LT3452448T - Integruoto signalinio kelio streso moduliatoriai - Google Patents
Integruoto signalinio kelio streso moduliatoriaiInfo
- Publication number
- LT3452448T LT3452448T LTEPPCT/US2017/031360T LTUS2017031360T LT3452448T LT 3452448 T LT3452448 T LT 3452448T LT US2017031360 T LTUS2017031360 T LT US2017031360T LT 3452448 T LT3452448 T LT 3452448T
- Authority
- LT
- Lithuania
- Prior art keywords
- modulators
- integrated stress
- stress pathway
- pathway
- integrated
- Prior art date
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/18—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having at least one of the singly-bound oxygen atoms further bound to a carbon atom of a six-membered aromatic ring, e.g. phenoxyacetamides
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/65—One oxygen atom attached in position 3 or 5
- C07D213/66—One oxygen atom attached in position 3 or 5 having in position 3 an oxygen atom and in each of the positions 4 and 5 a carbon atom bound to an oxygen, sulphur, or nitrogen atom, e.g. pyridoxal
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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| US201662332278P | 2016-05-05 | 2016-05-05 | |
| PCT/US2017/031360 WO2017193034A1 (en) | 2016-05-05 | 2017-05-05 | Modulators of the integrated stress pathway |
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| US20210145771A1 (en) * | 2017-07-03 | 2021-05-20 | Glaxosmithkline Intellectual Property Development Limited | N-(3-(2-(4-chlorophenoxy)acetamido)bicyclo[1.1.1] pentan-1-yl)-2-cyclobutane-1- carboxamide derivatives and related compounds as atf4 inhibitors for treating cancer and other diseases |
| CN111094233B (zh) | 2017-08-09 | 2024-03-15 | ę“ēŗ³ē«å¶čÆå ¬åø | ååē©ćē»åē©åę¹ę³ |
| PT3676297T (pt) | 2017-09-01 | 2023-08-29 | Denali Therapeutics Inc | Compostos, composiƧƵes e mƩtodos |
| JP2021501785A (ja) | 2017-11-02 | 2021-01-21 | ć«ćŖć³ ć©ć¤ć ćµć¤ćØć³ć·ć¼ćŗ ćØć«ćØć«ć·ć¼ | ēµ±åēć¹ćć¬ć¹ēµč·Æć®čŖæēÆå¤ |
| UY37956A (es) * | 2017-11-02 | 2019-05-31 | Abbvie Inc | Moduladores de la vĆa de estrĆ©s integrada |
| UY37958A (es) * | 2017-11-02 | 2019-05-31 | Abbvie Inc | Moduladores de la vĆa de estrĆ©s integrada |
| RU2020122711A (ru) * | 2017-12-13 | 2022-01-17 | ŠŠ ŠŠŠ”ŠŠ” ŠŠŠŠŠ¢ŠŠ ŠŠ»ŠŠ»Š”Šø | ŠŠ½Š³ŠøŠ±ŠøŃоŃŃ ŠæŃŃŠø ŠøŠ½ŃŠµŠ³ŃŠøŃŠ¾Š²Š°Š½Š½Š¾Š¹ ŃŠµŠ°ŠŗŃŠøŠø на ŃŃŃŠµŃŃ |
| US20210130308A1 (en) * | 2018-03-23 | 2021-05-06 | Denali Therapeutics Inc. | Modulators of eukaryotic initiation factor 2 |
| SG11202011014VA (en) | 2018-06-05 | 2020-12-30 | Praxis Biotech LLC | Inhibitors of integrated stress response pathway |
| JP2021529814A (ja) * | 2018-07-09 | 2021-11-04 | ć°ć©ćÆć½ć¹ćć¹ćÆć©ć¤ć³ćć¤ć³ćć¬ćÆćć„ć¢ć«ćććććć£ć¼ććć£ććććć”ć³ćććŖććććļ¼§ļ½ļ½ļ½ļ½ļ½ļ½ļ½ļ½ļ½ļ½ļ½ļ½ļ½ļ½ Iļ½ļ½ļ½ ļ½ļ½ļ½ ļ½ļ½ļ½ļ½ļ½ ļ¼°ļ½ļ½ļ½ļ½ ļ½ļ½ļ½ ļ¼¤ļ½ ļ½ļ½ ļ½ļ½ļ½ļ½ļ½ ļ½ļ½ Lļ½ļ½ļ½ļ½ļ½ ļ½ | åå¦ååē© |
| TWI832295B (zh) * | 2018-10-11 | 2024-02-11 | ē¾ååä¾å ēå½ē§åøęéč²¬ä»»å ¬åø | ę“åęęæč·Æå¾ä¹åč„čŖæēÆå |
| MA54959A (fr) | 2019-02-13 | 2021-12-22 | Denali Therapeutics Inc | ComposƩs, compositions et procƩdƩs |
| CA3129609A1 (en) * | 2019-02-13 | 2020-08-20 | Denali Therapeutics Inc. | Eukaryotic initiation factor 2b modulators |
| KR20210134351A (ko) * | 2019-02-25 | 2021-11-09 | ķė½ģģ¤ ė°ģ“ģ¤ķ ķ¬ ģģģØ | ķµķ© ģ¤ķøė ģ¤ ė°ģ ź²½ė”ģ ģµģ ģ |
| EA202192900A1 (ru) | 2019-04-23 | 2022-03-18 | ŠŠ²Š¾Ńек ŠŠ½ŃŠµŃнеŃнл ŠŠ¼Š±Ń | ŠŠ¾Š“ŃŠ»ŃŃŠ¾ŃŃ ŠæŃŃŠø ŠøŠ½ŃŠµŠ³ŃŠøŃŠ¾Š²Š°Š½Š½Š¾Š¹ ŃŠµŠ°ŠŗŃŠøŠø на ŃŃŃŠµŃŃ |
| AU2020261234A1 (en) | 2019-04-23 | 2021-11-11 | Evotec International Gmbh | Modulators of the integrated stress response pathway |
| AU2020266592A1 (en) * | 2019-04-30 | 2021-12-02 | Abbvie Inc. | Substituted cyclolakyls as modulators of the integrated stress pathway |
| PH12021552759A1 (en) * | 2019-04-30 | 2022-07-04 | Abbvie Inc | Substituted cycloalkyls as modulators of the integrated stress pathway |
| CA3142748A1 (en) | 2019-06-12 | 2020-12-17 | Praxis Biotech LLC | Modulators of integrated stress response pathway |
| PH12022551379A1 (en) * | 2019-12-06 | 2023-05-03 | Vertex Pharma | Substituted tetrahydrofurans as modulators of sodium channels |
| KR20220133252A (ko) | 2020-01-28 | 2022-10-04 | ģ볓ķ ģøķ°ė“ģ ė ź²ģ ė² ķ | ķµķ© ģ¤ķøė ģ¤ ė°ģ ź²½ė”ģ ģ”°ģ ģ |
| JP2023517944A (ja) | 2020-03-11 | 2023-04-27 | ćØć“ć©ćććÆć»ć¤ć³ćæć¼ćć·ć§ćć«ć»ć²ć¼ć«ć·ć£ććć»ćććć»ćć·ć„ć¬ć³ćÆćć«ć»ćććć³ć° | ēµ±åēć¹ćć¬ć¹åæēēµč·Æć®čŖæēÆå å |
| US11351149B2 (en) | 2020-09-03 | 2022-06-07 | Pfizer Inc. | Nitrile-containing antiviral compounds |
| AU2021366303A1 (en) | 2020-10-22 | 2023-06-22 | Evotec International Gmbh | Modulators of the integrated stress response pathway |
| US20230391763A1 (en) | 2020-10-22 | 2023-12-07 | Evotec International Gmbh | Modulators of the integrated stress response pathway |
| CA3195290A1 (en) | 2020-10-22 | 2022-04-28 | Holly Victoria Atton | Modulators of the integrated stress response pathway |
| JP2023553149A (ja) * | 2020-12-10 | 2023-12-20 | ć¢ćøć§ćć»ćć¤ćŖćć”ć¼ćć·ć„ć¼ćć£ć«ć«ćŗć»ćć¼ć«ćć£ć³ć°ć¹ć»ć¤ć³ć³ć¼ćć¬ć¤ććć | ē®č転移ę§ćććę²»ēććę¹ę³ |
| KR20250122004A (ko) * | 2024-02-05 | 2025-08-13 | ģ¬ėØė²ģø ėźµ¬ź²½ė¶ģ²ØėØģė£ģ°ģ ģ§ķ„ģ¬ėØ | ģ ź·ķ eIF2B ģģ©ģ ė° ģ“넼 ķ¬ķØķė ėģ¬ģ§ķ ģė°© ėė ģ¹ė£ģ© ģ”°ģ±ė¬¼ |
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| US4911920A (en) | 1986-07-30 | 1990-03-27 | Alcon Laboratories, Inc. | Sustained release, comfort formulation for glaucoma therapy |
| FR2588189B1 (fr) | 1985-10-03 | 1988-12-02 | Merck Sharp & Dohme | Composition pharmaceutique de type a transition de phase liquide-gel |
| EP0495421B1 (en) | 1991-01-15 | 1996-08-21 | Alcon Laboratories, Inc. | Use of carrageenans in topical ophthalmic compositions |
| JP2007517868A (ja) | 2004-01-07 | 2007-07-05 | ć¢ć¹ćć©ć¼ćć« ć¢ćÆććć©ć° | ę²»ēč¬ļ½ |
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| AU2005267093B2 (en) | 2004-07-23 | 2009-10-01 | Nuada Llc | Peptidase inhibitors |
| GB0516314D0 (en) * | 2005-08-08 | 2005-09-14 | Argenta Discovery Ltd | Compound |
| RU2442771C2 (ru) * | 2005-08-08 | 2012-02-20 | ŠŃŠ“Š¶ŠµŠ½ŃŠ° ŠŠøŃŠŗŠ°Š²ŠµŃŠø ŠŃŠ“ | ŠŃŠ¾ŠøŠ·Š²Š¾Š“Š½ŃŠµ Š±ŠøŃŠøŠŗŠ»Š¾[2,2,1]гепŃ-7-иламина Šø ŠøŃ ŠæŃŠøŠ¼ŠµŠ½ŠµŠ½ŠøŃ |
| WO2007017752A1 (en) * | 2005-08-10 | 2007-02-15 | Pfizer Limited | Substituted triazole derivatives as oxytocin antagonists |
| MX2010003249A (es) * | 2007-09-25 | 2010-11-09 | Takeda Pharmaceutical | Inhibidores de quinasas sĆmil polo. |
| US8741894B2 (en) * | 2010-03-17 | 2014-06-03 | Axikin Pharmaceuticals, Inc. | Arylsulfonamide CCR3 antagonists |
| CN103025725B (zh) | 2010-08-10 | 2015-09-16 | å®ęÆę³°ę„å¶čÆęéå ¬åø | ęēÆååē© |
| AR084457A1 (es) * | 2010-12-22 | 2013-05-15 | Lundbeck & Co As H | Derivados de biciclo[3,2,1]octilamida |
| AU2014233520B2 (en) * | 2013-03-15 | 2019-02-21 | The Regents Of The University Of California | Modulators of the eIF2alpha pathway |
| WO2015038778A1 (en) * | 2013-09-11 | 2015-03-19 | The Brigham And Women's Hospital, Inc. | SUBSTITUTED UREA EIF2α KINASE ACTIVATORS |
| EP3489232A3 (en) * | 2014-04-04 | 2019-07-31 | Syros Pharmaceuticals, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
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