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公开(公告)号:US20100234388A1
公开(公告)日:2010-09-16
申请号:US12303720
申请日:2007-06-08
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K31/4985 , C07D471/14 , A61P9/12 , A61P15/00 , C12N9/99
CPC分类号: C07D471/14 , C07B2200/05
摘要: Provided herein are substituted PDE5 inhibitors of Formula (1), and processes of preparation and pharmaceutical compositions thereof. Also provided are methods of their use for the treatment and/or management of hypertension, erectile dysfunction, and/or the inability to maintain improved erectile function. The compounds are deuterated tadalafil derivatives.
摘要翻译: 本文提供了式(1)的取代的PDE5抑制剂及其制备方法及其药物组合物。 还提供了它们用于治疗和/或治疗高血压,勃起功能障碍和/或不能维持改善的勃起功能的方法。 化合物是氘化的他达拉非衍生物。
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公开(公告)号:US20100144657A1
公开(公告)日:2010-06-10
申请号:US12633511
申请日:2009-12-08
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K31/445 , C07D211/44 , A61K31/7028 , A61K31/46 , A61P1/00
CPC分类号: C07D211/52
摘要: The present invention relates to new phenylpiperidine modulators of opioid μ-receptors, pharmaceutical compositions thereof, and methods of use thereof.
摘要翻译: 本发明涉及阿片样物质μ受体的新的苯基哌啶调节剂,其药物组合物及其使用方法。
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公开(公告)号:US20100137244A1
公开(公告)日:2010-06-03
申请号:US12373228
申请日:2007-07-12
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K31/695 , C07D309/10 , C07F7/02 , A61P3/00 , A61P9/00 , A61P25/16 , A61P25/28 , A61P35/00
CPC分类号: C07D309/30
摘要: Chemical syntheses and medical uses of novel modulators of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase and diastereomeric mixtures of isomers, individual diastereomers, pharmaceutically acceptable salts, solvates, or prodrugs thereof, the chemical synthesis thereof, and the medical use of such compounds for the treatment and/or management of hypercholesterolemia, dyslipidemia, coronary artery disease, atherosclerosis, metabolic syndrome, a hyperproliferative disease such as colorectal cancer, prostate cancer, and melanoma, a neurodegenerative disease such as cerebral ischemia, Alzheimer's disease, and Parkinson's disease are described.
摘要翻译: 3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶和异构体的非对映异构体混合物,其各自的非对映异构体,药学上可接受的盐,溶剂合物或前药的新型调节剂的化学合成和医学用途,其化学合成和 用于治疗和/或治疗高胆固醇血症,血脂异常,冠状动脉疾病,动脉粥样硬化,代谢综合征,过度增殖性疾病如结肠直肠癌,前列腺癌和黑素瘤的医学用途,神经变性疾病如脑缺血,阿尔茨海默病 ,帕金森氏病。
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公开(公告)号:US20100120861A1
公开(公告)日:2010-05-13
申请号:US12616848
申请日:2009-11-12
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K31/445 , C07D211/32 , A61P3/10
CPC分类号: C07D295/135
摘要: The present invention relates to new benzoic acid inhibitors of ATP-sensitive potassium channel activity, pharmaceutical compositions thereof, and methods of use thereof.
摘要翻译: 本发明涉及ATP敏感钾通道活性的新型苯甲酸抑制剂及其药物组合物及其使用方法。
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公开(公告)号:US20100119624A1
公开(公告)日:2010-05-13
申请号:US12561646
申请日:2009-09-17
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K33/00 , A61K31/554 , A61K31/55 , A61K31/5375 , A61K31/495 , C07D239/22 , A61P25/18 , A61P25/24
CPC分类号: A61K31/495 , A61K31/4375 , A61K31/5375 , A61K31/55 , A61K31/554 , A61K45/06 , C07D471/04 , A61K2300/00
摘要: The present invention relates to new benzisoxazole modulators of D2 receptors and/or 5-HT2A receptors, pharmaceutical compositions thereof, and methods of use thereof.
摘要翻译: 本发明涉及D2受体和/或5-HT2A受体的新的苯并异恶唑调节剂,其药物组合物及其使用方法。
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公开(公告)号:US20100076087A1
公开(公告)日:2010-03-25
申请号:US12422834
申请日:2009-04-13
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K31/137 , A61P25/24
CPC分类号: C07C217/74 , A61K31/137 , C07C2601/14
摘要: Disclosed herein are methods for the reduction of inter-patient variability of a drug, such as in one or more parameters including half-life (t1/2), maximum plasma concentration (Cmax), time at maximal plasma concentration (Tmax), area under the time-versus-concentration curve (AUC). Also provided are methods of reducing side effects associated with drugs.
摘要翻译: 本文公开了用于减少药物的患者间变异性的方法,例如在包括半衰期(t1 / 2),最大血浆浓度(Cmax),最大血浆浓度(Tmax)时间),面积 在时间 - 浓度曲线(AUC)下。 还提供减少与药物相关的副作用的方法。
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公开(公告)号:US20090258897A1
公开(公告)日:2009-10-15
申请号:US12082470
申请日:2008-04-11
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K31/437 , C07D471/04 , C07D211/94 , C07D221/00 , A61P1/04
CPC分类号: C07D471/04 , C07D213/61 , C07D213/89
摘要: Disclosed herein are substituted benzimidazole-based proton pump modulators of Formula I, processes of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
摘要翻译: 本文公开了式I的取代的基于苯并咪唑的质子泵调节剂,其制备方法,其药物组合物及其使用方法。
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公开(公告)号:US20090247628A1
公开(公告)日:2009-10-01
申请号:US12409420
申请日:2009-03-23
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K31/24 , C07C229/28 , C07C229/34
CPC分类号: C07C219/20 , C07B59/001 , C07C2601/14
摘要: Disclosed herein are substituted phenylcyclohexylglycolate-based muscarinic acetylcholine receptor modulators of Formula I, processes of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
摘要翻译: 本文公开了式I的取代苯基环己基乙醇酸酯基毒蕈碱性乙酰胆碱受体调节剂,其制备方法,其药物组合物及其使用方法。
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公开(公告)号:US20090209592A1
公开(公告)日:2009-08-20
申请号:US12413323
申请日:2009-03-27
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K31/4439 , C07D401/12 , A61P1/04 , A61P1/00
CPC分类号: C07D401/12
摘要: Chemical syntheses and medical uses of novel inhibitors of the gastric H+, K+-ATPase for the treatment and/or management of duodenal ulcers, heartburn, acid reflux, other conditions mediated by gastric acid secretion and/or psoriasis are described.
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公开(公告)号:US20090191183A1
公开(公告)日:2009-07-30
申请号:US12181929
申请日:2008-07-29
申请人: Thomas G. Gant , Sepehr Sarshar
发明人: Thomas G. Gant , Sepehr Sarshar
IPC分类号: A61K31/404 , C07D209/20 , A61K31/727 , A61K39/395 , A61K31/46 , A61K31/436 , A61K31/522 , A61K31/47 , A61K31/41 , A61K31/575
CPC分类号: C07D209/24
摘要: Disclosed herein are substituted indole cysteinyl leukotriene receptor modulators of Formula I, process of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
摘要翻译: 本文公开了式I的取代的吲哚半胱氨酰白三烯受体调节剂,其制备方法,其药物组合物及其使用方法。
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