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公开(公告)号:EP2471803A1
公开(公告)日:2012-07-04
申请号:EP12161249.3
申请日:2003-09-05
申请人: Alchemia Limited
发明人: Meutermans, Wim , Schafer, Karl , West, Michael Leo , Muldoon, Craig , Foley, Fiona , Bouloc, Natalie , Tometzki, Gerald
IPC分类号: C07H17/02 , C07H17/08 , A61K31/7056 , A61K31/7076 , A61K31/4184 , A61P9/00 , A61P29/00 , A61K31/708
CPC分类号: C07H17/02 , A61K31/7056 , A61K31/7076 , A61K31/708 , C07H17/08
摘要: The present invention relates to a method of inhibiting or effecting the activity of protein kinase activity which comprises contacting a protein kinase with a compound of formula (I) being a derivate of a furanose or pyronase from of a monosaccharide, or a pharmaceutically acceptable salt thereof.
摘要翻译: 本发明涉及一种抑制或影响蛋白激酶活性活性的方法,该方法包括使蛋白激酶与由单糖或其药学上可接受的盐形成的呋喃糖或pyronase衍生物的式(I)化合物 。
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公开(公告)号:EP1549325A1
公开(公告)日:2005-07-06
申请号:EP03747740.3
申请日:2003-10-10
申请人: Alchemia Limited
发明人: MEUTERMANS, Wim , LE THANH, Giang , ABBENANTE, Giovani , TOMETZKI, Gerald , HALLIDAY, Judy , ZEUGG, Johannes
IPC分类号: A61K31/7008 , A61K31/70
CPC分类号: A61K31/7008 , A61K31/7034 , A61K31/7036 , A61K31/7052
摘要: A method of inhibiting or effecting the activity of a GPCR which comprises contacting a GPCR with a compound of general formula (I), or a pharmaceutically acceptable salt thereof General Formula (I).
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公开(公告)号:EP1487812A1
公开(公告)日:2004-12-22
申请号:EP03745223.2
申请日:2003-03-28
申请人: Alchemia Limited
发明人: MEUTERMANS, Wim , WEST, Michael, Leo , THANH LE, Giang , ADAMSON, George , SCHAFER, Karl , ABBENANTE, Giovani
IPC分类号: C07D307/20 , C07D307/22 , C07D307/24 , C07D309/08 , C07D309/10 , C07D309/14 , C07H5/04 , C07H7/02 , C07H7/04
CPC分类号: C07D405/12 , C07D309/14 , C07F7/1856 , C07H15/12
摘要: A compound of formula (I), wherein, n is 0 or 1; R6 and R7 are h ydrogen, or together form a carbonyl oxygen; R1 is selected from the group consisting of hydrogen; -N(Z)Y and -C(Z)Y wherein; When R1 is -N(Z)Y, then: Y is selected from hydrogen, or the following, where G denotes the point of connection to the nitrogen atom in N(Y)Z (i-v); Z is selected from hydrogen or X1; Q is selected from hydrogen or W; The groups W are independently selected from the group consisting of alkyl, alkenyl, alkynyl, heteroalkyl, aryl, heteroaryl, arylalkyl and heteroarylalkyl of 1 to 20 atoms , The groups X1 are independently selected from the group consisting of alkyl, alkenyl, alkynyl, heteroalkyl, acyl, arylacyl, heteroarylacyl, aryl, heteroaryl, arylalkyl and heteroarylalkyl of 1 to 20 atoms , When R1 is -C(Z)Y, then: Y is selected from the group consisting of two hydrogen atoms, a double bonded oxygen (=O) to form a carbonyl, and a triple bonded nitrogen to form a nitrile, Z is absent, or is selected from hydrogen or U, Wherein U is selected from the group consisting of alkyl, alkenyl, alkynyl, heteroalkyl, aminoalkyl, aminoaryl, aryloxy, alkoxy, heteroaryloxy, aminoaryl, aminoheteroaryl, thioalkyl, thioaryl or thioheteroaryl, acyl, arylacyl, heteroarylacyl, aryl, heteroaryl, arylalkyl and heteroarylalkyl of 1 to 20 atoms, . When R1 is H, at least two of the groups R2, R3, R4 and R5 are selected from the group consisting of -OX2 or -N(T)Y, and the others are independently selected from hydrogen, -OH, -OX2, -N(T)Y, wherein Y is as defined above, T is selected from hydrogen or X2; and X2 is independently selected from alkyl, alkenyl, alkynyl, heteroalkyl, aryl, heteroaryl, arylalkyl or heteroarylalkyl of 1 to 20 atoms, When R1 is N(Z)Y or C(Z)Y, at least one of the groups R2, R3, R4 and R5 are selected from the group consisting of -OX2 or -N(T)Y, and the others are independently selected from hydrogen, -OH, -OX2, -N(T)Y, wherein Y is as defined above, T is selected from hydrogen or X2; and X2 is independently selected from alkyl, alkenyl, alkynyl, heteroalkyl, aryl, heteroaryl, arylalkyl or heteroarylalkyl of 1 to 20 atoms.
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公开(公告)号:EP1440077A1
公开(公告)日:2004-07-28
申请号:EP02766941.5
申请日:2002-09-06
申请人: Alchemia Limited
发明人: SEIFERT, Joachim , SINGH, Latika , RAMSDALE, Tracie, Elizabeth , WEST, Michael, Leo , DRINNAN, Nicholas, Barry
IPC分类号: C07H3/02 , C07H3/04 , C07H3/06 , A61K31/702 , A61P7/02
CPC分类号: C07H9/00 , C07H3/06 , C07H5/04 , C07H7/033 , C07H11/00 , C07H13/04 , C07H13/08 , C07H15/10 , C07H15/18
摘要: Preparation of synthetic monosaccharides, disaccharides, trisaccharides, tetrasaccharides and pentasaccharides for use in the preparation of synthetic heparinoids.
摘要翻译: 制备用于制备合成类肝素的合成单糖,二糖,三糖,四糖和五糖。
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公开(公告)号:EP2471803B1
公开(公告)日:2013-11-27
申请号:EP12161249.3
申请日:2003-09-05
申请人: Alchemia Limited
发明人: Meutermans, Wim , Schafer, Karl , West, Michael Leo , Muldoon, Craig , Foley, Fiona , Bouloc, Natalie , Tometzki, Gerald
IPC分类号: C07H17/02 , C07H17/08 , A61K31/7056 , A61K31/7076 , A61K31/4184 , A61P9/00 , A61P29/00 , A61K31/708
CPC分类号: C07H17/02 , A61K31/7056 , A61K31/7076 , A61K31/708 , C07H17/08
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公开(公告)号:EP2557086A2
公开(公告)日:2013-02-13
申请号:EP12188642.8
申请日:2002-09-06
申请人: Alchemia Limited
发明人: Seifert, Joachim , Singh, Latika , Ramsdale, Tracie Elizabeth , West, Michael Leo , Drinnan, Nicholas Barry
IPC分类号: C07H3/02 , C07H3/04 , C07H3/06 , A61K31/702 , A61P7/02
CPC分类号: C07H9/00 , C07H3/06 , C07H5/04 , C07H7/033 , C07H11/00 , C07H13/04 , C07H13/08 , C07H15/10 , C07H15/18
摘要: Preparation of synthetic monosaccharides, disaccharides and trisaccharides for use in the preparation of synthetic heparinoids.
摘要翻译: 制备用于制备合成类肝素的合成单糖,二糖和三糖。
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公开(公告)号:EP1546167A1
公开(公告)日:2005-06-29
申请号:EP03793479.1
申请日:2003-09-05
申请人: Alchemia Limited
发明人: MEUTERMANS, Wim , SCHAFER, Karl , WEST, Michael, Leo , MULDOON, Craig , FOLEY, Fiona , BOULOC, Natalie , TOMETZKI, Gerald
IPC分类号: C07H17/02 , C07H17/08 , A61K31/7056 , A61K31/7076 , A61K31/4184 , A61P9/00 , A61P29/00
CPC分类号: C07H17/02 , A61K31/7056 , A61K31/7076 , A61K31/708 , C07H17/08
摘要: A method of inhibiting or effecting the activity of protein kinase activity which comprises contacting a protein kinase with a compound of formula (I) being a derivative of a furanose or pyranose form of a monosaccharide, or a pharmaceutically acceptable salt thereof.
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公开(公告)号:EP1539780A1
公开(公告)日:2005-06-15
申请号:EP03783843.0
申请日:2003-08-08
申请人: Alchemia Limited
发明人: WEST, Michael, Leo , ANDREWS, Peter , RAMSDALE, Tracie, Elizabeth , MEUTERMANS, Wim , THANH LE, Giang , CLARK, Chris , ABBENANTE, Giovani , LIU, Ligong
摘要: New compounds and methods for the preparation of combinatorial libraries of potentially biologically active compounds are based on monosaccharides of formula (I) being a derivative of a furanose or pyranose form of a monosaccharide.
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公开(公告)号:EP2545923A1
公开(公告)日:2013-01-16
申请号:EP12182570.7
申请日:2006-12-20
申请人: Alchemia Limited
发明人: Meutermans, Wim , McKeveney, Declan , Zuegg, Johannes , Premraj, Rajaratnam , Muldoon, Craig , Le Thanh, Giang
IPC分类号: A61K31/70 , A61K31/351 , A61K31/34 , A61P31/04 , C07D235/30 , C07D235/32 , C07D249/06
CPC分类号: A61K31/34 , A61K31/351 , A61K31/70 , C07D235/30 , C07D235/32 , C07D249/06 , Y02A50/473
摘要: The present invention relates to monosaccharide compounds of formula (I)
as described herein which are suitable for inhibiting bacterial growth.摘要翻译: 本发明涉及适用于抑制细菌生长的如本文所述的式(I)的单糖化合物。
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公开(公告)号:EP1962864A1
公开(公告)日:2008-09-03
申请号:EP06828045.2
申请日:2006-12-20
申请人: Alchemia Limited
发明人: MEUTERMANS, Wim , MCKEVENEY, Declan , ZUEGG, Johannes , PREMRAJ, Rajaratnam , MULDOON, Craig , LE THANH, Gaing
IPC分类号: A61K31/70 , A61K31/351 , A61K31/34 , A61P31/04
CPC分类号: A61K31/34 , A61K31/351 , A61K31/70 , C07D235/30 , C07D235/32 , C07D249/06 , Y02A50/473
摘要: The present invention relates to monosaccharide compounds of formula (I) as described herein which are suitable for inhibiting bacterial growth.
摘要翻译: 一方面,本发明提供了通过使细菌与有效量的如本文所述的式(1)的至少一种单糖化合物接触来抑制细菌生长的方法:
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