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1. 发明申请

WO2007054139A2 STYRYLSULFONAMIDES, THEIR MANUFACTURE AND USE AS PHARMACEUTICAL AGENTS 审中-公开
标题翻译：酪氨酸聚糖，其制造和用作药物代理
公开(公告)号：WO2007054139A2
公开(公告)日：2007-05-18
申请号：PCT/EP2006/004756
申请日：2006-05-19
申请人： F. HOFFMANN-LA ROCHE AG , BOYD, Edward , BROOKFIELD, Frederick , GRIDLEY, Jonathan , KOERNER, Matthias , KUBBIES, Manfred , LAU, Raymond , REIFF, Ulrike , TIEFENTHALER, Georg , VON DER SAAL, Wolfgang , WOODCOCK, Timothy
发明人： BOYD, Edward , BROOKFIELD, Frederick , GRIDLEY, Jonathan , KOERNER, Matthias , KUBBIES, Manfred , LAU, Raymond , REIFF, Ulrike , TIEFENTHALER, Georg , VON DER SAAL, Wolfgang , WOODCOCK, Timothy
IPC分类号： C07C311/51 , C07C303/40 , A61K31/18
CPC分类号： C07C311/51
摘要： Objects of the present invention are the compounds of formula (I) Their pharmaceutically acceptable salts, enantiomeric forms, diastereoisomers and racemates, the preparation of the above compounds, medicaments containing them and their manufacture, as well as the use of the above compounds in the control or prevention of illnesses such as cancer.
摘要翻译：本发明的目的是式（I）的化合物：其药学上可接受的盐，对映体形式，非对映异构体和外消旋体，上述化合物的制备，含有它们的药物及其制备，以及上述化合物在控制或预防癌症等疾病。

2. 发明申请

WO2007006459A1 HETEROARYLETHENYL DERIVATIVES, THEIR MANUFACTURE AND USE AS PHARMACEUTICAL AGENTS 审中-公开
标题翻译：异丙肾上腺素衍生物，其制造和用作药物代理
公开(公告)号：WO2007006459A1
公开(公告)日：2007-01-18
申请号：PCT/EP2006/006523
申请日：2006-07-05
申请人： F.HOFFMANN-LA ROCHE AG , BOYD, Edward , BROOKFIELD, Frederick , GRIDLEY, Jonathan , KUBBIES, Manfred , LAU, Raymond , REIFF, Ulrike , TIEFENTHALER, Georg , VON DER SAAL, Wolfgang , VON HIRSCHHEYDT, Thomas , WOODCOCK, Timothy
发明人： BOYD, Edward , BROOKFIELD, Frederick , GRIDLEY, Jonathan , KUBBIES, Manfred , LAU, Raymond , REIFF, Ulrike , TIEFENTHALER, Georg , VON DER SAAL, Wolfgang , VON HIRSCHHEYDT, Thomas , WOODCOCK, Timothy
IPC分类号： C07D333/24 , C07D213/59 , A61K31/38 , A61P35/00 , A61K31/44
CPC分类号： A61K31/38 , A61K31/381 , A61K31/44 , C07D213/59 , C07D333/24
摘要： Objects of the present invention are the compounds of formula (I) their pharmaceutically acceptable salts, enantiomeric forms, diastereoisomers and racemates, the preparation of the above compounds, pharmaceutical compositions containing them and their manufacture, as well as the use of the above compounds in the control or prevention of illnesses such as cancer.
摘要翻译：本发明的目的是式（I）化合物的药学上可接受的盐，对映体形式，非对映异构体和外消旋体，上述化合物的制备，含有它们的药物组合物及其制备方法，以及上述化合物在控制或预防癌症等疾病。

3. 发明申请

WO2007014707A1 HETEROCYCLIC BENZYLAMINO DERIVATIVES, THEIR MANUFACTURE AND USE AS PHARMACEUTICAL AGENTS 审中-公开
标题翻译：杂环烷基苯胺衍生物及其制备和用作药物代理
公开(公告)号：WO2007014707A1
公开(公告)日：2007-02-08
申请号：PCT/EP2006/007479
申请日：2006-07-28
申请人： F. HOFFMANN-LA ROCHE AG , BOYD, Edward , BROOKFIELD, Frederick , GRIDLEY, Jonathan , HONOLD, Konrad , LAU, Raymond , SCHEIBLICH, Stefan
发明人： BOYD, Edward , BROOKFIELD, Frederick , GRIDLEY, Jonathan , HONOLD, Konrad , LAU, Raymond , SCHEIBLICH, Stefan
IPC分类号： C07D471/04 , A61K31/437 , A61P35/00
CPC分类号： C07D471/04
摘要： Objects of the present invention are the compounds of formula (I) their pharmaceutically acceptable salts, enantiomeric forms, diastereoisomers and racemates, the preparation of the above-mentioned compounds, pharmaceutical compositions containing them and their manufacture, as well as the use of the above-mentioned compounds in the control or prevention of illnesses such as cancer.
摘要翻译：本发明的目的是式（I）化合物的药学上可接受的盐，对映体形式，非对映异构体和外消旋体，上述化合物的制备，含有它们的药物组合物及其制备方法以及上述用途所述化合物可用于控制或预防诸如癌症等疾病。

4. 发明申请

WO2006032518A1 NOVEL PHTHALAZINONE DERIVATIVES, AS AURORA-A KINASE INHIBITORS 审中-公开
标题翻译：新型苯乙烯酮衍生物，作为AURORA-KINASE抑制剂
公开(公告)号：WO2006032518A1
公开(公告)日：2006-03-30
申请号：PCT/EP2005/010311
申请日：2005-09-23
申请人： F. HOFFMANN-LA ROCHE AG , BOYD, Edward , BROOKFIELD, Frederick , GEORGES, Guy , GOLLER, Bernhard , HUENSCH, Sabine , RUEGER, Petra , RUETH, Matthias , SCHEIBLICH, Stefan , SCHUELL, Christine , VON DER SAAL, Wolfgang , WARNE, Justin , WEIGAND, Stefan
发明人： BOYD, Edward , BROOKFIELD, Frederick , GEORGES, Guy , GOLLER, Bernhard , HUENSCH, Sabine , RUEGER, Petra , RUETH, Matthias , SCHEIBLICH, Stefan , SCHUELL, Christine , VON DER SAAL, Wolfgang , WARNE, Justin , WEIGAND, Stefan
IPC分类号： C07D403/12
CPC分类号： C07D403/12
摘要： Objects of the present invention are the compounds of formula (I) their pharmaceutically acceptable salts, enantiomeric forms, diastereoisomers and racemates, the preparation of the above-mentioned compounds, medicaments containing them and their manufacture, as well as the use of the above-mentioned compounds in the control or prevention of illnesses such as cancer.
摘要翻译：本发明的目的是式（I）化合物的药学上可接受的盐，对映体形式，非对映异构体和外消旋体，上述化合物的制备，含有它们的药物及其制备方法，以及上述用途，提及的化合物在控制或预防诸如癌症的疾病中。

5. 发明申请

WO2007107298A1 PHTHALAZINONE PYRAZOLE DERIVATIVES, THEIR MANUFACTURE AND USE AS PHARMACEUTICAL AGENTS 审中-公开
标题翻译：苯并噻唑酮衍生物及其制备方法及用作药物代理
公开(公告)号：WO2007107298A1
公开(公告)日：2007-09-27
申请号：PCT/EP2007/002332
申请日：2007-03-16
申请人： F. HOFFMANN-LA ROCHE AG , BOYD, Edward , BROOKFIELD, Frederick , COURTNEY, Steve , GEORGES, Guy , GOLLER, Bernhard , LIMBERG, Anja , PRIME, Michael , RUEGER, Petra , RUETH, Matthias
发明人： BOYD, Edward , BROOKFIELD, Frederick , COURTNEY, Steve , GEORGES, Guy , GOLLER, Bernhard , LIMBERG, Anja , PRIME, Michael , RUEGER, Petra , RUETH, Matthias
IPC分类号： C07D403/12 , C07D401/14 , A61K31/495 , A61P35/00
CPC分类号： C07D403/12 , C07D401/14
摘要： Objects of the present invention are the compounds of formula (I) their pharmaceutically acceptable salts, enantiomeric forms, diastereoisomers and racemates, the preparation of the above-mentioned compounds, medicaments containing them and their manufacture, as well as the use of the above-mentioned compounds in the control or prevention of illnesses such as cancer.
摘要翻译：本发明的目的是式（I）化合物的药学上可接受的盐，对映体形式，非对映异构体和外消旋体，上述化合物的制备，含有它们的药物及其制备方法，以及上述用途，提及的化合物在控制或预防诸如癌症的疾病中。

6. 发明公开

EP1912987A1 HETEROCYCLIC BENZYLAMINO DERIVATIVES, THEIR MANUFACTURE AND USE AS PHARMACEUTICAL AGENTS 审中-公开
标题翻译：杂环BENZYLAMINODERIVATE，制备方法及其作为药剂
公开(公告)号：EP1912987A1
公开(公告)日：2008-04-23
申请号：EP06776480.3
申请日：2006-07-28
申请人： F. Hoffmann-La Roche AG
发明人： BOYD, Edward , BROOKFIELD, Frederick , GRIDLEY, Jonathan , HONOLD, Konrad , LAU, Raymond , SCHEIBLICH, Stefan
IPC分类号： C07D471/04 , A61K31/437 , A61P35/00
CPC分类号： C07D471/04
摘要： Objects of the present invention are the compounds of formula (I) their pharmaceutically acceptable salts, enantiomeric forms, diastereoisomers and racemates, the preparation of the above-mentioned compounds, pharmaceutical compositions containing them and their manufacture, as well as the use of the above-mentioned compounds in the control or prevention of illnesses such as cancer.

7. 发明申请

WO2005086950A2 METHOD FOR DATA ENCRYPTION IN AN ETHERNET PASSIVE OPTICAL NETWORK 审中-公开
标题翻译：用于以太网被动光网络中数据加密的方法
公开(公告)号：WO2005086950A2
公开(公告)日：2005-09-22
申请号：PCT/US2005/008150
申请日：2005-03-10
申请人： TEKNOVUS, INC., , KRAMER, Glen , DAVIS, Lawrence , BOYD, Edward , HIRTH, Ryan , HO, Ngo Thanh
发明人： KRAMER, Glen , DAVIS, Lawrence , BOYD, Edward , HIRTH, Ryan , HO, Ngo Thanh
IPC分类号： H04L9/00 , H04L9/12
CPC分类号： H04L9/12 , H04L9/0637
摘要： One embodiment of the present invention provides a system that decrypts downstream data in an Ethernet passive optical network (EPON). During operation, the system receives a data frame which is encrypted based on a remote input block and a session key, wherein the remote input block is constructed based on a remote cipher counter and a remote block counter. The system adjusts a local cipher counter based on a received checksum located in a preamble of the data frame, wherein the local cipher counter is substantially synchronized with the remote cipher counter. In addition, the system truncates the local cipher counter by discarding n least significant bits thereof. The system then constructs a local input block based on the truncated cipher counter and a local block counter for the received data frame. Next, the system decrypts the data frame based on the local input block and the session key.
摘要翻译：本发明的一个实施例提供一种解密以太网无源光网络（EPON）中的下游数据的系统。在操作期间，系统接收基于远程输入块和会话密钥加密的数据帧，其中基于远程密码计数器和远程块计数器构建远程输入块。该系统基于位于数据帧的前导码中的接收到的校验和来调整本地密码计数器，其中本地密码计数器基本上与远程密码计数器同步。此外，系统通过丢弃其最低有效位来截断本地密码计数器。然后，系统基于截断的密码计数器和接收到的数据帧的本地块计数器构建本地输入块。接下来，系统基于本地输入块和会话密钥来解密数据帧。

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