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公开(公告)号:US20080255188A1
公开(公告)日:2008-10-16
申请号:US11995433
申请日:2006-07-11
申请人: Naresh Kumar , Mohammad Salman , Kirandeep Kaur , Anita Chugh , Sandeep Sinha
发明人: Naresh Kumar , Mohammad Salman , Kirandeep Kaur , Anita Chugh , Sandeep Sinha
IPC分类号: A61K31/472 , C07D217/26
CPC分类号: C07D471/08
摘要: This present invention generally relates to muscarinic receptor antagonists of Formula (I), which are useful, among other uses, for the treatment of various diseases of the respiratory, urinary and gastrointestinal systems mediated through muscarinic receptors. The invention also relates to the process for the preparation of disclosed compounds, pharmaceutical compositions containing the disclosed compounds, and the methods for treating diseases mediated through muscarinic receptors.
摘要翻译: 本发明一般涉及式(I)的毒蕈碱受体拮抗剂,其可用于治疗通过毒蕈碱受体介导的呼吸,泌尿和胃肠系统的各种疾病。 本发明还涉及制备所公开的化合物的方法,含有所公开的化合物的药物组合物,以及用于治疗通过毒蕈碱受体介导的疾病的方法。
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公开(公告)号:US20080207536A1
公开(公告)日:2008-08-28
申请号:US11572754
申请日:2005-07-13
申请人: Biswajit Das , Rita Katoch , Atul Kashinath Hajare , Gobind Singh Kapkoti , Anish Bandyopadhyay , Ramadass Venkataramanan , Rajesh Kumar , Santosh Haribhau Kurhade , Sujata Rathy , Anjan Chakrabarti , Yogesh Baban Surase , Mohammad Salman , Ashok Rattan
发明人: Biswajit Das , Rita Katoch , Atul Kashinath Hajare , Gobind Singh Kapkoti , Anish Bandyopadhyay , Ramadass Venkataramanan , Rajesh Kumar , Santosh Haribhau Kurhade , Sujata Rathy , Anjan Chakrabarti , Yogesh Baban Surase , Mohammad Salman , Ashok Rattan
IPC分类号: A61K31/7048 , C07H17/08 , A61P31/04
CPC分类号: C07H17/08
摘要: The present invention provides acylide derivatives, which can be used as antibacterial agents. Compounds disclosed herein can be used for the treatment or prevention of a condition caused by or contributed to by Gram-positive, Gram-negative or anaerobic bacteria, more particularly against bacterium such as Staphylococci, Streptococci, Enterococci, Haemophilus, Moraxalla spp., Chlamydia spp., Mycoplasm, Legionella spp., Myobacterium, Helicobacter, Clostridium, Bacteroides, Corynebacterium, Baccillus or Enterobactericeae. Processes for the preparation of disclosed compounds, pharmaceutical compositions thereof, and method of treating bacterial infections, are also provided.
摘要翻译: 本发明提供可用作抗菌剂的酰化物衍生物。 本文公开的化合物可用于治疗或预防由革兰氏阳性,革兰氏阴性或厌氧细菌引起的或由其贡献的病症,特别是针对细菌如葡萄球菌,链球菌,肠球菌,嗜血杆菌,莫萨拉氏菌,衣原体 肉豆蔻,军团菌属,Myobacterium,Helicobacter,Clostridium,拟杆菌属,棒状杆菌属,Baccillus或肠杆菌属。 还提供了制备所公开的化合物的方法,其药物组合物和治疗细菌感染的方法。
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公开(公告)号:US20080188470A1
公开(公告)日:2008-08-07
申请号:US11911576
申请日:2006-04-12
申请人: Biswajit Das , Sonali Rudra , Sangita Sangita , Mohammad Salman , Ashok Rattan
发明人: Biswajit Das , Sonali Rudra , Sangita Sangita , Mohammad Salman , Ashok Rattan
IPC分类号: A61K31/5383 , C07D498/04 , A61P31/04
CPC分类号: Y02A50/478 , Y02P20/55
摘要: Provided herein are novel substituted phenyl oxazolidinones and to processes for the synthesis thereof. Also provided are pharmaceutical compositions comprising one or more compounds described herein The compounds described can be useful antimicrobial agents, which can be effective against a number of human and veterinary pathogens, including gram-positive aerobic bacteria such as multiple-resistant staphylococci, streptococci and enterococci, as well as, anaerobic organisms, such as Bacterioides spp. and Clostridia spp. species, and acid fast organisms, such as Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp.
摘要翻译: 本文提供了新的取代的苯基恶唑烷酮,以及其合成方法。 还提供了包含本文所述的一种或多种化合物的药物组合物。所述化合物可以是有用的抗微生物剂,其可以对许多人和兽医病原体有效,包括革兰氏阳性好氧细菌如多重耐药性葡萄球菌,链球菌和肠球菌 ,以及厌氧生物,如细菌属。 和梭菌属(Clostridia spp。) 物种和酸性快速生物,如结核分枝杆菌,鸟分枝杆菌和分枝杆菌。
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公开(公告)号:US20080114031A1
公开(公告)日:2008-05-15
申请号:US11692362
申请日:2007-03-28
申请人: Viswajanani Sattigeri , Sudershan Arora , Mohammad Salman , Venkata Palle , Ashis Mukherji , Ashwani Verna , Sanjay Malhotra , Sankaranarayanan Dharmarajan , Abhijit Ray , Raj Shirumalla
发明人: Viswajanani Sattigeri , Sudershan Arora , Mohammad Salman , Venkata Palle , Ashis Mukherji , Ashwani Verna , Sanjay Malhotra , Sankaranarayanan Dharmarajan , Abhijit Ray , Raj Shirumalla
IPC分类号: A61K31/4525 , A61K31/34 , A61P17/00 , A61P29/00 , A61P3/10 , A61P35/00 , A61P37/00 , A61P9/00 , C07D307/20 , C07D405/02 , C07D405/14 , C07D413/02
摘要: The present invention relates to monosaccharide derivatives as anti-inflammatory agents. The compounds disorder herein can be useful for inhibition and prevention of inflammation and associated pathologies including inflammatory and autoimmune diseases such as bronchial asthma, rheumatoid arthritis, type I diabetes, multiple sclerosis, allograft rejection, psoriasis, inflammatory bowel disease, Ulcerative colitis, acne, atherosclerosis, cancer, pruritis and allergic rhinitis. Pharmacological compositions containing compounds disclosed herein and the methods of treating bronchial asthma, chronic obstructive pulmonary disease, rheumatoid arthritis, multiple sclerosis, type I diabetes, psoriasis, allograft rejection, inflammatory bowel disease, Ulcerative colitis, acne, atherosclerosis, cancer, pruritis, allergic rhinitis and other inflammatory and/or autoimmune disorders, using the compounds are also provided.
摘要翻译: 本发明涉及作为抗炎剂的单糖衍生物。 本文中的化合物障碍可用于抑制和预防炎症和相关病理,包括炎症和自身免疫性疾病,例如支气管哮喘,类风湿性关节炎,I型糖尿病,多发性硬化,同种异体移植排斥,牛皮癣,炎性肠病,溃疡性结肠炎,痤疮, 动脉粥样硬化,癌症,瘙痒和过敏性鼻炎。 包含本文公开的化合物的药理学组合物和治疗支气管哮喘,慢性阻塞性肺病,类风湿性关节炎,多发性硬化,I型糖尿病,牛皮癣,同种异体移植物排斥反应,炎症性肠病,溃疡性结肠炎,痤疮,动脉粥样硬化,癌症,瘙痒,过敏性 还提供使用该化合物的鼻炎和其它炎性和/或自身免疫性疾病。
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公开(公告)号:US20070021487A1
公开(公告)日:2007-01-25
申请号:US10552503
申请日:2004-01-06
IPC分类号: A61K31/403 , C07D209/02
CPC分类号: C07D209/52 , C07D403/06
摘要: This invention generally relates to muscarinic receptor antagonists of formula (I) which are useful, among other uses, for the treatment of various diseases of the respiratory, urinary and gastrointestinal systems mediated through muscarinic receptors. Specifically, the invention relates to derivatives of azabicyclo compounds, including, for example, 6-substituted azabicyclo[3.1.0]hexanes, as well as pharmaceutical compositions containing such compounds and methods of treating diseases mediated through muscarinic receptors.
摘要翻译: 本发明一般涉及式(I)的毒蕈碱受体拮抗剂,其可用于治疗通过毒蕈碱受体介导的呼吸,尿和胃肠道系统的各种疾病。 具体地,本发明涉及氮杂二环化合物的衍生物,包括例如6-取代的氮杂双环[3.1.0]己烷,以及含有这些化合物的药物组合物和治疗通过毒蕈碱受体介导的疾病的方法。
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公开(公告)号:US20060241114A1
公开(公告)日:2006-10-26
申请号:US10546462
申请日:2003-02-20
申请人: Jasbir Arora , Nidhi Gupta , Mohammad Salman , Jang Gupta , Upendra Pandit
发明人: Jasbir Arora , Nidhi Gupta , Mohammad Salman , Jang Gupta , Upendra Pandit
IPC分类号: A61K31/53 , A61K31/454 , C07D403/02
CPC分类号: C07D401/06 , C07D211/46 , C07D211/76 , C07D401/12 , C07D409/12
摘要: Certain derivatives of azasugars, useful in the treatment of cancer, are presented. This invention also relates to pharmacological compositions containing the compounds of present invention and treatment of cancer, including tumor or other neoplasm, with an azasugar.
摘要翻译: 介绍了可用于治疗癌症的某些衍生物,如氮杂酮。 本发明还涉及含有本发明化合物的药理学组合物,以及用氮杂十四烷治疗癌症,包括肿瘤或其他肿瘤。
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公开(公告)号:US20060111425A1
公开(公告)日:2006-05-25
申请号:US10520572
申请日:2003-04-11
申请人: Mohammad Salman , Anita Mehta , Pakala Kumara Sarma , Shankar Shetty , Sankaranarayanan Dharmarajan , Naresh Kumar , Arundutt Silamkoti , Anita Chugh
发明人: Mohammad Salman , Anita Mehta , Pakala Kumara Sarma , Shankar Shetty , Sankaranarayanan Dharmarajan , Naresh Kumar , Arundutt Silamkoti , Anita Chugh
IPC分类号: A61K31/403 , C07D403/02 , C07D209/02
CPC分类号: C07D401/12 , C07D209/52 , C07D403/12 , C07D413/12 , C07D417/12
摘要: This invention generally relates to muscarinic receptor antagonists which are useful, among other uses, for the treatment of various diseases of the respiratory, urinary and gastrointestinal systems mediated through muscarinic receptors. Specifically, the invention relates to derivatives of azabicyclo compounds, including, for example, 6-substituted azabicyclo[3.1.0] hexanes, and 2,4,6-trisubstituted derivatives. The invention also relates to pharmaceutical compositions containing the compounds and the methods of treating the diseases mediated through muscarinic receptors.
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公开(公告)号:US20050107614A1
公开(公告)日:2005-05-19
申请号:US10490275
申请日:2002-09-24
申请人: Purna Ray , Jayachandra Babu , Mohammad Salman
发明人: Purna Ray , Jayachandra Babu , Mohammad Salman
IPC分类号: C07D295/12 , A61P3/10 , C07D295/135 , C07D211/32
CPC分类号: C07D295/135
摘要: The present invention relates to a cost effective and industrially advantageous process for the preparation of repaglinide.
摘要翻译: 本发明涉及用于制备瑞格列奈的成本效益和工业上有利的方法。
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公开(公告)号:US06441226B1
公开(公告)日:2002-08-27
申请号:US09467201
申请日:1999-12-20
IPC分类号: C07C6116
CPC分类号: C07C403/20 , C07C51/09 , C07C51/353 , C07C2601/16 , C07D309/32 , C07C57/26
摘要: The present invention relates to a process for the preparation of 13-cis isomer of Vitamin A acid, commonly known as isotretinoin, in a single step.
摘要翻译: 本发明涉及在单一步骤中制备维生素A酸(通常称为异维A酸)的13-顺式异构体的方法。
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