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公开(公告)号:US07345144B2
公开(公告)日:2008-03-18
申请号:US11174851
申请日:2005-07-05
CPC分类号: A61K38/12 , C07K5/0821 , C07K5/1024 , C07K7/06 , C07K7/56 , C07K7/60 , Y10S436/811
摘要: A highly selective melanocortin-4 receptor antagonist cyclic hexapeptide of the formula where R1, R2, R3a, R3b, R4, R5, x, y and z are as defined in the specification, and a method of treating body weight disorders, including cachexia, sarcopenia and wasting syndrome or disease, and treating inflammation and immune disorders.
摘要翻译: 具有下式的高选择性黑皮质素-4受体拮抗剂环状六肽其中R 1,R 2,R 3a,R 3b, R 3,R 5,R 5,x,y和z如说明书中所定义,以及治疗体重紊乱的方法,包括恶病质,肌肉减少症和 浪费综合征或疾病,以及治疗炎症和免疫疾病。
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公开(公告)号:US07718802B2
公开(公告)日:2010-05-18
申请号:US11099814
申请日:2005-04-05
申请人: Shubh D. Sharma , Yi-Qun Shi , Ramesh Rajpurohit , Zhijun Wu
发明人: Shubh D. Sharma , Yi-Qun Shi , Ramesh Rajpurohit , Zhijun Wu
IPC分类号: C07D241/04 , C07D403/06 , C07D295/023
CPC分类号: C07D241/04 , C07D403/06
摘要: Melanocortin receptor-specific compounds of the general formulas and pharmaceutically acceptable salts thereof, where J is a substituted or unsubstituted monocyclic or bicyclic ring structure, L is a linker, W is a heteroatom unit with at least one cationic center, hydrogen bond donor or hydrogen bond acceptor, Q includes a substituted or unsubstituted aromatic carbocyclic ring, R6, R7, y and z are as defined in the specification, and the carbon atom marked with an asterisk can have any stereochemical configuration, and optionally with one or two additional ring substituents as defined, which compounds bind to one or more melanocortin receptors and are optionally an agonist, a partial agonist, an antagonist, an inverse agonist or an antagonist of an inverse agonist, and may be employed for treatment of one or more melanocortin receptor-associated conditions or disorders, and methods for the use of the compounds of the invention.
摘要翻译: 其中J为取代或未取代的单环或双环结构的黑皮质素受体特异性化合物及其药学上可接受的盐,L为连接基,W为至少一个阳离子中心,氢键供体或氢的杂原子单元 键接受体,Q包括取代或未取代的芳族碳环,R6,R7,y和z如说明书中所定义,并且具有星号的碳原子可以具有任何立体化学构型,并且任选具有一个或两个另外的环取代基 定义为哪些化合物结合一种或多种黑皮质素受体,并且任选地是激动剂,部分激动剂,拮抗剂,反向激动剂的反向激动剂或拮抗剂,并且可用于治疗一种或多种黑皮质素受体相关 条件或障碍,以及使用本发明化合物的方法。
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公开(公告)号:US07601753B2
公开(公告)日:2009-10-13
申请号:US11680932
申请日:2007-03-01
申请人: Shubh D. Sharma , Yi-Qun Shi , Zhijun Wu , Ramesh Rajpurohit
发明人: Shubh D. Sharma , Yi-Qun Shi , Zhijun Wu , Ramesh Rajpurohit
IPC分类号: A61K31/40 , C07D207/04
CPC分类号: C07D487/04 , A61K38/12 , C07D207/16 , C07D241/04 , C07D241/08 , C07D317/72 , C07D401/12 , C07D403/06 , C07D403/12 , C07D417/12 , C07K5/0202 , C07K5/021 , C07K5/06078 , C07K5/06191 , C07K5/081 , C07K5/0821 , C07K5/0823 , C07K5/0827 , C07K5/1008 , C07K5/101 , G06F19/16 , G06F19/706
摘要: Melanocortin receptor-specific pyrrolidine compounds having the structure: and stereoisomer and pharmaceutically acceptable salts thereof, where R1, R2, and R3 are as described in the specification, preferably where R3 is a D-amino acid with at least one substituted or unsubstituted phenyl or naphthyl aromatic ring, and where R3 optionally further includes an amine capping group or from one to three additional amino acid residues, optionally with an amine capping group, which compounds are agonists, antagonists or mixed agonists and antagonists at one or more melanocortin receptors, and having utility in the treatment of melanocortin receptor-related disorders and conditions. Methods of synthesis of compounds of structure (I), pharmaceutical compositions containing a compound of structure (I) and methods relating to the use thereof are also disclosed.
摘要翻译: 具有以下结构的黑皮质素受体特异性吡咯烷化合物及其立体异构体和药学上可接受的盐,其中R 1,R 2和R 3如说明书中所述,优选其中R 3是具有至少一个取代或未取代的苯基的D-氨基酸或 并且其中R 3任选地进一步包括胺封端基团或一至三个另外的氨基酸残基,任选地具有胺封端基团,所述化合物是一种或多种黑皮质素受体的激动剂,拮抗剂或混合激动剂和拮抗剂,以及 可用于治疗黑皮质素受体相关疾病和病症。 还公开了结构(I)化合物的合成方法,含有结构(I)化合物的药物组合物及其使用方法。
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公开(公告)号:US07342089B2
公开(公告)日:2008-03-11
申请号:US11174845
申请日:2005-07-05
CPC分类号: C07K7/06 , A61K38/12 , C07K5/0821 , C07K5/1024 , C07K7/60 , Y10S436/811
摘要: A highly selective melanocortin-4 receptor antagonist cyclic peptide of the formula where R1, R2, R3, R4a, R4b, R5, R6, R7, x, y and z are as defined in the specification, and a method of treating body weight disorders, including cachexia, sarcopenia and wasting syndrome or disease, and treating inflammation and immune disorders.
摘要翻译: 下式的高选择性黑皮质素-4受体拮抗剂环肽其中R 1,R 2,R 3,R 4a, R 4b,R 5,R 6,R 7,x,y和z分别为 如本说明书中所定义的,以及治疗体重障碍(包括恶病质,肌营养不良和消瘦综合征或疾病)以及治疗炎症和免疫疾病的方法。
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公开(公告)号:US07964601B2
公开(公告)日:2011-06-21
申请号:US12131822
申请日:2008-06-02
申请人: Shubh D. Sharma , Yi-Qun Shi , Ramesh Rajpurohit , Zhijun Wu , Papireddy Purma , Annette M. Shadiack , Kevin D. Burris
发明人: Shubh D. Sharma , Yi-Qun Shi , Ramesh Rajpurohit , Zhijun Wu , Papireddy Purma , Annette M. Shadiack , Kevin D. Burris
IPC分类号: A61K31/497 , C07D403/06 , C07D241/04 , C07D241/06
CPC分类号: C07D403/10 , C07D241/04 , C07D403/06
摘要: A melanocortin receptor-specific compound of the general formula of structure I: where X, R1, R2a, R2b, R3, R4a, R4b, R5a and R5b are as defined in the specification, which compound binds with high affinity to one or more melanocortin receptors and is optionally an agonist, an antagonist, an inverse agonist or an antagonist of an inverse agonist, and may be employed for treatment of one or melanocortin receptor-associated conditions or disorders, and methods for the use of the compounds of the invention.
摘要翻译: 结构I通式的黑皮质素受体特异性化合物:其中X,R1,R2a,R2b,R3,R4a,R4b,R5a和R5b如本说明书中所定义,该化合物以高亲和力结合一种或多种黑皮质素 受体,并且任选地是激动剂,拮抗剂,反向激动剂的反向激动剂或拮抗剂,并且可以用于治疗一种或黑皮质素受体相关病症或病症,以及使用本发明化合物的方法。
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公开(公告)号:US07456184B2
公开(公告)日:2008-11-25
申请号:US10837519
申请日:2004-04-30
申请人: Shubh D. Sharma , Yi-Qun Shi , Zhijun Wu , Ramesh Rajpurohit , Annette M. Shadiack , Papireddy Purma , Kevin D. Burris
发明人: Shubh D. Sharma , Yi-Qun Shi , Zhijun Wu , Ramesh Rajpurohit , Annette M. Shadiack , Papireddy Purma , Kevin D. Burris
IPC分类号: A61K31/497 , C07D403/02
CPC分类号: C07D403/10 , C07D241/04 , C07D403/06
摘要: A melanocortin receptor-specific compound of the general formula of structure I: where X, R1, R2a, R2b, R3, R4a, R4b, R5a and R5b are as defined in the specification, which compound binds with high affinity to one or more melanocortin receptors and is optionally an agonist, an antagonist, an inverse agonist or an antagonist of an inverse agonist, and may be employed for treatment of one or melanocortin receptor-associated conditions or disorders, and methods for the use of the compounds of the invention.
摘要翻译: 结构I的通式的黑皮质素受体特异性化合物:其中X,R 1,R 2a,R 2b,R SUB R 3,R 4a,R 4b,R 5a和R 5b如本文所定义。 说明书,该化合物以高亲和力结合一种或多种黑皮质素受体,并且任选地是反向激动剂的激动剂,拮抗剂,反向激动剂或拮抗剂,并且可用于治疗一种或黑皮质素受体相关病症或 病症和使用本发明化合物的方法。
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公开(公告)号:US20080234289A1
公开(公告)日:2008-09-25
申请号:US12131822
申请日:2008-06-02
申请人: Shubh D. Sharma , Yi-Qun Shi , Ramesh Rajpurohit , Zhijun Wu , Papireddy Purma , Annette M. Shadiack , Kevin D. Burris
发明人: Shubh D. Sharma , Yi-Qun Shi , Ramesh Rajpurohit , Zhijun Wu , Papireddy Purma , Annette M. Shadiack , Kevin D. Burris
IPC分类号: A61K31/495 , C07D241/04 , A61K31/496 , A61P3/04 , C07D403/06
CPC分类号: C07D403/10 , C07D241/04 , C07D403/06
摘要: A melanocortin receptor-specific compound of the general formula of structure I: where X, R1, R2a, R2b, R3, R4a, R4b, R5a and R5b are as defined in the specification, which compound binds with high affinity to one or more melanocortin receptors and is optionally an agonist, an antagonist, an inverse agonist or an antagonist of an inverse agonist, and may be employed for treatment of one or melanocortin receptor-associated conditions or disorders, and methods for the use of the compounds of the invention.
摘要翻译: 结构I的通式的黑皮质素受体特异性化合物:其中X,R 1,R 2a,R 2b,R SUB R 3,R 4a,R 4b,R 5a和R 5b如本文所定义。 说明书,该化合物以高亲和力结合一种或多种黑皮质素受体,并且任选地是反向激动剂的激动剂,拮抗剂,反向激动剂或拮抗剂,并且可用于治疗一种或黑皮质素受体相关病症或 病症和使用本发明化合物的方法。
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公开(公告)号:US07189755B2
公开(公告)日:2007-03-13
申请号:US10776657
申请日:2004-02-10
申请人: Shubh D. Sharma , Yi-Qun Shi , Zhijun Wu , Ramesh Rajpurohit
发明人: Shubh D. Sharma , Yi-Qun Shi , Zhijun Wu , Ramesh Rajpurohit
IPC分类号: A61K31/4025 , C07D207/04
CPC分类号: C07D487/04 , A61K38/12 , C07D207/16 , C07D241/04 , C07D241/08 , C07D317/72 , C07D401/12 , C07D403/06 , C07D403/12 , C07D417/12 , C07K5/0202 , C07K5/021 , C07K5/06078 , C07K5/06191 , C07K5/081 , C07K5/0821 , C07K5/0823 , C07K5/0827 , C07K5/1008 , C07K5/101 , G06F19/16 , G06F19/706
摘要: Melanocortin receptor-specific pyrrolidine compounds having the structure: and stereoisomer and pharmaceutically acceptable salts thereof, where R1, R2, and R3 are as described in the specification, preferably where R3 is a D-amino acid with at least one substituted or unsubstituted phenyl or naphthyl aromatic ring, and where R3 optionally further includes an amine capping group or from one to three additional amino acid residues, optionally with an amine capping group, which compounds are agonists, antagonists or mixed agonists and antagonists at one or more melanocortin receptors, and having utility in the treatment of melanocortin receptor-related disorders and conditions. Methods of synthesis of compounds of structure (I), pharmaceutical compositions containing a compound of structure (I) and methods relating to the use thereof are also disclosed.
摘要翻译: 具有以下结构的黑皮质素受体特异性吡咯烷化合物及其立体异构体和药学上可接受的盐,其中R 1,R 2和R 3是 如说明书中所述,优选其中R 3是具有至少一个取代或未取代的苯基或萘基芳环的D-氨基酸,并且其中R 3'任选地进一步包括 胺封端基团或一至三个另外的氨基酸残基,任选具有胺封端基团,该化合物是一种或多种黑皮质素受体的激动剂,拮抗剂或混合激动剂和拮抗剂,并且可用于治疗黑皮质素受体相关 疾病和病症。 还公开了结构(I)化合物的合成方法,含有结构(I)化合物的药物组合物及其使用方法。
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公开(公告)号:US07417027B2
公开(公告)日:2008-08-26
申请号:US10756212
申请日:2004-01-12
CPC分类号: C07K7/06 , A61K38/00 , C07K5/1008 , C07K5/1013 , C07K5/1027 , C07K7/56 , C07K14/68
摘要: Linear and cyclic peptides are provided specific to one or melanocortin receptors, and which exhibit agonist, antagonist, or mixed agonist-antagonist activity. In one embodiment, a linear peptide of the following general formula is provided:
摘要翻译: 线性和环肽提供特异于一种或黑皮质素受体,并且其表现出激动剂,拮抗剂或混合的激动剂 - 拮抗剂活性。 在一个实施方案中,提供以下通式的线性肽:
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公开(公告)号:US07795378B2
公开(公告)日:2010-09-14
申请号:US11031898
申请日:2005-01-07
CPC分类号: C07K5/0827 , A61K38/00 , C07K5/0806 , C07K5/081 , C07K5/1024
摘要: A peptide of the structural formula: or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5, R6, m and n are as defined. Further provided are methods for treatment of sexual dysfunction, including erectile dysfunction and female sexual dysfunction, and combination drugs and method of use thereof, including a peptide of the invention and one or more second sexual dysfunction pharmaceutical agents.
摘要翻译: 结构式的肽或其药学上可接受的盐,其中R 1,R 2,R 3,R 4,R 5,R 6,m和n如上所定义。 还提供了治疗性功能障碍的方法,包括勃起功能障碍和女性性功能障碍,以及联合药物及其使用方法,包括本发明的肽和一种或多种第二性功能障碍药剂。
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