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公开(公告)号:EP1679305B1
公开(公告)日:2012-02-08
申请号:EP06007501.7
申请日:2001-06-29
发明人: Nelson, Mark, L. , Frechette, Roger , Viski, Peter , Ismail, Mohamed , Bowser, Todd , Dumornay, Jimmy , Rennie, Glen , Liu, Gui , Koza, Darrell , Sheahan, Paul , Stapleton, Karen , Hawkins, Paul , Bhatia, Beena , Verma, Atul , Mcintyre, Laura , Warchol, Tad
IPC分类号: C07C237/26 , A61K31/65
CPC分类号: A61K31/65 , C07C237/26 , C07C255/59 , C07C271/22 , C07C271/28 , C07C271/30 , C07C271/58 , C07C275/30 , C07C275/34 , C07C275/38 , C07C275/40 , C07C275/42 , C07C275/50 , C07C275/54 , C07C311/06 , C07C311/21 , C07C333/08 , C07C335/22 , C07C381/10 , C07C2601/08 , C07C2601/10 , C07C2601/14 , C07C2601/16 , C07C2603/46 , C07D295/155 , C07F9/4006 , C07F9/4056 , Y02A50/473 , Y02A50/481
摘要: The present invention pertains, at least in part, to novel 9- substituted minocycline compounds. These minocycline compounds can be used to treat numerous tetracycline compound-responsive states, such as bacterial infections and neoplasms, as well as other known applications for minocycline and tetracycline compounds in general, such as blocking tetracycline compounds in general, such as blocking tetracycline efflux and modulation of gene expression.
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公开(公告)号:EP2308832B1
公开(公告)日:2018-09-12
申请号:EP10182900.0
申请日:2001-06-29
发明人: Nelson, Mark L. , Frechette, Roger , Viski, Peter , Ismail, Mohamed Y , Bowser, Todd , Dumornay, Jimmy , Rennie, Glen , Liu, Gui , Koza, Darrell , Sheahan, Paul , Stapleton, Karen , Hawkins, Paul , Bhatia, Beena , Verma, Atul , McIntyre, Laura , Warchol, Ted
IPC分类号: C07C237/26 , A61K31/65 , A61P31/04 , A61P17/00
CPC分类号: A61K31/65 , C07C237/26 , C07C255/59 , C07C271/22 , C07C271/28 , C07C271/30 , C07C271/58 , C07C275/30 , C07C275/34 , C07C275/38 , C07C275/40 , C07C275/42 , C07C275/50 , C07C275/54 , C07C311/06 , C07C311/21 , C07C333/08 , C07C335/22 , C07C381/10 , C07C2601/08 , C07C2601/10 , C07C2601/14 , C07C2601/16 , C07C2603/46 , C07D295/155 , C07F9/4006 , C07F9/4056 , Y02A50/473 , Y02A50/481
摘要: The present invention pertains, at least in part, to novel 9- substituted minocycline compounds. These minocycline compounds can be used to treat numerous tetracycline compound-responsive states, such as bacterial infections and neoplasms, as well as other known applications for minocycline and tetracycline compounds in general, such as blocking tetracycline compounds in general, such as blocking tetracycline efflux and modulation of gene expression.
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公开(公告)号:EP2308832A1
公开(公告)日:2011-04-13
申请号:EP10182900.0
申请日:2001-06-29
发明人: Nelson, Mark L. , Frechette, Roger , Viski, Peter , Ismail, Mohamed Y , Bowser, Todd , Dumornay, Jimmy , Rennie, Glen , Liu, Gui , Koza, Darrell , Sheahan, Paul , Stapleton, Karen , Hawkins, Paul , Bhatia, Beena , Verma, Atul , McIntyre, Laura , Warchol, Ted
IPC分类号: C07C237/26 , A61K31/65
CPC分类号: A61K31/65 , C07C237/26 , C07C255/59 , C07C271/22 , C07C271/28 , C07C271/30 , C07C271/58 , C07C275/30 , C07C275/34 , C07C275/38 , C07C275/40 , C07C275/42 , C07C275/50 , C07C275/54 , C07C311/06 , C07C311/21 , C07C333/08 , C07C335/22 , C07C381/10 , C07C2601/08 , C07C2601/10 , C07C2601/14 , C07C2601/16 , C07C2603/46 , C07D295/155 , C07F9/4006 , C07F9/4056 , Y02A50/473 , Y02A50/481
摘要: The present invention pertains, at least in part, to novel 9- substituted minocycline compounds. These minocycline compounds can be used to treat numerous tetracycline compound-responsive states, such as bacterial infections and neoplasms, as well as other known applications for minocycline and tetracycline compounds in general, such as blocking tetracycline compounds in general, such as blocking tetracycline efflux and modulation of gene expression.
摘要翻译: 本发明至少部分涉及新的9-取代的米诺环素化合物。 这些米诺环素化合物可用于治疗许多四环素化合物应答状态,例如细菌感染和肿瘤,以及一般的米诺环素和四环素化合物的其它已知应用,例如一般阻断四环素化合物,如阻断四环素外排和 基因表达的调节。
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公开(公告)号:EP2308832B8
公开(公告)日:2019-04-24
申请号:EP10182900.0
申请日:2001-06-29
发明人: Nelson, Mark L. , Frechette, Roger , Viski, Peter , Ismail, Mohamed Y , Bowser, Todd , Dumornay, Jimmy , Rennie, Glen , Liu, Gui , Koza, Darrell , Sheahan, Paul , Stapleton, Karen , Hawkins, Paul , Bhatia, Beena , Verma, Atul , Honeyman, Laura , Warchol, Ted
IPC分类号: C07C237/26 , A61K31/65 , A61P31/04 , A61P17/00
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公开(公告)号:EP2289871A1
公开(公告)日:2011-03-02
申请号:EP10183426.5
申请日:2001-06-29
发明人: Nelson, Mark L. , Frechette, Roger , Viski, Peter , Ismail, Mohamed , Bowser, Todd , Bhatia, Beena , Messersmith, David , McIntyre, Laura , Koza, Darrell , Rennie, Glen , Sheahan, Paul , Hawkins, Paul , Verma, Atul , Warchol, Tad , Bandarage, Upul
IPC分类号: C07C237/26 , C07C311/06 , A61K31/65
CPC分类号: C07D213/64 , C07C237/26 , C07C251/24 , C07C251/48 , C07C271/22 , C07C271/28 , C07C271/58 , C07C275/24 , C07C311/06 , C07C2601/02 , C07C2601/04 , C07C2601/08 , C07C2601/10 , C07C2601/14 , C07C2603/46 , C07D207/22 , C07D213/50 , C07D213/56 , C07D239/36 , C07D261/18 , C07D277/30 , C07D277/42 , C07D295/096 , C07D295/135 , C07D295/155 , C07D307/54 , C07D307/68 , C07D307/79 , C07D317/60 , C07D333/24 , C07D333/28 , C07D333/60 , C07F9/2475
摘要: The present invention pertains, at least in part, to novel 7-substituted tetracycline compounds. These tetracycline compounds can be used to treat numerous tetracycline compound-responsive states, such as bacterial infections and neoplasms, as well as other known applications for minocycline and tetracycline compounds in general, such as blocking tetracycline efflux and modulation of gene expression.
摘要翻译: 本发明至少部分地涉及新的7-取代四环素化合物。 这些四环素化合物可用于治疗多种四环素化合物反应状态,例如细菌感染和肿瘤,以及其它已知的米诺环素和四环素化合物的一般应用,例如阻断四环素外排和调节基因表达。
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公开(公告)号:EP1679305A1
公开(公告)日:2006-07-12
申请号:EP06007501.7
申请日:2001-06-29
发明人: Nelson, Mark, L. , Frechette, Roger , Viski, Peter , Ismail, Mohamed , Bowser, Todd , Dumornay, Jimmy , Rennie, Glen , Liu, Gui , Koza, Darrell , Sheahan, Paul , Stapleton, Karen , Hawkins, Paul , Bhatia, Beena , Verma, Atul , Mcintyre, Laura , Warchol, Tad
IPC分类号: C07C237/26 , A61K31/65
CPC分类号: A61K31/65 , C07C237/26 , C07C255/59 , C07C271/22 , C07C271/28 , C07C271/30 , C07C271/58 , C07C275/30 , C07C275/34 , C07C275/38 , C07C275/40 , C07C275/42 , C07C275/50 , C07C275/54 , C07C311/06 , C07C311/21 , C07C333/08 , C07C335/22 , C07C381/10 , C07C2601/08 , C07C2601/10 , C07C2601/14 , C07C2601/16 , C07C2603/46 , C07D295/155 , C07F9/4006 , C07F9/4056 , Y02A50/473 , Y02A50/481
摘要: The present invention pertains, at least in part, to novel 9- substituted minocycline compounds. These minocycline compounds can be used to treat numerous tetracycline compound-responsive states, such as bacterial infections and neoplasms, as well as other known applications for minocycline and tetracycline compounds in general, such as blocking tetracycline compounds in general, such as blocking tetracycline efflux and modulation of gene expression.
摘要翻译: 本发明至少部分地涉及新的9-取代的米诺环素化合物。 这些米诺环素化合物可用于治疗许多四环素化合物反应状态,例如细菌感染和肿瘤,以及通常其他已知的米诺环素和四环素化合物的应用,例如通常阻断四环素化合物,例如阻断四环素外排和 调节基因表达。
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公开(公告)号:EP2298732A1
公开(公告)日:2011-03-23
申请号:EP10184631.9
申请日:2001-06-29
发明人: Hawkins, Paul , Bhatia, Been , Warhol, Tad , Nelson, Mark L. , Frechette, Roger , Viski, Peter , Ismail, Mohammed , Bowser, Todd , McIntyre, Laura , Reddy, Laxma , Stapleton, Karen , Sheahan, Paul
IPC分类号: C07C237/26 , A61K31/65
CPC分类号: C07C237/26 , B32B37/0007 , B32B37/003 , B32B37/1284 , C07C2601/14 , C07C2601/16 , C07C2603/46 , C07D209/48 , C07D213/82 , C07D215/14 , C07D307/24 , C07D317/60
摘要: A 7, 9-substituted tetracycline selected from:
摘要翻译: A选自7,9取代四环素:
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公开(公告)号:EP2301913A1
公开(公告)日:2011-03-30
申请号:EP10184559.2
申请日:2001-06-29
发明人: Hawkins, Paul , Bhatia, Beena , Warchol, Tad , Nelson, Mark, L. , Frechette, Roger , Viski, Peter , Ismail, Mohamed , Bowser, Todd , McIntyre, Laura , Reddy, Laxma , Stapleton, Karen , Sheahan, Paul
IPC分类号: C07C237/26 , A61K31/65
CPC分类号: C07C237/26 , B32B37/0007 , B32B37/003 , B32B37/1284 , C07C2601/14 , C07C2601/16 , C07C2603/46 , C07D209/48 , C07D213/82 , C07D215/14 , C07D307/24 , C07D317/60
摘要: A 7, 9-substituted tetracycline compound of Formula I:
wherein:
X is CH 2 ;
R 4' and R 4" are each independently alkyl;
R 4 is NR 4' R 4" ;
R 2 , R 2' , R 3 , R 8 , R 10 , R 11 and R 12 are each hydrogen;
R 5 is hydrogen or hydroxyl;
R 7 is alkyl, alkenyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, arylalkyl, amino, acyl or -(CH 2 ) 0-3 NR 7c C(=W')WR 7a ;
R 9 is nitro, alkyl, alkenyl, alkynyl, aryl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, arylalkyl, amino, arylalkenyl, arylalkynyl, thionitroso, acyl or -(CH 2 ) 0-3 NR 9c C(=Z')ZR 9a ;
Z is CR 9d R 9e , S, NR 9b or O;
Z' is O, S or NR 9f ;
W is CR 7d R 7e , S, NR 7b or O;
W' is O, S or NR 7f ; and
R 7a , R 7b , R 7c , R 7d , R 7e , R 7f , R 9a , R 9b , R 9c , R 9d , R 9e and R 9f are each independently hydrogen, acyl, alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, arylalkyl, aryl, heterocyclic or heteroaromatic;
or a 7, 9-substituted tetracycline compound selected from:
and摘要翻译: 7,9-取代的式I的四环素化合物:其中:X是CH 2; R 4'和R 4“各自独立地为烷基; R 4为NR 4'R 4”; R 2,R 2',R 3,R 8,R 10,R 11和R 12各自为氢; R 5是氢或羟基; R 7是烷基,烯基,烷氧基,烷硫基,烷基亚磺酰基,烷基磺酰基,芳基烷基,氨基,酰基或 - (CH 2)0-3 NR 7c C(= W')WR 7a; R 9是硝基,烷基,烯基,炔基,芳基,烷氧基,烷硫基,烷基亚磺酰基,烷基磺酰基,芳烷基,氨基,芳基烯基,芳基炔基,亚硫基,酰基或 - (CH 2)0-3 NR 9c C(= Z' 9a; Z为CR 9d R 9e,S,NR 9b或O; Z'是O,S或NR 9f; W是CR 7d R 7e,S,NR 7b或O; W'是O,S或NR 7f; R 7a,R 7b,R 7c,R 7d,R 7e,R 7f,R 9a,R 9b,R 9c,R 9d,R 9e和R 9f各自独立地为氢,酰基,烷基,烯基,炔基,烷氧基 烷硫基,烷基亚磺酰基,烷基磺酰基,烷基氨基,芳基烷基,芳基,杂环或杂芳族; 或选自以下的7,9取代的四环素化合物
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公开(公告)号:EP1955996A1
公开(公告)日:2008-08-13
申请号:EP08005899.3
申请日:2001-06-29
发明人: Hawkins, Paul , Bhatia, Beena , Warchol, Tad , Nelson, Mark, L. , Frechette, Roger , Viski, Peter , Ismail, Mohamed , Bowser, Todd , McIntyre, Laura , Reddy, Laxma , Stapleton, Karen , Sheahan, Paul
IPC分类号: C07C237/26 , A61K31/65
CPC分类号: C07C237/26 , B32B37/0007 , B32B37/003 , B32B37/1284 , C07C2601/14 , C07C2601/16 , C07C2603/46 , C07D209/48 , C07D213/82 , C07D215/14 , C07D307/24 , C07D317/60
摘要: The present invention pertains to novel 7,9- substituted tetracycline compounds. These tetracycline compounds can be used to treat numerous tetracycline compound-responsive states, such as bacterial infections and neoplasms, as well as other known applications for minocycline and tetracycline compounds in general, such as blocking tetracycline efflux and modulation of gene expression.
摘要翻译: 本发明涉及新的7,9-取代的四环素化合物。 这些四环素化合物可用于治疗多种四环素化合物反应状态,例如细菌感染和肿瘤,以及其它已知的米诺环素和四环素化合物的一般应用,例如阻断四环素外排和调节基因表达。
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公开(公告)号:EP2301914A1
公开(公告)日:2011-03-30
申请号:EP10184615.2
申请日:2001-06-29
发明人: Hawkins, Paul , Bhatia, Beena , Warchol, Tad , Nelson, Mark, L. , Frechette, Roger , Viski, Peter , Ismail, Mohamed , Bowser, Todd , Mcintyre, Laura , Reddy, Laxma , Stapleton, Karen , Sheahan, Paul
IPC分类号: C07C237/26 , A61K31/65
CPC分类号: C07C237/26 , B32B37/0007 , B32B37/003 , B32B37/1284 , C07C2601/14 , C07C2601/16 , C07C2603/46 , C07D209/48 , C07D213/82 , C07D215/14 , C07D307/24 , C07D317/60
摘要: A 7, 9-substituted tetracycline compound of Formula I:
wherein:
X is CH 2 ;
R 4' and R 4" are each independently alkyl;
R 4 is NR 4' R 4" ;
R 2 , R 2' , R 3 , R 8 , R 10 , R 11 and R 12 are each hydrogen;
R 5 is hydrogen or hydroxyl;
R 7 is nitro;
R 9 is alkyl, alkenyl, alkynyl, aryl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, arylalkyl, amino, arylalkenyl, arylalkynyl, thionitroso, acyl or-(CH 2 ) 0-3 NR 9c (=Z')ZR 9a ;
Z is CR 9d R 9e , S, NR 9b or O;
Z' is O, S or NR 9f ; and
R 9a , R 9b , R 9c , R 9d , R 9e and R 9f are each independently hydrogen, acyl, alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, arylalkyl, aryl, heterocyclic or heteroaromatic.摘要翻译: 7,9-取代的式I的四环素化合物:其中:X是CH 2; R 4'和R 4“各自独立地为烷基; R 4为NR 4'R 4”; R 2,R 2',R 3,R 8,R 10,R 11和R 12各自为氢; R 5是氢或羟基; R 7是硝基; R 9是烷基,烯基,炔基,芳基,烷氧基,烷硫基,烷基亚磺酰基,烷基磺酰基,芳基烷基,氨基,芳基烯基,芳基炔基,亚硫基,酰基或 - (CH 2)0-3 NR 9c(= Z')ZR 9a; Z为CR 9d R 9e,S,NR 9b或O; Z'是O,S或NR 9f; R 9a,R 9b,R 9c,R 9d,R 9e和R 9f各自独立地为氢,酰基,烷基,烯基,炔基,烷氧基,烷硫基,烷基亚磺酰基,烷基磺酰基,烷基氨基,芳烷基,芳基,杂环或杂芳族。
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