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公开(公告)号:US20240173307A1
公开(公告)日:2024-05-30
申请号:US18330171
申请日:2023-06-06
发明人: Kathleen Ann Martin , Carmela Sidrauski , Marina Pliushchev , Jennifer M. Frost , Yunsong Tong , Xiangdong Xu , Lei Shi , Qingwei Zhang , Zhaoming Xiong , Ramzi Farah Sweis , Michael J. Dart , Kathleen J. Murauski
IPC分类号: A61K31/44 , A61K31/165 , A61K31/18 , A61K31/341 , A61K31/35 , A61K31/381 , A61K31/4045 , A61K31/415 , A61K31/4184 , A61K31/42 , A61K31/421 , A61K31/4245 , A61K31/426 , A61K31/437 , A61K31/439 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/443 , A61K31/444 , A61K31/4965 , A61K31/50 , A61K31/505 , A61K45/06 , A61P25/28 , C07C237/24 , C07C311/46 , C07C323/40 , C07D213/40 , C07D213/64 , C07D213/71 , C07D213/75 , C07D213/85 , C07D231/12 , C07D233/64 , C07D235/14 , C07D237/14 , C07D239/34 , C07D239/47 , C07D241/12 , C07D261/08 , C07D263/32 , C07D271/06 , C07D277/28 , C07D307/52 , C07D333/20 , C07D401/12 , C07D405/12 , C07D471/04 , C07D471/08 , C07D493/08
CPC分类号: A61K31/44 , A61K31/165 , A61K31/18 , A61K31/341 , A61K31/35 , A61K31/381 , A61K31/4045 , A61K31/415 , A61K31/4184 , A61K31/42 , A61K31/421 , A61K31/4245 , A61K31/426 , A61K31/437 , A61K31/439 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/443 , A61K31/444 , A61K31/4965 , A61K31/50 , A61K31/505 , A61K45/06 , A61P25/28 , C07C237/24 , C07C311/46 , C07C323/40 , C07D213/40 , C07D213/64 , C07D213/71 , C07D213/75 , C07D213/85 , C07D231/12 , C07D233/64 , C07D235/14 , C07D237/14 , C07D239/34 , C07D239/47 , C07D241/12 , C07D261/08 , C07D263/32 , C07D271/06 , C07D277/28 , C07D307/52 , C07D333/20 , C07D401/12 , C07D405/12 , C07D471/04 , C07D471/08 , C07D493/08
摘要: Provided herein are compounds, compositions, and methods useful for modulating the integrated stress response (ISR) and for treating related diseases; disorders and conditions.
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公开(公告)号:US20230144411A1
公开(公告)日:2023-05-11
申请号:US17841570
申请日:2022-06-15
发明人: Jillian Basinger Thompson , Brett C. Bookser , Scott Burley , Pablo Garcia-Reynaga , Andrew Hudson , Marco Peters , Benjamin Pratt , Aaron Thompson , Joe Tran , Lino Valdez
IPC分类号: C07D405/12 , A61P25/28 , C07C211/40 , C07C237/24 , C07C255/46 , C07D207/14 , C07D207/273 , C07D211/58 , C07D211/76 , C07D211/96 , C07D213/38 , C07D309/14 , C07D401/12
CPC分类号: C07D405/12 , A61P25/28 , C07C211/40 , C07C237/24 , C07C255/46 , C07D207/14 , C07D207/273 , C07D211/58 , C07D211/76 , C07D211/96 , C07D213/38 , C07D309/14 , C07D401/12 , C07C2601/08 , C07C2601/16 , C07C2601/14
摘要: Substituted cyclohexyl chemical entities of Formula (I):
wherein Ra, G, and Rb have any of the values described herein, and compositions comprising such chemical entities; methods of making them; and their use in a wide range of methods, including metabolic and reaction kinetic studies; detection and imaging techniques; radioactive therapies; modulating and treating disorders mediated by nociceptin activity or dopamine signaling; treating neurological disorders, neurodegenerative diseases, depression, and schizophrenia; enhancing the efficiency of cognitive and motor training; and treating peripheral disorders, including renal, respiratory, gastrointestinal, liver, genitourinary, metabolic, and inflammatory disorders.-
公开(公告)号:US20180273468A1
公开(公告)日:2018-09-27
申请号:US15523560
申请日:2015-11-03
IPC分类号: C07C231/12 , C07C231/02
CPC分类号: C07C231/12 , C07B2200/07 , C07C231/02 , C07C231/18 , C07C2601/02 , C07C237/24 , C07C235/40
摘要: The invention relates to a process for the preparation of Levomilnacipran or salts thereof, compounds useful in the treatment of depression, with high yield.
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公开(公告)号:US20180244606A1
公开(公告)日:2018-08-30
申请号:US15758709
申请日:2016-09-16
申请人: Metacrine, Inc.
IPC分类号: C07C233/54 , A61K45/06 , A61K31/216 , C07C271/28 , A61K31/27 , C07C255/57 , A61K31/277 , C07D309/08 , A61K31/351 , A61K31/337 , C07D305/08 , C07D335/02 , A61K31/382 , C07D205/04 , A61K31/397 , C07D265/30 , A61K31/5375 , C07C323/50 , C07C317/44 , C07D211/94 , A61K31/45 , C07C235/04 , C07C235/40 , C07D211/06 , A61K31/4453 , C07C235/82 , C07D231/12 , A61K31/415 , C07D213/40 , A61K31/4406 , C07D261/08 , A61K31/42 , C07D295/135 , A61K31/402 , C07D231/56 , A61K31/416 , A61K31/404 , C07D209/04 , C07D317/58 , A61K31/36 , C07D295/26 , C07D295/195 , C07D277/28 , A61K31/426 , A61K31/4184 , C07D235/08 , C07D249/18 , A61K31/4192 , C07D239/42 , A61K31/505 , C07D241/20 , A61K31/4965 , C07D237/20 , A61K31/50 , A61P1/16
CPC分类号: C07C233/54 , A61K31/16 , A61K31/216 , A61K31/27 , A61K31/277 , A61K31/337 , A61K31/351 , A61K31/36 , A61K31/382 , A61K31/397 , A61K31/402 , A61K31/404 , A61K31/415 , A61K31/416 , A61K31/4184 , A61K31/4192 , A61K31/42 , A61K31/426 , A61K31/4406 , A61K31/4453 , A61K31/45 , A61K31/4965 , A61K31/50 , A61K31/505 , A61K31/5375 , A61K45/06 , A61P1/16 , C07C233/63 , C07C233/65 , C07C233/81 , C07C233/87 , C07C235/04 , C07C235/16 , C07C235/40 , C07C235/56 , C07C235/64 , C07C235/82 , C07C237/24 , C07C255/57 , C07C255/60 , C07C271/24 , C07C271/28 , C07C311/07 , C07C311/08 , C07C317/32 , C07C317/44 , C07C323/50 , C07C323/61 , C07C2601/04 , C07C2601/08 , C07C2601/14 , C07C2601/18 , C07C2602/16 , C07C2602/42 , C07C2603/74 , C07D205/04 , C07D209/04 , C07D211/06 , C07D211/62 , C07D211/76 , C07D211/94 , C07D211/96 , C07D213/40 , C07D231/12 , C07D231/56 , C07D235/04 , C07D235/08 , C07D237/20 , C07D239/42 , C07D241/20 , C07D249/18 , C07D261/08 , C07D265/30 , C07D277/28 , C07D295/088 , C07D295/135 , C07D295/195 , C07D295/26 , C07D305/08 , C07D309/08 , C07D317/58 , C07D319/12 , C07D335/02 , A61K2300/00
摘要: Described herein are compounds that are farnesoid X receptor agonists, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders associated with farnesoid X receptor activity.
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公开(公告)号:US20180237385A1
公开(公告)日:2018-08-23
申请号:US15754838
申请日:2016-08-31
申请人: KUEN-FENG CHEN , CHUNG-WAI SHIAU
发明人: KUEN-FENG CHEN , CHUNG-WAI SHIAU
IPC分类号: C07C275/36 , C07C235/82 , C07D213/84 , C07D401/12
CPC分类号: C07C275/36 , A61K31/155 , C07C235/82 , C07C237/16 , C07C237/24 , C07C317/26 , C07D213/84 , C07D265/36 , C07D401/12
摘要: Some novel compounds are provided in this disclosure. These novel compounds have potential SHP-1 agonist activity for being used in treating cancer.
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公开(公告)号:US20180111894A1
公开(公告)日:2018-04-26
申请号:US15846198
申请日:2017-12-18
申请人: Mark G. DeGiacomo
发明人: Hassan Pajouhesh , Richard Holland , Lingyun Zhang , Hossein Pajouhesh , Jason Lamontagne , Brendan Whelan
IPC分类号: C07C237/06 , C07C237/22 , C07D265/30 , C07D231/14 , C07C237/04 , C07D241/08 , C07D413/06 , C07D401/12 , C07D205/04 , C07D413/04 , C07D403/06 , C07D403/04 , C07D401/04 , C07D235/14 , C07D211/60 , C07D207/16 , C07C237/24
CPC分类号: C07C237/06 , A61K31/401 , A61K31/454 , A61K31/5377 , C07C237/04 , C07C237/22 , C07C237/24 , C07C2601/02 , C07C2601/14 , C07D205/04 , C07D207/16 , C07D211/60 , C07D231/14 , C07D235/14 , C07D241/08 , C07D265/30 , C07D401/04 , C07D401/12 , C07D403/04 , C07D403/06 , C07D413/04 , C07D413/06
摘要: The invention relates to compounds useful in treating conditions associated with voltage-gated ion channel function, particularly conditions associated with sodium channel activity. More specifically, the invention concerns compounds (e.g., compounds according to any of Formulas (I)-(XIII) and in particular Formula (X), and Compounds (1)-(236) of Table 1) that are useful in treatment of a variety of diseases and conditions.
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公开(公告)号:US09701620B2
公开(公告)日:2017-07-11
申请号:US14880739
申请日:2015-10-12
申请人: Dow AgroSciences LLC
发明人: William C. Lo , James E. Hunter , Gerald B. Watson , Akshay Patny , Pravin S. Iyer , Joshodeep Boruwa
IPC分类号: C07C233/66 , C07C327/46 , A01N61/00 , A01N37/18 , A01N53/00 , A01N37/34 , C07C237/24 , C07C255/46 , C07D401/10 , A01N43/08 , A01N43/16 , A01N43/20 , A01N43/40 , A01N43/50 , A01N43/60 , A01N43/78 , A01N43/82 , C07C233/65 , C07C255/57 , C07C63/70 , C07D207/16 , C07D213/61 , C07D295/12 , C07D331/04 , A01N43/54 , A01N43/653 , A01N47/32 , A61K31/166 , A61K31/17 , A61K31/4196 , A61K31/4245 , A61K31/426 , A61K31/4965 , A61K31/505 , A61K31/5375 , C07C243/14 , C07C335/14 , C07D239/26 , C07D241/12 , C07D249/14 , C07D271/10 , C07D277/32 , C07D295/192 , A01N37/20 , A01N37/28 , A01N41/10 , A01N47/22 , A01N47/38 , A01N37/46 , A01N47/10 , A01N47/28 , A01N47/36 , A61K45/06 , A61K31/167 , C07C259/08 , C07C271/22 , C07C271/24 , C07C275/24 , C07C211/27 , C07C211/29 , C07C211/30 , C07C211/42 , C07C233/13 , C07C233/56 , C07C233/83 , C07C237/06 , C07C239/08 , C07C243/22 , C07C243/32 , C07C251/44 , A01N43/10 , A01N43/56
CPC分类号: C07C233/66 , A01N37/10 , A01N37/18 , A01N37/20 , A01N37/28 , A01N37/34 , A01N37/46 , A01N41/10 , A01N43/08 , A01N43/10 , A01N43/16 , A01N43/20 , A01N43/36 , A01N43/40 , A01N43/50 , A01N43/54 , A01N43/56 , A01N43/60 , A01N43/653 , A01N43/78 , A01N43/82 , A01N43/84 , A01N47/10 , A01N47/22 , A01N47/28 , A01N47/32 , A01N47/36 , A01N47/38 , A01N53/00 , A01N61/00 , A61K31/166 , A61K31/167 , A61K31/17 , A61K31/4196 , A61K31/4245 , A61K31/426 , A61K31/4965 , A61K31/505 , A61K31/5375 , A61K45/06 , C07C63/70 , C07C211/27 , C07C211/29 , C07C211/30 , C07C211/42 , C07C233/13 , C07C233/56 , C07C233/65 , C07C233/83 , C07C237/06 , C07C237/24 , C07C239/08 , C07C243/14 , C07C243/22 , C07C243/32 , C07C251/44 , C07C255/46 , C07C255/57 , C07C259/08 , C07C271/22 , C07C271/24 , C07C275/24 , C07C327/46 , C07C335/14 , C07C2601/02 , C07C2601/04 , C07C2602/08 , C07C2602/10 , C07D207/16 , C07D207/26 , C07D209/08 , C07D209/48 , C07D211/58 , C07D213/40 , C07D213/61 , C07D237/32 , C07D239/26 , C07D241/12 , C07D249/08 , C07D249/14 , C07D271/10 , C07D277/28 , C07D277/32 , C07D277/64 , C07D295/108 , C07D295/12 , C07D295/192 , C07D307/06 , C07D307/52 , C07D331/04 , C07D401/10 , C07D405/04
摘要: This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.
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68.AMINOCYCLOBUTANE DERIVATIVES, METHOD FOR PREPARING SAME AND THE USE THEREOF AS DRUGS 审中-公开
标题翻译: 氨基胆碱衍生物,其制备方法及其作为药物的用途公开(公告)号:US20170065543A1
公开(公告)日:2017-03-09
申请号:US15262885
申请日:2016-09-12
发明人: Bernard VACHER , Elodie BLANC , Ronan DEPOORTERE
IPC分类号: A61K31/165
CPC分类号: A61K31/165 , C07C231/14 , C07C235/40 , C07C237/24 , C07C2601/04 , C07D307/00
摘要: The present inventions concerns derivatives of aminocyclobutane, particularly as NMDA receptor antagonists, their application in human therapy and their method of preparation.These compounds correspond to the general formula (1): wherein: X1 represents a hydrogen atom or fluorine atom; X2 is a hydrogen atom or fluorine atom or chlorine atom; R1 represents a hydrogen atom or fluorine atom or chlorine atom or methyl group or methoxy group or cyano group; R2 represents independently or together a methyl group or ethyl group.
摘要翻译: 本发明涉及氨基环丁烷的衍生物,特别是作为NMDA受体拮抗剂,它们在人类治疗中的应用及其制备方法。 这些化合物对应于通式(1):其中:X1表示氢原子或氟原子; X2是氢原子或氟原子或氯原子; R1表示氢原子或氟原子或氯原子或甲基或甲氧基或氰基; R2独立地表示甲基或乙基。
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69.Compound having ability to inhibit 11Beta-HSD1 enzyme or pharmaceutically acceptable salt thereof, method for producing same, and pharmaceutical composition containing same as active ingredient 有权
标题翻译: 具有抑制11Beta-HSD1酶或其药学上可接受的盐的能力的化合物,其制备方法和含有作为活性成分的药物组合物公开(公告)号:US09464044B2
公开(公告)日:2016-10-11
申请号:US14409414
申请日:2013-06-04
申请人: AHN-GOOK PHARMACEUTICAL CO., LTD. , BAMICHEM Co., Ltd. , INCHEON UNIVERSITY INDUSTRY ACADEMIC COOPERATION FOUNDATION
发明人: Soon Kil Ahn , Jin Auh , Nam Song Choi , Chang Kyun Han , Tae-Jeong Kim , Kamsa Pae , Young June Shin , Dong-Oh Han , Cheol Kyu Han
IPC分类号: C07C311/19 , C07C311/21 , C07C275/28 , C07C311/08 , C07C311/29 , C07C237/24 , C07D213/82 , C07D215/08 , C07D217/06 , C07D231/18 , C07D333/34 , C07C311/14 , C07D239/42 , C07D241/42 , C07D417/12 , C07D275/06 , C07D277/36 , C07D209/08 , C07D277/56 , C07D295/215 , C07D213/70 , C07D307/64
CPC分类号: C07C311/21 , C07C237/24 , C07C275/28 , C07C311/08 , C07C311/14 , C07C311/19 , C07C311/29 , C07C2601/02 , C07C2601/18 , C07C2602/42 , C07C2603/74 , C07D209/08 , C07D213/70 , C07D213/82 , C07D215/08 , C07D217/06 , C07D231/18 , C07D239/42 , C07D241/42 , C07D275/06 , C07D277/36 , C07D277/56 , C07D295/215 , C07D307/64 , C07D333/34 , C07D417/12
摘要: The present invention relates to a novel compound or a pharmaceutically acceptable salt thereof inhibiting 11β-HSD1 enzyme activity, a preparation method of the same, and a pharmaceutical composition comprising the same as an active ingredient. Since the compound of the present invention selectively inhibits the activity of 11β-HSD1 (11β-Hydroxysteroid dehydrogenase type 1), the compound of the invention can be effectively used as a therapeutic agent for the treatment of diseases caused by the over-activation of 11β-HSD1 such as non-insulin dependent type II diabetes, insulin resistance, obesity, lipid disorder, metabolic syndrome, and other diseases or condition mediated by the excessive activity of glucocorticoid.
摘要翻译: 本发明涉及抑制11β-HSD1酶活性的新型化合物或其药学上可接受的盐,其制备方法以及含有该活性成分的药物组合物。 由于本发明化合物选择性地抑制11β-HSD1(11β-羟基类固醇脱氢酶1型)的活性,本发明化合物可有效地用作治疗由11β过度活化引起的疾病的治疗剂 -HSD1如非胰岛素依赖型II型糖尿病,胰岛素抵抗,肥胖症,脂质障碍,代谢综合征等疾病或由糖皮质激素过度活性介导的病症。
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公开(公告)号:US09403767B2
公开(公告)日:2016-08-02
申请号:US13803295
申请日:2013-03-14
申请人: Grünenthal GmbH
发明人: Bert Nolte , Wolfgang Schröder , Klaus Linz , Werner Englberger , Hans Schick , Heinz Graubaum , Birgit Braun , Sigrid Ozegowski , József Bálint , Helmut Sonnenschein
IPC分类号: C07C211/00 , C07D209/20 , C07C211/40 , C07C215/14 , C07C215/42 , C07C217/74 , C07C223/04 , C07C229/16 , C07C233/36 , C07C233/40 , C07C233/41 , C07C233/62 , C07C233/79 , C07C235/54 , C07C237/06 , C07C275/24 , C07C311/07 , C07C311/18 , C07D209/12 , C07D209/14 , C07D211/62 , C07D213/12 , C07D213/82 , C07D231/14 , C07D251/54 , C07D295/135 , C07D309/08 , C07D333/20 , C07D403/08 , C07D409/08 , A61K31/135 , A61K45/06 , A61K31/136 , A61K31/165 , A61K31/18 , A61K31/404 , A61K31/53 , A61K31/5377 , C07C211/54 , C07C237/24 , C07C311/37 , C07D251/48
CPC分类号: C07D209/20 , A61K31/135 , A61K31/136 , A61K31/165 , A61K31/18 , A61K31/404 , A61K31/53 , A61K31/5377 , A61K45/06 , C07C211/40 , C07C211/54 , C07C215/14 , C07C215/42 , C07C217/74 , C07C223/04 , C07C229/16 , C07C233/36 , C07C233/40 , C07C233/41 , C07C233/62 , C07C233/79 , C07C235/54 , C07C237/06 , C07C237/24 , C07C275/24 , C07C311/07 , C07C311/18 , C07C311/37 , C07C2601/08 , C07C2601/14 , C07C2601/16 , C07D209/12 , C07D209/14 , C07D211/62 , C07D213/12 , C07D213/82 , C07D231/14 , C07D251/48 , C07D251/54 , C07D295/135 , C07D309/08 , C07D333/20 , C07D403/08 , C07D409/08
摘要: The invention relates to compounds that have an affinity to the μ-opioid receptor and the ORL 1-receptor, methods for their production, medications containing these compounds and the use of these compounds for the treatment of pain and other conditions.
摘要翻译: 本发明涉及对μ-阿片受体和ORL1-受体具有亲和力的化合物,其生产方法,含有这些化合物的药物以及这些化合物用于治疗疼痛和其它病症的用途。
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