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公开(公告)号:US5807867A
公开(公告)日:1998-09-15
申请号:US211120
申请日:1994-05-23
申请人: Fumitaka Ito , Hiroshi Kondo , Masami Nakane , Kaoru Shimada , John Adams Lowe, III , Terry Jay Rosen
发明人: Fumitaka Ito , Hiroshi Kondo , Masami Nakane , Kaoru Shimada , John Adams Lowe, III , Terry Jay Rosen
IPC分类号: C07D453/02 , A01N43/90 , A61K20060101 , A61K31/395 , A61K31/435 , A61K31/439 , A61K31/44 , A61K31/445 , A61P1/00 , A61P1/16 , A61P11/00 , A61P25/00 , A61P25/04 , A61P25/20 , A61P25/24 , A61P29/00 , A61P43/00 , C07D20060101 , C07D453/00 , C07D453/04 , C07D471/10
CPC分类号: C07D453/02
摘要: Compounds of the formula ##STR1## wherein R.sup.1 is methoxy and R.sup.2 is selected from the group consisting of methyl, ethyl, isopropyl, sec-butyl and tert-butyl; and the pharmaceutically acceptable salts of such compounds. These compounds are substance P antagonists and useful in the treatment of gastrointestinal disorders, inflammatory disorders, central nervous system disorders and pain.
摘要翻译: PCT No.PCT / US92 / 03317。 371日期1994年5月23日 102(e)日期1994年5月23日PCT提交1992年4月28日PCT公布。 出版物WO92 / 21677 日期:1992年12月10日化学式为其中R 1为甲氧基且R 2选自甲基,乙基,异丙基,仲丁基和叔丁基的式 和这些化合物的药学上可接受的盐。 这些化合物是物质P拮抗剂,可用于治疗胃肠道疾病,炎性疾病,中枢神经系统疾病和疼痛。
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公开(公告)号:US5939433A
公开(公告)日:1999-08-17
申请号:US846909
申请日:1997-04-30
申请人: Fumitaka Ito , Hiroshi Kondo , Masami Nakane , Kaoru Shimada , John Adams Lowe, III , Terry Jay Rosen
发明人: Fumitaka Ito , Hiroshi Kondo , Masami Nakane , Kaoru Shimada , John Adams Lowe, III , Terry Jay Rosen
IPC分类号: C07D453/02 , A01N43/90 , A61K20060101 , A61K31/395 , A61K31/435 , A61K31/439 , A61K31/44 , A61K31/445 , A61P1/00 , A61P1/16 , A61P11/00 , A61P25/00 , A61P25/04 , A61P25/20 , A61P25/24 , A61P29/00 , A61P43/00 , C07D20060101 , C07D453/00 , C07D453/04 , C07D471/10
CPC分类号: C07D453/02
摘要: Compounds of the formula ##STR1## wherein R.sup.1 is methoxy and R.sup.2 is selected from the group consisting of methyl, ethyl, isopropyl, sec-butyl and tert-butyl; and the pharmaceutically acceptable salts of such compounds.These compounds are substance P antagonists and useful in the treatment of gastrointestinal disorders, inflammatory disorders, central nervous system disorders and pain.
摘要翻译: 下式的化合物其中R1是甲氧基,R2选自甲基,乙基,异丙基,仲丁基和叔丁基; 和这些化合物的药学上可接受的盐。 这些化合物是物质P拮抗剂,可用于治疗胃肠道疾病,炎性疾病,中枢神经系统疾病和疼痛。
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公开(公告)号:US06222038B1
公开(公告)日:2001-04-24
申请号:US08377552
申请日:1995-01-24
申请人: Fumitaka Ito , Hiroshi Kondo , Masami Nakane , John Adams Lowe, III , Terry Jay Rosen , Kaoru Shimada
发明人: Fumitaka Ito , Hiroshi Kondo , Masami Nakane , John Adams Lowe, III , Terry Jay Rosen , Kaoru Shimada
IPC分类号: C07D45302
CPC分类号: C07D453/02
摘要: Compounds of the formula wherein R1 is methoxy and R2 is selected from the group consisting of methyl, ethyl, isopropyl, sec-butyl and tert-butyl; and the pharmaceutically acceptable salts of such compounds. These compounds are substance P antagonists and useful in the treatment of gastrointestinal disorders, inflammatory disorders, central nervous system disorders and pain.
摘要翻译: 甲酰基赖氨酸R1的化合物是甲氧基,R2选自甲基,乙基,异丙基,仲丁基和叔丁基; 和这些化合物的药学上可接受的盐。这些化合物是物质P拮抗剂,可用于治疗胃肠疾病,炎性疾病,中枢神经系统疾病和疼痛。
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4.
公开(公告)号:US5744480A
公开(公告)日:1998-04-28
申请号:US443418
申请日:1995-05-22
IPC分类号: A61K31/445 , A61K31/435 , A61K31/439 , A61K31/451 , A61K31/47 , A61K31/473 , A61K31/55 , A61P25/00 , A61P25/18 , A61P25/20 , A61P25/24 , A61P25/26 , A61P29/00 , A61P37/08 , C07C45/44 , C07C45/51 , C07C45/67 , C07C45/71 , C07C47/55 , C07C47/575 , C07D207/14 , C07D209/52 , C07D211/56 , C07D211/76 , C07D215/42 , C07D221/04 , C07D453/00 , C07D453/02 , C07D471/08 , C07D471/18 , C07D487/08 , C07D498/18 , C07D513/18 , A61K31/44
CPC分类号: C07D453/02 , C07C45/44 , C07C45/513 , C07C45/673 , C07C45/71 , C07C47/575 , C07D211/56
摘要: The present invention relates to novel fluoroalkoxybenzylamino derivatives of nitrogen containing heterocyclic compounds, and specifically, to compounds of the formula ##STR1## wherein Q, X.sup.1, X.sup.2 and X.sup.3 are as defined below. These novel compounds are useful in the treatment of inflammatory and central nervous system disorders, as well as other disorders.
摘要翻译: 本发明涉及含氮杂环化合物的新的氟代烷氧基苄基氨基衍生物,具体地说,涉及式I,其中Q,X 1,X 2和X 3如下所定义的化合物。 这些新型化合物可用于治疗炎性和中枢神经系统疾病以及其它疾病。
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5.
公开(公告)号:US5773450A
公开(公告)日:1998-06-30
申请号:US167881
申请日:1993-12-14
IPC分类号: A61K31/445 , A61K31/435 , A61K31/439 , A61K31/451 , A61K31/47 , A61K31/473 , A61K31/55 , A61P25/00 , A61P25/18 , A61P25/20 , A61P25/24 , A61P25/26 , A61P29/00 , A61P37/08 , C07C45/44 , C07C45/51 , C07C45/67 , C07C45/71 , C07C47/55 , C07C47/575 , C07D207/14 , C07D209/52 , C07D211/56 , C07D211/76 , C07D215/42 , C07D221/04 , C07D453/00 , C07D453/02 , C07D471/08 , C07D471/18 , C07D487/08 , C07D498/18 , C07D513/18
CPC分类号: C07D453/02 , C07C45/44 , C07C45/513 , C07C45/673 , C07C45/71 , C07C47/575 , C07D211/56
摘要: The present invention relates to novel fluoroalkoxybenzylamino derivatives of nitrogen containing heterocyclic compounds, and specifically, to compounds of the formula ##STR1## wherein Q, X.sup.1, x.sup.2 and X.sup.3 are as defined below. These novel compounds are useful in the treatment of inflammatory and central nervous system disorders, as well as other disorders.
摘要翻译: PCT No.PCT / US92 / 03571 Sec。 371日期1993年12月14日第 102(e)日期1993年12月14日PCT提交1992年5月5日PCT公布。 出版物WO92 / 06079 日期:1992年04月16日本发明涉及含氮杂环化合物的新的氟代烷氧基苄基氨基衍生物,具体地说,涉及下式的化合物,其中Q,X1,X2和X3定义如下。 这些新型化合物可用于治疗炎性和中枢神经系统疾病以及其它疾病。
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6.
公开(公告)号:US06362195B1
公开(公告)日:2002-03-26
申请号:US09381887
申请日:2000-03-28
申请人: John Adams Lowe, III
发明人: John Adams Lowe, III
IPC分类号: C07D40110
CPC分类号: C07D213/73 , C07D401/10
摘要: The present invention relates to 6-phenyl-pyridin-2-ylamine derivatives of the formula wherein R1, R2, R3 and R4 are defined as in the specification, that exhibit activity as nitric oxide synthase (NOS) inhibitors, to pharmaceutical compositions containing them and to their use in the treatment and prevention of central nervous system and other disorders.
摘要翻译: 本发明涉及式I的化合物,其中R 1,R 2,R 3和R 4的6-苯基 - 吡啶-2-基胺衍生物如说明书中所定义,其表现出作为一氧化氮合酶(NOS)抑制剂的活性,含有它们的药物组合物, 用于治疗和预防中枢神经系统等疾病。
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公开(公告)号:US5854256A
公开(公告)日:1998-12-29
申请号:US821500
申请日:1997-03-21
申请人: John Adams Lowe, III
发明人: John Adams Lowe, III
IPC分类号: A61K31/435 , A61K31/495 , A61K31/535 , A61K31/54 , A61P1/00 , A61P25/00 , A61P25/04 , A61P29/00 , C07B59/00 , C07D453/00 , C07D453/02 , C07D471/08 , C07D471/18 , C07D491/18 , C07D495/18 , C07D498/18 , C07D513/18 , A61K31/44 , C07D221/06 , C07D221/22
CPC分类号: C07D471/08 , C07B59/00 , C07D453/02
摘要: Quinuclidine derivatives of the formula ##STR1## and the pharmaceutically acceptable salts thereof, wherein m, P, Z, Y, R.sup.1, R.sup.2 and R.sup.3 are as defined below. The compounds are substance P antagonists and, therefore, are useful in treating gastrointestinal disorders, central nervous system disorders, inflammatory diseases, pain and migraine.
摘要翻译: 式III的奎宁环衍生物及其药学上可接受的盐,其中m,P,Z,Y,R 1,R 2和R 3如下所定义。 这些化合物是物质P拮抗剂,因此可用于治疗胃肠疾病,中枢神经系统疾病,炎性疾病,疼痛和偏头痛。
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公开(公告)号:US5698568A
公开(公告)日:1997-12-16
申请号:US403967
申请日:1995-03-14
申请人: John Adams Lowe, III
发明人: John Adams Lowe, III
IPC分类号: A61K31/435 , A61K31/495 , A61K31/535 , A61K31/54 , A61P1/00 , A61P25/00 , A61P25/04 , A61P29/00 , C07B59/00 , C07D453/00 , C07D453/02 , C07D471/08 , C07D471/18 , C07D491/18 , C07D495/18 , C07D498/18 , C07D513/18 , A61K31/44 , C07D487/08 , C07D491/08 , C07D495/08
CPC分类号: C07D471/08 , C07B59/00 , C07D453/02
摘要: Quinuclidine derivatives of the formula ##STR1## and the pharmaceutically acceptable salts thereof, wherein m, P, Z, Y, R.sup.1, R.sup.2 and R.sup.3 are as defined below. The compounds are substance P antagonists and, therefore, are useful in treating gastrointestinal disorders, central nervous system disorders, inflammatory diseases, pain and migraine.
摘要翻译: 其中m,P,Z,Y,R 1,R 2和R 3如下所定义,具有下式的喹啉衍生物或其药学上可接受的盐。 这些化合物是物质P拮抗剂,因此可用于治疗胃肠疾病,中枢神经系统疾病,炎性疾病,疼痛和偏头痛。
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公开(公告)号:US07012078B2
公开(公告)日:2006-03-14
申请号:US10313446
申请日:2002-12-06
申请人: John Adams Lowe, III
发明人: John Adams Lowe, III
IPC分类号: C07D471/10 , C07D401/10 , C07D401/14 , A61K31/438 , A61K31/4427
CPC分类号: C07D213/73 , C07D401/10 , C07D401/12 , C07D401/14 , C07D405/12 , C07D405/14 , C07D451/06 , C07D453/02 , C07D471/04 , C07D491/04
摘要: The present invention relates to 2-aminopyridine derivatives of the formula wherein G, R1 and R2 are defined as in the specification, that exhibit activity as nitric oxide synthase (NOS) inhibitors, to pharmaceutical compositions containing them and to their use in the treatment and prevention of central nervous system and other disorders.
摘要翻译: 本发明涉及下式的2-氨基吡啶衍生物,其中G,R 1和R 2 2如本说明书所定义,表现出作为一氧化氮合酶(NOS) )抑制剂,含有它们的药物组合物及其在治疗和预防中枢神经系统和其他疾病中的用途。
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公开(公告)号:US08883812B2
公开(公告)日:2014-11-11
申请号:US13808355
申请日:2011-06-20
申请人: Michelle Marie Claffey , Jennifer Elizabeth Davoren , John Adams Lowe, III , Robert Joseph Mather
发明人: Michelle Marie Claffey , Jennifer Elizabeth Davoren , John Adams Lowe, III , Robert Joseph Mather
IPC分类号: C07D401/04 , A61K31/4523 , A61K31/506 , A61K45/06
CPC分类号: A61K31/506 , A61K31/4523 , A61K45/06 , C07D401/04
摘要: The present invention relates to compounds of Formula (I) as described herein or a pharmaceutically acceptable salt thereof, pharmaceutical composition comprising a compound of Formula (I) or a pharmaceutically acceptable salt thereof and methods of treating, or manufacture of a medicament to treat, a disease, disorder, or condition of the central nervous system, including bipolar disorder, depressive disorders, anxiety disorders, cognitive disorders, pain disorders, urogentital disorder, and epilepsy, among the other diseases, disorders or conditions discussed herein as mono-therapy or in combination with another active pharmaceutical ingredient.
摘要翻译: 本发明涉及本文所述的式(I)化合物或其药学上可接受的盐,包含式(I)化合物或其药学上可接受的盐的药物组合物和治疗或制造药物的方法, 其中包括双相情感障碍,抑郁障碍,焦虑障碍,认知障碍,疼痛障碍,泌尿功能障碍和癫痫在内的其他疾病,疾病或病症中的疾病,病症或状况, 与另一种活性药物成分组合。
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