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公开(公告)号:US10941151B2
公开(公告)日:2021-03-09
申请号:US16880337
申请日:2020-05-21
申请人: Ogeda SA
发明人: Hamid R. Hoveyda , Guillaume Dutheuil , Graeme Lovat Fraser , Marie-Odile Roy , Mohamed El Bousmaqui , Frederic Batt
IPC分类号: C07D241/08 , C07D487/04
摘要: The present invention relates to novel compounds of Formula I and their use in therapeutic treatments. The invention further relates to a novel chiral synthesis of 5,6,7,(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines using N-sp3 protective groups. The invention also provides intermediates for use in the synthesis of compounds of Formula I.
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公开(公告)号:US20200222399A1
公开(公告)日:2020-07-16
申请号:US16796422
申请日:2020-02-20
申请人: OGEDA SA
发明人: Hamid HOVEYDA , Graeme FRASER
IPC分类号: A61K31/4985 , A61K31/4725 , A61K31/495 , A61K31/472 , A61P3/04
摘要: Disclosed is use of NK3R antagonists for the therapeutic treatment leptin-related disease.
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公开(公告)号:US10683295B2
公开(公告)日:2020-06-16
申请号:US16047740
申请日:2018-07-27
申请人: Ogeda SA
发明人: Hamid R. Hoveyda , Guillaume Dutheuil , Graeme Lovat Fraser , Marie-Odile Roy , Mohamed El Bousmaqui , Frederic Batt
IPC分类号: C07D241/38 , C07D487/04
摘要: The present invention relates to novel compounds of Formula I and their use in therapeutic treatments. The invention further relates to a novel chiral synthesis of 5,6,7,(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines using N-sp3 protective groups. The invention also provides intermediates for use in the synthesis of compounds of Formula I.
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公开(公告)号:US10214533B2
公开(公告)日:2019-02-26
申请号:US15956311
申请日:2018-04-18
申请人: OGEDA SA
发明人: Hamid Hoveyda , Guillaume Dutheuil , Graeme Fraser
IPC分类号: C07D487/04 , A61K31/4985
摘要: Novel compounds of Formula I and their use in therapeutic treatments.
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公开(公告)号:US20180289705A1
公开(公告)日:2018-10-11
申请号:US15557832
申请日:2016-03-16
申请人: OGEDA SA
发明人: Hamid HOVEYDA , Graeme FRASER
IPC分类号: A61K31/4985 , A61P3/04
摘要: Disclosed is use of NK3R antagonists for the therapeutic treatment of pathological excess body fat and/or prevention of body fat gain in patients. Also disclosed is a cosmetic method for stimulating the loss of excess of body fat, including the administration of a NK-3 receptor antagonist.
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公开(公告)号:US20180194772A1
公开(公告)日:2018-07-12
申请号:US15906268
申请日:2018-02-27
申请人: Ogeda SA
IPC分类号: C07D487/04 , A61K31/407 , A61K31/4985
CPC分类号: C07D487/04 , A61K31/407 , A61K31/4985
摘要: The present invention is directed to novel compounds of formula I and their use as therapeutic compounds.
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公开(公告)号:US20240199618A1
公开(公告)日:2024-06-20
申请号:US18235976
申请日:2023-08-21
申请人: Ogeda SA
发明人: Hamid Hoveyda , Guillaume Dutheuil , Graeme Fraser
IPC分类号: C07D487/04
CPC分类号: C07D487/04
摘要: A method for treating and/or preventing polycystic ovary syndrome (PCOS) including the administration, to a patient in need thereof, of a pharmaceutically effective amount of a compound of Formula I
or a pharmaceutically acceptable solvate thereof.-
公开(公告)号:US11731974B2
公开(公告)日:2023-08-22
申请号:US17066086
申请日:2020-10-08
申请人: Ogeda SA
IPC分类号: C07D487/04
CPC分类号: C07D487/04
摘要: A method for treating and/or preventing polycystic ovary syndrome (PCOS) including the administration, to a patient in need thereof, of a pharmaceutically effective amount of a compound of Formula I
or a pharmaceutically acceptable solvate thereof.-
公开(公告)号:US11078203B2
公开(公告)日:2021-08-03
申请号:US16629710
申请日:2018-07-12
申请人: OGEDA SA
发明人: Hamid Hoveyda
IPC分类号: C07D487/04 , A61P5/08 , A61P5/24
摘要: Deuterated fezolinetant (R)-(4-fluorophenyl)-(8-methyl-3-(3-(methyl-d3)-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]trizolo[4,3-a]pyrazin-7(8H)-yl)methanone: or a pharmaceutically acceptable salt or solvate thereof, as an NK-3 antagonist. Also, methods of modulating NK-3 receptor activity including administering an effective amount of the compound or pharmaceutically acceptable salt or solvate thereof. Additionally, a process for manufacturing the compound or pharmaceutically acceptable salt or solvate thereof.
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公开(公告)号:US20200270254A1
公开(公告)日:2020-08-27
申请号:US16629710
申请日:2018-07-12
申请人: OGEDA SA
发明人: Hamid HOVEYDA
IPC分类号: C07D487/04 , A61P5/08 , A61P5/24
摘要: Deuterated fezolinetant (R)-(4-fluorophenyl)-(8-methyl-3-(3-(methyl-d3)-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]trizolo[4,3-a]pyrazin-7(8H)-yl)methanone: or a pharmaceutically acceptable salt or solvate thereof, as an NK-3 antagonist. Also, methods of modulating NK-3 receptor activity including administering an effective amount of the compound or pharmaceutically acceptable salt or solvate thereof. Additionally, a process for manufacturing the compound or pharmaceutically acceptable salt or solvate thereof.
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