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公开(公告)号:US20060217414A1
公开(公告)日:2006-09-28
申请号:US11259765
申请日:2005-10-27
申请人: David Sawutz , Philippe Brianceau , Ana Bercovici , Ginny Ho , Deen Tulshian
发明人: David Sawutz , Philippe Brianceau , Ana Bercovici , Ginny Ho , Deen Tulshian
IPC分类号: C07D453/02 , A61K31/46
CPC分类号: C07D451/02
摘要: The compound of the formula or a pharmaceutically acceptable salt or solvate thereof, pharmaceutical compositions therefore, and the use of said compounds as nociceptin receptor inhibitors useful in the treatment of anxiety are disclosed.
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公开(公告)号:US07485650B2
公开(公告)日:2009-02-03
申请号:US11259765
申请日:2005-10-27
IPC分类号: A61K31/46
CPC分类号: C07D451/02
摘要: The compound of the formula or a pharmaceutically acceptable salt or solvate thereof, pharmaceutical compositions therefore, and the use of said compounds as nociceptin receptor inhibitors useful in the treatment of anxiety are disclosed.
摘要翻译: 公开了式的化合物或其药学上可接受的盐或溶剂化物,因此药物组合物以及所述化合物作为治疗焦虑症的伤害感受肽受体抑制剂的用途。
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公开(公告)号:US06716846B2
公开(公告)日:2004-04-06
申请号:US10155277
申请日:2002-05-23
申请人: Deen Tulshian , Ginny D. Ho , Lisa S. Silverman , Julius J. Matasi , Robbie L. McLeod , John A. Hey , Richard W. Chapman , Ana Bercovici , Francis M. Cuss
发明人: Deen Tulshian , Ginny D. Ho , Lisa S. Silverman , Julius J. Matasi , Robbie L. McLeod , John A. Hey , Richard W. Chapman , Ana Bercovici , Francis M. Cuss
IPC分类号: C07D40306
CPC分类号: A61K45/06 , A61K31/00 , A61K31/438 , A61K31/439 , A61K31/451 , A61K31/4535 , A61K31/454
摘要: Novel compounds of the formula or a pharmaceutically acceptable salt or solvate thereof, wherein: the dotted line represents an optional double bond; X1 is optionally substituted alkyl, cycloalkyl, aryl, heteroaryl or heterocycloalkyl; X2 is —CHO, —CN, optionally substituted amino, alkyl, or aryl; or X1 is optionally substituted benzofused heterocyclyl and X2 is hydrogen; or X1 and X2 together form an optionally benzofused spiro heterocyclyl group R1, R2, R3 and R4 are independently H and alkyl, or (R1 and R4) or (R2 and R3) or (R1 and R3) or (R2 and R4) together can form an alkylene bridge of 1 to 3 carbon atoms; Z1 is optionally substituted alkyl, aryl, heteroaryl, cycloalkyl or heterocycloalkyl, or —CO2(alkyl or substituted amino) or CN; Z2 is H or Z1; Z3 is H oralkyl; or Z1, Z2 and Z3, together with the carbon to which they are attached, form bicyclic saturated or unsaturated rings; pharmaceutical compositions therefore, and the use of said compounds as nociceptin receptor inhibitors useful in the treatment of pain, anxiety, cough, asthma, depression and alcohol abuse are disclosed.
摘要翻译: 式的新型化合物或其药学上可接受的盐或溶剂合物,其中:虚线表示任选的双键; X 1为任选取代的烷基,环烷基,芳基,杂芳基或杂环烷基; X 2为-CHO, - CN,任选取代的氨基,烷基或芳基;或X 1是任选取代的苯并稠合的杂环基,X 2是氢;或X 1和X 2一起形成任选的苯并稠合的螺杂环基R 1, R 2,R 3和R 4独立地为H和烷基,或(R 1和R 4)或(R 2和R 3)或(R 1) >和R 3)或(R 2和R 4)可以一起形成1至3个碳原子的亚烷基桥; Z 1是任选取代的烷基,芳基,杂芳基,环烷基或杂环烷基,或 -CO 2(烷基或取代的氨基)或CN; Z 2是H或Z 1; Z 3是H或烷基; 或Z 1,Z 2和Z 3与它们所连接的碳一起形成双环饱和或不饱和环; 因此,公开了用于治疗疼痛,焦虑,咳嗽,哮喘,抑郁和酒精滥用的所述化合物作为伤害感受肽受体抑制剂的用途。
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公开(公告)号:US07094784B2
公开(公告)日:2006-08-22
申请号:US10761977
申请日:2004-01-21
申请人: Deen Tulshian , Ginny D. Ho , Lisa S. Silverman , Julius J. Matasi , Robbie L. McLeod , John A. Hey , Richard W. Chapman , Ana Bercovici , Francis M. Cuss
发明人: Deen Tulshian , Ginny D. Ho , Lisa S. Silverman , Julius J. Matasi , Robbie L. McLeod , John A. Hey , Richard W. Chapman , Ana Bercovici , Francis M. Cuss
IPC分类号: C07D401/04 , A61K31/46
CPC分类号: A61K45/06 , A61K31/00 , A61K31/438 , A61K31/439 , A61K31/451 , A61K31/4535 , A61K31/454
摘要: Novel compounds of the formula or a pharmaceutically acceptable salt or solvate thereof, wherein: the dotted line represents an optional double bond; X1 is optionally substituted alkyl, cycloalkyl, aryl, heteroaryl or heterocycloalkyl; X2 is —CHO, —CN, optionally substituted amino, alkyl, or aryl; or X1 is optionally substituted benzofused heterocyclyl and X2 is hydrogen; or X1 and X2 together form an optionally benzofused spiro heterocyclyl group R1, R2, R3 and R4 are independently H and alkyl, or (R1 and R4) or (R2 and R3) or (R1 and R3) or (R2 and R4) together can form an alkylene bridge of 1 to 3 carbon atoms; Z1 is optionally substituted alkyl, aryl, heteroaryl, cycloalkyl or heterocycloalkyl, or —CO2(alkyl or substituted amino) or CN ; Z2 is H or Z1; Z3 is H oralkyl; or Z1, Z2 and Z3, together with the carbon to which they are attached, form bicyclic saturated or unsaturated rings; pharmaceutical compositions therefore, and the use of said compounds as nociceptin receptor inhibitors useful in the treatment of pain, anxiety, cough, asthma, depression and alcohol abuse are disclosed.
摘要翻译: 新型式的化合物或其药学上可接受的盐或溶剂合物,其中:虚线表示任选的双键; X 1是任选取代的烷基,环烷基,芳基,杂芳基或杂环烷基; X 2是-CHO,-CN,任选取代的氨基,烷基或芳基; 或X 1是任选取代的苯并稠合的杂环基,X 2是氢; 或X 1和X 2一起形成任选的苯并稠合的螺杂环基R 1,R 2,R 2, 或者R 4和R 4独立地是H和烷基,或者(R 1和R 4)和(R 0) 或者R 2和R 3)或(R 1和R 3)或(R 2) 和R 4)可以形成1至3个碳原子的亚烷基桥; Z 1是任选取代的烷基,芳基,杂芳基,环烷基或杂环烷基或-CO 2(烷基或取代的氨基)或CN; Z 2是H或Z 1; Z 3是H或烷基; 或Z 1,Z 2和Z 3与它们所连接的碳一起形成双环饱和或不饱和环; 因此,公开了用于治疗疼痛,焦虑,咳嗽,哮喘,抑郁和酒精滥用的所述化合物作为伤害感受肽受体抑制剂的用途。
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公开(公告)号:US06455527B2
公开(公告)日:2002-09-24
申请号:US09769824
申请日:2001-01-25
申请人: Deen Tulshian , Ginny D. Ho , Lisa S. Silverman , Julius J. Matasi , Robbie L. McLeod , John A. Hey , Richard W. Chapman , Ana Bercovici , Francis M. Cuss
发明人: Deen Tulshian , Ginny D. Ho , Lisa S. Silverman , Julius J. Matasi , Robbie L. McLeod , John A. Hey , Richard W. Chapman , Ana Bercovici , Francis M. Cuss
IPC分类号: A61K31445
CPC分类号: A61K45/06 , A61K31/00 , A61K31/438 , A61K31/439 , A61K31/451 , A61K31/4535 , A61K31/454
摘要: Novel compounds of the formula or a pharmaceutically acceptable salt or solvate thereof, wherein: the dotted line represents an optional double bond; X1 is optionally substituted alkyl, cycloalkyl, aryl, heteroaryl or heterocycloalkyl; X2 is —CHO, —CN, optionally substituted amino, alkyl, or aryl; or X1 is optionally substituted benzofused heterocyclyl and X2 is hydrogen; or X1 and X2 together form an optionally benzofused spiro heterocyclyl group R1, R2, R3 and R4 are independently H and alkyl, or (R1 and R4) or (R2 and R3) or (R1 and R3) or (R2 and R4) together can form an alkylene bridge of 1 to 3 carbon atoms; Z1 is optionally substituted alkyl, aryl, heteroaryl, cycloalkyl or heterocycloalkyl, or —CO2(alkyl or substituted amino) or CN ; Z2 is H or Z1; Z3 is H oralkyl; or Z1, Z2 and Z3, together with the carbon to which they are attached, form bicyclic saturated or unsaturated rings; pharmaceutical compositions therefore, and the use of said compounds as nociceptin receptor inhibitors useful in the treatment of pain, anxiety, cough, asthma, depression and alcohol abuse are disclosed.
摘要翻译: 式的新型化合物或其药学上可接受的盐或溶剂化物,其中:虚线表示任选的双键; X 1为任选取代的烷基,环烷基,芳基,杂芳基或杂环烷基; X 2为-CHO,-CN,任选取代的氨基, 烷基或芳基;或X 1是任选取代的苯并稠合的杂环基,并且X 2是氢;或者X 1和X 2一起形成任选的苯并稠合的螺杂环基R1,R2,R3和R4独立地是H和烷基,或(R1和R4)或 和(R 3和R 3)或(R 1和R 3)或(R 2和R 4)在一起可以形成1至3个碳原子的亚烷基桥; Z 1是任选取代的烷基,芳基,杂芳基,环烷基或杂环烷基,或-CO 2(烷基或取代的氨基 )或CN; Z2是H或Z1; Z 3是H或烷基; 或Z 1,Z 2和Z 3与它们所连接的碳一起形成双环饱和或不饱和环;因此,药物组合物以及所述化合物用作疼痛,焦虑,咳嗽,哮喘的伤害感受肽受体抑制剂的用途 ,公开抑郁症和酗酒。
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公开(公告)号:US06262066B1
公开(公告)日:2001-07-17
申请号:US09359771
申请日:1999-07-26
申请人: Deen Tulshian , Ginny D. Ho , Lisa S. Silverman , Julius J. Matasi , Robbie L. McLeod , John A. Hey , Richard W. Chapman , Ana Bercovici , Francis M. Cuss
发明人: Deen Tulshian , Ginny D. Ho , Lisa S. Silverman , Julius J. Matasi , Robbie L. McLeod , John A. Hey , Richard W. Chapman , Ana Bercovici , Francis M. Cuss
IPC分类号: C07D22122
CPC分类号: A61K45/06 , A61K31/00 , A61K31/438 , A61K31/439 , A61K31/451 , A61K31/4535 , A61K31/454
摘要: Novel compounds of the formula or a pharmaceutically acceptable salt or solvate thereof, wherein: the dotted line represents an optional double bond; X1 is optionally substituted alkyl, cycloalkyl, aryl, heteroaryl or heterocycloalkyl; X2 is —CHO, —CN, optionally substituted amino, alkyl, or aryl; or X1 is optionally substituted benzofused heterocyclyl and X2 is hydrogen; or X1 and X2 together form an optionally benzofused Spiro heterocyclyl group R1, R2, R3 and R4 are independently H and alkyl, or (R1 and R4) or (R2 and R3) or (R1 and R3) or (R2 and R4) together can form an alkylene bridge of 1 to 3 carbon atoms; Z1 is optionally substituted alkyl, aryl, heteroaryl, cycloalkyl or heterocycloalkyl, or —CO2(alkyl or substituted amino) or CN; Z2 is H or Z1; Z3 is H oralkyl; or Z1, Z2 and Z3, together with the carbon to which they are attached, form bicyclic saturated or unsaturated rings; pharmaceutical compositions therefore, and the use of said compounds as nociceptin receptor inhibitors useful in the treatment of pain, anxiety, cough, asthma, depression and alcohol abuse are disclosed.
摘要翻译: 式的新型化合物或其药学上可接受的盐或溶剂化物,其中:虚线表示任选的双键; X 1为任选取代的烷基,环烷基,芳基,杂芳基或杂环烷基; X 2为-CHO,-CN,任选取代的氨基, 烷基或芳基;或X 1为任选取代的苯并稠合的杂环基,且X 2为氢;或X 1和X 2一起形成任选的苯并稠合的螺杂环基R1,R2,R3和R4独立地为H和烷基,或(R1和R4)或 和(R 3和R 3)或(R 1和R 3)或(R 2和R 4)在一起可以形成1至3个碳原子的亚烷基桥; Z 1是任选取代的烷基,芳基,杂芳基,环烷基或杂环烷基,或-CO 2(烷基或取代的氨基 )或CN; Z2是H或Z1; Z 3是H或烷基; 或Z 1,Z 2和Z 3与它们所连接的碳一起形成双环饱和或不饱和环; 因此,公开了用于治疗疼痛,焦虑,咳嗽,哮喘,抑郁和酒精滥用的所述化合物作为伤害感受肽受体抑制剂的用途。
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