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公开(公告)号:US20200270266A1
公开(公告)日:2020-08-27
申请号:US16871532
申请日:2020-05-11
发明人: Ippei SATO , Takashi KAMIKUBO , Masanori MIURA , Yuji MATSUSHIMA , Hiroaki TANAKA , Yasuhiro SHIINA , Susumu YAMAKI , Tomoyuki SAITO , Hiroshi KIYOHARA , Munemichi OHE , Kayoko MIHARA , Bradley Paul MORGAN , Fady MALIK , Scott Emile COLLIBEE , Luke ASHCRAFT , Pu-Ping LU , Jeffrey Michael WARRINGTON , Marc GARARD
IPC分类号: C07D491/20 , C07D491/107 , C07D217/24 , C07D471/04 , C07D217/26 , C07D471/10 , A61P21/00
摘要: Novel tetrahydroisoquinoline derivative compounds are disclosed herein that may be used as an active ingredient for a pharmaceutical composition, and in particular, for a pharmaceutical composition useful for preventing or treating a disease or condition responsive to modulation of the contractility of the skeletal sarcomere. This may be accomplished, for example, by modulation of the troponin complex of the fast skeletal muscle sarcomere through one or more of fast skeletal myosin, actin, tropomyosin, troponin C, troponin I, and troponin T, and fragments and isoforms thereof. The tetrahydroisoquinoline derivative compounds can thus be used as an agent for preventing or treating 1) neuromuscular disorders, 2) disorders of voluntary muscle, 3) CNS disorders in which muscle weakness, atrophy, and fatigue are prominent symptoms, 4) muscle symptoms stemming from systemic disorders, and 5) dysfunctions of pelvic floor and urethral/anal sphincter muscle.
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公开(公告)号:US20170233402A1
公开(公告)日:2017-08-17
申请号:US15429738
申请日:2017-02-10
发明人: Ippei SATO , Takashi KAMIKUBO , Masanori MIURA , Yuji MATSUSHIMA , Hiroaki TANAKA , Yasuhiro SHllNA , Susumu YAMAKI , Tomoyuki SAITO , Hiroshi KIYOHARA , Munemichi OHE , Kayoko MIHARA , Bradley Paul MORGAN , Fady MALIK , Scott Emile COLLIBEE , Luke ASHCRAFT , Pu-Ping LU , Jeffrey Michael WARRINGTON , Marc GARARD
IPC分类号: C07D491/20 , C07D471/10 , C07D471/04 , C07D217/26 , C07D491/107 , C07D217/24
CPC分类号: C07D491/20 , C07D217/24 , C07D217/26 , C07D471/04 , C07D471/10 , C07D491/107
摘要: Novel tetrahydroisoquinoline derivative compounds are disclosed herein that may be used as an active ingredient for a pharmaceutical composition, and in particular, for a pharmaceutical composition useful for preventing or treating a disease or condition responsive to modulation of the contractility of the skeletal sarcomere. This may be accomplished, for example, by modulation of the troponin complex of the fast skeletal muscle sarcomere through one or more of fast skeletal myosin, actin, tropomyosin, troponin C, troponin I, and troponin T, and fragments and isoforms thereof. The tetrahydroisoquinoline derivative compounds can thus be used as an agent for preventing or treating 1) neuromuscular disorders, 2) disorders of voluntary muscle, 3) CNS disorders in which muscle weakness, atrophy, and fatigue are prominent symptoms, 4) muscle symptoms stemming from systemic disorders, and 5) dysfunctions of pelvic floor and urethral/anal sphincter muscle.
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公开(公告)号:US20230125280A1
公开(公告)日:2023-04-27
申请号:US17944060
申请日:2022-09-13
发明人: Ippei SATO , Takashi KAMIKUBO , Masanori MIURA , Yuji MATSUSHIMA , Hiroaki TANAKA , Yasuhiro SHIINA , Susumu YAMAKI , Tomoyuki SAITO , Hiroshi KIYOHARA , Munemichi OHE , Kayoko MIHARA , Bradley Paul MORGAN , Fady MALIK , Scott Emile COLLIBEE , Luke ASHCRAFT , Pu-Ping LU , Jeffrey Michael WARRINGTON , Marc GARARD
IPC分类号: C07D491/20 , C07D491/107 , C07D217/24 , C07D471/04 , C07D217/26 , C07D471/10 , A61P21/00
摘要: Novel tetrahydroisoquinoline derivative compounds are disclosed herein that may be used as an active ingredient for a pharmaceutical composition, and in particular, for a pharmaceutical composition useful for preventing or treating a disease or condition responsive to modulation of the contractility of the skeletal sarcomere. This may be accomplished, for example, by modulation of the troponin complex of the fast skeletal muscle sarcomere through one or more of fast skeletal myosin, actin, tropomyosin, troponin C, troponin I, and troponin T, and fragments and isoforms thereof. The tetrahydroisoquinoline derivative compounds can thus be used as an agent for preventing or treating 1) neuromuscular disorders, 2) disorders of voluntary muscle, 3) CNS disorders in which muscle weakness, atrophy, and fatigue are prominent symptoms, 4) muscle symptoms stemming from systemic disorders, and 5) dysfunctions of pelvic floor and urethral/anal sphincter muscle.
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公开(公告)号:US20140038983A1
公开(公告)日:2014-02-06
申请号:US13946353
申请日:2013-07-19
发明人: Bradley Paul MORGAN , Alex MUCI , Pu-Ping LU , Erica Anne KRAYNACK , Todd TOCHIMOTO , David J. MORGANS
IPC分类号: C07D213/75
CPC分类号: C07D213/75 , C07D211/56 , C07D239/42 , C07D261/14 , C07D263/48 , C07D271/113 , C07D295/26 , C07D401/10 , C07D401/12 , C07D417/00 , C07D417/10 , C07D417/12 , C07D487/04 , C07D491/04 , C07D513/04
摘要: Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.
摘要翻译: 某些取代的脲衍生物选择性地调节心肌肉瘤,例如通过增强心肌肌球蛋白,并且可用于治疗包括充血性心力衰竭的收缩性心力衰竭。
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