C07D233/02 , C07D239/00 , C07D249/08 , C07D263/02 , C07D277/02 , C07D307/02
CPC分类号: C07D207/333 , C07C49/84 , C07D207/335 , C07D213/50 , C07D213/64 , C07D231/12 , C07D233/54 , C07D233/64 , C07D239/26 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/40 , C07D307/46 , C07D307/52 , C07D333/20 , C07D333/22 , C07D401/10 , C07D403/10 , C07D405/10 , C07D405/12 , C07D407/10 , C07D409/10 , C07D413/10 , C07D417/04 , C07D417/10
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3.NOVEL COMPOUNDS FOR SELECTIVE HISTONE DEACETYLASE INHIBITORS, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME 审中-公开
标题翻译: 新化合物选择性蛋白去乙酰化酶和药物成分,以便公开(公告)号:EP2991982A4
公开(公告)日:2016-09-14
申请号:EP14792173
申请日:2014-04-29
发明人: LEE CHANGSIK , YANG HYUN-MO , CHOI HOJIN , KIM DOHOON , KIM SOYOUNG , HA NINA , LIM HYOJIN , KO EUNHEE , YOON SEONGAE , BAE DAEKWON
IPC分类号: C07D413/12 , A61K31/5377 , A61P29/00 , A61P35/00
CPC分类号: C07D231/56 , C07D207/08 , C07D207/10 , C07D209/08 , C07D209/14 , C07D211/26 , C07D211/46 , C07D211/52 , C07D213/40 , C07D213/74 , C07D213/75 , C07D215/12 , C07D239/26 , C07D239/42 , C07D265/30 , C07D295/215 , C07D309/08 , C07D309/10 , C07D317/58 , C07D319/18 , C07D401/12 , C07D403/12 , C07D405/12 , C07D407/12 , C07D413/12 , C07D417/12
摘要: The present invention relates to novel urea derivatives and, more particularly, to novel urea derivatives with histone deacetylase (HDAC) inhibitory activity, isomers thereof, pharmaceutically acceptable salts thereof, their use for the preparation of a medicaments comprising the same, a pharmaceutical composition comprising the same, a treatment method using the composition, and a method for preparing novel urea derivatives. The novel urea derivatives as selective histone deacetylase (HDAC) inhibitors are effective for the treatment of histone deacetylase-mediated diseases such as malignant tumors, inflammatory diseases, rheumatoid arthritis, neurodegeneration, etc.
摘要翻译: 本发明涉及新颖的脲衍生物,并且更具体地涉及具有组蛋白脱乙酰酶(HDAC)抑制活性的,它们的异构体,其药学上可接受的盐,它们的用于药物的包含其的制备使用新颖的脲衍生物,药物组合物,其包括 同样,使用该组合物的处理方法,以及用于制备新颖的脲衍生物的方法。 新颖的脲衍生物作为选择性组蛋白脱乙酰酶(HDAC)抑制剂是有效的组蛋白脱乙酰介导的疾病的治疗:如恶性肿瘤,炎症性疾病,类风湿性关节炎,神经变性,等
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