MA32684B1 - Dérivés de picolinamide en tant qu'inhibiteurs de kinase - Google Patents
Dérivés de picolinamide en tant qu'inhibiteurs de kinaseInfo
- Publication number
- MA32684B1 MA32684B1 MA33733A MA33733A MA32684B1 MA 32684 B1 MA32684 B1 MA 32684B1 MA 33733 A MA33733 A MA 33733A MA 33733 A MA33733 A MA 33733A MA 32684 B1 MA32684 B1 MA 32684B1
- Authority
- MA
- Morocco
- Prior art keywords
- kinase
- compositions
- compounds
- kinase inhibitors
- inhibiting
- Prior art date
Links
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical class NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 title abstract 2
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract 3
- 102100036077 Serine/threonine-protein kinase pim-1 Human genes 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 230000002401 inhibitory effect Effects 0.000 abstract 2
- 208000005623 Carcinogenesis Diseases 0.000 abstract 1
- 101001059454 Homo sapiens Serine/threonine-protein kinase MARK2 Proteins 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 102000004278 Receptor Protein-Tyrosine Kinases Human genes 0.000 abstract 1
- 108090000873 Receptor Protein-Tyrosine Kinases Proteins 0.000 abstract 1
- 102100028904 Serine/threonine-protein kinase MARK2 Human genes 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000036952 cancer formation Effects 0.000 abstract 1
- 231100000504 carcinogenesis Toxicity 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 230000010469 pro-virus integration Effects 0.000 abstract 1
Classifications
-
- 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
- C07D213/60—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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- 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
- A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
-
- 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
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente invention concerne de nouveaux composés de picolinamide, des compositions et des procédés d'inhibition de l'activité kinase d'intégration de provirus de Maloney (kinase PIM) associée à la cancérogenèse chez un sujet humain ou animal. Dans certains modes de réalisation, les composés et compositions sont efficaces pour inhiber l'activité d'au moins une kinase PIM. Les nouveaux composés et compositions peuvent être utilisés seuls ou en combinaison avec au moins un agent additionnel pour le traitement d'un trouble véhiculé par une sérine/thréonine kinase ou un récepteur tyrosine kinase, tel que le cancer.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9366608P | 2008-09-02 | 2008-09-02 | |
| US22566009P | 2009-07-15 | 2009-07-15 | |
| PCT/EP2009/061205 WO2010026124A1 (fr) | 2008-09-02 | 2009-08-31 | Dérivés de picolinamide en tant qu’inhibiteurs de kinase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA32684B1 true MA32684B1 (fr) | 2011-10-02 |
Family
ID=41228825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA33733A MA32684B1 (fr) | 2008-09-02 | 2011-04-01 | Dérivés de picolinamide en tant qu'inhibiteurs de kinase |
Country Status (38)
| Country | Link |
|---|---|
| US (4) | US8329732B2 (fr) |
| EP (1) | EP2344474B1 (fr) |
| JP (2) | JP5412519B2 (fr) |
| KR (1) | KR101345920B1 (fr) |
| CN (3) | CN102203079B (fr) |
| AU (1) | AU2009289319C1 (fr) |
| BR (1) | BRPI0918268B1 (fr) |
| CA (1) | CA2734415C (fr) |
| CL (1) | CL2011000454A1 (fr) |
| CO (1) | CO6351725A2 (fr) |
| CR (1) | CR20110114A (fr) |
| DK (1) | DK2344474T3 (fr) |
| DO (1) | DOP2011000067A (fr) |
| EA (1) | EA020136B1 (fr) |
| EC (1) | ECSP11010859A (fr) |
| ES (1) | ES2551900T3 (fr) |
| GE (1) | GEP20135849B (fr) |
| HN (1) | HN2011000629A (fr) |
| HR (1) | HRP20151410T1 (fr) |
| HU (1) | HUE026381T2 (fr) |
| IL (1) | IL211291A (fr) |
| MA (1) | MA32684B1 (fr) |
| ME (1) | ME01291A (fr) |
| MX (1) | MX2011002365A (fr) |
| MY (1) | MY150136A (fr) |
| NI (1) | NI201100052A (fr) |
| NZ (1) | NZ591449A (fr) |
| PE (1) | PE20110298A1 (fr) |
| PL (1) | PL2344474T3 (fr) |
| PT (1) | PT2344474E (fr) |
| RS (1) | RS54506B1 (fr) |
| SI (1) | SI2344474T1 (fr) |
| SM (1) | SMT201600005B (fr) |
| SV (1) | SV2011003849A (fr) |
| TW (1) | TWI434843B (fr) |
| UY (1) | UY32085A (fr) |
| WO (1) | WO2010026124A1 (fr) |
| ZA (1) | ZA201101118B (fr) |
Families Citing this family (92)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2455382B1 (fr) | 2005-12-13 | 2016-10-26 | Incyte Holdings Corporation | Pyrrolo[2,3-b]pyridines et pyrrolo[2,3-b]pyrimidines à substitution hétéroaryle en tant qu'inhibiteurs de la janus kinase |
| US20140249135A1 (en) * | 2007-03-01 | 2014-09-04 | Novartis Ag | Pim kinase inhibitors and methods of their use |
| EP3070090B1 (fr) | 2007-06-13 | 2018-12-12 | Incyte Holdings Corporation | Utilisation des sels de l'inhibiteur de janus kinase (r)-3-(4- (7h-pyrrolo [2,3-d] pyrimidin-4-yl)-1h-pyrazol-1-yl) -3-cyclopentylpropanenitrile |
| WO2010026121A1 (fr) * | 2008-09-02 | 2010-03-11 | Novartis Ag | Inhibiteurs bicycliques des kinases |
| MX2011002365A (es) | 2008-09-02 | 2011-04-04 | Novartis Ag | Derivados de picolinamida como inhibidres de cinasa. |
| JP5775070B2 (ja) | 2009-05-22 | 2015-09-09 | インサイト・コーポレイションIncyte Corporation | ヤヌスキナーゼ阻害剤としてのピラゾール−4−イル−ピロロ[2,3−d]ピリミジンおよびピロール−3−イル−ピロロ[2,3−d]ピリミジンのN−(ヘテロ)アリール−ピロリジン誘導体 |
| SG176111A1 (en) | 2009-05-22 | 2011-12-29 | Incyte Corp | 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octane- or heptane-nitrile as jak inhibitors |
| AR078012A1 (es) | 2009-09-01 | 2011-10-05 | Incyte Corp | Derivados heterociclicos de las pirazol-4-il- pirrolo (2,3-d) pirimidinas como inhibidores de la quinasa janus |
| PT3354652T (pt) | 2010-03-10 | 2020-07-20 | Incyte Holdings Corp | Derivados de piperidin-4-ilazetidina como inibidores de jak1 |
| JP6161537B2 (ja) * | 2010-04-07 | 2017-07-12 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | ピラゾール−4−イル−ヘテロシクリル−カルボキサミド化合物及び使用の方法 |
| RS54824B1 (sr) | 2010-05-21 | 2016-10-31 | Incyte Holdings Corp | Topikalna formulacija za inhibiciju jak-a |
| JP2013530199A (ja) * | 2010-07-06 | 2013-07-25 | ノバルティス アーゲー | キナーゼ阻害剤として有用な環状エーテル化合物 |
| CA2818542A1 (fr) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Derives pyrrolopyridine et pyrrolopyrimidine a substitution cyclobutyle utilises comme inhibiteurs des jak |
| WO2012068440A1 (fr) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Pyrrolopyridines et pyrrolopyrimidines à substitution hétérocyclique utilisées en tant qu'inhibiteurs des jak |
| EP2675816A4 (fr) * | 2011-02-14 | 2014-08-13 | Univ Alberta | Catalyseurs à base d'acide boronique et procédés d'utilisation associés pour l'activation et la transformation d'acides carboxyliques |
| WO2012120415A1 (fr) * | 2011-03-04 | 2012-09-13 | Novartis Ag | Composés de cyclohexyle tétrasubstitués à titre d'inhibiteurs de kinases |
| UY33930A (es) * | 2011-03-04 | 2012-10-31 | Novartis Ag | Inhibidores novedosos de quinasas |
| JP2014516941A (ja) | 2011-04-29 | 2014-07-17 | アムジェン インコーポレイテッド | Pim阻害剤としての二環式ピリダジン化合物 |
| MY165963A (en) | 2011-06-20 | 2018-05-18 | Incyte Holdings Corp | Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors |
| EP2734205B1 (fr) | 2011-07-21 | 2018-03-21 | Tolero Pharmaceuticals, Inc. | Inhibiteurs de protéine kinase hétérocycliques |
| US9458151B2 (en) * | 2011-08-11 | 2016-10-04 | Jikai Biosciences, Inc. | Isothiazole derivatives as PIM kinase inhibitors and preparation methods and use in medicinal manufacture thereof |
| US9453003B2 (en) * | 2011-08-11 | 2016-09-27 | Jikai Biosciences, Inc. | Pyrimidine derivatives as PIM kinase inhibitors and preparation methods and use in medicinal manufacture thereof |
| TW201313721A (zh) | 2011-08-18 | 2013-04-01 | Incyte Corp | 作為jak抑制劑之環己基氮雜環丁烷衍生物 |
| UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
| TW201406761A (zh) | 2012-05-18 | 2014-02-16 | Incyte Corp | 做爲jak抑制劑之哌啶基環丁基取代之吡咯并吡啶及吡咯并嘧啶衍生物 |
| US9173883B2 (en) | 2012-05-21 | 2015-11-03 | Novartis Ag | Ring-substituted N-pyridinyl amides as kinase inhibitors |
| WO2014033631A1 (fr) | 2012-08-31 | 2014-03-06 | Novartis Ag | N- (3-pyridyl)-biarylamides en tant qu'inhibiteurs de kinase |
| WO2014033630A1 (fr) | 2012-08-31 | 2014-03-06 | Novartis Ag | Nouveaux carboxamides d'aminothiazole en tant qu'inhibiteurs de kinase |
| DK2900657T3 (da) | 2012-09-26 | 2020-05-04 | Hoffmann La Roche | Cykliske etherpyrazol-4-yl-heterocyclyl-carboxamidforbindelser og fremgangsmåder til anvendelse |
| CN103724301A (zh) * | 2012-10-10 | 2014-04-16 | 上海特化医药科技有限公司 | (2r)-2-脱氧-2,2-二取代-1,4-核糖内酯及其制备方法和用途 |
| CN113384546A (zh) | 2012-11-15 | 2021-09-14 | 因赛特公司 | 鲁索利替尼的缓释剂型 |
| US20150336960A1 (en) | 2012-12-19 | 2015-11-26 | Novartis Ag | Aryl-substituted fused bicyclic pyridazine compounds |
| JP6437452B2 (ja) * | 2013-01-14 | 2018-12-12 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Pimキナーゼ阻害剤として有用な二環式芳香族カルボキサミド化合物 |
| RS60244B1 (sr) | 2013-01-15 | 2020-06-30 | Incyte Holdings Corp | Jedinjenja tiazolkarboksamida i piridinkarboksamida korisna kao inhibitori pim kinaze |
| WO2014138168A1 (fr) | 2013-03-06 | 2014-09-12 | Incyte Corporation | Procédés et intermédiaires pour la génération d'un inhibiteur de jak |
| US9113629B2 (en) * | 2013-03-15 | 2015-08-25 | Dow Agrosciences Llc | 4-amino-6-(4-substituted-phenyl)-picolinates and 6-amino-2-(4-substituted-phenyl)-pyrimidine-4-carboxylates and their use as herbicides |
| SG10201801069QA (en) | 2013-08-07 | 2018-03-28 | Incyte Corp | Sustained release dosage forms for a jak1 inhibitor |
| JP2016527305A (ja) * | 2013-08-08 | 2016-09-08 | ノバルティス アーゲー | Pimキナーゼ阻害剤の組合せ |
| CN105658653A (zh) | 2013-08-23 | 2016-06-08 | 因赛特公司 | 可用作pim激酶抑制剂的呋喃并-和噻吩并-吡啶甲酰胺化合物 |
| US10570204B2 (en) | 2013-09-26 | 2020-02-25 | The Medical College Of Wisconsin, Inc. | Methods for treating hematologic cancers |
| AU2014354821A1 (en) | 2013-11-27 | 2016-05-26 | Novartis Ag | Combination therapy comprising an inhibitor of JAK, CDK and PIM |
| SG10201900002QA (en) | 2014-01-24 | 2019-02-27 | Dana Farber Cancer Institue Inc | Antibody molecules to pd-1 and uses thereof |
| EP3099717B1 (fr) | 2014-01-31 | 2019-03-27 | Novartis AG | Molécules d'anticorps anti-tim-3 et leurs utilisations |
| US20150259420A1 (en) | 2014-03-14 | 2015-09-17 | Novartis Ag | Antibody molecules to lag-3 and uses thereof |
| JP6554480B2 (ja) | 2014-03-18 | 2019-07-31 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | オキセパン−2−イル−ピラゾール−4−イル−ヘテロシクリル−カルボキサミド化合物と使用方法 |
| US9498467B2 (en) | 2014-05-30 | 2016-11-22 | Incyte Corporation | Treatment of chronic neutrophilic leukemia (CNL) and atypical chronic myeloid leukemia (aCML) by inhibitors of JAK1 |
| WO2016010897A1 (fr) | 2014-07-14 | 2016-01-21 | Incyte Corporation | Composés carboxamide hétéroaromatiques bicycliques utiles en tant qu'inhibiteurs de kinases pim |
| US9580418B2 (en) | 2014-07-14 | 2017-02-28 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors |
| JO3589B1 (ar) * | 2014-08-06 | 2020-07-05 | Novartis Ag | مثبطات كيناز البروتين c وطرق استخداماتها |
| ES2771926T3 (es) | 2014-09-13 | 2020-07-07 | Novartis Ag | Terapias de combinación |
| AU2015327868A1 (en) | 2014-10-03 | 2017-04-20 | Novartis Ag | Combination therapies |
| MA41044A (fr) | 2014-10-08 | 2017-08-15 | Novartis Ag | Compositions et procédés d'utilisation pour une réponse immunitaire accrue et traitement contre le cancer |
| TWI716362B (zh) | 2014-10-14 | 2021-01-21 | 瑞士商諾華公司 | 針對pd-l1之抗體分子及其用途 |
| HK1248603A1 (zh) | 2015-03-10 | 2018-10-19 | Aduro Biotech, Inc. | 用於活化"干扰素基因的刺激剂"依懒性信号传导的组合物和方法 |
| WO2016196244A1 (fr) | 2015-05-29 | 2016-12-08 | Incyte Corporation | Composés de pyridineamine utiles en tant qu'inhibiteurs de kinase pim |
| US20180222982A1 (en) | 2015-07-29 | 2018-08-09 | Novartis Ag | Combination therapies comprising antibody molecules to pd-1 |
| DK3317301T3 (da) | 2015-07-29 | 2021-06-28 | Immutep Sas | Kombinationsterapier omfattende antistofmolekyler mod lag-3 |
| EP3878465A1 (fr) | 2015-07-29 | 2021-09-15 | Novartis AG | Polythérapies comprenant des molécules d'anticorps tim-3 |
| TWI734699B (zh) | 2015-09-09 | 2021-08-01 | 美商英塞特公司 | Pim激酶抑制劑之鹽 |
| CN105254624B (zh) * | 2015-09-18 | 2019-08-09 | 上海吉铠医药科技有限公司 | 异噻唑衍生物pim激酶抑制剂及其制备方法与在制药中的应用 |
| CN105130959B (zh) * | 2015-09-18 | 2018-08-03 | 上海吉铠医药科技有限公司 | 嘧啶衍生物pim激酶抑制剂及其制备方法与在制药中的应用 |
| US9920032B2 (en) | 2015-10-02 | 2018-03-20 | Incyte Corporation | Heterocyclic compounds useful as pim kinase inhibitors |
| EP3370768B9 (fr) | 2015-11-03 | 2022-03-16 | Janssen Biotech, Inc. | Anticorps se liant spécifiquement à pd-1 et leurs utilisations |
| WO2017106656A1 (fr) | 2015-12-17 | 2017-06-22 | Novartis Ag | Molécules d'anticorps anti-pd-1 et leurs utilisations |
| CN107519175A (zh) * | 2016-06-21 | 2017-12-29 | 上海方予健康医药科技有限公司 | 一种嘧啶化合物或其盐在制备用于预防和/或治疗与flt3相关的疾病或障碍的药物中的应用 |
| CN107522696B (zh) * | 2016-06-21 | 2019-02-19 | 上海方予健康医药科技有限公司 | 一种嘧啶类化合物的盐酸盐及其制备方法和用途 |
| CN107522695B (zh) * | 2016-06-21 | 2018-09-14 | 上海方予健康医药科技有限公司 | 一种pim激酶抑制剂的盐酸盐及其制备方法和用途 |
| WO2018009466A1 (fr) | 2016-07-05 | 2018-01-11 | Aduro Biotech, Inc. | Composés dinucléotidiques cycliques d'acide nucléique bloqué et leurs utilisations |
| UY37695A (es) | 2017-04-28 | 2018-11-30 | Novartis Ag | Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo |
| WO2018237173A1 (fr) | 2017-06-22 | 2018-12-27 | Novartis Ag | Molécules d'anticorps dirigées contre cd73 et utilisations correspondantes |
| EP3645008A4 (fr) * | 2017-06-30 | 2020-12-09 | Bristol-Myers Squibb Company | Composés quinolinycyclohexylpropanamide substitués et procédés améliorés pour leur préparation |
| AR113922A1 (es) | 2017-12-08 | 2020-07-01 | Incyte Corp | Terapia de combinación de dosis baja para el tratamiento de neoplasias mieloproliferativas |
| US12398209B2 (en) | 2018-01-22 | 2025-08-26 | Janssen Biotech, Inc. | Methods of treating cancers with antagonistic anti-PD-1 antibodies |
| EA202091830A1 (ru) | 2018-01-30 | 2020-12-29 | Инсайт Корпорейшн | Способы и промежуточные соединения для получения ингибитора jak |
| BR112020018094A2 (pt) | 2018-03-08 | 2020-12-22 | Incyte Corporation | Compostos de aminopirazina diol como inibidores de pi3k-¿ |
| MD3773593T2 (ro) | 2018-03-30 | 2024-10-31 | Incyte Corp | Tratament hidradenitei supurative utilizând inhibitori ai JAK |
| CN117838695A (zh) | 2018-04-13 | 2024-04-09 | 住友制药肿瘤公司 | 用于治疗骨髓增殖性肿瘤和与癌症相关的纤维化的pim激酶抑制剂 |
| AR126019A1 (es) | 2018-05-30 | 2023-09-06 | Novartis Ag | Anticuerpos frente a entpd2, terapias de combinación y métodos de uso de los anticuerpos y las terapias de combinación |
| MX2020013085A (es) | 2018-06-05 | 2021-03-02 | Crinetics Pharmaceuticals Inc | Antagonistas del receptor de subtipo 2 de melanocortina (mc2r) y usos de los mismos. |
| US11046658B2 (en) | 2018-07-02 | 2021-06-29 | Incyte Corporation | Aminopyrazine derivatives as PI3K-γ inhibitors |
| NZ778055A (en) | 2019-02-12 | 2025-11-28 | Sumitomo Pharma America Inc | Formulations comprising heterocyclic protein kinase inhibitors |
| CN110078706B (zh) * | 2019-05-31 | 2022-02-01 | 浙江师范大学 | 一种伊马替尼衍生物及其制备方法和用途 |
| CN110452164B (zh) * | 2019-09-10 | 2022-07-22 | 上海皓鸿生物医药科技有限公司 | Pim447关键中间体的制备方法 |
| US20220348651A1 (en) | 2019-09-18 | 2022-11-03 | Novartis Ag | Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies |
| US12479825B2 (en) | 2019-11-07 | 2025-11-25 | Crinetics Pharmaceuticals, Inc. | Melanocortin subtype-2 receptor (MC2R) antagonists and uses thereof |
| EP4077307B1 (fr) | 2019-12-18 | 2025-03-12 | Crinetics Pharmaceuticals, Inc. | Antagonistes du récepteur du sous-type 2 de la mélanocortine (mc2r) à pipéridine à double substitution gem et leurs utilisations |
| WO2021133563A1 (fr) | 2019-12-23 | 2021-07-01 | Crinetics Pharmaceuticals, Inc. | Antagonistes du récepteur du sous-type 2 de la mélanocortine à base de pipéridine spirocyclique (mc2r) et leurs utilisations |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
| CN112915086B (zh) * | 2021-01-27 | 2022-04-12 | 广州市力鑫药业有限公司 | 一种含有Akt靶向激酶抑制剂的药物组合物 |
| JP2024510260A (ja) | 2021-03-19 | 2024-03-06 | クリネティックス ファーマシューティカルズ,インク. | 疾患の治療のためのメラノコルチンサブタイプ-2受容体(mc2r)アンタゴニスト |
| WO2023003014A1 (fr) * | 2021-07-21 | 2023-01-26 | 中外製薬株式会社 | Procédé de production d'un dérivé arylamide |
| EP4611753A1 (fr) | 2022-10-31 | 2025-09-10 | Sumitomo Pharma America, Inc. | Inhibiteur de pim-1 pour le traitement de néoplasmes myéloprolifératifs |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2398478A1 (fr) | 2000-01-26 | 2001-08-02 | Kunio Atsumi | Nouveaux derives de carbapenem de type sel quaternaire |
| AU2001231143A1 (en) * | 2000-01-27 | 2001-08-07 | Cytovia, Inc. | Substituted nicotinamides and analogs as activators of caspases and inducers of apoptosis and the use thereof |
| US8618085B2 (en) | 2000-04-28 | 2013-12-31 | Koasn Biosciences Incorporated | Therapeutic formulations of desoxyepothilones |
| MXPA03008560A (es) | 2001-03-22 | 2004-06-30 | Abbot Gmbh & Co Kg | Pirazolopirimidinas como agentes terapeuticos. |
| KR100557093B1 (ko) | 2003-10-07 | 2006-03-03 | 한미약품 주식회사 | 다약제 내성 저해 활성을 갖는 테트라졸 유도체 및 그의제조방법 |
| TW200523252A (en) | 2003-10-31 | 2005-07-16 | Takeda Pharmaceutical | Pyridine compounds |
| AU2004297235A1 (en) | 2003-12-04 | 2005-06-23 | Vertex Pharmaceuticals Incorporated | Quinoxalines useful as inhibitors of protein kinases |
| US7459562B2 (en) | 2004-04-23 | 2008-12-02 | Bristol-Myers Squibb Company | Monocyclic heterocycles as kinase inhibitors |
| US20060004197A1 (en) | 2004-07-02 | 2006-01-05 | Thomas Thrash | Sulfonamide-based compounds as protein tyrosine kinase inhibitors |
| CR9465A (es) | 2005-03-25 | 2008-06-19 | Surface Logix Inc | Compuestos mejorados farmacocineticamente |
| EP1910385B1 (fr) | 2005-08-04 | 2013-07-24 | Sirtris Pharmaceuticals, Inc. | Benzothiazols et thiazolopyridines en tant que modulateurs de sirtuine |
| US8053454B2 (en) | 2005-10-06 | 2011-11-08 | Exelixis, Inc. | Pyridopyrimidinone inhibitors of PIM-1 and/or PIM-3 |
| GB0520657D0 (en) * | 2005-10-11 | 2005-11-16 | Ludwig Inst Cancer Res | Pharmaceutical compounds |
| HRPK20050957B3 (en) * | 2005-11-11 | 2008-09-30 | Džanko Nikša | Collapsible hanger |
| AR063531A1 (es) * | 2006-10-31 | 2009-01-28 | Schering Corp | Derivados de anilinopiperazina y composicion farmaceutica |
| CA2668210C (fr) * | 2006-10-31 | 2013-03-12 | Schering Corporation | Derives d'anilinopiperazine et leurs methodes d'utilisation |
| MX2009009304A (es) * | 2007-03-01 | 2009-11-18 | Novartis Ag | Inhibidores de cinasa pim y metodos para su uso. |
| JP5241834B2 (ja) * | 2007-07-19 | 2013-07-17 | メルク・シャープ・アンド・ドーム・コーポレーション | プロテインキナーゼ阻害剤としての複素環アミド化合物 |
| EP2195286A2 (fr) | 2007-09-10 | 2010-06-16 | Cipla Limited | Procédé de préparation d'un inhibiteur de la kinase raf et intermédiaires utilisables dans ledit procédé |
| AR070531A1 (es) * | 2008-03-03 | 2010-04-14 | Novartis Ag | Inhibidores de cinasa pim y metodos para su uso |
| MX2011002365A (es) | 2008-09-02 | 2011-04-04 | Novartis Ag | Derivados de picolinamida como inhibidres de cinasa. |
| WO2011016234A1 (fr) | 2009-08-04 | 2011-02-10 | Raqualia Pharma Inc. | Dérivés de picolinamide bloqueurs de ttx-s |
| US8859546B2 (en) | 2011-01-21 | 2014-10-14 | Abbvie Inc. | Picolinamide inhibitors of kinases |
-
2009
- 2009-08-31 MX MX2011002365A patent/MX2011002365A/es active IP Right Grant
- 2009-08-31 US US12/584,158 patent/US8329732B2/en active Active
- 2009-08-31 AU AU2009289319A patent/AU2009289319C1/en active Active
- 2009-08-31 CN CN200980143187.8A patent/CN102203079B/zh active Active
- 2009-08-31 PE PE2011000444A patent/PE20110298A1/es active IP Right Grant
- 2009-08-31 JP JP2011524408A patent/JP5412519B2/ja active Active
- 2009-08-31 CN CN201410461060.3A patent/CN104311480A/zh active Pending
- 2009-08-31 HR HRP20151410TT patent/HRP20151410T1/hr unknown
- 2009-08-31 RS RS20150730A patent/RS54506B1/sr unknown
- 2009-08-31 KR KR1020117007556A patent/KR101345920B1/ko active Active
- 2009-08-31 EP EP09782396.7A patent/EP2344474B1/fr active Active
- 2009-08-31 PL PL09782396T patent/PL2344474T3/pl unknown
- 2009-08-31 GE GEAP2009012163 patent/GEP20135849B/en unknown
- 2009-08-31 NZ NZ591449A patent/NZ591449A/xx not_active IP Right Cessation
- 2009-08-31 EA EA201100425A patent/EA020136B1/ru not_active IP Right Cessation
- 2009-08-31 HU HUE09782396A patent/HUE026381T2/en unknown
- 2009-08-31 CN CN2013102514039A patent/CN103333157A/zh active Pending
- 2009-08-31 DK DK09782396.7T patent/DK2344474T3/en active
- 2009-08-31 WO PCT/EP2009/061205 patent/WO2010026124A1/fr not_active Ceased
- 2009-08-31 PT PT97823967T patent/PT2344474E/pt unknown
- 2009-08-31 SI SI200931330T patent/SI2344474T1/sl unknown
- 2009-08-31 MY MYPI2011000927A patent/MY150136A/en unknown
- 2009-08-31 ES ES09782396.7T patent/ES2551900T3/es active Active
- 2009-08-31 BR BRPI0918268-3A patent/BRPI0918268B1/pt active IP Right Grant
- 2009-08-31 ME MEP-2011-37A patent/ME01291A/fr unknown
- 2009-08-31 CA CA2734415A patent/CA2734415C/fr active Active
- 2009-09-01 UY UY0001032085A patent/UY32085A/es not_active Application Discontinuation
- 2009-09-01 TW TW098129413A patent/TWI434843B/zh not_active IP Right Cessation
-
2011
- 2011-02-11 ZA ZA2011/01118A patent/ZA201101118B/en unknown
- 2011-02-17 IL IL211291A patent/IL211291A/en active IP Right Grant
- 2011-03-01 NI NI201100052A patent/NI201100052A/es unknown
- 2011-03-01 CL CL2011000454A patent/CL2011000454A1/es unknown
- 2011-03-02 CR CR20110114A patent/CR20110114A/es unknown
- 2011-03-02 DO DO2011000067A patent/DOP2011000067A/es unknown
- 2011-03-02 EC EC2011010859A patent/ECSP11010859A/es unknown
- 2011-03-02 HN HN2011000629A patent/HN2011000629A/es unknown
- 2011-03-03 SV SV2011003849A patent/SV2011003849A/es unknown
- 2011-03-08 CO CO11028419A patent/CO6351725A2/es active IP Right Grant
- 2011-04-01 MA MA33733A patent/MA32684B1/fr unknown
- 2011-12-15 US US13/327,358 patent/US8592455B2/en active Active
-
2013
- 2013-06-25 JP JP2013132978A patent/JP5813701B2/ja active Active
- 2013-11-15 US US14/081,132 patent/US9079889B2/en active Active
-
2015
- 2015-07-13 US US14/797,534 patent/US20150315150A1/en not_active Abandoned
-
2016
- 2016-01-05 SM SM201600005T patent/SMT201600005B/it unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA32684B1 (fr) | Dérivés de picolinamide en tant qu'inhibiteurs de kinase | |
| MA29915B1 (fr) | Benzimidazoles substitues utilises en tant qu'inhibiteurs de kinases | |
| MA32232B1 (fr) | Nouveaux compoés hétérocycliques et leurs utilisations | |
| EA201100426A1 (ru) | Бициклические ингибиторы киназы | |
| EA200900828A1 (ru) | Соединения и композиции в качестве ингибиторов активности каннабиноидного рецептора 1 | |
| MA30607B1 (fr) | N-phenylmethyl -5-oxo-proline-2-amides substitues tenant lieu d'antagonistes du recepteur p2x7 et procedes d'utilisation | |
| BRPI0515532A (pt) | composto, composição farmacêutica, métodos de inibir a ligação de ligandos endógenos ao receptor de crth-2 em uma célula, de tratar, melhorar ou prevenir um distúrbio responsivo à inibição da ligação de ligandos endógenos ao receptor de crt-2 e de preparar um composto, e, kit | |
| MA33178B1 (fr) | Pipéridines substituées comme antagonistes de ccr3 | |
| MA35459B1 (fr) | Composés et compositions pouvant être utilisés en tant qu'inhibiteurs de la kinase c-kit | |
| MA31761B1 (fr) | Nouveaux inhibiteurs de seh et leur utilisation | |
| EA200701036A1 (ru) | Лактамные соединения и их применение в качестве фармацевтических препаратов | |
| ATE516803T1 (de) | Aryl-spirohydantoin-cgrp-rezeptor-antagonisten | |
| MA30358B1 (fr) | Quinazolines pour l'inhibition de pdk1 | |
| MA30333B1 (fr) | Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete. | |
| ATE556060T1 (de) | Monocyclische anilidspirohydantoine als cgrp- rezeptorantagonisten | |
| DE602007008434D1 (de) | Rezeptoren | |
| MA31158B1 (fr) | Composes tricycliques et leur utilisation comme modulateurs du recepteur de glucocorticoïdes | |
| MA30906B1 (fr) | Composes et compositions en tant quinhibiteurs des proteines kinases | |
| MA31016B1 (fr) | Composes de diazepan substitues comme antagonistes des recepteurs de l'orexine. | |
| TNSN07305A1 (fr) | Agonistes de pyy et leurs utilisations | |
| EP1606286A4 (fr) | Antagonistes benodiazepine spirohydantoin des recepteurs de cgrp | |
| MA29160B1 (fr) | Derives de triazole substitues, servant d'antagonistes d'ocytocine | |
| MA27565A1 (fr) | Derives de 4-tetrazolyl-4-phenylpiperidine utilises pour le traitement de la douleur | |
| ATE394400T1 (de) | Bicyclische anilidspirohydantoine als cgrp- rezeptorantagonisten | |
| MA30988B1 (fr) | Composes destines a inhiber la progression mitotique |