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公开(公告)号:US20090217579A1
公开(公告)日:2009-09-03
申请号:US11991022
申请日:2006-08-25
CPC分类号: A01H5/10 , C12N9/14 , C12N9/2414 , C12N9/2422 , C12N9/2425 , C12N9/2434 , C12N9/2451
摘要: The invention relates to a process for increasing the amount of enzymes in a grain by germinating the grain in conditions in which the grain is wounded. The invention also relates to hydrolases obtainable from grains for use in food processing and manufacturing industries, to the germination of grains such as barley and to isolation of enzymes from grains.
摘要翻译: 本发明涉及通过在谷物受伤的条件下发芽而增加谷粒中酶的量的方法。 本发明还涉及可从用于食品加工和制造工业的谷物获得的水解酶,对谷物如大麦的发芽和从谷物中分离酶。
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公开(公告)号:US07459448B2
公开(公告)日:2008-12-02
申请号:US11242413
申请日:2005-10-03
申请人: Christopher Blackburn , Christopher F. Claiborne , Courtney A. Cullis , Natalie A. Dales , Michael Patane , Matthew Stirling , Omar Stradella , Gabriel S. Weatherhead
发明人: Christopher Blackburn , Christopher F. Claiborne , Courtney A. Cullis , Natalie A. Dales , Michael Patane , Matthew Stirling , Omar Stradella , Gabriel S. Weatherhead
IPC分类号: C07D487/04 , A61K31/55
CPC分类号: C07D491/14 , C07D471/14 , C07D487/04 , C07D495/14
摘要: The present invention provides novel compounds useful as inhibitors of protein kinases. The invention also provides pharmaceutical compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various diseases.
摘要翻译: 本发明提供了可用作蛋白激酶抑制剂的新化合物。 本发明还提供包含本发明化合物的药物组合物和使用该组合物治疗各种疾病的方法。
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公开(公告)号:US20070293498A1
公开(公告)日:2007-12-20
申请号:US11878708
申请日:2007-07-26
IPC分类号: A61K31/40 , A61K31/166 , A61K31/4025 , A61K31/495 , A61P19/08 , A61P3/04 , C07D207/09 , C07D233/64 , C07D239/70 , C07D413/06 , C07D409/12 , C07D401/06 , C07D333/38 , C07D295/145 , C07D239/14 , C07D233/48 , C07C235/42 , A61P25/00 , A61K31/5375 , A61K31/4164 , A61K31/381
CPC分类号: C07C279/22 , C07C317/32 , C07C2601/02 , C07C2601/08 , C07C2601/14 , C07C2602/10 , C07D207/12 , C07D207/14 , C07D207/16 , C07D207/22 , C07D209/14 , C07D211/26 , C07D211/34 , C07D211/60 , C07D211/62 , C07D213/40 , C07D217/02 , C07D231/12 , C07D233/56 , C07D233/88 , C07D239/16 , C07D239/42 , C07D249/08 , C07D295/13 , C07D295/185 , C07D307/79 , C07D333/20 , C07D333/38 , C07D401/06 , C07D407/12 , C07D409/12 , C07D451/04 , C07D453/02 , C07D471/10
摘要: This invention provides compounds and methods for treating melanocortin receptor associated disorders, such as weight loss disorders including cachexia resulting from cancer and other chronic illnesses. The compounds are represented by formula I: wherein X is oxygen or sulfur; G is G1 or G2: L1, L2, L3 and Q are linker groups, and Rings A, B and C, and R1-R14 are described in the specification. The compounds are antagonists of melanocortin receptors.
摘要翻译: 本发明提供了用于治疗黑皮质素受体相关疾病的化合物和方法,例如包括由癌症和其它慢性疾病引起的恶病质的体重减轻障碍。 化合物由式I表示:其中X是氧或硫; G是G1或G2:L 1,L 2,L 3和Q是连接基,环A,B和C和 在说明书中描述了R 1〜R 14。 这些化合物是黑皮质素受体的拮抗剂。
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公开(公告)号:US07045532B2
公开(公告)日:2006-05-16
申请号:US09999781
申请日:2001-10-31
申请人: Susan L. Acton , Timothy D. Ocain , Alexandra E. Gould , Natalie A. Dales , Bing Guan , James A. Brown , Michael Patane , Vivek J. Kadambi , Michael Solomon , Alain Stricker-Krongrad
发明人: Susan L. Acton , Timothy D. Ocain , Alexandra E. Gould , Natalie A. Dales , Bing Guan , James A. Brown , Michael Patane , Vivek J. Kadambi , Michael Solomon , Alain Stricker-Krongrad
IPC分类号: A61K31/194 , A61K31/198 , A61K31/39 , A61K31/415 , A61K31/4172
CPC分类号: C07D231/12 , A61K31/00 , A61K31/195 , A61K31/196 , A61K31/341 , A61K31/36 , A61K31/381 , A61K31/40 , A61K31/4035 , A61K31/4164 , A61K31/42 , A61K31/421 , A61K31/422 , A61K31/426 , A61K31/433 , A61K31/44 , A61K31/4439 , C07B2200/07 , C07C229/16 , C07C229/24 , C07C229/26 , C07C229/36 , C07C271/20 , C07C275/24 , C07C323/52 , C07C323/58 , C07C2601/02 , C07C2601/14 , C07D209/20 , C07D213/55 , C07D233/64 , C07D235/16 , C07D249/08 , C07D261/08 , C07D277/06 , C07D277/30 , C07D277/40 , C07D277/42 , C07D333/24 , C07D405/06 , C07K16/40
摘要: ACE-2 inhibitors for the treatment of body weight and related disorders are disclosed. ACE-2 inhibitors include peptides and small molecules. Examples of small molecule ACE-2 inhibitors include compounds of formula (I): Z-Λ (I) Wherein Z is a zinc coordinating moiety and Λ is an amino-acid mimicking moiety, and pharmaceutically acceptabale salts thereof. Methods of using the inhibitors and pharmaceutical compositions containing the inhibitors to treat a body weight disorder, to decrease appetite, to increase muscle mass, to decrease body fat, to treat diabetes and to treat a state associated with altered lipid metabolism, are also described.
摘要翻译: 公开了用于治疗体重和相关疾病的ACE-2抑制剂。 ACE-2抑制剂包括肽和小分子。 小分子ACE-2抑制剂的实例包括式(I)的化合物:<?in-line-formula description =“In-line formula”end =“lead”?> Z-Lambda(I) formula description =“In-line Formulas”end =“tail”?>其中Z是锌配位部分,Lambda是氨基酸模拟部分及其药学上可接受的盐。 还描述了使用抑制剂和含有抑制剂的药物组合物治疗体重紊乱,降低食欲,增加肌肉量,降低体脂肪,治疗糖尿病和治疗与脂质代谢改变相关的状态的方法。
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公开(公告)号:US20090123987A1
公开(公告)日:2009-05-14
申请号:US11991059
申请日:2006-08-25
IPC分类号: C12N9/14
CPC分类号: C12Y302/01041 , C12N9/2451 , C12N9/2457
摘要: The invention relates to improved methods for extracting and purifying limit dextrinase enzymes from cells, in particular plant cells. The process of the invention includes heating a cell homogenate at 4O° C., in the presence of divalent cations thus increasing the specific activity of the limit dextrinase.
摘要翻译: 本发明涉及从细胞,特别是植物细胞中提取和纯化极限糊精酶的改进方法。 本发明的方法包括在二价阳离子存在下在40℃加热细胞匀浆,从而增加极限糊精酶的比活性。
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公开(公告)号:US20080269217A1
公开(公告)日:2008-10-30
申请号:US12149440
申请日:2008-05-01
申请人: Tricia J. Vos , Michael E. Solomon , Christopher F. Claiborne , Martin P. Maguire , Mingshi Dai , Michael Patane , Thoma H. Marsilje
发明人: Tricia J. Vos , Michael E. Solomon , Christopher F. Claiborne , Martin P. Maguire , Mingshi Dai , Michael Patane , Thoma H. Marsilje
IPC分类号: A61K31/5377 , A61K31/505 , C07D239/06 , A61K31/4184 , C07D235/02 , C07D233/24 , A61K31/4174 , C07D413/02
CPC分类号: C07D471/04 , A61K31/4164 , A61K31/4174 , A61K31/4184 , A61K31/505 , A61K31/5377 , C07C211/27 , C07C211/29 , C07C211/30 , C07C237/38 , C07C257/18 , C07C271/20 , C07C275/26 , C07D233/06 , C07D233/10 , C07D233/18 , C07D233/20 , C07D233/22 , C07D233/26 , C07D233/30 , C07D233/42 , C07D233/48 , C07D235/12 , C07D235/18 , C07D239/06 , C07D295/073 , C07D295/088 , C07D295/13 , C07D295/135 , C07D401/04 , C07D403/14 , C07D405/10 , C07D405/14 , C07D409/04 , C07D409/10 , C07D409/12 , C07D487/04 , C07D513/04
摘要: Provided are MC4-R binding compounds of the formula XVII: wherein L2 is a linker group, and P1, P2, P3, P4, Z1, Z2, Z3, Z4, Z5, t, s, and R are as described in the specification. Methods of using the compounds to treat MC4-R associated disorders, such as disorders associated with weight loss, are also provided.
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公开(公告)号:US07365070B2
公开(公告)日:2008-04-29
申请号:US10727997
申请日:2003-12-04
IPC分类号: A61K31/40 , A61K31/415 , A61K31/381 , A61K31/535 , A61K31/445 , C07D211/26 , C07D207/04 , C07D333/22 , C07D265/30 , C07D233/66 , C07D241/04 , C07D409/12 , C07D221/20
CPC分类号: C07C279/22 , C07C317/32 , C07C2601/02 , C07C2601/08 , C07C2601/14 , C07C2602/10 , C07D207/12 , C07D207/14 , C07D207/16 , C07D207/22 , C07D209/14 , C07D211/26 , C07D211/34 , C07D211/60 , C07D211/62 , C07D213/40 , C07D217/02 , C07D231/12 , C07D233/56 , C07D233/88 , C07D239/16 , C07D239/42 , C07D249/08 , C07D295/13 , C07D295/185 , C07D307/79 , C07D333/20 , C07D333/38 , C07D401/06 , C07D407/12 , C07D409/12 , C07D451/04 , C07D453/02 , C07D471/10
摘要: This invention provides compounds and methods for treating melanocortin receptor associated disorders, such as weight loss disorders including cachexia resulting from cancer and other chronic illnesses. The compounds are represented by formula I: wherein X is oxygen or sulfur; G is G1 or G2: L1, L2, L3 and Q are linker groups, and Rings A, B and C, and R1-R14 are described in the specification. The compounds are antagonists of melanocortin receptors.
摘要翻译: 本发明提供了用于治疗黑皮质素受体相关疾病的化合物和方法,例如包括由癌症和其它慢性疾病引起的恶病质的体重减轻障碍。 化合物由式I表示:其中X是氧或硫; G是G1或G2:L 1,L 2,L 3和Q是连接基,环A,B和C和 在说明书中描述了R 1〜R 14。 这些化合物是黑皮质素受体的拮抗剂。
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公开(公告)号:US20070031957A1
公开(公告)日:2007-02-08
申请号:US11544908
申请日:2006-10-05
申请人: Michael Patane
发明人: Michael Patane
IPC分类号: C12N9/16
CPC分类号: C12N9/16 , Y10S435/814
摘要: A process for purifying a phosphodiesterase 1 (PDE-1) from a cell including heating an extract of a cell formed from a solution including at least on divalent cation, to increase the specific activity of PDE-1 in the extract.
摘要翻译: 一种从细胞中纯化磷酸二酯酶1(PDE-1)的方法,包括加热由至少包含二价阳离子的溶液形成的细胞的提取物,以提高提取物中PDE-1的比活性。
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29.
公开(公告)号:US20050143372A1
公开(公告)日:2005-06-30
申请号:US10490223
申请日:2002-10-30
申请人: Shomir Ghosh , Michael Patane , Kenneth Carson , I-Cheng Chi , Qing Ye , Amy Elder , Tracy Jenkins
发明人: Shomir Ghosh , Michael Patane , Kenneth Carson , I-Cheng Chi , Qing Ye , Amy Elder , Tracy Jenkins
IPC分类号: A61K31/445 , A61K31/495 , A61K31/55 , C07D205/04 , C07D207/14 , C07D211/26 , C07D211/28 , C07D211/52 , C07D211/56 , C07D211/58 , C07D211/62 , C07D223/16 , C07D243/08 , C07D295/185 , C07D295/205 , C07D295/26 , C07D295/30 , C07D295/32 , C07D401/04 , C07D401/08 , C07D401/10 , C07D401/12 , C07D405/04 , C07D409/12 , C07D413/04 , C07D413/10 , C07D417/04 , C07D471/10 , C07D471/18 , C07D491/10 , C07D498/10
CPC分类号: C07D223/16 , C04B35/632 , C07D205/04 , C07D207/14 , C07D211/26 , C07D211/28 , C07D211/52 , C07D211/56 , C07D211/58 , C07D211/62 , C07D243/08 , C07D295/185 , C07D295/205 , C07D295/26 , C07D295/30 , C07D295/32 , C07D401/04 , C07D401/08 , C07D401/10 , C07D401/12 , C07D405/04 , C07D409/12 , C07D413/04 , C07D413/10 , C07D417/04 , C07D471/10 , C07D491/10
摘要: The invention relates to compounds having the formula (I). Preferred compounds are antagonists of C—C chemokine receptor 8. The invention also relates to a method for treating a subjected having an inflammatory disorder or viral disorder comprising administering to a subject in need thereof an effective amount of a compound of the invention.
摘要翻译: 本发明涉及具有式(I)的化合物。 优选的化合物是C-C趋化因子受体8的拮抗剂。本发明还涉及一种用于治疗患有炎性病症或病毒病症的受试者的方法,其包括向有需要的受试者施用有效量的本发明化合物。
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公开(公告)号:US07935694B2
公开(公告)日:2011-05-03
申请号:US12231661
申请日:2008-09-04
申请人: Christopher Blackburn , Christopher F. Claiborne , Courtney A. Cullis , Natalie A. Dales , Michael Patane , Matthew Stirling , Omar Stradella , Gabriel S. Weatherhead
发明人: Christopher Blackburn , Christopher F. Claiborne , Courtney A. Cullis , Natalie A. Dales , Michael Patane , Matthew Stirling , Omar Stradella , Gabriel S. Weatherhead
IPC分类号: A61P35/00
CPC分类号: C07D491/14 , C07D471/14 , C07D487/04 , C07D495/14
摘要: The present invention provides novel compounds useful as inhibitors of protein kinases. The invention also provides pharmaceutical compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various diseases.
摘要翻译: 本发明提供了可用作蛋白激酶抑制剂的新化合物。 本发明还提供包含本发明化合物的药物组合物和使用该组合物治疗各种疾病的方法。
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