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公开(公告)号:US08716309B2
公开(公告)日:2014-05-06
申请号:US13980819
申请日:2012-01-30
申请人: Cheol Young Maeng , Young Koo Jang , Su Bong Cha , Hye Won Shin , Chan Mi Joung , Hwa Ryun Cha , Eun Jung Yi
发明人: Cheol Young Maeng , Young Koo Jang , Su Bong Cha , Hye Won Shin , Chan Mi Joung , Hwa Ryun Cha , Eun Jung Yi
IPC分类号: A01N43/90 , A61K31/44 , C07D453/02
CPC分类号: C07D453/02
摘要: A pyridone derivative compound and a pharmaceutically acceptable salt, isomer, solvate or hydrate thereof, and a preventive or therapeutic pharmaceutical composition for cognitive disorders that includes the pyridone derivative compound or a pharmaceutically acceptable salt, isomer, solvate or hydrate thereof.
摘要翻译: 吡啶酮衍生物化合物及其药学上可接受的盐,异构体,溶剂合物或水合物,以及包括吡啶酮衍生化合物或其药学上可接受的盐,异构体,溶剂化物或水合物的认知障碍的预防或治疗药物组合物。
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公开(公告)号:US20130317059A1
公开(公告)日:2013-11-28
申请号:US13980819
申请日:2012-01-30
申请人: Cheol Young Maeng , Young Koo Jang , Su Bong Cha , Hye Won Shin , Chan Mi Joung , Hwa Ryun Cha , Eun Jung Yi
发明人: Cheol Young Maeng , Young Koo Jang , Su Bong Cha , Hye Won Shin , Chan Mi Joung , Hwa Ryun Cha , Eun Jung Yi
IPC分类号: C07D453/02
CPC分类号: C07D453/02
摘要: A pyridone derivative compound and a pharmaceutically acceptable salt, isomer, solvate or hydrate thereof, and a preventive or therapeutic pharmaceutical composition for cognitive disorders that includes the pyridone derivative compound or a pharmaceutically acceptable salt, isomer, solvate or hydrate thereof.
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公开(公告)号:US08952165B2
公开(公告)日:2015-02-10
申请号:US13980821
申请日:2012-01-30
申请人: Cheol Young Maeng , Young Koo Jang , Su Bong Cha , Hye Won Shin , Chan Mi Joung , Eun Jung Yi
发明人: Cheol Young Maeng , Young Koo Jang , Su Bong Cha , Hye Won Shin , Chan Mi Joung , Eun Jung Yi
IPC分类号: C07D453/02 , C07D417/14 , C07D471/08 , A61K31/4748
CPC分类号: A61K31/439 , A61K9/0053 , A61K31/4709 , A61K31/4725 , A61K31/497 , C07D453/02
摘要: A pyridone derivative compound and a pharmaceutically acceptable salt, isomer, solvate or hydrate thereof, and a preventive or therapeutic pharmaceutical composition for cognitive disorders that includes the pyridone derivative compound or a pharmaceutically acceptable salt, isomer, solvate or hydrate thereof.
摘要翻译: 吡啶酮衍生物化合物及其药学上可接受的盐,异构体,溶剂合物或水合物,以及包括吡啶酮衍生化合物或其药学上可接受的盐,异构体,溶剂化物或水合物的认知障碍的预防或治疗药物组合物。
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公开(公告)号:US08039634B2
公开(公告)日:2011-10-18
申请号:US11795303
申请日:2006-01-13
申请人: Jeong-woo Cho , Sang-chul Lim , Cheol-young Maeng , Sun-gwan Hwang , Sung-jin Bae , Eun-ae Kim
发明人: Jeong-woo Cho , Sang-chul Lim , Cheol-young Maeng , Sun-gwan Hwang , Sung-jin Bae , Eun-ae Kim
IPC分类号: C07D213/16 , C07D263/32
CPC分类号: C07D263/32 , C07D413/04
摘要: Provided are an oxazole hydroxamic acid derivatives and pharmaceutically useful salt thereof as a histone deacetylase inhibitor. The oxazole hydroxamic acid derivative and pharmaceutically useful salt thereof, prepared in accordance with the present invention, can treat and/or prevent various cancers and inflammatory diseases caused by histone deacetylase.
摘要翻译: 提供了恶唑异羟肟酸衍生物及其药学上有用的盐作为组蛋白脱乙酰酶抑制剂。 根据本发明制备的恶唑异羟肟酸衍生物及其药用盐可以治疗和/或预防由组蛋白脱乙酰酶引起的各种癌症和炎性疾病。
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公开(公告)号:US20090209596A1
公开(公告)日:2009-08-20
申请号:US11795303
申请日:2006-01-13
申请人: Jeong-woo Cho , Sang-chul Lim , Cheol-young Maeng , Sun-gwan Hwang , Sung-jin Bae , Eun-ae Kim
发明人: Jeong-woo Cho , Sang-chul Lim , Cheol-young Maeng , Sun-gwan Hwang , Sung-jin Bae , Eun-ae Kim
IPC分类号: A61K31/421 , C07D263/32 , C07D413/04 , A61K31/4439 , A61P35/00 , A61P29/00
CPC分类号: C07D263/32 , C07D413/04
摘要: Provided are an oxazole hydroxamic acid derivative and a pharmaceutically useful salt thereof as a histone deacetylase inhibitor The oxazole hydroxamic acid derivative and pharmaceutically useful salt thereof, prepared in accordance with the present invention, can treat and/or prevent various cancers and inflammatory diseases caused by histone deacetylase.
摘要翻译: 提供了作为组蛋白脱乙酰酶抑制剂的恶唑异羟肟酸衍生物及其药学上可用的盐。根据本发明制备的恶唑异羟肟酸衍生物及其药学上可用的盐可以治疗和/或预防各种癌症和由 组蛋白脱乙酰酶。
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公开(公告)号:US20130296340A1
公开(公告)日:2013-11-07
申请号:US13980821
申请日:2012-01-30
申请人: Cheol Young Maeng , Young Koo Jang , Su Bong Cha , Hye Won Shin , Chan Mi Joung , Eun Jung Yi
发明人: Cheol Young Maeng , Young Koo Jang , Su Bong Cha , Hye Won Shin , Chan Mi Joung , Eun Jung Yi
IPC分类号: C07D453/02
CPC分类号: A61K31/439 , A61K9/0053 , A61K31/4709 , A61K31/4725 , A61K31/497 , C07D453/02
摘要: A pyridone derivative compound and a pharmaceutically acceptable salt, isomer, solvate or hydrate thereof, and a preventive or therapeutic pharmaceutical composition for cognitive disorders that includes the pyridone derivative compound or a pharmaceutically acceptable salt, isomer, solvate or hydrate thereof.
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公开(公告)号:US08420353B2
公开(公告)日:2013-04-16
申请号:US10508759
申请日:2003-03-22
申请人: Hyo Jeong Hong , Cheol-Young Maeng , Gi-Hyeok Yang , Meong Hee Jang , Mee Sook Oh , Jin-Soo Song , Young Kug Jang
发明人: Hyo Jeong Hong , Cheol-Young Maeng , Gi-Hyeok Yang , Meong Hee Jang , Mee Sook Oh , Jin-Soo Song , Young Kug Jang
IPC分类号: A61K39/395 , C07K16/00
CPC分类号: C07K16/464 , A61K2039/505 , C07K16/082 , C07K16/461 , C07K2317/565 , C07K2317/92
摘要: A humanized antibody is produced by process comprising the steps of: (a) selecting a specificity determining residue (SDR) of the complementarity determining region (CDR) of murine monoclonal antibody heavy chain and light chain variable regions; and (b) grafting said SDR to at least one of the corresponding amino acid sequences in human antibody variable regions.
摘要翻译: 通过包括以下步骤的方法制备人源化抗体:(a)选择鼠单克隆抗体重链和轻链可变区的互补决定区(CDR)的特异性测定残基(SDR); 和(b)将所述SDR移植到人抗体可变区中的至少一个相应的氨基酸序列。
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公开(公告)号:US20090208508A1
公开(公告)日:2009-08-20
申请号:US12094955
申请日:2006-11-24
申请人: Kong Joo Lee , Hyun Jung Kim , Jeong Woo Cho , Cheol Young Maeng , You Kyung Nam , Sang Mi Lim , Young Mee Kim
发明人: Kong Joo Lee , Hyun Jung Kim , Jeong Woo Cho , Cheol Young Maeng , You Kyung Nam , Sang Mi Lim , Young Mee Kim
IPC分类号: A61K39/395 , A61K31/7105 , C12Q1/68
CPC分类号: A61K31/70 , C07K14/4703 , C12N15/1137 , C12N2310/14 , C12N2310/53 , C12Q1/6886 , C12Q2600/136
摘要: The present invention relates to a composition for diagnosing cancer metastasis comprising Ubiquitin C-terminal hydrolase-L1 (UCH-L1), a use of UCH-L1 for diagnosing cancer metastasis and a method for diagnosing cancer metastasis using the same; a composition for suppressing cancer metastasis comprising an inhibitor of UCH-L1, a use of an inhibitor of UCH-L1 for suppressing cancer metastasis and a method of suppressing cancer metastasis using the same; a composition for screening a cancer metastasis inhibitor comprising UCH-L1 protein, a use of UCH-L1 protein for screening a cancer metastasis inhibitor and a method of screening cancer metastasis inhibitor using the same; a composition for screening a cancer metastasis inhibitor comprising UCH-L1 gene, a use of UCH-L1 gene for screening a cancer metastasis inhibitor, a method of screening cancer metastasis inhibitor using the same.UCH-L1 is a key molecule to modulate cell migration including the cancer invasion according to their expressing level. Thus, the monoclonal and polyclonal antibodies and the substrate of UCH-L1 can be used for diagnosis of cancer metastasis.Also, the cancer metastasis can be suppressed by inhibiting of the expression of UCH-L1 or activity of the enzyme, thus we can screen and develop an inhibitor of UCH-L1 and use it as an adjuvant drug for anticancer therapy.
摘要翻译: 本发明涉及用于诊断癌转移的组合物,其包含泛素C末端水解酶-L1(UCH-L1),UCH-L1用于诊断癌症转移的用途和使用该组合物诊断癌症转移的方法。 用于抑制癌转移的组合物,其包含UCH-L1抑制剂,UCH-L1抑制剂用于抑制癌症转移的用途及使用其抑制癌转移的方法; 用于筛选包含UCH-L1蛋白的癌症转移抑制剂的组合物,UCH-L1蛋白用于筛选癌症转移抑制剂的方法和使用该组合物筛选癌症转移抑制剂的方法; 用于筛选包含UCH-L1基因的癌转移抑制剂的组合物,使用UCH-L1基因筛选癌症转移抑制剂,使用该组合物筛选癌症转移抑制剂的方法。 UCH-L1是根据其表达水平调节细胞迁移的关键分子,包括癌症侵袭。 因此,单克隆抗体和多克隆抗体以及UCH-L1的底物可用于癌症转移的诊断。 此外,可以通过抑制UCH-L1的表达或酶的活性来抑制癌症转移,从而可以筛选和开发UCH-L1的抑制剂,并将其用作抗癌治疗的辅助药物。
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