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公开(公告)号:US20070225361A1
公开(公告)日:2007-09-27
申请号:US11695268
申请日:2007-04-02
申请人: Derek Demaine , Haydn Jones , Simon MacDonald , Andrew Mason , Stephen Shanahan
发明人: Derek Demaine , Haydn Jones , Simon MacDonald , Andrew Mason , Stephen Shanahan
IPC分类号: A61K31/351
CPC分类号: A61K45/06 , A61K31/13 , A61K31/351 , A61K31/7056 , A61K47/54 , A61K47/55 , C07D309/28 , A61K2300/00
摘要: The invention relates to compounds of general formula (I), in which: R is an amino or guanidino group; R2 is acetyl or trifluoroacetyl; n and q are either the same or different and selected from 0, 1 or 2; and X is an optionally substituted phenyl, optionally substituted naphthyl or optionally substituted phenyl-Y-optionally substituted phenyl in which Y is selected from a covalent bond, CH2, CH2CH2, O or SO2, or a pharmaceutically acceptable derivative thereof, with the proviso that when X is phenyl or naphthyl, n and q are both 2 and when X is phenyl-Y-phenyl in which Y is a covalent bond, then n and q are not both 0, methods for their preparation, pharmaceutical formulations containing them or their use in the prevention or treatment of a viral infection.
摘要翻译: 本发明涉及通式(I)的化合物,其中:R是氨基或胍基; R 2是乙酰基或三氟乙酰基; n和q相同或不同,选自0,1或2; 并且X是任选取代的苯基,任选取代的萘基或任选取代的苯基-Y-任选取代的苯基,其中Y选自共价键,CH 2,CH 2, CH 2,O或SO 2,或其药学上可接受的衍生物,条件是当X是苯基或萘基时,n和q都是2,当X是 苯基-Y-苯基,其中Y是共价键,则n和q都不为0,其制备方法,含有它们的药物制剂或其用于预防或治疗病毒感染。
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公开(公告)号:US20050054718A1
公开(公告)日:2005-03-10
申请号:US10494242
申请日:2002-11-08
IPC分类号: C12Q1/04 , A61K9/12 , A61K31/13 , A61K31/21 , A61K31/351 , A61K31/7056 , A61K45/00 , A61K45/06 , A61K47/48 , A61P31/12 , A61P31/14 , A61P31/16 , C07D309/28 , C07D407/12 , C12Q1/70 , A61K31/35 , C07D49/02
CPC分类号: A61K45/06 , A61K31/13 , A61K31/351 , A61K31/7056 , A61K47/54 , A61K47/55 , C07D309/28 , A61K2300/00
摘要: The invention relates to compounds of general formula (I), in which: R is an amino or guanidino group; R2 is acetyl or trifluoroacetyl; n and q are either the same or different and selected from 0, 1 or 2; and X is an optionally substituted phenyl, optionally substituted naphthyl or optionally substituted phenyl-Y-optionally substituted phenyl in which Y is selected from a covalent bond, CH2, CH2CH2, O or SO2, or a pharmaceutically acceptable derivative thereof, with the proviso that when X is phenyl or naphthyl, n and q are both 2 and when X is phenyl-Y-phenyl in which Y is a covalent bond, then n and q are not both 0, methods for their preparation, pharmaceutical formulations containing them or their use in the prevention or treatment of a viral infection.
摘要翻译: 本发明涉及通式(I)的化合物,其中:R是氨基或胍基; R 2是乙酰基或三氟乙酰基; n和q相同或不同,选自0,1或2; CH 2,CH 2 CH 2,O或SO 2,或其药学上可接受的衍生物,其中Y是任选取代的苯基,任选取代的萘基或任选取代的苯基-Y-任选取代的苯基,其中Y选自共价键, 当X是苯基或萘基时,n和q都是2,当X是其中Y是共价键的苯基-Y-苯基时,n和q都不是0,它们的制备方法,含有它们的药物制剂或它们 用于预防或治疗病毒感染。
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公开(公告)号:US20070225358A1
公开(公告)日:2007-09-27
申请号:US11734394
申请日:2007-04-12
申请人: Betty JIN , Simon MacDonald , Darryl McConnell , Van Nguyen , Stephen Shanahan , Wen-Yang Wu
发明人: Betty JIN , Simon MacDonald , Darryl McConnell , Van Nguyen , Stephen Shanahan , Wen-Yang Wu
IPC分类号: A61K31/35
CPC分类号: A61K31/351 , A61K31/13 , A61K31/7056 , A61K38/00 , A61K45/06 , A61K47/54 , A61K47/55 , C07D309/28 , C07K5/06104 , A61K2300/00
摘要: The invention relates to compounds of general formula (I); in which R is an amino or guanidino group; R2 is acetyl or trifluoroacetyl; X is CONH, NHCO or O; n is an integer from 2 to 6; and Y is C2-C9 alkyl C3-8 cycloalkyl, C1-C4 alkoxyalkyl, an amino acid or dipeptide, or a pharmaceutically acceptable derivative thereof, methods for their preparation, pharmaceutical formulations containing them or their use in the prevention or treatment of a viral infection.
摘要翻译: 本发明涉及通式(I)的化合物; 其中R是氨基或胍基; R 2是乙酰基或三氟乙酰基; X是CONH,NHCO或O; n为2-6的整数; 且Y为C 2 -C 9烷基C 3-8环烷基,C 1 -C 3烷基, 4烷氧基烷基,氨基酸或二肽或其药学上可接受的衍生物,其制备方法,含有它们的药物制剂或其在预防或治疗病毒感染中的用途。
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公开(公告)号:US20050043399A1
公开(公告)日:2005-02-24
申请号:US10494241
申请日:2002-11-08
申请人: Derek Demaine , Graham Inglis , Simon MacDonald , Stephen Shanahan , Simon Tucker , Keith Watson , Wen-Yang Wu
发明人: Derek Demaine , Graham Inglis , Simon MacDonald , Stephen Shanahan , Simon Tucker , Keith Watson , Wen-Yang Wu
IPC分类号: A61K9/12 , A61K9/72 , A61K31/13 , A61K31/215 , A61K31/351 , A61K31/7052 , A61K31/7056 , A61K45/00 , A61K45/06 , A61K47/48 , A61M15/00 , A61P3/12 , A61P11/00 , A61P27/16 , A61P31/00 , A61P31/04 , A61P31/12 , A61P31/16 , A61P43/00 , C07B53/00 , C07D309/28 , A61K31/35 , C07D45/02
CPC分类号: A61K31/7056 , A61K31/13 , A61K31/351 , A61K45/06 , A61K47/54 , A61K47/55 , C07D309/28 , A61K2300/00
摘要: The invention relates to compounds of general formula (I); in which R is an amino or guanidino group; R2 is acetyl or trifluoroacetyl; and n is an integer from 10 to 18 or a pharmaceutically acceptable derivative thereof, methods for their preparation, pharmaceutical formulations containing them or their use in the prevention or treatment of a viral infection.
摘要翻译: 本发明涉及通式(I)的化合物; 其中R是氨基或胍基; R 2是乙酰基或三氟乙酰基; 并且n为10至18的整数或其药学上可接受的衍生物,其制备方法,含有它们的药物制剂或其在预防或治疗病毒感染中的用途。
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公开(公告)号:US20050038108A1
公开(公告)日:2005-02-17
申请号:US10494243
申请日:2002-11-08
申请人: Michael Dowle , Betty Jin , Simon Macdonald , Andrew McM Mason , Darryl Mcconnell , Van Nguyen , Stepehn Shanahan , Wen-Yang Wu
发明人: Michael Dowle , Betty Jin , Simon Macdonald , Andrew McM Mason , Darryl Mcconnell , Van Nguyen , Stepehn Shanahan , Wen-Yang Wu
IPC分类号: A61K9/12 , A61K9/14 , A61K31/13 , A61K31/351 , A61K31/7052 , A61K45/00 , A61P31/04 , A61P31/12 , A61P31/16 , A61P43/00 , C07D309/28 , A61K31/34 , C07D45/02
CPC分类号: C07D309/28
摘要: The invention relates to compounds of general formula (I); in which R is an amino or guanidino group; R2 is acetyl or trifluoroacetyl; X is CONH, SO2NH, NHCO or NHCONH; m is either 0 or 1; n is an integer from 2 to 6; q is an integer from 0 to 3; and Y is hydrogen or an aromatic substituent, or a pharmaceutically acceptable derivative thereof; methods for their preparation, pharmaceutical formulations containing them or their use in the prevention or treatment of a viral infection.
摘要翻译: 本发明涉及通式(I)的化合物; 其中R是氨基或胍基; R 2是乙酰基或三氟乙酰基; X是CONH,SO2NH,NHCO或NHCONH; m为0或1; n为2-6的整数; q是0至3的整数; Y为氢或芳香族取代基,或其药学上可接受的衍生物; 其制备方法,含有它们的药物制剂或其在预防或治疗病毒感染中的用途。
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公开(公告)号:US20070293564A1
公开(公告)日:2007-12-20
申请号:US11607872
申请日:2006-12-04
申请人: Michael Dowle , Betty Jin , Simon MacDonald , Andrew Mason , Darryl McConnell , Van Nguyen , Stephen Shanahan , Wen-Yang Wu
发明人: Michael Dowle , Betty Jin , Simon MacDonald , Andrew Mason , Darryl McConnell , Van Nguyen , Stephen Shanahan , Wen-Yang Wu
IPC分类号: A61K31/35
CPC分类号: C07D309/28
摘要: A method for the prevention of an orthomyxovirus or paramyxovirus infection comprising the step of administration to a subject in need thereof of an effective amount of a compound of formula (I)
摘要翻译: 一种用于预防正粘病毒或副粘病毒感染的方法,包括向有需要的受试者施用有效量的式(I)化合物的步骤,
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公开(公告)号:US20070225359A1
公开(公告)日:2007-09-27
申请号:US11751269
申请日:2007-05-21
申请人: Derek DEMAINE , Graham Inglis , Simon MacDonald , Stephen Shanahan , Simon Tucker , Keith Watson , Wen-Yang Wu
发明人: Derek DEMAINE , Graham Inglis , Simon MacDonald , Stephen Shanahan , Simon Tucker , Keith Watson , Wen-Yang Wu
IPC分类号: A61K31/35
CPC分类号: A61K31/7056 , A61K31/13 , A61K31/351 , A61K45/06 , A61K47/54 , A61K47/55 , C07D309/28 , A61K2300/00
摘要: The invention relates to compounds of general formula (I); in which R is an amino or guanidino group; R2 is acetyl or trifluoroacetyl; and n is an integer from 10 to 18 or a pharmaceutically acceptable derivative thereof, methods for their preparation, pharmaceutical formulations containing them or their use in the prevention or treatment of a viral infection.
摘要翻译: 本发明涉及通式(I)的化合物; 其中R是氨基或胍基; R 2是乙酰基或三氟乙酰基; 并且n为10至18的整数或其药学上可接受的衍生物,其制备方法,含有它们的药物制剂或其在预防或治疗病毒感染中的用途。
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公开(公告)号:US20050054719A1
公开(公告)日:2005-03-10
申请号:US10494260
申请日:2002-11-08
申请人: Betty Jin , Simon MacDonald , Darryl McConnell , Van Nguyen , Stephen Shanahan , Wen-Yang Wu
发明人: Betty Jin , Simon MacDonald , Darryl McConnell , Van Nguyen , Stephen Shanahan , Wen-Yang Wu
IPC分类号: A61K31/13 , A61K31/351 , A61K31/7052 , A61K31/7056 , A61K38/00 , A61K45/06 , A61K47/48 , A61P11/00 , A61P31/04 , A61P31/12 , A61P31/16 , C07D309/28 , C07K5/072 , C07D45/02 , A61K31/35
CPC分类号: A61K31/351 , A61K31/13 , A61K31/7056 , A61K38/00 , A61K45/06 , A61K47/54 , A61K47/55 , C07D309/28 , C07K5/06104 , A61K2300/00
摘要: The invention relates to compounds of general formula (1); in which R is an amino or guanidino group; R2 is acetyl or trifluoroacetyl; X is CONH, NHCO or O; n is an integer from 2 to 6; and Y is C2-C8 alkyl C3-8 cycloalkyl, C1-C4 alkoxyalkyl, an amino acid or dipeptide, or a pharmaceutically acceptable derivative thereof, methods for their preparation, pharmaceutical formulations containing them or their use in the prevention or treatment of a viral infection.
摘要翻译: 本发明涉及通式(1)的化合物; 其中R是氨基或胍基; R 2是乙酰基或三氟乙酰基; X为CONH,NHCO或O; n为2-6的整数; 并且Y是C 2 -C 8烷基C 3-8环烷基,C 1 -C 4烷氧基烷基,氨基酸或二肽或其药学上可接受的衍生物,其制备方法,含有它们的药物制剂或其用于预防或治疗病毒 感染。
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公开(公告)号:US20050032853A1
公开(公告)日:2005-02-10
申请号:US10488791
申请日:2002-08-30
申请人: Brian Judkins , Simon MacDonald , Derek Demaine , Graham Inglis , Julie Hamblin
发明人: Brian Judkins , Simon MacDonald , Derek Demaine , Graham Inglis , Julie Hamblin
IPC分类号: C07D309/28 , C07D407/06 , C07D413/02 , A61K31/4245
CPC分类号: C07D407/06 , C07D309/28 , Y02P20/55
摘要: Compounds of formula (I), methods for their preparation and their use in the manufacture of neuraminidase inhibitor conjugates. Wherein R represents as carboxylic acid protecting group; P1 and P2 can be the same or different and are selected from amine protecting groups; P3 represents a protecting group for 1, 2 diols; and LG represents a leaving group.
摘要翻译: 式(I)的化合物,其制备方法及其在制备神经氨酸酶抑制剂缀合物中的用途。 其中R表示羧酸保护基; P1和P2可以相同或不同,并且选自胺保护基; P3表示1,2二醇的保护基; LG代表离职团体。
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