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公开(公告)号:WO2012158308A3
公开(公告)日:2012-11-22
申请号:PCT/US2012/034656
申请日:2012-04-23
申请人: ACTRACE, LLC , ZENG, Lei
发明人: ZENG, Lei
摘要: Described are pipetting systems that automatically track the dispensing and extracting of reagents to and from arrays of well locations. The systems track the position of a pipette with respect to the well locations, and selectively illuminate those locations to indicate the progress of pipetting operations. Control logic can shepherd pipetting processes, indicating errors and guiding the user.
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公开(公告)号:WO2012158308A2
公开(公告)日:2012-11-22
申请号:PCT/US2012034656
申请日:2012-04-23
申请人: ACTRACE LLC , ZENG LEI
发明人: ZENG LEI
CPC分类号: G01N35/00584 , B01L3/0237 , B01L3/527 , B01L2200/025 , B01L2200/143 , B01L2200/148 , B01L2300/027 , B01L2300/0654 , B01L2300/0829 , G01N35/00722 , G01N35/1002 , G01N35/1011 , G01N2035/0091
摘要: Described are pipetting systems that automatically track the dispensing and extracting of reagents to and from arrays of well locations. The systems track the position of a pipette with respect to the well locations, and selectively illuminate those locations to indicate the progress of pipetting operations. Control logic can shepherd pipetting processes, indicating errors and guiding the user.
摘要翻译: 描述了移液系统,其自动跟踪从井阵列阵列排出和提取试剂。 系统跟踪移液器相对于井位置的位置,并且选择性地照亮那些位置以指示移液操作的进展。 控制逻辑可以吸取移液过程,指示错误并引导用户。
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公开(公告)号:WO2007084625A9
公开(公告)日:2007-09-13
申请号:PCT/US2007001350
申请日:2007-01-19
申请人: SINAI SCHOOL MEDICINE , ZHOU MING-MING , SACHCHIDANAND D PHIL , ZENG LEI , MANFREDI JAMES J , RESNICK-SILVERMAN LOIS , AARONSON STUART
发明人: ZHOU MING-MING , SACHCHIDANAND D PHIL , ZENG LEI , MANFREDI JAMES J , RESNICK-SILVERMAN LOIS , AARONSON STUART
IPC分类号: A61K31/473 , A61K31/403
CPC分类号: C07C317/40 , C07C233/05 , C07C233/07 , C07C233/18 , C07C233/25 , C07C233/54 , C07C323/52 , C07D209/12 , C07D209/38 , C07D209/88 , C07D215/08 , C07D221/08
摘要: The present invention features compounds and pharmaceutical compositions comprising the same that are useful for modulating p53 activity. The invention further provides methods for inhibiting the biological activity of p53 and for treating diseases such as, for instance, cancer, cell death caused all or in part by cancer treatments such as chemotherapy or radiation thereapy, neuron cell death, stroke, Alzheimer's Disease and Parkinson's Disease.
摘要翻译: 本发明的特征在于包含其可用于调节p53活性的化合物和药物组合物。 本发明还提供了抑制p53的生物学活性和治疗诸如癌症,全部或部分地由癌症治疗如化学疗法或放射治疗,神经元细胞死亡,中风,阿尔茨海默氏病等引起的细胞死亡的疾病的方法,以及 帕金森病
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公开(公告)号:WO2007084625A3
公开(公告)日:2007-12-13
申请号:PCT/US2007001350
申请日:2007-01-19
申请人: SINAI SCHOOL MEDICINE , ZHOU MING-MING , SACHCHIDANAND D PHIL , ZENG LEI , MANFREDI JAMES J , RESNICK-SILVERMAN LOIS , AARONSON STUART
发明人: ZHOU MING-MING , SACHCHIDANAND D PHIL , ZENG LEI , MANFREDI JAMES J , RESNICK-SILVERMAN LOIS , AARONSON STUART
IPC分类号: A61K31/425 , A61K31/415 , A61K31/42
CPC分类号: C07C317/40 , C07C233/05 , C07C233/07 , C07C233/18 , C07C233/25 , C07C233/54 , C07C323/52 , C07D209/12 , C07D209/38 , C07D209/88 , C07D215/08 , C07D221/08
摘要: The present invention features compounds and pharmaceutical compositions comprising the same that are useful for modulating p53 activity. The invention further provides methods for inhibiting the biological activity of p53 and for treating diseases such as, for instance, cancer, cell death caused all or in part by cancer treatments such as chemotherapy or radiation thereapy, neuron cell death, stroke, Alzheimer's Disease and Parkinson's Disease.
摘要翻译: 本发明的特征在于包含其用于调节p53活性的化合物和药物组合物。 本发明进一步提供了抑制p53的生物学活性和治疗疾病例如癌症,全部或部分由癌症治疗例如化学疗法或辐射,神经元细胞死亡,中风,阿尔茨海默氏病和 帕金森病。
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公开(公告)号:WO2007084625A2
公开(公告)日:2007-07-26
申请号:PCT/US2007/001350
申请日:2007-01-19
申请人: MOUNT SINAI SCHOOL OF MEDICINE , ZHOU, Ming-Ming , SACHCHIDANAND, D., Phil , ZENG, Lei , MANFREDI, James, J. , RESNICK-SILVERMAN, Lois , AARONSON, Stuart
发明人: ZHOU, Ming-Ming , SACHCHIDANAND, D., Phil , ZENG, Lei , MANFREDI, James, J. , RESNICK-SILVERMAN, Lois , AARONSON, Stuart
IPC分类号: A61K31/473 , A61K31/403
CPC分类号: C07C317/40 , C07C233/05 , C07C233/07 , C07C233/18 , C07C233/25 , C07C233/54 , C07C323/52 , C07D209/12 , C07D209/38 , C07D209/88 , C07D215/08 , C07D221/08
摘要: The present invention features compounds and pharmaceutical compositions comprising the same that are useful for modulating p53 activity. The invention further provides methods for inhibiting the biological activity of p53 and for treating diseases such as, for instance, cancer, cell death caused all or in part by cancer treatments such as chemotherapy or radiation thereapy, neuron cell death, stroke, Alzheimer's Disease and Parkinson's Disease.
摘要翻译: 本发明的特征在于用于调节p53活性的化合物和包含其的药物组合物。 本发明进一步提供了抑制p53的生物学活性和治疗疾病例如癌症,全部或部分由癌症治疗例如化学疗法或辐射,神经元细胞死亡,中风,阿尔茨海默氏病和 帕金森病。 p>
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公开(公告)号:WO2006083692A2
公开(公告)日:2006-08-10
申请号:PCT/US2006/002840
申请日:2006-01-27
发明人: ZHOU, Ming-ming , ZENG, Lei , WANG, Zhiyong
IPC分类号: A61K31/277
CPC分类号: C07C215/16 , C07C211/29 , C07C211/53 , C07C217/20 , C07C229/18 , C07C229/42 , C07C255/58 , C07D311/08 , C07D311/16 , C07D311/18
摘要: The present invention features compounds of the following general formula (I) wherein R 1 is selected from the group consisting of hydrogen, lower alkyl, aryl, aralkyl; substituted aralkyl, heteroaryl; substituted heteroaryl, phenyl, SO 2 , NH 2 , NO 2 , SO 2 , CH 2 , CH 2 CH 3 , OCH 3 , OCOCH 3 , CH 2 COCH 3 , and OH, CN and halogen; R 2 is selected from the group consisting of hydrogen; lower alkyl, aryl, phenyl, aralkyl; substituted aralkyl, heteroaryl; substituted heteroaryl, SO 2 NH 2 NH 3 + NO 2 , SO 2 , CH 3 , CH 2 CH 3 , OCH 3 , OCOCH 3 , CH 2 COCH 3, and OH, halogen, carboxy, and alkoxy; X is selected from the group consisting of lower alkyl, SO 2 , NH, NO 2 , , CH 3 , CH 2 CH 3 , OCH 3 , OCOCH 3 , CH 2 COCH 3 , and OH, carboxy, and alkoxy; and n is an integer from O to 10 and their pharmaceutically acceptable salts of acids or bases as well as pharmaceutical compositions comprising these compounds. The invention further provides methods for preventing or inhibiting the binding of bromodomains to acetyl-lysine residues of proteins and methods for treating HIV infection and HW related disease. The present invention also features compounds of the following general formula (II) wherein: R 1 R 2 and R 3 are independently selected from the group consisting of hydrogen; lower alkyl, aryl, phenyl, aralkyl; substituted aralkyl, heteroaryl; substituted heteroaryl, SO 2 , NH 2 , NH 3 + NO 2, SO 2 , CH 3 , CH 2 CH 3 , OCH 3 , OCOCH 3 , CH 2 COCH 3 , OH, SH, halogen, carboxy; and R 4 is selected from the group consisting of lower alkyl, aryl, SO 2 , NH, NO 2 , CH 3 , CH 2 CH 3 , OCH 3 , OCOCH 3 , CH 2 COCH 3 , OH, carboxy, and alkoxy as well as pharmaceutical compositions comprising these compounds. The invention further provides methods for preventing or inhibiting the binding of bromodomains to acetyl-lysine residues of proteins and methods f treating HW infection and HIY related disease. The present invention also features compounds of formula (III) wherein R 1 , R 2 , R 3 , R 4 R 5 , and R 6 are independently selected from the group consisting of hydrogen; lower alkyl, aryl, phenyl, aralkyl; substituted aralkyl, heteroaryl, substituted heteroaryl, SO 2 NH 2 , NH 3 + , NO 2 , SO 2 , CH 3 , CH 2 CH 3 , OCH 3 , OCOCH 3 , CH 2 COCH 3 , OCH 2 CH 3 , OCH(CH 3 ) 2 , OCH 2 COOH, OCHCH 3 COOH, OCH 2 COCH 3 , OCH 2 CONH 2 , OCOCH(CH 3 ) 2 , OCH 2 CH 2 OH, OCH 2 CH 2 CH 3 , O(CH 2 ) 3 CH 3 , OCHCH 3 COOCH 3 , OCH 2 CON(CH 3 ) 2 ,NH(CH 2 ) 3 N(CH 3 ) 2 , NH(CH 2 ) 2 N(CH 3 ) 2 , NH(CH 2 ) 2 OH, NH(CH 2 ) 3 CH 3 , NHCH 3 , SH, halogen, carboxy, and alkoxy as well as pharmaceutical compositions comprising these compounds. The invention further provides methods for preventing or inhibiting the binding of bromodomains to acetyl-lysine residues of proteins and methods for treating HIV infection and HIV related disease.
摘要翻译: 本发明的特征在于以下通式(I)的化合物,其中R 1选自氢,低级烷基,芳基,芳烷基; 取代的芳烷基,杂芳基; 取代的杂芳基,苯基,SO 2,NH 2,NO 2,SO 2,CH 2 CH 2,CH 3,OCH 3,OCOCH 3,CH 2, CO,SO 3,OH,CN和卤素; R 2选自氢; 低级烷基,芳基,苯基,芳烷基; 取代的芳烷基,杂芳基; 取代的杂芳基,SO 2 NH 2 NH 3,
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公开(公告)号:WO2006083692A3
公开(公告)日:2007-01-11
申请号:PCT/US2006002840
申请日:2006-01-27
发明人: ZHOU MING-MING , ZENG LEI , WANG ZHIYONG
IPC分类号: A61K31/35 , A61K31/135 , A61K31/16 , A61K31/195 , A61K31/24 , A61K31/275 , C07C205/06 , C07C205/12 , C07C205/37 , C07C211/27 , C07C211/29 , C07C217/56 , C07C217/60 , C07C217/62 , C07C255/58 , C07D311/12 , C07D311/14 , C07D311/16 , C07D311/18
CPC分类号: C07C215/16 , C07C211/29 , C07C211/53 , C07C217/20 , C07C229/18 , C07C229/42 , C07C255/58 , C07D311/08 , C07D311/16 , C07D311/18
摘要: The present invention features compounds of the following general formula (I) wherein R 1 is selected from the group consisting of hydrogen, lower alkyl, aryl, aralkyl; substituted aralkyl, heteroaryl; substituted heteroaryl, phenyl, SO 2 , NH 2 , NO 2 , SO 2 , CH 2 , CH 2 CH 3 , OCH 3 , OCOCH 3 , CH 2 COCH 3 , and OH, CN and halogen; R 2 is selected from the group consisting of hydrogen; lower alkyl, aryl, phenyl, aralkyl; substituted aralkyl, heteroaryl; substituted heteroaryl, SO 2 NH 2 NH 3 + N
摘要翻译: 本发明的特征在于以下通式(I)的化合物,其中R 1选自氢,低级烷基,芳基,芳烷基; 取代的芳烷基,杂芳基; 取代的杂芳基,苯基,SO 2,NH 2,NO 2,SO 2,CH 2 CH 2,CH 3,OCH 3,OCOCH 3,CH 2, CO,SO 3,OH,CN和卤素; R 2选自氢; 低级烷基,芳基,苯基,芳烷基; 取代的芳烷基,杂芳基; 取代的杂芳基,SO 2 NH 2 NH 3,N,N,N,N,
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公开(公告)号:WO2005004178A1
公开(公告)日:2005-01-13
申请号:PCT/US2004/019896
申请日:2004-06-22
IPC分类号: H01F27/08
CPC分类号: H01F27/085 , H01F17/045 , H01F27/322 , H01F27/324 , H01F37/00
摘要: An inductor includes an elongate magnetic core, a coil wrapped around the core and a spacer that separates the coil from the core to provide a coolant passage between the coil and the core. The coolant passage may include an air passage that extends substantially parallel to an axis of the core and that has first and second openings proximate respective first and second ends of the core. The coil may include a twisted bundle of individually insulated conductors. The inductor may be housed in a flux-tolerant compartment, i.e., a conductive aluminum structure that supports eddy currents with relatively acceptable resistive losses.
摘要翻译: 电感器包括细长的磁芯,缠绕在芯上的线圈和将线圈与芯分离以在线圈和芯之间提供冷却剂通道的间隔件。 冷却剂通道可以包括空气通道,空气通道基本上平行于芯的轴线延伸,并且具有靠近芯的相应的第一和第二端的第一和第二开口。 线圈可以包括单独绝缘导体的扭绞束。 电感器可以容纳在容许容纳室中,即支持具有相对可接受的电阻损耗的涡流的导电铝结构。
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