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1.
公开(公告)号:US20100137300A1
公开(公告)日:2010-06-03
申请号:US12530929
申请日:2007-03-21
申请人: George Hynd , Nicholas Charles Ray , Harry Finch , John Gary Montana , Michael Colin Cramp , Trevor Keith Harrison , Rosa Arienzo , Paul Blaney , Yann Griffon , David Middlemiss
发明人: George Hynd , Nicholas Charles Ray , Harry Finch , John Gary Montana , Michael Colin Cramp , Trevor Keith Harrison , Rosa Arienzo , Paul Blaney , Yann Griffon , David Middlemiss
IPC分类号: A61K31/5377 , A61K31/435 , A61K31/4709 , C07D413/12 , C07D221/04 , C07D215/14 , A61P1/00 , A61P11/06 , A61P11/00 , A61P1/04
CPC分类号: C07D471/04
摘要: The specific compounds of this list: {7-cyano-2-methyl-1-[4-(morpholine-4-sutfonyl)benzyl]indolizin-3-yl}acetic acid, {1-(3-chloro-4-ethanesulfonylbenzyl)-7-cyano-2-methylindolizin-3-yl}acetic acid, {1-[3-chloro4-(morpholine-4-sulfonyl)benzyl]-7-cyano-2-methylindolizin-3-yl}acetic acid, {1-(3-chloro-4-ethanesulfonylphenylsulfanyl)-7-cyano-2-methylindolizin-3-yl}acetic acid, {1-[3-chloro-4-(morpholine-4-sutfonyl)phenylsutfanyl]-7-cyano-2-methylindolizin-3-yl}acetic acid, {7-cyano-1-(6-fluoroquinolin-2-ylmethyl)-2-methylindolizin-3-yl}acetic acid are ligands of the CRTH2 receptor and are useful in the treatment of respiratory diseases.
摘要翻译: 该列表的具体化合物:{7-氰基-2-甲基-1- [4-(吗啉-4-磺酰基)苄基]中氮茚-3-基}乙酸,{1-(3-氯-4-乙磺酰基苄基 )-7-氰基-2-甲基吲哚啉-3-基}乙酸{1- [3-氯-4-(吗啉-4-磺酰基)苄基] -7-氰基-2-甲基吲哚啉-3-基}乙酸, {1-(3-氯-4-乙磺酰基苯基硫烷基)-7-氰基-2-甲基吲哚啉-3-基}乙酸{1- [3-氯-4-(吗啉-4-磺基)苯基f烷基] 氰基-2-甲基吲哚啉-3-基}乙酸,{7-氰基-1-(6-氟喹啉-2-基甲基)-2-甲基吲哚啉-3-基}乙酸是CRTH2受体的配体,可用于 治疗呼吸系统疾病。
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公开(公告)号:US20080306109A1
公开(公告)日:2008-12-11
申请号:US12065963
申请日:2006-09-14
申请人: George Hynd , Nicholas Charles Ray , Harry Finch , John Gary Montana , Michael Colin Cramp , Trevor Keith Harrison , Rosa Arienzo , Paul Blaney , Yann Griffon , David Middlemiss
发明人: George Hynd , Nicholas Charles Ray , Harry Finch , John Gary Montana , Michael Colin Cramp , Trevor Keith Harrison , Rosa Arienzo , Paul Blaney , Yann Griffon , David Middlemiss
IPC分类号: A61K31/44 , C07D455/02 , A61P43/00
CPC分类号: C07D471/04
摘要: Compounds of formula (I) are CRTH2 antagonists, useful in the treatment of, for example, asthma, chronic obstructive pulmonary disease, rhinitis, allergic airway syndrome, and allergic rhinobronchitis. Formula (I) wherein R1, R2. R3 and R4 each independently are hydrogen, C1-C6alkyl, fully or partially fluorinated C1-C6alkyl, halo, —S(O)nR10, —SO2N(R10)2, —N(R10)2, —C(O)N(R10)2, —NR10C(O)R9, —CO2R10, —C(O)R9, —NO2, —CN or —OR11; wherein each R9 is independently C1-C6alkyl, aryl, heteroaryl; R10 is independently hydrogen, C1-C6alkyl, aryl, or heteroaryl; R11 is hydrogen, C1-C6alkyl, fully or partially fluorinated C1-C6alkyl or a group —SO2R10; n is 0, 1 or 2; R5 is C1-C6alkyl, fully or partially fluorinated C1-C6alkyl, C1-C6alkenyl, C1-C6alkynyl, optionally substituted aryl, or optionally substituted heteroaryl; R6 is hydrogen, C1-C6alkyl or fully or partially fluorinated C1-C6alkyl; R7 and R8 are independently hydrogen or C1-C6alkyl, or R7 and R8 together with the atom to which they are attached form a cycloalkyl group; and X is —CHR6—, —S(O)n—, —C(O)—, —NR6SO2— or —SO2NR6- wherein n is 0, 1 or 2.
摘要翻译: 式(I)化合物是CRTH2拮抗剂,可用于治疗例如哮喘,慢性阻塞性肺病,鼻炎,过敏性气道综合征和过敏性鼻炎支原体炎。 式(I)其中R1,R2。 完全或部分氟化的C 1 -C 6烷基,卤素,-S(O)n R 10,-SO 2 N(R 10)2,-N(R 10)2,-C(O)N( R 10)2,-NR 10 C(O)R 9,-CO 2 R 10,-C(O)R 9,-NO 2,-CN或-OR 11; 其中每个R 9独立地是C 1 -C 6烷基,芳基,杂芳基; R 10独立地是氢,C 1 -C 6烷基,芳基或杂芳基; R 11是氢,C 1 -C 6烷基,完全或部分氟化的C 1 -C 6烷基或基团-SO 2 R 10; n为0,1或2; R 5是C 1 -C 6烷基,完全或部分氟化的C 1 -C 6烷基,C 1 -C 6烯基,C 1 -C 6炔基,任选取代的芳基或任选取代的杂芳基; R6是氢,C1-C6烷基或完全或部分氟化的C1-C6烷基; R 7和R 8独立地是氢或C 1 -C 6烷基,或者R 7和R 8与它们所连接的原子一起形成环烷基; 且X为-CHR 6 - , - S(O)n - , - C(O) - , - NR 6 SO 2 - 或-SO 2 NR 6 - ,其中n为0,1或2。
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公开(公告)号:US20070281928A1
公开(公告)日:2007-12-06
申请号:US10591884
申请日:2005-03-09
申请人: Robin Clark , Nicholas Ray , Paul Blaney , Christopher Hurley , Karen Williams
发明人: Robin Clark , Nicholas Ray , Paul Blaney , Christopher Hurley , Karen Williams
IPC分类号: A61K31/415 , A61K31/5377 , A61P43/00 , C07D401/02 , C07D413/14
CPC分类号: C07D471/04
摘要: The present invention provides a novel class of fused ring azadecalin compounds and methods of using the compounds as glucocorticoid receptor modulators.
摘要翻译: 本发明提供了一类新颖的稠环氮杂环丁烷化合物和使用该化合物作为糖皮质激素受体调节剂的方法。
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公开(公告)号:US20070203179A1
公开(公告)日:2007-08-30
申请号:US10596998
申请日:2005-01-10
申请人: Robin Clark , Nicholas Ray , Paul Blaney , Christopher Hurley , Hazel Hunt , David Clark , Karen Williams
发明人: Robin Clark , Nicholas Ray , Paul Blaney , Christopher Hurley , Hazel Hunt , David Clark , Karen Williams
IPC分类号: A61K31/47 , C07D217/04 , C07D217/08
CPC分类号: C07D217/04 , C07D217/02 , C07D217/06 , C07D217/08 , C07D401/10 , C07D401/12 , C07D405/06 , C07D409/12 , C07D409/14 , C07D413/12 , C07D413/14 , C07D417/12 , C07D491/10 , C07D513/04 , C07D513/06
摘要: The present invention provides a novel class of azadecalin compounds and methods of using the compounds as glucocorticoid receptor modulators.
摘要翻译: 本发明提供了一类新颖的氮杂环丁烷化合物和使用该化合物作为糖皮质激素受体调节剂的方法。
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公开(公告)号:US07678813B2
公开(公告)日:2010-03-16
申请号:US10596998
申请日:2005-01-10
申请人: Robin D. Clark , Nicholas C. Ray , Paul Blaney , Christopher Hurley , Hazel Hunt , David Clark , Karen Williams
发明人: Robin D. Clark , Nicholas C. Ray , Paul Blaney , Christopher Hurley , Hazel Hunt , David Clark , Karen Williams
IPC分类号: A61K31/47 , C07D217/02 , C07D417/12
CPC分类号: C07D217/04 , C07D217/02 , C07D217/06 , C07D217/08 , C07D401/10 , C07D401/12 , C07D405/06 , C07D409/12 , C07D409/14 , C07D413/12 , C07D413/14 , C07D417/12 , C07D491/10 , C07D513/04 , C07D513/06
摘要: The present invention provides a novel class of azadecalin compounds and methods of using the compounds as glucocorticoid receptor modulators.
摘要翻译: 本发明提供了一类新颖的氮杂环丁烷化合物和使用该化合物作为糖皮质激素受体调节剂的方法。
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公开(公告)号:US20050159484A1
公开(公告)日:2005-07-21
申请号:US10846217
申请日:2004-05-14
申请人: Peter Fischer , Jan Sarek , Paul Blaney , Piers Collier , John Ferguson , Jonathan Hull
发明人: Peter Fischer , Jan Sarek , Paul Blaney , Piers Collier , John Ferguson , Jonathan Hull
IPC分类号: A61P35/00 , C07J63/00 , C07J71/00 , A61K31/225 , C07C67/02
CPC分类号: C07J63/008 , C07J71/0005
摘要: The present invention relates to 3β,28-diacetoxy-18-oxo-19,20,21,29,30-pentanorlupan-22-oic acid methanol solvate, its use in medicine and processes for its preparation.
摘要翻译: 本发明涉及3β,28-二乙酰氧基-18-氧代-19,20,21,29,30-戊酰氧基-22-酸甲醇溶剂合物,其用于医药及其制备方法。
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公开(公告)号:US08324203B2
公开(公告)日:2012-12-04
申请号:US12691684
申请日:2010-01-21
申请人: Robin D. Clark , Nicholas C. Ray , Paul Blaney , Christopher Hurley , Hazel Hunt , David Clark , Karen Williams
发明人: Robin D. Clark , Nicholas C. Ray , Paul Blaney , Christopher Hurley , Hazel Hunt , David Clark , Karen Williams
IPC分类号: A61K31/538 , A61K31/47 , A61K31/5377 , A61K31/506 , A61K31/497
CPC分类号: C07D217/04 , C07D217/02 , C07D217/06 , C07D217/08 , C07D401/10 , C07D401/12 , C07D405/06 , C07D409/12 , C07D409/14 , C07D413/12 , C07D413/14 , C07D417/12 , C07D491/10 , C07D513/04 , C07D513/06
摘要: The present invention provides a novel class of azadecalin compounds and methods of using the compounds as glucocorticoid receptor modulators.
摘要翻译: 本发明提供了一类新颖的氮杂环丁烷化合物和使用该化合物作为糖皮质激素受体调节剂的方法。
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