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公开(公告)号:US11701409B2
公开(公告)日:2023-07-18
申请号:US16074330
申请日:2017-02-01
申请人: Adepthera LLC
发明人: Sheau Yu Teddy Hsu
IPC分类号: A61K38/22 , A61K47/54 , A61K31/704 , A61P9/04 , A61P9/12
CPC分类号: A61K38/22 , A61K31/704 , A61K47/542 , A61P9/04 , A61P9/12
摘要: Long-acting agonistic analogs for CLR/RAMP receptors are provided that have an extended half-live in vivo. The agonists are delivered to an individual at a dose sufficient to reduce hypertension and ischemic injury, and to reduce cardiotoxicity associated with chemotherapeutic agents.
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公开(公告)号:US20220340633A1
公开(公告)日:2022-10-27
申请号:US17316153
申请日:2021-05-10
申请人: Adepthera LLC
发明人: Sheau Yu Teddy Hsu
IPC分类号: C07K14/575 , C07K19/00 , C07K16/26
摘要: Analogs for CLR/RAMP receptor ligands are provided that have agonist, superagonist, antagonist or superantagonist activity. The analogs can be selective for one or more CLR/RAMP receptors, or can be pan-specific.
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公开(公告)号:US20220324935A1
公开(公告)日:2022-10-13
申请号:US17837736
申请日:2022-06-10
申请人: Adepthera LLC
发明人: Sheau Yu Teddy Hsu
IPC分类号: C07K14/575 , C07K14/585 , A61K47/60 , A61K47/54 , A61K45/06 , C07K14/47 , C07K14/655
摘要: Analogs for CLR/RAMP receptor ligands are provided that have agonist, superagonist, antagonist, super-antagonist, or multiple receptor modulatng activity. The analogs can be selective for one or more CLR/RAMP receptors, or can be pan-specific for multiple G protein-coupled receptors.
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公开(公告)号:US20210000922A1
公开(公告)日:2021-01-07
申请号:US16074330
申请日:2017-02-01
申请人: Adepthera LLC
发明人: Sheau Yu Teddy Hsu
IPC分类号: A61K38/22 , A61K47/54 , A61K31/704 , A61P9/04 , A61P9/12
摘要: Long-acting agonistic analogs for CLR/RAMP receptors are provided that have an extended half-live in vivo. The agonists are delivered to an individual at a dose sufficient to reduce hypertension and ischemic injury, and to reduce cardiotoxicity associated with chemotherapeutic agents.
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公开(公告)号:US12110318B2
公开(公告)日:2024-10-08
申请号:US17837736
申请日:2022-06-10
申请人: Adepthera LLC
发明人: Sheau Yu Teddy Hsu
IPC分类号: C07K14/575 , A61K38/00 , A61K45/06 , A61K47/54 , A61K47/60 , C07K14/47 , C07K14/585 , C07K14/655 , A61K9/00
CPC分类号: C07K14/575 , A61K45/06 , A61K47/542 , A61K47/60 , C07K14/47 , C07K14/57527 , C07K14/585 , C07K14/655 , A61K9/0019 , A61K38/00 , C07K2319/00
摘要: Analogs for CLR/RAMP receptor ligands are provided that have agonist, superagonist, antagonist, super-antagonist, or multiple receptor modulating activity. The analogs can be selective for one or more CLR/RAMP receptors, or can be pan-specific for multiple G protein-coupled receptors.
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公开(公告)号:US11034745B2
公开(公告)日:2021-06-15
申请号:US16066609
申请日:2017-01-04
申请人: Adepthera LLC
发明人: Sheau Yu Teddy Hsu
IPC分类号: C07K14/575 , C07K19/00 , C07K16/26 , A61K38/00
摘要: Analogs for CLR/RAMP receptor ligands are provided that have agonist, superagonist, antagonist or superantagonist activity. The analogs can be selective for one or more CLR/RAMP receptors, or can be pan-specific.
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公开(公告)号:US20200339649A1
公开(公告)日:2020-10-29
申请号:US16922850
申请日:2020-07-07
申请人: Adepthera LLC
发明人: Sheau Yu Teddy Hsu
IPC分类号: C07K14/575 , C07K14/585 , A61K47/60 , A61K47/54 , A61K45/06 , C07K14/47 , C07K14/655
摘要: Analogs for CLR/RAMP receptor ligands are provided that have agonist, superagonist, antagonist, super-antagonist, or multiple receptor modulatng activity. The analogs can be selective for one or more CLR/RAMP receptors, or can be pan-specific for multiple G protein-coupled receptors.
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公开(公告)号:US20190153059A1
公开(公告)日:2019-05-23
申请号:US16016235
申请日:2018-06-22
申请人: Adepthera LLC
发明人: Sheau Yu Teddy Hsu
IPC分类号: C07K14/575 , A61K47/60 , C07K14/585
摘要: Analogs for CLR/RAMP receptor ligands are provided that have agonist, superagonist, antagonist, super-antagonist, or multiple receptor modulatng activity. The analogs can be selective for one or more CLR/RAMP receptors, or can be pan-specific for multiple G protein-coupled receptors.
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公开(公告)号:US20190010203A1
公开(公告)日:2019-01-10
申请号:US16066609
申请日:2017-01-04
申请人: Adepthera LLC
发明人: Sheau Yu Teddy Hsu
IPC分类号: C07K14/575 , C07K16/26
摘要: Analogs for CLR/RAMP receptor ligands are provided that have agonist, superagonist, antagonist or superantagonist activity. The analogs can be selective for one or more CLR/RAMP receptors, or can be pan-specific.
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