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公开(公告)号:US20210309702A1
公开(公告)日:2021-10-07
申请号:US17164624
申请日:2021-02-01
发明人: Xuedong Liu , Xiaojuan Zhang , Zeyu Liu , Quanbin Xu
IPC分类号: C07K14/005 , A61K9/51 , C12N7/00 , C12N15/11 , C12N9/22 , A61K38/46 , A61K31/7088
摘要: The invention includes systems, methods, and compositions for designing secreted fusogenic ectosome vesicles, or gectosomes, that selectively encapsulate specific target proteins, nucleic acids and/or other small molecules in a predetermined manner. These engineered gectosomes can be used to deliver desired cargos to receipt cells in vitro, ex vivo, or in vivo and may further reprogram target cellular phenotypes in a dose-dependent manner, as well as perform genome editing functions, among others.
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公开(公告)号:US20210244686A1
公开(公告)日:2021-08-12
申请号:US17255214
申请日:2019-06-24
发明人: Xuedong Liu , Douglas Chapnick , William Old
IPC分类号: A61K31/05 , A61K31/352 , A61K31/192 , A61K31/09 , A61K45/06 , A61K31/445 , A61K31/13 , A61K31/27 , A61K31/55 , A61P3/06
摘要: The invention includes the use of cannabidiol (CBD), and cannabidiol analogs, as therapeutic compounds or formulations for the increase of lipid order in the cell membranes of a patient. This increase in membrane lipid order may cause downstream therapeutic effects that may ameliorate certain disease conditions such as cardio vascular disease, high-cholesterol and Alzheimer's disease.
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公开(公告)号:USRE47690E1
公开(公告)日:2019-11-05
申请号:US15968188
申请日:2018-05-01
IPC分类号: C07D513/04 , C07D473/16 , C07D473/34 , C07D487/04
摘要: The present invention relates to novel hydroxamic acids which are specific histone deacetylase (HDAC) inhibitors and/or TTK/Mps1 kinase inhibitors, including pharmaceutically acceptable salts thereof, which are useful for modulating HDAC and/or TTK/Mps1 kinase activity, pharmaceutical compositions comprising these compounds, and processes for their preparation.
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公开(公告)号:US20180306800A1
公开(公告)日:2018-10-25
申请号:US15959158
申请日:2018-04-20
发明人: Xuedong Liu , Gail Eckhardt , Gan Zhang , Conggang Zhang , Zeyu Liu , Eric Bunker
IPC分类号: G01N33/574 , A61P35/00 , A61K31/44 , A61K31/495 , A61K31/704 , A61K39/395 , A61K38/15 , A61K31/277 , C12Q1/6886
CPC分类号: G01N33/57492 , A61K31/277 , A61K31/44 , A61K31/495 , A61K31/704 , A61K38/15 , A61K39/39558 , A61P35/00 , C12Q1/6886 , C12Q2600/106 , C12Q2600/158
摘要: Methods and materials involved in assessing samples (e.g., cancer cells) for the status of PINK1-Parkin pathway biomarkers, as well as materials and methods for identifying cancer patients likely to respond to a particular cancer treatment regimen.
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公开(公告)号:US20180044352A1
公开(公告)日:2018-02-15
申请号:US15654662
申请日:2017-07-19
IPC分类号: C07D513/04 , C07D487/04 , C07D473/16 , C07D473/34
摘要: The present invention relates to novel hydroxamic acids which are specific histone deacetylase (HDAC) inhibitors and/or TTK/Mps1 kinase inhibitors, including pharmaceutically acceptable salts thereof, which are useful for modulating HDAC and/or TTK/Mps1 kinase activity, pharmaceutical compositions comprising these compounds, and processes for their preparation.
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公开(公告)号:US20170081343A1
公开(公告)日:2017-03-23
申请号:US15310743
申请日:2015-05-14
IPC分类号: C07D513/04 , C07D487/04 , C07D473/16
CPC分类号: C07D513/04 , C07D473/16 , C07D473/34 , C07D487/04
摘要: The present invention relates to novel hydroxamic acids which are specific histone deacetylase (HDAC) inhibitors and/or TTK/Mps1 kinase inhibitors, including pharmaceutically acceptable salts thereof, which are useful for modulating HDAC and/or TTK/Mps1 kinase activity, pharmaceutical compositions comprising these compounds, and processes for their preparation.
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公开(公告)号:US20150010541A1
公开(公告)日:2015-01-08
申请号:US14289877
申请日:2014-05-29
CPC分类号: C07K11/02 , A61K31/425 , A61K38/005 , A61K38/15 , A61K39/3955 , A61K45/06 , C07K5/0821 , C07K11/00
摘要: The present invention provides a novel macrocyclic compound of general Formula (I) having histone deacetylase (HDAC) inhibitory activity, a pharmaceutical composition comprising the compound, and a method useful to treat diseases using the compound.
摘要翻译: 本发明提供了具有组蛋白脱乙酰酶(HDAC)抑制活性的通式(I)的新型大环化合物,包含该化合物的药物组合物和可用于使用该化合物治疗疾病的方法。
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公开(公告)号:US20240102991A1
公开(公告)日:2024-03-28
申请号:US18386764
申请日:2023-11-03
IPC分类号: G01N33/50 , C12M1/34 , C12Q1/6825 , G01N21/64 , G01N33/542 , G01N33/554 , G01N33/58
CPC分类号: G01N33/5008 , C12M1/3476 , C12Q1/6825 , G01N21/64 , G01N21/6428 , G01N21/6452 , G01N33/542 , G01N33/554 , G01N33/582 , B01L2300/0636 , C12Q2500/00 , C12Q2560/00 , C12Q2563/107 , C12Q2563/179 , C12Q2565/1015 , C12Q2600/136 , G01N2500/04 , G01N2800/52
摘要: Provided are FRET-based biosensor constructs, and multiplexed platforms or arrays of these biosensor constructs useful for screening candidate drug molecules for efficacy and/or specificity of drug activity. Optionally the biosensor constructs may be located on an inner membrane within a cell or engineered to be located on the cell's surface. The cells or cell lines displaying the biosensors on a cell surface may be arranged as an array of cells for high throughput evaluation of the efficacy and/or specificity of drug candidates, such as a library of candidate drug compounds.
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公开(公告)号:US20210181181A1
公开(公告)日:2021-06-17
申请号:US16954100
申请日:2018-12-14
摘要: Provided are FRET-based biosensor constructs, and multiplexed platforms or arrays of these biosensor constructs useful for screening candidate drug molecules for efficacy and/or specificity of drug activity. Optionally the biosensor constructs may be located on an inner membrane within a cell or engineered to be located on the cell's surface. The cells or cell lines displaying the biosensors on a cell surface may be arranged as an array of cells for high throughput evaluation of the efficacy and/or specificity of drug candidates, such as a library of candidate drug compounds.
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公开(公告)号:US10508122B2
公开(公告)日:2019-12-17
申请号:US15654662
申请日:2017-07-19
IPC分类号: C07D513/04 , C07D473/34 , C07D487/04 , C07D473/16
摘要: The present invention relates to novel hydroxamic acids which are specific histone deacetylase (HDAC) inhibitors and/or TTK/Mps1 kinase inhibitors, including pharmaceutically acceptable salts thereof, which are useful for modulating HDAC and/or TTK/Mps1 kinase activity, pharmaceutical compositions comprising these compounds, and processes for their preparation.
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