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1.7-[(7-ALKOXY)-CHROM-3-EN-6-YL]-HEPTATRIENOIC ACID AND 7-[(3-ALKOXY)-5,6-DIHYDRONAPHTHALEN-2-YL]-HEPTATRIENOIC ACID DERIVATIVES HAVING SERUM GLUCOSE REDUCING ACTIVITY 失效
标题翻译: 7 - [(7-烷氧基)-CHROM-3-EN-6-YL] - 庚酸和7 - [(3-烷氧基)-5,6-二氢萘-2-基] - 嘌呤酸衍生物具有减少血清葡萄糖 活动公开(公告)号:US20050096380A1
公开(公告)日:2005-05-05
申请号:US10696748
申请日:2003-10-29
申请人: Richard Beard , Tien Duong , Janet Takeuchi , Ling Li , Kwok Tsang , Xiaoxia Liu , Jayasree Vasudevan , Liming Wang , Santosh Sinha , Haiqing Yuan , Roshantha Chandraratna
发明人: Richard Beard , Tien Duong , Janet Takeuchi , Ling Li , Kwok Tsang , Xiaoxia Liu , Jayasree Vasudevan , Liming Wang , Santosh Sinha , Haiqing Yuan , Roshantha Chandraratna
IPC分类号: A61K31/21 , A61K31/335 , C07C59/72 , C07C69/587 , C07C69/734 , C07D311/58 , A61K31/353 , A61K31/192 , C07C65/105
CPC分类号: C07C69/734 , C07C59/72 , C07C2601/02 , C07C2602/28 , C07D311/58
摘要: Compounds of the formula where the variables have the meaning defined in the specification are capable of reducing serum glucose levels in diabetic mammals without the undesirable side effects of transiently increasing triglyceride levels and reducing serum thyroxine levels.
摘要翻译: 其中变量具有本说明书中定义的含义的式的化合物能够降低糖尿病哺乳动物中的血清葡萄糖水平,而没有瞬时增加甘油三酯水平和降低血清甲状腺素水平的不良副作用。
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2.Compounds having selective cytochrome P450RAI-1 or selective cytochrome P450RAI-2 inhibitory activity and methods of obtaining the same 失效
标题翻译: 具有选择性细胞色素P450RAI-1或选择性细胞色素P450RAI-2抑制活性的化合物及其获得方法公开(公告)号:US20080004455A1
公开(公告)日:2008-01-03
申请号:US11728313
申请日:2007-03-23
申请人: Jayasree Vasudevan , Liming Wang , Xiaoxia Liu , Kwok Tsang , Ling Li , Janet Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Vidyasagar Vuligonda , Roshantha Chandraratna
发明人: Jayasree Vasudevan , Liming Wang , Xiaoxia Liu , Kwok Tsang , Ling Li , Janet Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Vidyasagar Vuligonda , Roshantha Chandraratna
IPC分类号: C07D311/96 , C07C229/44 , C07C63/331 , C07D311/04
CPC分类号: C07C69/73 , C07C57/42 , C07C59/64 , C07C59/86 , C07C69/753 , C07C69/76 , C07C229/34 , C07C229/38 , C07C229/46 , C07C229/50 , C07C275/42 , C07C2601/02 , C07C2602/10 , C07D311/58 , C07D311/64 , C07D311/96
摘要: Compounds of formulas 1 through 17 provided in the specification specifically or selectively inhibit either the cytochrome P450RAI-1 enzyme or the cytochrome P450RAI-2 enzyme.
摘要翻译: 在说明书中提供的式1至17的化合物具体地或选择性地抑制细胞色素P450RAI-1酶或细胞色素P450RAI-2酶。
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3.Compounds having selective cytochrome P450RAI-1 or selective cytochrome P450RAI-2 inhibitory activity and methods of obtaining the same 失效
标题翻译: 具有选择性细胞色素P450RAI-1或选择性细胞色素P450RAI-2抑制活性的化合物及其获得方法公开(公告)号:US20050176689A1
公开(公告)日:2005-08-11
申请号:US11014460
申请日:2004-12-16
申请人: Jayasree Vasudevan , Liming Wang , Xiaoxia Liu , Kwok Tsang , Ling Li , Janet Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Vidyasagar Vuligonda , Roshantha Chandraratna
发明人: Jayasree Vasudevan , Liming Wang , Xiaoxia Liu , Kwok Tsang , Ling Li , Janet Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Vidyasagar Vuligonda , Roshantha Chandraratna
IPC分类号: C07C57/42 , C07C59/64 , C07C59/86 , C07C69/18 , C07C69/73 , C07C69/753 , C07C69/76 , C07C229/34 , C07C229/38 , C07C229/46 , C07C229/50 , C07C275/42 , C07D311/58 , C07D311/64 , C07D311/96 , A61K31/655 , A61K31/4747 , A61K31/497 , A61K31/502 , A61K31/506
CPC分类号: C07C69/73 , C07C57/42 , C07C59/64 , C07C59/86 , C07C69/753 , C07C69/76 , C07C229/34 , C07C229/38 , C07C229/46 , C07C229/50 , C07C275/42 , C07C2601/02 , C07C2602/10 , C07D311/58 , C07D311/64 , C07D311/96
摘要: Compounds of formulas 1 through 17 provided in the specification specifically or selectively inhibit either the cytochrome P450RAI-1 enzyme or the cytochrome P450RAI-2 enzyme.
摘要翻译: 在说明书中提供的式1至17的化合物具体地或选择性地抑制细胞色素P450RAI-1酶或细胞色素P450RAI-2酶。
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4.Methods for treating retinoid responsive disorders using selective inhibitors of CYP26A and CYP26B 失效
标题翻译: 使用CYP26A和CYP26B的选择性抑制剂治疗类视黄醇应答障碍的方法公开(公告)号:US20050187298A1
公开(公告)日:2005-08-25
申请号:US11010953
申请日:2004-12-13
申请人: Jayasree Vasudevan , Rong Yang , Liming Wang , Xiaoxia Liu , Kwok-Yin Tsang , Ling Li , Janet Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Roshantha Chandraratna
发明人: Jayasree Vasudevan , Rong Yang , Liming Wang , Xiaoxia Liu , Kwok-Yin Tsang , Ling Li , Janet Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Roshantha Chandraratna
IPC分类号: A61K31/19 , A61K31/192 , A61K31/35 , A61K31/38
CPC分类号: A61K31/19 , A61K31/192 , A61K31/35 , A61K31/38
摘要: The invention provides methods for treating an individual having a retinoid responsive disorder. In one embodiment, a method involves administering to the individual an effective amount of a selective CYP26B inhibitor, the selective CYP26B inhibitor having at least 10-fold selectivity for CYP26B relative to CYP26A. In another embodiment, a method involves administering to the individual an effective amount of a selective CYP26A inhibitor, the selective CYP26A inhibitor having a chemical formula set forth in the specification. The invention further provides screening methods for identifying a selective CYP26A inhibitor or selective CYP26B inhibitor.
摘要翻译: 本发明提供了治疗患有类视黄醇反应性障碍的个体的方法。 在一个实施方案中,一种方法涉及向个体施用有效量的选择性CYP26B抑制剂,所述选择性CYP26B抑制剂相对于CYP26A对CYP26B具有至少10倍的选择性。 在另一个实施方案中,一种方法包括向个体施用有效量的选择性CYP26A抑制剂,该选择性CYP26A抑制剂具有说明书中阐述的化学式。 本发明还提供用于鉴定选择性CYP26A抑制剂或选择性CYP26B抑制剂的筛选方法。
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5.Methods for treating retinoid responsive disorders using selective inhibitors of CYP26A and CYP26B 失效
标题翻译: 使用CYP26A和CYP26B的选择性抑制剂治疗类视黄醇应答障碍的方法公开(公告)号:US07468391B2
公开(公告)日:2008-12-23
申请号:US11010953
申请日:2004-12-13
申请人: Jayasree Vasudevan , Rong Yang , Liming Wang , Xiaoxia Liu , Kwok-Yin Tsang , Ling Li , Janet Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Roshantha A. Chandraratna
发明人: Jayasree Vasudevan , Rong Yang , Liming Wang , Xiaoxia Liu , Kwok-Yin Tsang , Ling Li , Janet Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Roshantha A. Chandraratna
IPC分类号: A01N31/00 , A61K9/00 , A61K31/415 , A61K9/20 , A61K9/48
CPC分类号: A61K31/19 , A61K31/192 , A61K31/35 , A61K31/38
摘要: The invention provides methods for treating an individual having a retinoid responsive disorder. In one embodiment, a method involves administering to the individual an effective amount of a selective CYP26B inhibitor, the selective CYP26B inhibitor having at least 10-fold selectivity for CYP26B relative to CYP26A. In another embodiment, a method involves administering to the individual an effective amount of a selective CYP26A inhibitor, the selective CYP26A inhibitor having a chemical formula set forth in the specification. The invention further provides screening methods for identifying a selective CYP26A inhibitor or selective CYP26B inhibitor.
摘要翻译: 本发明提供了治疗患有类视黄醇反应性障碍的个体的方法。 在一个实施方案中,一种方法涉及向个体施用有效量的选择性CYP26B抑制剂,所述选择性CYP26B抑制剂相对于CYP26A对CYP26B具有至少10倍的选择性。 在另一个实施方案中,一种方法包括向个体施用有效量的选择性CYP26A抑制剂,该选择性CYP26A抑制剂具有说明书中阐述的化学式。 本发明还提供用于鉴定选择性CYP26A抑制剂或选择性CYP26B抑制剂的筛选方法。
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6.7-[(7-Alkoxy)-chrom-3-en-6-yl]-heptatrienoic acid and 7-[(3-alkoxy)-5,6-dihydronaphthalen-2-yl]-heptatrienoic acid derivatives having serum glucose reducing activity 失效
标题翻译: 7 - [(7-烷氧基) - 色烯-3-烯-6-基] - 庚三烯酸和具有血清葡萄糖降低的7 - [(3-烷氧基)-5,6-二氢萘-2-基] - 庚二酸衍生物 活动公开(公告)号:US06887896B1
公开(公告)日:2005-05-03
申请号:US10696748
申请日:2003-10-29
申请人: Richard L. Beard , Tien T. Duong , Janet A. Takeuchi , Ling Li , Kwok Yin Tsang , Xiaoxia Liu , Jayasree Vasudevan , Liming Wang , Santosh C. Sinha , Haiqing Yuan , Roshantha A. Chandraratna
发明人: Richard L. Beard , Tien T. Duong , Janet A. Takeuchi , Ling Li , Kwok Yin Tsang , Xiaoxia Liu , Jayasree Vasudevan , Liming Wang , Santosh C. Sinha , Haiqing Yuan , Roshantha A. Chandraratna
IPC分类号: A61K31/21 , A61K31/335 , C07C59/72 , C07C69/587 , C07C69/734 , C07D311/58 , A61K31/35 , A61K31/19 , A61K31/235
CPC分类号: C07C69/734 , C07C59/72 , C07C2601/02 , C07C2602/28 , C07D311/58
摘要: Compounds of the formula where the variations have the meaning defined in the specification are capable of reducing serum glucose levels in diabetic mammals without the undesirable side effects of transiently increasing triglyceride levels and reducing serum thyroxine levels.
摘要翻译: 其中变化具有本说明书中定义的含义的式的化合物能够降低糖尿病哺乳动物中的血清葡萄糖水平,而没有暂时增加甘油三酯水平和降低血清甲状腺素水平的不良副作用。
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7.Compounds having selective cytochrome P450RAI-1 or selective cytochrome P450RAI-2 inhibitory activity and methods of obtaining the same 失效
标题翻译: 具有选择性细胞色素P450RAI-1或选择性细胞色素P450RAI-2抑制活性的化合物及其获得方法公开(公告)号:US07226951B2
公开(公告)日:2007-06-05
申请号:US11014460
申请日:2004-12-16
申请人: Jayasree Vasudevan , Liming Wang , Xiaoxia Liu , Kwok Yin Tsang , Ling Li , Janet A. Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Vidyasagar Vuligonda , Roshantha A. Chandraratna
发明人: Jayasree Vasudevan , Liming Wang , Xiaoxia Liu , Kwok Yin Tsang , Ling Li , Janet A. Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Vidyasagar Vuligonda , Roshantha A. Chandraratna
IPC分类号: A61K31/135 , C07C62/00 , C07C69/52 , C07C211/16
CPC分类号: C07C69/73 , C07C57/42 , C07C59/64 , C07C59/86 , C07C69/753 , C07C69/76 , C07C229/34 , C07C229/38 , C07C229/46 , C07C229/50 , C07C275/42 , C07C2601/02 , C07C2602/10 , C07D311/58 , C07D311/64 , C07D311/96
摘要: Compounds of formulas 1 through 17 provided in the specification specifically or selectively inhibit either the cytochrome P450RAI-1 enzyme or the cytochrome P450RAI-2 enzyme.
摘要翻译: 在说明书中提供的式1至17的化合物具体地或选择性地抑制细胞色素P450RAI-1酶或细胞色素P450RAI-2酶。
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8.Compounds having selective cytochrome P450RAI-1 or selective cytochrome P450RAI-2 inhibitory activity and methods of obtaining the same 失效
标题翻译: 具有选择性细胞色素P450RAI-1或选择性细胞色素P450RAI-2抑制活性的化合物及其获得方法公开(公告)号:US07638648B2
公开(公告)日:2009-12-29
申请号:US11728313
申请日:2007-03-23
申请人: Jayasree Vasudevan , Liming Wang , Xiaoxia Liu , Kwok Yin Tsang , Ling Li , Janet A. Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Vidyasagar Vuligonda , Roshantha A. Chandraratna
发明人: Jayasree Vasudevan , Liming Wang , Xiaoxia Liu , Kwok Yin Tsang , Ling Li , Janet A. Takeuchi , Thong Vu , Richard Beard , Smita Bhat , Vidyasagar Vuligonda , Roshantha A. Chandraratna
IPC分类号: C07D265/06 , C07D263/02 , C07D277/02 , C07D213/02 , C07D333/04 , C07D307/34 , C07C229/34
CPC分类号: C07C69/73 , C07C57/42 , C07C59/64 , C07C59/86 , C07C69/753 , C07C69/76 , C07C229/34 , C07C229/38 , C07C229/46 , C07C229/50 , C07C275/42 , C07C2601/02 , C07C2602/10 , C07D311/58 , C07D311/64 , C07D311/96
摘要: Compounds of formulas 1 through 17 provided in the specification specifically or selectively inhibit either the cytochrome P450RAI-1 enzyme or the cytochrome P450RAI-2 enzyme.
摘要翻译: 本说明书中提供的式1至17的化合物具体地或选择性地抑制细胞色素P450RAI-1酶或细胞色素P450RAI-2酶。
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9.AROMATIC COMPOUNDS HAVING SPHINGOSINE-1-PHOSPHONATE (S1P) RECEPTOR ACTIVITY 失效
标题翻译: 具有丝氨酸1-磷酸(S1P)受体活性的芳香化合物公开(公告)号:US20130018019A1
公开(公告)日:2013-01-17
申请号:US13569243
申请日:2012-08-08
申请人: Janet A. Takeuchi , Ling Li , Xiaoxia Liu
发明人: Janet A. Takeuchi , Ling Li , Xiaoxia Liu
IPC分类号: A61K31/675 , A61K31/661 , A61P29/00 , A61P19/02 , A61P37/06 , A61P9/00 , A61P27/02 , A61P1/00 , A61P17/00 , A61P25/00 , A61K31/662 , A61P17/06
CPC分类号: C07F9/3808 , C07F9/5355 , C07F9/572 , C07F9/58 , C07F9/65583 , C07F9/65586
摘要: Novel aromatic compounds which are useful as sphingosine-1-phosphate modulators and useful for treating a wide variety of disorders associated with modulation of sphingosine-1-phosphate receptors.
摘要翻译: 可用作鞘氨醇-1-磷酸调节剂的新型芳族化合物,可用于治疗与调节鞘氨醇-1-磷酸受体相关的各种疾病。
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10.Aromatic compounds having sphingosine-1-phosphonate (S1P) receptor activity 失效
标题翻译: 具有鞘氨醇-1-膦酸酯(S1P)受体活性的芳族化合物公开(公告)号:US08513220B2
公开(公告)日:2013-08-20
申请号:US13569243
申请日:2012-08-08
申请人: Janet A. Takeuchi , Ling Li , Xiaoxia Liu
发明人: Janet A. Takeuchi , Ling Li , Xiaoxia Liu
IPC分类号: A61K31/675 , A61K31/661 , A61K31/662 , A61P1/00 , A61P9/00 , A61P17/00 , A61P17/06 , A61P19/02 , A61P25/00 , A61P27/02 , A61P29/00 , A61P37/06
CPC分类号: C07F9/3808 , C07F9/5355 , C07F9/572 , C07F9/58 , C07F9/65583 , C07F9/65586
摘要: Novel aromatic compounds which are useful as sphingosine-1-phosphate modulators and useful for treating a wide variety of disorders associated with modulation of sphingosine-1-phosphate receptors.
摘要翻译: 可用作鞘氨醇-1-磷酸调节剂的新型芳族化合物,可用于治疗与调节鞘氨醇-1-磷酸受体相关的各种疾病。
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