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公开(公告)号:US20220185801A1
公开(公告)日:2022-06-16
申请号:US17587304
申请日:2022-01-28
发明人: Mark FEINBERG , Santosh A. KHEDKAR
IPC分类号: C07D409/12 , C07D239/38 , C07D311/62 , C07D239/52 , C07D207/44 , C07C251/86 , C07C49/84 , C07C39/15 , C07C205/45 , C07C217/48
摘要: The invention relates to compositions and methods for inhibiting Krüppel-like Factor 10 (KLF10) for modulation of T regulatory cells and cancer immunotherapy.
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公开(公告)号:US11084784B2
公开(公告)日:2021-08-10
申请号:US15128932
申请日:2015-03-25
发明人: Rajiv Sharma , Bichismita Sahu , Sunil Vasantrao Mali , Deepak Singh , Pramod Bhaskar Kumar , Mahesh Dawange , Hitesh Mistry
IPC分类号: C07C317/32 , C07D311/22 , C07D335/06 , C07D265/36 , C07D207/27 , C07D295/26 , C07C233/29 , C07C237/22 , A61K31/18 , A61K31/351 , C07C217/88 , C07C317/24 , C07C311/08 , C07C255/46 , C07C233/54 , C07C217/48 , C07C211/45 , C07C215/70 , C07C255/50 , A61K31/277 , C07C309/89 , C07C225/22 , C07C229/42 , C07C317/44 , A61K31/165 , C07C323/09 , A61K31/5375 , C07C311/37 , C07F5/02 , A61K31/402 , C07D317/72 , C07C217/76 , C07C205/36 , A61K31/382 , C07F7/18 , C07C237/52 , C07C311/21 , C07C381/10 , C07D211/14 , C07D213/30 , C07D231/12 , C07D233/58 , C07D257/04 , C07D295/088 , C07D295/135 , C07D295/192 , C07D305/08
摘要: The present invention relates to a compound of formula I, or an isotopic form, stereoisomer, a tautomer, a pharmaceutically acceptable salt, a solvate, a polymorph, a prodrug, N-oxide or S-oxide thereof; and processes for their preparation. The invention further relates to pharmaceutical compositions containing the compounds and their use in the treatment of diseases or disorders mediated by RORγ.
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公开(公告)号:US10947180B2
公开(公告)日:2021-03-16
申请号:US16679026
申请日:2019-11-08
申请人: vTv Therapeutics LLC
发明人: Per Sauerberg , Pavel Pihera , Zdenek Polivka , Miroslav Havranek , Ingrid Petterson , John Patrick Mogensen
IPC分类号: C07C69/736 , A61K31/5375 , A61K31/415 , C07C59/70 , C07C217/48 , C07C323/16 , C07C323/32 , C07D211/46 , C07D213/30 , C07D231/12 , C07D295/096 , C07D307/79 , C07D333/16 , C07D333/54 , C07D265/30 , C07D213/36 , C07D295/112 , C07D307/81 , C07D333/20 , A61K31/192 , A61K31/195 , A61K31/343 , A61K31/381 , A61K31/40 , A61K31/4025 , A61K31/4402 , A61K31/445 , A61K31/495 , A61K31/5377
摘要: Phenoxy acetic acids and phenyl propionic acids and their use in improving mitochondrial energy output in a subject are provided herein. The present compounds are activators of PPARδ and may be useful for treating conditions mediated by the same.
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公开(公告)号:US10471066B2
公开(公告)日:2019-11-12
申请号:US15817470
申请日:2017-11-20
申请人: vTv Therapeutics LLC
发明人: Per Sauerberg , Pavel Pihera , Zdenek Polivka , Miroslav Havranek , Ingrid Pettersson , John Patrick Mogensen
IPC分类号: A61K31/415 , A61K31/5375 , A61K31/5377 , C07C59/70 , C07C217/48 , C07C323/16 , C07C323/32 , C07D211/46 , C07D213/30 , C07D231/12 , C07D295/096 , C07D307/79 , C07D333/16 , C07D333/54 , C07D265/30 , C07D213/36 , C07D295/112 , C07D307/81 , C07D333/20 , A61K31/192 , A61K31/195 , A61K31/343 , A61K31/381 , A61K31/40 , A61K31/4025 , A61K31/4402 , A61K31/445 , A61K31/495
摘要: Phenoxy acetic acids and phenyl propionic acids and their use in improving mitochondrial energy output in a subject are provided herein. The present compounds are activators of PPARδ and may be useful for treating conditions mediated by the same.
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公开(公告)号:US20180321226A1
公开(公告)日:2018-11-08
申请号:US16021941
申请日:2018-06-28
申请人: Roger GIESE , Poguang WANG
发明人: Roger GIESE , Poguang WANG
IPC分类号: G01N33/52 , C07C217/48 , C07C217/58
CPC分类号: G01N33/52 , C07C217/48 , C07C217/58 , G01N2458/15 , G01N2560/00
摘要: The invention provides methods of detecting an analyte by multi-stage mass spectrometry with improved S/N ratio. An analyte is labeled with a positively-charged mass tag to form a precursor ion that leads by anchimeric assistance to a greatly enhanced, analyte-characteristic first product ion that can, in turn, lead to a greatly enhanced, analyte-characteristic second product ion in a mass spectrometer. Either a three stage mass spectrometer (true MS3) or a two-stage mass spectrometer (MS2) operated in a pseudo MS3 mode can be used. The precursor ion is split via an anchimeric-assisted reaction to form a first product ion, which in turn can be fragmented to form the second product ion. The methods offer extreme ultrasensitivity, at the low amol level. The invention also provides anchimeric mass tags for use in the methods. A wide variety of previously undetectable analytes of biological or environmental origin can be detected and quantified.
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公开(公告)号:US10071967B2
公开(公告)日:2018-09-11
申请号:US15101380
申请日:2014-12-04
发明人: Pierre Cristau , Philippe Desbordes , Julie Geist , Lionel Nicolas , Philippe Rinolfi , Jan-Peter Schmidt , Tomoki Tsuchiya , Jean-Pierre Vors , Ulrike Wachendorff-Neumann
IPC分类号: C07D231/12 , A01N33/04 , C07D231/14 , C07D231/16 , C07D233/28 , A01N35/04 , A01N37/34 , A01N43/10 , A01N43/56 , A01N43/647 , A01N43/76 , A01N55/00 , C07C22/04 , C07C47/54 , C07C47/55 , C07C47/575 , C07C211/27 , C07C217/48 , C07C255/46 , C07D249/06 , C07D263/32 , C07D307/38 , C07D307/54 , C07F7/08
CPC分类号: C07D231/12 , A01N33/04 , A01N35/04 , A01N37/34 , A01N43/10 , A01N43/56 , A01N43/647 , A01N43/76 , A01N55/00 , C07C22/04 , C07C47/54 , C07C47/55 , C07C47/575 , C07C211/27 , C07C217/48 , C07C255/46 , C07C2601/02 , C07D231/14 , C07D231/16 , C07D233/28 , C07D249/06 , C07D263/32 , C07D307/38 , C07D307/54 , C07F7/0803
摘要: The present invention relates to fungicidal N-cycloalkyl-N-{[2-(1-substitutedcycloalkyl)phenyl]methylene} carboxamide derivatives and their thiocarbonyl derivatives, their process of preparation and intermediate compounds for their preparation, their use as fungicides, particularly in the form of fungicidal compositions and methods for the control of phytopathogenic fungi of plants using these compounds or their compositions.
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公开(公告)号:US09944618B2
公开(公告)日:2018-04-17
申请号:US14776397
申请日:2014-03-10
申请人: Mayo Foundation for Medical Education and Research , Virginia Tech Intellectual Properties, Inc.
IPC分类号: C07D333/28 , C07C259/06 , C07C211/30 , A61K31/138 , C07C215/28 , C07C215/68 , C07C217/48 , C07C217/62 , C07C217/64 , C07C233/43 , C07C235/06 , C07C235/08 , C07D317/58 , C07D319/18 , C07D333/20 , C07D261/08 , C07D265/06 , C07D267/10 , C07D207/12 , C07D271/06 , C07D295/135 , C07D295/185 , C07D213/30 , C07D213/61 , C07D213/64 , C07D213/65 , C07C215/30 , C07C235/14 , C07C323/32 , C07D205/04 , C07D213/38 , C07D215/06 , C07D295/192
CPC分类号: C07D333/28 , A61K31/138 , C07C211/30 , C07C215/28 , C07C215/30 , C07C215/68 , C07C217/48 , C07C217/62 , C07C217/64 , C07C233/43 , C07C235/06 , C07C235/08 , C07C235/14 , C07C259/06 , C07C323/32 , C07C2601/02 , C07C2601/04 , C07D205/04 , C07D207/12 , C07D213/30 , C07D213/38 , C07D213/61 , C07D213/64 , C07D213/65 , C07D215/06 , C07D261/08 , C07D265/06 , C07D267/10 , C07D271/06 , C07D295/135 , C07D295/185 , C07D295/192 , C07D317/58 , C07D319/18 , C07D333/20
摘要: This document relates to compounds as well as methods and materials involved in modulating neurotransmitter reuptake. For example, compounds, methods for synthesizing compounds, and methods for inhibiting neurotransmitter reuptake are provided. Specifically gamma-amino alcohol derivatives that inhibit the reuptake of neurotransmitters such as dopamine, serotonin, epinephrine or norepinephrine are provided as therapeutic agents for the treatment of depression or anxiety in a mammalian subject.
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公开(公告)号:US20160326120A1
公开(公告)日:2016-11-10
申请号:US15101380
申请日:2014-12-04
发明人: Pierre CRISTAU , Philippe DESBORDES , Julie GEIST , Lionel NICOLAS , Philippe RINOLFI , Jan-Peter SCHMIDT , Tomoki TSUCHIYA , Jean-Pierre VORS , Ulrike WACHENDORFF-NEUMANN
IPC分类号: C07D231/12 , C07D249/06 , C07D307/38 , C07D263/32 , C07C211/27 , C07C217/48 , C07F7/08 , C07C255/46 , C07C47/54 , C07C47/55 , C07C47/575 , C07C22/04 , A01N43/56 , A01N43/647 , A01N43/10 , A01N43/76 , A01N33/04 , A01N55/00 , A01N37/34 , A01N35/04 , C07D307/54
CPC分类号: C07D231/12 , A01N33/04 , A01N35/04 , A01N37/34 , A01N43/10 , A01N43/56 , A01N43/647 , A01N43/76 , A01N55/00 , C07C22/04 , C07C47/54 , C07C47/55 , C07C47/575 , C07C211/27 , C07C217/48 , C07C255/46 , C07C2601/02 , C07D231/14 , C07D231/16 , C07D233/28 , C07D249/06 , C07D263/32 , C07D307/38 , C07D307/54 , C07F7/0803
摘要: The present invention relates to fungicidal N-cycloalkyl-N-{[2-(1-substitutedcycloalkyl)phenyl]methylene} carboxamide derivatives and their thiocarbonyl derivatives, their process of preparation and intermediate compounds for their preparation, their use as fungicides, particularly in the form of fungicidal compositions and methods for the control of phytopathogenic fungi of plants using these compounds or their compositions.
摘要翻译: 本发明涉及杀真菌N-环烷基-N - {[2-(1-取代环烷基)苯基]亚甲基]甲酰胺衍生物及其硫代羰基衍生物,其制备方法及其制备中间体化合物,它们用作杀真菌剂,特别是在 使用这些化合物或其组合物的杀真菌组合物和控制植物病原性真菌的方法。
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公开(公告)号:US09447310B2
公开(公告)日:2016-09-20
申请号:US14810106
申请日:2015-07-27
申请人: Thomas P. Daly
发明人: Thomas P. Daly
IPC分类号: C07C229/22 , C07C229/12 , C07C309/14 , C07C217/08 , C07C215/08 , C07C217/48 , C07C219/22 , C07C205/40 , C07C205/15 , C09K3/00 , C07D213/74 , C07F9/58 , C07F9/09 , C07F9/38
CPC分类号: C09K3/00 , C07C205/15 , C07C205/40 , C07C215/08 , C07C217/08 , C07C217/28 , C07C217/48 , C07C219/06 , C07C219/22 , C07C229/12 , C07C229/22 , C07C309/14 , C07D213/74 , C07D295/088 , C07D295/15 , C07F9/091 , C07F9/3808 , C07F9/3817 , C07F9/58 , C11D1/66
摘要: Amines and amine derivatives that improve the buffering range, and/or reduce the chelation and other negative interactions of the buffer and the system to be buffered. The reaction of amines or polyamines with various molecules to form polyamines with differing pKa's will extend the buffering range, derivatives that result in polyamines that have the same pKa yields a greater buffering capacity. Derivatives that result in zwitterionic buffers improve yield by allowing a greater range of stability.
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公开(公告)号:US20150336876A1
公开(公告)日:2015-11-26
申请号:US14761897
申请日:2014-01-21
IPC分类号: C07C217/48 , C07D333/20 , C07D277/28 , C07C217/72 , C07D215/233 , C07D213/68 , C07C255/54 , C07C255/37 , C07D215/26 , C07D209/48 , C07D401/12 , C07D409/06 , C07D405/06 , C07D417/06 , C07D413/06 , C07C271/16
CPC分类号: C07C217/48 , C07C211/09 , C07C217/04 , C07C217/72 , C07C255/37 , C07C255/54 , C07C271/16 , C07C271/20 , C07C317/22 , C07C317/28 , C07C323/20 , C07C323/25 , C07D209/48 , C07D213/68 , C07D215/22 , C07D215/233 , C07D215/26 , C07D263/32 , C07D277/28 , C07D295/08 , C07D307/52 , C07D333/20 , C07D401/12 , C07D403/12 , C07D405/04 , C07D405/06 , C07D409/04 , C07D409/06 , C07D413/04 , C07D413/06 , C07D417/04 , C07D417/06
摘要: The invention provides a compound having a selective inhibitory activity against highly-expressed LAT-1 in tumor cell. The compound is represented by the formula (I): wherein each symbol is as defined in the specification, or a salt thereof, and a LAT-1 inhibitor comprising the same.
摘要翻译: 本发明提供对肿瘤细胞中高表达LAT-1具有选择性抑制活性的化合物。 化合物由式(I)表示:其中每个符号如说明书中所定义,或其盐,和含有该化合物的LAT-1抑制剂。
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