MA35861B1 - Inhibiteur de la kinase régulant les signaux de l'apoptose - Google Patents
Inhibiteur de la kinase régulant les signaux de l'apoptoseInfo
- Publication number
- MA35861B1 MA35861B1 MA37202A MA37202A MA35861B1 MA 35861 B1 MA35861 B1 MA 35861B1 MA 37202 A MA37202 A MA 37202A MA 37202 A MA37202 A MA 37202A MA 35861 B1 MA35861 B1 MA 35861B1
- Authority
- MA
- Morocco
- Prior art keywords
- apoptosis
- signals
- kinase inhibitor
- regulating
- inhibitor regulating
- Prior art date
Links
- 230000006907 apoptotic process Effects 0.000 title abstract 2
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- 230000001105 regulatory effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000007342 Diabetic Nephropathies Diseases 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 208000033679 diabetic kidney disease Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 208000017169 kidney disease Diseases 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 201000002793 renal fibrosis Diseases 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4436—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—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
- C07D213/02—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
- 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
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/56—Amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Nutrition Science (AREA)
- Physiology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Gastroenterology & Hepatology (AREA)
- Urology & Nephrology (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Physical Education & Sports Medicine (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Virology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
Abstract
La présente invention concerne un composé de formule (i). Le composé possède une activité inhibitrice de la kinase régulant les signaux de l'apoptose (« ask 1 ») et est donc utile dans le traitement de maladies telles que la néphropathie, la néphropathie diabétique et la fibrose rénale.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261591710P | 2012-01-27 | 2012-01-27 | |
| PCT/US2013/022997 WO2013112741A1 (fr) | 2012-01-27 | 2013-01-24 | Inhibiteur de la kinase régulant les signaux de l'apoptose |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA35861B1 true MA35861B1 (fr) | 2014-12-01 |
Family
ID=47684038
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA37202A MA35861B1 (fr) | 2012-01-27 | 2014-07-11 | Inhibiteur de la kinase régulant les signaux de l'apoptose |
Country Status (39)
| Country | Link |
|---|---|
| US (7) | US8742126B2 (fr) |
| EP (1) | EP2807151B1 (fr) |
| JP (1) | JP5770950B2 (fr) |
| KR (5) | KR101799739B1 (fr) |
| CN (2) | CN104080771B (fr) |
| AP (1) | AP2014007836A0 (fr) |
| AR (2) | AR089818A1 (fr) |
| AU (1) | AU2013201586C1 (fr) |
| BR (1) | BR112014018355B1 (fr) |
| CA (3) | CA3026700C (fr) |
| CL (1) | CL2014001988A1 (fr) |
| CO (1) | CO7061073A2 (fr) |
| CR (1) | CR20140405A (fr) |
| CY (1) | CY1117201T1 (fr) |
| DK (1) | DK2807151T3 (fr) |
| EA (1) | EA024746B1 (fr) |
| ES (1) | ES2558203T3 (fr) |
| HR (1) | HRP20151399T1 (fr) |
| HU (1) | HUE028641T2 (fr) |
| IL (3) | IL233598A (fr) |
| IN (1) | IN2014DN06174A (fr) |
| MA (1) | MA35861B1 (fr) |
| MD (1) | MD4601B1 (fr) |
| ME (1) | ME02322B (fr) |
| MX (3) | MX2014009075A (fr) |
| NZ (1) | NZ739339A (fr) |
| PE (1) | PE20141822A1 (fr) |
| PH (1) | PH12014501697A1 (fr) |
| PL (1) | PL2807151T3 (fr) |
| PT (1) | PT2807151E (fr) |
| RS (1) | RS54492B1 (fr) |
| SG (1) | SG11201404348UA (fr) |
| SI (1) | SI2807151T1 (fr) |
| SM (1) | SMT201600047B (fr) |
| TW (4) | TWI487523B (fr) |
| UA (1) | UA112098C2 (fr) |
| UY (1) | UY34573A (fr) |
| WO (1) | WO2013112741A1 (fr) |
| ZA (1) | ZA201405260B (fr) |
Families Citing this family (151)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI598347B (zh) | 2009-07-13 | 2017-09-11 | 基利科學股份有限公司 | 調節細胞凋亡信號之激酶的抑制劑 |
| EP2651417B1 (fr) | 2010-12-16 | 2016-11-30 | Calchan Limited | Dérivés pyrrolopyrimidine inhibant ask1 |
| UY34573A (es) | 2012-01-27 | 2013-06-28 | Gilead Sciences Inc | Inhibidor de la quinasa que regula la señal de la apoptosis |
| AU2014354769A1 (en) | 2013-11-26 | 2016-05-26 | Gilead Sciences, Inc. | Therapies for treating myeloproliferative disorders |
| AU2015206194A1 (en) | 2014-01-20 | 2016-07-28 | Gilead Sciences, Inc. | Therapies for treating cancers |
| US20150342943A1 (en) * | 2014-06-03 | 2015-12-03 | Gilead Sciences, Inc. | Methods of treating liver disease |
| TW201618781A (zh) | 2014-08-13 | 2016-06-01 | 吉李德科學股份有限公司 | 治療肺高血壓之方法 |
| KR20190035960A (ko) * | 2014-09-24 | 2019-04-03 | 길리애드 사이언시즈, 인코포레이티드 | 간 질환의 치료 방법 |
| MA41252A (fr) * | 2014-12-23 | 2017-10-31 | Gilead Sciences Inc | Formes solides d'un inhibiteur d'ask 1 |
| EP4276095A3 (fr) | 2014-12-23 | 2024-01-17 | Gilead Sciences, Inc. | Procédés de préparation d'inhibiteurs ask1 |
| TW201639573A (zh) | 2015-02-03 | 2016-11-16 | 吉李德科學股份有限公司 | 有關治療癌症之合併治療 |
| EP3722297A1 (fr) | 2015-03-04 | 2020-10-14 | Gilead Sciences, Inc. | Composés modulateurs de récepteurs de type toll |
| SI3191470T1 (sl) | 2015-07-06 | 2019-04-30 | Gilead Sciences, Inc. | Modulatorji COT in postopki njihove uporabe |
| ES2900482T3 (es) | 2015-10-01 | 2022-03-17 | Gilead Sciences Inc | Combinación de un inhibidor de Btk y un inhibidor de punto de control para el tratamiento del cáncer |
| AU2016329075A1 (en) * | 2015-10-02 | 2018-04-26 | Gilead Sciences, Inc. | Combinations of the BTK inhibitor GS-4059 with inhibitors selected from a JAK, ASK1, BRD and/or MMP9 inhibitor to treat cancer, allergic disorders, autoimmune diseases or inflammatory diseases |
| EP3394044A1 (fr) | 2015-12-17 | 2018-10-31 | Gilead Sciences, Inc. | Composés inhibiteurs de kinases se liant à tank |
| JP2019510752A (ja) | 2016-03-04 | 2019-04-18 | ギリアード サイエンシーズ, インコーポレイテッド | オートタキシン阻害剤の組成物及び合剤 |
| WO2017177179A1 (fr) | 2016-04-08 | 2017-10-12 | Gilead Sciences, Inc. | Compositions et méthodes de traitement du cancer, de maladies inflammatoires et de maladies autoimmunes |
| MX2018015584A (es) | 2016-06-13 | 2019-09-18 | I Mab | Anticuerpos anti-pd-l1 y usos de los mismos. |
| WO2018026835A1 (fr) | 2016-08-04 | 2018-02-08 | Gilead Sciences, Inc. | Cobicistat destiné à être utilisé dans des traitements du cancer |
| EP3507288B1 (fr) | 2016-09-02 | 2020-08-26 | Gilead Sciences, Inc. | Dérivés de 4,6-diamino-pyrido[3,2-d]pyrimidine en tant que modulateurs du recepteur de type toll |
| PT3507276T (pt) | 2016-09-02 | 2022-01-11 | Gilead Sciences Inc | Compostos moduladores do recetor de tipo toll |
| US20180133212A1 (en) | 2016-11-03 | 2018-05-17 | Gilead Sciences, Inc. | Combination of a bcl-2 inhibitor and a bromodomain inhibitor for treating cancer |
| WO2018089212A1 (fr) | 2016-11-11 | 2018-05-17 | Gilead Sciences, Inc. | Procédé de traitement d'une maladie hépatique |
| WO2018097977A1 (fr) | 2016-11-22 | 2018-05-31 | Gilead Sciences, Inc. | Formes cristallines d'un complexe phosphate d'un inhibiteur de bet |
| AR110252A1 (es) | 2016-11-30 | 2019-03-13 | Gilead Sciences Inc | Compuestos heterocíclicos fusionados como inhibidores de la quinasa cam |
| SG11201906579UA (en) * | 2017-01-22 | 2019-08-27 | Fujian Cosunter Pharmaceutical Co Ltd | Pyridine derivative as ask1 inhibitor and preparation method and use thereof |
| US10787435B2 (en) | 2017-01-22 | 2020-09-29 | Fuijan Cosunter Pharmaceutical Co. Ltd. | ASK1 inhibitor and preparation method and use thereof |
| SI3383916T1 (sl) | 2017-01-24 | 2022-06-30 | I-Mab Biopharma Us Limited | Protitelesa proti-CD73 in njihove uporabe |
| US10370381B2 (en) | 2017-02-24 | 2019-08-06 | Gilead Sciences, Inc. | Inhibitors of bruton'S tyrosine kinase |
| US10314844B2 (en) | 2017-02-24 | 2019-06-11 | Gilead Sciences, Inc. | Inhibitors of Bruton's tyrosine kinase |
| WO2018157277A1 (fr) * | 2017-02-28 | 2018-09-07 | Eli Lilly And Company | Composés d'isoquinoléine et de naphtydrine |
| US11136324B2 (en) | 2017-03-03 | 2021-10-05 | Jiangsu Hansoh Pharmaceutical Group Co., Ltd. | Substituted imidazoles as apoptosis signal regulating kinase 1 inhibitors |
| JOP20180017A1 (ar) | 2017-03-14 | 2019-01-30 | Gilead Sciences Inc | مثبط كيناز منظم لإشارة تلاشي خلايا |
| CA3056925A1 (fr) | 2017-03-28 | 2018-10-04 | Gilead Sciences, Inc. | Methodes de traitement d'une maladie hepatique |
| CA3059883A1 (fr) | 2017-04-12 | 2018-10-18 | Gilead Sciences, Inc. | Methodes de traitement d'une maladie hepatique |
| JOP20180040A1 (ar) | 2017-04-20 | 2019-01-30 | Gilead Sciences Inc | مثبطات pd-1/pd-l1 |
| JP7377718B2 (ja) | 2017-05-12 | 2023-11-10 | エナンタ ファーマシューティカルズ インコーポレイテッド | アポトーシスシグナル調節キナーゼ1阻害剤およびその使用方法 |
| US10450301B2 (en) | 2017-05-25 | 2019-10-22 | Enanta Pharmaceuticals, Inc. | Apoptosis signal-regulating kinase 1 inhibitors and methods of use thereof |
| WO2018218044A2 (fr) * | 2017-05-25 | 2018-11-29 | Enanta Pharmaceuticals Inc | Inhibiteurs de la kinase 1 de régulation de signal d'apoptose et leurs méthodes d'utilisation |
| US10253018B2 (en) | 2017-05-25 | 2019-04-09 | Enanta Pharmaceuticals, Inc. | Apoptosis signal-regulating kinase 1 inhibitors and methods of use thereof |
| US10495648B2 (en) | 2017-06-13 | 2019-12-03 | Gilead Sciences, Inc. | Methods of treating liver fibrosis |
| CN109265443B (zh) * | 2017-07-18 | 2022-11-29 | 南京圣和药业股份有限公司 | 作为ask抑制剂的杂环化合物及其应用 |
| WO2019046186A1 (fr) | 2017-08-28 | 2019-03-07 | Enanta Pharmaceuticals, Inc. | Inhibiteurs de la kinase 1 régulant le signal apoptotique contenant des tétrazoles et méthodes d'utilisation de ceux-ci |
| CN109456308B (zh) * | 2017-09-06 | 2022-11-29 | 南京圣和药业股份有限公司 | 作为ask抑制剂的杂环化合物及其应用 |
| WO2019047094A1 (fr) * | 2017-09-07 | 2019-03-14 | Eli Lilly And Company | Composés de cyclobutyle-imidazolidinone |
| US10370352B2 (en) | 2017-09-07 | 2019-08-06 | Eli Lilly And Company | Cyclobutyl-imidazolidinone compounds |
| CN111315380A (zh) | 2017-09-08 | 2020-06-19 | 弗朗塞拉美国制药有限责任公司 | 凋亡信号调节激酶抑制剂及其用途 |
| WO2019047161A1 (fr) * | 2017-09-08 | 2019-03-14 | Eli Lilly And Company | Composés d'imidazolidine |
| CN111518080A (zh) * | 2017-10-12 | 2020-08-11 | 深圳市塔吉瑞生物医药有限公司 | 一种1,2,4-三氮唑类化合物 |
| CN107793400B (zh) * | 2017-10-31 | 2020-01-31 | 武汉九州钰民医药科技有限公司 | 吡啶类化合物及其在制备治疗肝脏疾病的药物中的应用 |
| EP3710599B1 (fr) | 2017-11-13 | 2024-07-17 | Gilead Sciences, Inc. | Procédé de stadification de la fibrose hépatique chez les patients atteints de nash |
| CN111566120B (zh) | 2017-12-20 | 2023-09-29 | 捷克共和国有机化学与生物化学研究所 | 活化sting转接蛋白的具有膦酸酯键的3’3’环状二核苷酸 |
| US11203610B2 (en) | 2017-12-20 | 2021-12-21 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 2′3′ cyclic dinucleotides with phosphonate bond activating the sting adaptor protein |
| WO2019136025A1 (fr) | 2018-01-02 | 2019-07-11 | Seal Rock Therapeutics, Inc. | Composés inhibiteurs d'ask1 et utilisations associées |
| CR20200347A (es) | 2018-02-13 | 2020-09-23 | Gilead Sciences Inc | Inhibidores pd-1/pd-l1 |
| CN110294742B (zh) * | 2018-03-21 | 2023-01-31 | 山东轩竹医药科技有限公司 | 并环类ask1抑制剂及其应用 |
| TWI818007B (zh) | 2018-04-06 | 2023-10-11 | 捷克科學院有機化學與生物化學研究所 | 2'3'-環二核苷酸 |
| TW202005654A (zh) | 2018-04-06 | 2020-02-01 | 捷克科學院有機化學與生物化學研究所 | 2,2,─環二核苷酸 |
| TWI833744B (zh) | 2018-04-06 | 2024-03-01 | 捷克科學院有機化學與生物化學研究所 | 3'3'-環二核苷酸 |
| EP3773577B1 (fr) * | 2018-04-12 | 2024-11-20 | Terns, Inc. | Inhibiteurs d'ask1 tricycliques |
| KR102591947B1 (ko) | 2018-04-19 | 2023-10-25 | 길리애드 사이언시즈, 인코포레이티드 | Pd-1/pd-l1 억제제 |
| CN110407806B (zh) * | 2018-04-28 | 2021-08-17 | 深圳微芯生物科技股份有限公司 | 甲酰胺类化合物、其制备方法及其应用 |
| CN112312905B (zh) | 2018-05-02 | 2024-03-15 | 英安塔制药有限公司 | 含四唑的细胞凋亡信号调节激酶1抑制剂及其使用方法 |
| US10683289B2 (en) | 2018-05-02 | 2020-06-16 | Enanta Pharmaceuticals, Inc. | Apoptosis signal-regulating kinase 1 inhibitors and methods of use thereof |
| WO2019211799A1 (fr) | 2018-05-03 | 2019-11-07 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | Analogue de dinucléotide 2'3'-cyclique comprenant un nucléotide modifié par cyclopentanyle |
| EP3814272A4 (fr) | 2018-05-11 | 2022-03-02 | Phosphorex, Inc. | Microparticules et nanoparticules ayant des charges de surface négatives |
| WO2019222112A1 (fr) | 2018-05-14 | 2019-11-21 | Gilead Sciences, Inc. | Inhibiteurs de mcl-1 |
| US10654833B2 (en) | 2018-06-28 | 2020-05-19 | Hepatikos Therapeutics, Llc | ASK1 isoindolin-1-one inhibitors and methods of use thereof |
| PT3820572T (pt) | 2018-07-13 | 2023-11-10 | Gilead Sciences Inc | Inibidores pd-1/pd-l1 |
| JP7096460B2 (ja) * | 2018-07-20 | 2022-07-06 | 福建▲広▼生中霖生物科技有限公司 | Ask1阻害剤としての結晶形、その製造方法及び利用 |
| US10968199B2 (en) | 2018-08-22 | 2021-04-06 | Enanta Pharmaceuticals, Inc. | Cycloalkyl-containing apoptosis signal-regulating kinase 1 inhibitors and methods of use thereof |
| WO2020072656A1 (fr) | 2018-10-03 | 2020-04-09 | Gilead Sciences, Inc. | Dérivés d'imidozopyrimidine |
| KR102298546B1 (ko) | 2018-10-18 | 2021-09-08 | 에이치케이이노엔 주식회사 | 신규한 n-(이소프로필-트리아졸릴)피리디닐)-헤테로아릴-카르복사미드 유도체 및 이의 용도 |
| JP7158577B2 (ja) | 2018-10-24 | 2022-10-21 | ギリアード サイエンシーズ, インコーポレイテッド | Pd-1/pd-l1阻害剤 |
| EP4371987B9 (fr) | 2018-10-31 | 2025-11-26 | Gilead Sciences, Inc. | Composés de 6-azabenzimidazole substitués utilisés en tant qu'inhibiteurs de hpk1 |
| KR102658602B1 (ko) | 2018-10-31 | 2024-04-19 | 길리애드 사이언시즈, 인코포레이티드 | Hpk1 억제 활성을 갖는 치환된 6-아자벤즈이미다졸 화합물 |
| CN111170995A (zh) * | 2018-11-09 | 2020-05-19 | 山东轩竹医药科技有限公司 | Ask1抑制剂及其应用 |
| WO2020106707A1 (fr) | 2018-11-19 | 2020-05-28 | Enanta Pharmaceuticals, Inc. | Inhibiteurs de la kinase 1 régulant le signal d'apoptose et leurs méthodes d'utilisation |
| CN109608441A (zh) * | 2018-12-26 | 2019-04-12 | 都创(上海)医药科技有限公司 | 一种ask1抑制剂的合成工艺 |
| EP3911647B1 (fr) | 2019-01-15 | 2023-12-13 | Gilead Sciences, Inc. | Composé d'isoxazole comme agoniste de fxr et les compositions pharmaceutiques le comprenant. |
| CN109813915A (zh) * | 2019-02-15 | 2019-05-28 | 浠思(上海)生物技术有限公司 | 利用htrf一步法筛选激酶抑制剂的方法 |
| AU2020225225B2 (en) | 2019-02-19 | 2022-12-22 | Gilead Sciences, Inc. | Solid forms of FXR agonists |
| CN113543851B (zh) | 2019-03-07 | 2025-03-18 | 捷克共和国有机化学与生物化学研究所 | 2’3’-环二核苷酸及其前药 |
| US20220143061A1 (en) | 2019-03-07 | 2022-05-12 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3'3'-cyclic dinucleotides and prodrugs thereof |
| EP3935065A1 (fr) | 2019-03-07 | 2022-01-12 | Institute of Organic Chemistry and Biochemistry ASCR, V.V.I. | Analogue du dinucléotide 3'3'-cyclique comprenant un nucléotide modifié par cyclopentanyle utilisé en tant que modulateur de sting |
| JP7697885B2 (ja) | 2019-03-11 | 2025-06-24 | ギリアード サイエンシーズ, インコーポレイテッド | 化合物の製剤およびそれらの使用 |
| US11466033B2 (en) | 2019-03-25 | 2022-10-11 | Enanta Pharmaceuticals, Inc. | Substituted pyridines as apoptosis signal-regulating kinase 1 inhibitors |
| TWI751517B (zh) | 2019-04-17 | 2022-01-01 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
| TW202210480A (zh) | 2019-04-17 | 2022-03-16 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
| WO2020237025A1 (fr) | 2019-05-23 | 2020-11-26 | Gilead Sciences, Inc. | Exo-méthylène-oxindoles substitués qui sont des inhibiteurs de hpk1/map4k1 |
| TWI770527B (zh) | 2019-06-14 | 2022-07-11 | 美商基利科學股份有限公司 | Cot 調節劑及其使用方法 |
| CA3140708A1 (fr) | 2019-06-18 | 2020-12-24 | Helen Horton | Association de vaccins contre le virus de l'hepatite b (vhb) et de derives de pyridopyrimidine |
| WO2020263830A1 (fr) | 2019-06-25 | 2020-12-30 | Gilead Sciences, Inc. | Protéines de fusion flt3l-fc et procédés d'utilisation |
| WO2020261294A1 (fr) * | 2019-06-26 | 2020-12-30 | Mankind Pharma Ltd. | Nouveaux inhibiteurs de kinase 1 de régulation de signal d'apoptose |
| AR119594A1 (es) | 2019-08-09 | 2021-12-29 | Gilead Sciences Inc | Derivados de tienopirimidina como inhibidores acc y usos de los mismos |
| CN118178645A (zh) | 2019-10-18 | 2024-06-14 | 四十七公司 | 用于治疗骨髓增生异常综合征和急性髓系白血病的联合疗法 |
| KR20220091576A (ko) | 2019-10-31 | 2022-06-30 | 포티 세븐, 인코포레이티드 | 혈액암의 항-cd47 및 항-cd20 기반 치료 |
| TWI778443B (zh) | 2019-11-12 | 2022-09-21 | 美商基利科學股份有限公司 | Mcl1抑制劑 |
| KR102775995B1 (ko) | 2019-11-15 | 2025-03-11 | 길리애드 사이언시즈, 인코포레이티드 | Lpa 수용체 길항제로서의 트라이아졸 카르바메이트 피리딜 설폰아미드 및 이의 용도 |
| CN111018831B (zh) * | 2019-11-21 | 2022-05-31 | 中国药科大学 | 细胞凋亡信号调节激酶抑制剂及其应用 |
| WO2021133948A1 (fr) | 2019-12-23 | 2021-07-01 | Axcella Health Inc. | Compositions et méthodes pour le traitement de maladies et de troubles hépatiques |
| HRP20241518T1 (hr) | 2019-12-24 | 2025-01-03 | Carna Biosciences, Inc. | Spojevi koji moduliraju diacilglicerinkinazu |
| PH12022552122A1 (en) | 2020-02-14 | 2024-01-29 | Jounce Therapeutics Inc | Antibodies and fusion proteins that bind to ccr8 and uses thereof |
| JP2023520650A (ja) | 2020-03-30 | 2023-05-18 | ギリアード サイエンシーズ, インコーポレイテッド | (S)-6-(((1-(ビシクロ[1.1.1]ペンタン-1-イル)-1H-1,2,3-トリアゾール-4-イル)2-メチル-1-オキソ-1,2-ジヒドロイソキノリン-5-イル)メチル)))アミノ)8-クロロ-(ネオペンチルアミノ)キノリン-3-カルボニトリルCot阻害剤化合物の固体形態 |
| PL4126862T3 (pl) | 2020-04-02 | 2025-09-08 | Gilead Sciences, Inc. | Sposób wytwarzania związku będącego inhibitorem cot |
| US12110294B2 (en) | 2020-05-01 | 2024-10-08 | Gilead Sciences, Inc. | CD73 compounds |
| CA3185689A1 (fr) | 2020-06-03 | 2021-12-09 | Gilead Sciences, Inc. | Antagonistes du recepteur lpa et leurs utilisations |
| CN113831323B (zh) * | 2020-06-24 | 2025-08-29 | 武汉人福创新药物研发中心有限公司 | 芳杂环酰胺类化合物及其用途 |
| CN111808079A (zh) * | 2020-08-05 | 2020-10-23 | 中国药科大学 | 吲哚类ask1小分子抑制剂及其制备方法和应用 |
| CN114470217B (zh) * | 2020-11-24 | 2023-06-20 | 深圳微芯生物科技股份有限公司 | 预防和治疗代谢异常或炎症引起的组织损伤的药物组合物 |
| US12091404B2 (en) | 2021-03-11 | 2024-09-17 | Gilead Sciences, Inc. | GLP-1R modulating compounds |
| CN117120429A (zh) | 2021-03-29 | 2023-11-24 | 吉利德科学公司 | Khk抑制剂 |
| TW202302145A (zh) | 2021-04-14 | 2023-01-16 | 美商基利科學股份有限公司 | CD47/SIRPα結合及NEDD8活化酶E1調節次單元之共抑制以用於治療癌症 |
| CN114246866B (zh) * | 2021-04-28 | 2023-09-12 | 深圳微芯生物科技股份有限公司 | 用于治疗慢性肾病的药物及其用途 |
| AU2022273631B2 (en) | 2021-05-11 | 2025-04-17 | Gilead Sciences, Inc. | Lpa receptor antagonists and uses thereof |
| WO2022241023A1 (fr) | 2021-05-13 | 2022-11-17 | Gilead Sciences, Inc. | Antagonistes du récepteur lpa et leurs utilisations |
| WO2022245671A1 (fr) | 2021-05-18 | 2022-11-24 | Gilead Sciences, Inc. | Méthodes d'utilisation de protéines de fusion flt3l-fc |
| TW202345826A (zh) | 2021-06-04 | 2023-12-01 | 美商基利科學股份有限公司 | 治療nash之方法 |
| TW202311256A (zh) | 2021-06-18 | 2023-03-16 | 美商基利科學股份有限公司 | 用於治療fxr誘發之搔癢之il-31調節劑 |
| WO2022271659A1 (fr) | 2021-06-23 | 2022-12-29 | Gilead Sciences, Inc. | Composés modulant les diacylglycérol kinases |
| EP4359413A1 (fr) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Composés de modulation de la diacylglycérol kinase |
| US11976072B2 (en) | 2021-06-23 | 2024-05-07 | Gilead Sciences, Inc. | Diacylglycerol kinase modulating compounds |
| US11932634B2 (en) | 2021-06-23 | 2024-03-19 | Gilead Sciences, Inc. | Diacylglycerol kinase modulating compounds |
| US20230183216A1 (en) | 2021-10-28 | 2023-06-15 | Gilead Sciences, Inc. | Pyridizin-3(2h)-one derivatives |
| CR20240173A (es) | 2021-10-29 | 2024-06-20 | Gilead Sciences Inc | Compuestos de cd73 |
| CN118541360A (zh) | 2021-12-08 | 2024-08-23 | 吉利德科学公司 | Lpa受体拮抗剂及其用途 |
| WO2023107954A1 (fr) | 2021-12-08 | 2023-06-15 | Dragonfly Therapeutics, Inc. | Anticorps ciblant 5t4 et leurs utilisations |
| US20230203202A1 (en) | 2021-12-08 | 2023-06-29 | Dragonfly Therapeutics, Inc. | Proteins binding nkg2d, cd16 and 5t4 |
| CN118488948A (zh) | 2021-12-22 | 2024-08-13 | 吉利德科学公司 | Ikaros锌指家族降解剂及其用途 |
| JP2024546851A (ja) | 2021-12-22 | 2024-12-26 | ギリアード サイエンシーズ, インコーポレイテッド | Ikarosジンクフィンガーファミリー分解剤及びその使用 |
| TW202340168A (zh) | 2022-01-28 | 2023-10-16 | 美商基利科學股份有限公司 | Parp7抑制劑 |
| JP2025509610A (ja) | 2022-03-17 | 2025-04-11 | ギリアード サイエンシーズ, インコーポレイテッド | Ikarosジンクフィンガーファミリー分解剤及びその使用 |
| WO2023183817A1 (fr) | 2022-03-24 | 2023-09-28 | Gilead Sciences, Inc. | Polythérapie pour le traitement de cancers exprimant trop -2 |
| TWI876305B (zh) | 2022-04-05 | 2025-03-11 | 美商基利科學股份有限公司 | 用於治療結腸直腸癌之組合療法 |
| JP2025513258A (ja) | 2022-04-21 | 2025-04-24 | ギリアード サイエンシーズ, インコーポレイテッド | Kra g12d調節化合物 |
| IL317958A (en) | 2022-07-01 | 2025-02-01 | Gilead Sciences Inc | CD73 compounds |
| US20240091351A1 (en) | 2022-09-21 | 2024-03-21 | Gilead Sciences, Inc. | FOCAL IONIZING RADIATION AND CD47/SIRPa DISRUPTION ANTICANCER COMBINATION THERAPY |
| KR20250122479A (ko) | 2022-12-22 | 2025-08-13 | 길리애드 사이언시즈, 인코포레이티드 | Prmt5 억제제 및 이의 용도 |
| CN115844887B (zh) * | 2022-12-28 | 2023-09-08 | 中国人民解放军空军军医大学 | Selonsertib在制备治疗癌症的药物中的用途 |
| CN120882725A (zh) | 2023-04-11 | 2025-10-31 | 吉利德科学公司 | Kras调节化合物 |
| CN121079300A (zh) | 2023-04-21 | 2025-12-05 | 吉利德科学公司 | Prmt5抑制剂及其用途 |
| WO2024236595A1 (fr) * | 2023-05-18 | 2024-11-21 | Council Of Scientific And Industrial Research | Protac pour la dégradation de la protéine ask1 : préparation et utilisation associées |
| WO2025006720A1 (fr) | 2023-06-30 | 2025-01-02 | Gilead Sciences, Inc. | Composés modulateurs de kras |
| WO2025024663A1 (fr) | 2023-07-26 | 2025-01-30 | Gilead Sciences, Inc. | Inhibiteurs de parp7 |
| WO2025024811A1 (fr) | 2023-07-26 | 2025-01-30 | Gilead Sciences, Inc. | Inhibiteurs de parp7 |
| US20250101042A1 (en) | 2023-09-08 | 2025-03-27 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| US20250109147A1 (en) | 2023-09-08 | 2025-04-03 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| WO2025096589A1 (fr) | 2023-11-03 | 2025-05-08 | Gilead Sciences, Inc. | Inhibiteurs de prmt5 et leurs utilisations |
| WO2025137640A1 (fr) | 2023-12-22 | 2025-06-26 | Gilead Sciences, Inc. | Inhibiteurs azaspiro de wrn |
| US20250376484A1 (en) | 2024-05-21 | 2025-12-11 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6159731A (en) | 1997-02-12 | 2000-12-12 | Massachusetts Institute Of Technology | Daxx, a Fas-binding protein that activates JNK and apoptosis |
| EP1144600B1 (fr) | 1999-03-19 | 2008-07-30 | Aventis Pharmaceuticals Inc. | Acides nucleiques akt, polypeptides, et leurs utilisations |
| US6881555B2 (en) | 1999-03-19 | 2005-04-19 | Aventis Pharmaceuticals Inc. | AKT nucleic acids, polypeptides, and uses thereof |
| WO2001095410A1 (fr) * | 2000-06-07 | 2001-12-13 | Andelman Marc D | Cellules, systeme et procede electrochimiques de recyclage a connexion fluidique et electrique |
| US20070237770A1 (en) | 2001-11-30 | 2007-10-11 | Albert Lai | Novel compositions and methods in cancer |
| WO2005009470A1 (fr) | 2003-07-28 | 2005-02-03 | Osaka Industrial Promotion Organization | Traitement de l'insuffisance cardiaque contenant comme principe actif un inhibiteur d'ask1 et procede de criblage de celui-ci |
| CA2581375A1 (fr) | 2004-09-27 | 2006-04-06 | Kosan Biosciences Incorporated | Inhibiteurs de kinases specifiques |
| TW200628159A (en) | 2004-11-10 | 2006-08-16 | Synta Pharmaceuticals Corp | IL-12 modulatory compounds |
| EP1677113A1 (fr) | 2004-12-29 | 2006-07-05 | Max-Delbrück-Centrum für Molekulare Medizin (MDC) | Procédé d'identification des interactions protéine-protéine dans des réseaux de protéines associés aux maladies |
| US20070276050A1 (en) * | 2006-02-27 | 2007-11-29 | Gilead Sciences, Inc. | Methods for identifying ASK1 inhibitors useful for preventing and/or treating cardiovascular diseases |
| JPWO2008016131A1 (ja) | 2006-08-04 | 2009-12-24 | 武田薬品工業株式会社 | 縮合複素環化合物 |
| WO2008042867A2 (fr) | 2006-09-29 | 2008-04-10 | Emiliem Inc. | Modulateurs de kinases multiples |
| CA2671194A1 (fr) | 2006-12-08 | 2008-06-19 | Asuragen, Inc. | Genes et voies genetiques regules par le mir-20 en tant que cibles en vue d'une intervention therapeutique |
| EP1942104A1 (fr) | 2006-12-20 | 2008-07-09 | sanofi-aventis | Hétéroarylcyclopropanecarboxamide et leur utilisation pharmaceutique |
| US8104727B2 (en) | 2007-03-12 | 2012-01-31 | Denis Joanisse | Adjustable article support |
| US20090069288A1 (en) | 2007-07-16 | 2009-03-12 | Breinlinger Eric C | Novel therapeutic compounds |
| KR20100075881A (ko) | 2007-08-31 | 2010-07-05 | 메르크 세로노 에스. 에이. | 트리아졸로피리딘 화합물 및 ask 저해제로서 이의 용도 |
| EP2271646A1 (fr) | 2008-03-31 | 2011-01-12 | Takeda Pharmaceutical Company Limited | Inhibiteurs de kinase 1 de régulation de signal d'apoptose |
| WO2010008843A1 (fr) | 2008-06-24 | 2010-01-21 | Takeda Pharmaceutical Company Limited | Inhibiteurs de kinases 1 régulant le signal apoptotique |
| US20110263441A1 (en) | 2008-10-15 | 2011-10-27 | Golub Todd R | Compositions, kits, and methods for identification, assessment, prevention, and therapy of hepatic disorders |
| US20110294693A1 (en) | 2008-11-17 | 2011-12-01 | The George Washington University | Compositions and Methods for Identifying Autism Spectrum Disorders |
| WO2010111464A1 (fr) | 2009-03-27 | 2010-09-30 | Merck Sharp & Dohme Corp. | Inhibition par interférence arn de l'expression du gène kinase 1 de régulation du signal d'apoptose (ask1) au moyen d'un acide nucléique interférent court (ansi) |
| TWI598347B (zh) | 2009-07-13 | 2017-09-11 | 基利科學股份有限公司 | 調節細胞凋亡信號之激酶的抑制劑 |
| WO2011041293A1 (fr) | 2009-09-30 | 2011-04-07 | Takeda Pharmaceutical Company Limited | Dérivés pyrazolo [1, 5a] pyrimidines comme inhibiteurs de kinase 1 régulatrice de signal d'apoptose |
| US8802695B2 (en) | 2010-02-03 | 2014-08-12 | Takeda Pharmaceutical Company Limited | Apoptosis signal-regulating kinase 1 inhibitors |
| WO2011097594A2 (fr) | 2010-02-08 | 2011-08-11 | Kinagen, Inc. | Methodes therapeutiques et compositions impliquant l'inhibition de la kinase allosterique |
| EP2550266B1 (fr) | 2010-03-24 | 2018-05-09 | Amitech Therapeutics Solutions, Inc. | Composés hétérocycliques utiles pour l'inhibition de la kinase |
| CN102985418B (zh) | 2010-07-02 | 2015-09-09 | 吉利德科学股份有限公司 | 凋亡信号调节激酶抑制剂 |
| US20130236441A1 (en) | 2010-11-18 | 2013-09-12 | University Of Delaware | Methods of treating and preventing thrombotic diseases using ask1 inhibitors |
| EP2651417B1 (fr) | 2010-12-16 | 2016-11-30 | Calchan Limited | Dérivés pyrrolopyrimidine inhibant ask1 |
| AU2012220872A1 (en) | 2011-02-22 | 2013-09-12 | Caris Life Sciences Switzerland Holdings Gmbh | Circulating biomarkers |
| AU2012267884A1 (en) | 2011-06-07 | 2014-01-23 | Caris Life Sciences Switzerland Holdings Gmbh | Circulating biomarkers for cancer |
| UY34171A (es) | 2011-07-01 | 2013-01-31 | Gilead Sciences Inc | Compuestos heterocíclicos fusionados como moduladores del canal iónico |
| US8924765B2 (en) | 2011-07-03 | 2014-12-30 | Ambiq Micro, Inc. | Method and apparatus for low jitter distributed clock calibration |
| UY34573A (es) | 2012-01-27 | 2013-06-28 | Gilead Sciences Inc | Inhibidor de la quinasa que regula la señal de la apoptosis |
| EP4276095A3 (fr) | 2014-12-23 | 2024-01-17 | Gilead Sciences, Inc. | Procédés de préparation d'inhibiteurs ask1 |
| MA41252A (fr) | 2014-12-23 | 2017-10-31 | Gilead Sciences Inc | Formes solides d'un inhibiteur d'ask 1 |
-
2013
- 2013-01-11 UY UY0001034573A patent/UY34573A/es not_active Application Discontinuation
- 2013-01-24 CA CA3026700A patent/CA3026700C/fr active Active
- 2013-01-24 HU HUE13703675A patent/HUE028641T2/en unknown
- 2013-01-24 UA UAA201407926A patent/UA112098C2/uk unknown
- 2013-01-24 CN CN201380006957.0A patent/CN104080771B/zh active Active
- 2013-01-24 CA CA3026738A patent/CA3026738C/fr active Active
- 2013-01-24 DK DK13703675.2T patent/DK2807151T3/en active
- 2013-01-24 SG SG11201404348UA patent/SG11201404348UA/en unknown
- 2013-01-24 PL PL13703675T patent/PL2807151T3/pl unknown
- 2013-01-24 CA CA2862030A patent/CA2862030C/fr active Active
- 2013-01-24 MX MX2014009075A patent/MX2014009075A/es active IP Right Grant
- 2013-01-24 NZ NZ739339A patent/NZ739339A/en unknown
- 2013-01-24 EP EP13703675.2A patent/EP2807151B1/fr active Active
- 2013-01-24 KR KR1020177003620A patent/KR101799739B1/ko active Active
- 2013-01-24 US US13/748,901 patent/US8742126B2/en active Active
- 2013-01-24 KR KR1020177032774A patent/KR20170128622A/ko not_active Ceased
- 2013-01-24 SI SI201330109A patent/SI2807151T1/sl unknown
- 2013-01-24 JP JP2014554828A patent/JP5770950B2/ja active Active
- 2013-01-24 HR HRP20151399TT patent/HRP20151399T1/hr unknown
- 2013-01-24 PT PT137036752T patent/PT2807151E/pt unknown
- 2013-01-24 KR KR1020187037026A patent/KR20190000898A/ko not_active Ceased
- 2013-01-24 PE PE2014001153A patent/PE20141822A1/es active IP Right Grant
- 2013-01-24 ES ES13703675.2T patent/ES2558203T3/es active Active
- 2013-01-24 ME MEP-2016-5A patent/ME02322B/me unknown
- 2013-01-24 AU AU2013201586A patent/AU2013201586C1/en active Active
- 2013-01-24 WO PCT/US2013/022997 patent/WO2013112741A1/fr not_active Ceased
- 2013-01-24 EA EA201491283A patent/EA024746B1/ru unknown
- 2013-01-24 KR KR1020147023533A patent/KR101582065B1/ko active Active
- 2013-01-24 MD MDA20140082A patent/MD4601B1/ro not_active IP Right Cessation
- 2013-01-24 RS RS20160019A patent/RS54492B1/sr unknown
- 2013-01-24 MX MX2015009422A patent/MX365954B/es unknown
- 2013-01-24 BR BR112014018355-4A patent/BR112014018355B1/pt active IP Right Grant
- 2013-01-24 AP AP2014007836A patent/AP2014007836A0/xx unknown
- 2013-01-24 KR KR1020157036387A patent/KR101707764B1/ko active Active
- 2013-01-24 CN CN201811215092.XA patent/CN109438418B/zh active Active
- 2013-01-25 AR ARP130100241A patent/AR089818A1/es active IP Right Grant
- 2013-01-25 TW TW102102991A patent/TWI487523B/zh active
- 2013-01-25 TW TW105128669A patent/TWI634890B/zh active
- 2013-01-25 TW TW103125752A patent/TWI561514B/zh active
- 2013-01-25 TW TW107127139A patent/TW201916877A/zh unknown
-
2014
- 2014-04-16 US US14/254,342 patent/US9254284B2/en active Active
- 2014-04-16 US US14/254,359 patent/US9333197B2/en active Active
- 2014-07-10 IL IL233598A patent/IL233598A/en active IP Right Grant
- 2014-07-11 MA MA37202A patent/MA35861B1/fr unknown
- 2014-07-17 ZA ZA2014/05260A patent/ZA201405260B/en unknown
- 2014-07-22 IN IN6174DEN2014 patent/IN2014DN06174A/en unknown
- 2014-07-25 CL CL2014001988A patent/CL2014001988A1/es unknown
- 2014-07-25 MX MX2019007348A patent/MX2019007348A/es unknown
- 2014-07-25 PH PH12014501697A patent/PH12014501697A1/en unknown
- 2014-08-26 CO CO14186994A patent/CO7061073A2/es unknown
- 2014-08-29 CR CR20140405A patent/CR20140405A/es unknown
-
2015
- 2015-06-10 IL IL239311A patent/IL239311B/en active IP Right Grant
-
2016
- 2016-02-15 SM SM201600047T patent/SMT201600047B/it unknown
- 2016-02-16 CY CY20161100129T patent/CY1117201T1/el unknown
- 2016-04-27 US US15/140,204 patent/US9750730B2/en active Active
-
2017
- 2017-04-19 US US15/491,689 patent/US9873682B2/en active Active
- 2017-12-13 US US15/840,429 patent/US20180099950A1/en not_active Abandoned
-
2018
- 2018-03-07 IL IL257965A patent/IL257965A/en unknown
-
2019
- 2019-01-11 US US16/246,199 patent/US10508100B2/en active Active
- 2019-11-19 AR ARP190103385A patent/AR117113A2/es not_active Application Discontinuation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA35861B1 (fr) | Inhibiteur de la kinase régulant les signaux de l'apoptose | |
| MA46337A (fr) | Composé de pyridine | |
| PH12018502125A1 (en) | Bipyrazole derivatives as jak inhibitors | |
| MA35623B1 (fr) | Composés de 1-arylcarbonyl-4-oxypipéridine utiles pour le traitement de maladies neurodégénératives | |
| EA201100580A1 (ru) | Имидазопиридазинкарбонитрилы, используемые в качестве ингибиторов киназы | |
| EA201270373A1 (ru) | Ингибиторы jak2 и их применение для лечения миелопролиферативных заболеваний и злокачественной опухоли | |
| NZ628028A (en) | Processes for the preparation of (s)-1-(3-ethoxy-4-methoxyphenyl)-2-methanesulfonylethylamine | |
| EA201590224A1 (ru) | Имидазотриазинкарбонитрилы, используемые в качестве ингибиторов киназы | |
| MA38390B1 (fr) | Composés tétrahydropyrrolothiazines | |
| MX2010009207A (es) | Compuestos y composiciones heterociclicos como inhibidores de c-kit y pdgfr cinasa. | |
| EA201200373A1 (ru) | Соединения и композиции в качестве ингибиторов протеинкиназ | |
| TN2011000654A1 (fr) | Sulfonamides heterocycliques leurs utilisations et compositions pharmaceutiques les contenant | |
| EA201491747A1 (ru) | Замещенные пиридопиримидиновые соединения и их применение в качестве flt3 ингибиторов | |
| UA115052C2 (uk) | Конденсоване біциклічне 2,4-діамінопіримідинове похідне як подвійний alk- i fak-інгібітор | |
| MA39152A1 (fr) | Cyclopentanes substitués en 1,2 utilisés comme antagonistes du récepteur d'orexine | |
| MX2017000521A (es) | Pirimidinas novedosas 2,5-sustituidas como inhibidores de pde4. | |
| MX2017000522A (es) | Pirimidinas novedosas 2,5-sustituidas como inhibidores de pde. | |
| EA201690818A1 (ru) | Замещенные пиримидиновые соединения и их применение в качестве syk ингибиторов | |
| MY194604A (en) | Guanidinobenzoic acid ester compound | |
| EA201591369A1 (ru) | Новые производные пиримидина в качестве ингибиторов фосфодиэстеразы 10 (pde-10) | |
| EA201171030A1 (ru) | 2-МОРФОЛИНОПИРИДО[3,2-d]ПИРИМИДИНЫ | |
| MA38491A1 (fr) | Dérivé dihydropyridazine-3,5-dione | |
| MA38479B1 (fr) | 3-pyrimidin-4-yl-oxazolidin-2-ones comme inhibiteurs d'idh mutante | |
| MA35168B1 (fr) | Combinaison de panobinostat et de ruxolitinib dans le traitement du cancer tel qu'un néoplasme myéloprolifératif |