MA33926B1 - Aminopyrimidines en tant qu'inhibiteurs de la syk - Google Patents
Aminopyrimidines en tant qu'inhibiteurs de la sykInfo
- Publication number
- MA33926B1 MA33926B1 MA35069A MA35069A MA33926B1 MA 33926 B1 MA33926 B1 MA 33926B1 MA 35069 A MA35069 A MA 35069A MA 35069 A MA35069 A MA 35069A MA 33926 B1 MA33926 B1 MA 33926B1
- Authority
- MA
- Morocco
- Prior art keywords
- inhibitors
- aminopyrimidines
- syk
- copd
- asthma
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000005005 aminopyrimidines Chemical class 0.000 title 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 102000000551 Syk Kinase Human genes 0.000 abstract 1
- 108010016672 Syk Kinase Proteins 0.000 abstract 1
- -1 amine pyrimidines Chemical class 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 230000006806 disease prevention Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
- C07D451/06—Oxygen atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/08—Bridged systems
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- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
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- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
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- Orthopedic Medicine & Surgery (AREA)
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- Pain & Pain Management (AREA)
- Communicable Diseases (AREA)
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Abstract
La présente invention porte sur de nouvelles amines pyrimidines de formule (i) qui sont des inhibiteurs puissants de la tyrosine kinase de la rate, et sont utiles dans le traitement et la prévention de maladies à médiation par ladite enzyme, telle que l'asthme, la maladie pulmonaire obstructive chronique (copd) et l'arthrite rhumatoïde.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28726709P | 2009-12-17 | 2009-12-17 | |
| PCT/US2010/060463 WO2011075517A1 (fr) | 2009-12-17 | 2010-12-15 | Aminopyrimidines en tant qu'inhibiteurs de la syk |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA33926B1 true MA33926B1 (fr) | 2013-01-02 |
Family
ID=43502894
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA35069A MA33926B1 (fr) | 2009-12-17 | 2010-12-15 | Aminopyrimidines en tant qu'inhibiteurs de la syk |
Country Status (28)
| Country | Link |
|---|---|
| US (3) | US8551984B2 (fr) |
| EP (1) | EP2513098B1 (fr) |
| JP (2) | JP5242857B2 (fr) |
| KR (1) | KR101445012B1 (fr) |
| CN (1) | CN102858767B (fr) |
| AR (1) | AR080672A1 (fr) |
| AU (1) | AU2010331927B2 (fr) |
| BR (1) | BR112012014703B1 (fr) |
| CA (1) | CA2782889C (fr) |
| CL (1) | CL2012001627A1 (fr) |
| CO (1) | CO6551728A2 (fr) |
| CR (1) | CR20120331A (fr) |
| DO (1) | DOP2012000166A (fr) |
| EA (1) | EA022790B1 (fr) |
| EC (1) | ECSP12011982A (fr) |
| ES (1) | ES2609040T3 (fr) |
| GE (1) | GEP20146125B (fr) |
| GT (1) | GT201200202A (fr) |
| MA (1) | MA33926B1 (fr) |
| MX (1) | MX2012007154A (fr) |
| NI (1) | NI201200108A (fr) |
| NZ (1) | NZ600673A (fr) |
| PE (1) | PE20121480A1 (fr) |
| PH (1) | PH12012501225A1 (fr) |
| SG (1) | SG181803A1 (fr) |
| TN (1) | TN2012000288A1 (fr) |
| TW (1) | TW201132637A (fr) |
| WO (2) | WO2011075517A1 (fr) |
Families Citing this family (90)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8551984B2 (en) | 2009-12-17 | 2013-10-08 | Merck Sharp & Dohme Corp. | Aminopyrimidines as SYK inhibitors |
| WO2011075560A1 (fr) | 2009-12-17 | 2011-06-23 | Merck Sharp & Dohme Corp. | Aminopyrimidines en tant qu'inhibiteurs de la syk |
| PL2516434T3 (pl) | 2009-12-23 | 2015-11-30 | Takeda Pharmaceuticals Co | Skondensowane heteroaromatyczne pirolidynony jako inhibitory SYK |
| EA022188B1 (ru) | 2010-01-12 | 2015-11-30 | Аб Сьянс | Оксазольные ингибиторы киназы, содержащие их композиции и их применение |
| WO2012088266A2 (fr) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Imidazopyridazines et benzimidazoles substitués en tant qu'inhibiteurs de fgfr3 |
| JP5934782B2 (ja) | 2011-05-04 | 2016-06-15 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | アミノ−ピリジン含有脾臓チロシンキナーゼ(Syk)阻害薬 |
| US9120785B2 (en) | 2011-05-10 | 2015-09-01 | Merck Sharp & Dohme Corp. | Pyridyl aminopyridines as Syk inhibitors |
| WO2012154519A1 (fr) | 2011-05-10 | 2012-11-15 | Merck Sharp & Dohme Corp. | Aminopyrimidines en tant qu'inhibiteurs de syk |
| EP2706852B1 (fr) | 2011-05-10 | 2018-08-22 | Merck Sharp & Dohme Corp. | Bipyridylaminopyridines en tant qu'inhibiteurs de syk |
| JP2014159375A (ja) * | 2011-06-15 | 2014-09-04 | Takeda Chem Ind Ltd | アゼパン化合物 |
| US9056873B2 (en) | 2011-06-22 | 2015-06-16 | Takeda Pharmaceutical Company Limited | Substituted 6-aza-isoindolin-1-one derivatives |
| CN104125957B (zh) * | 2011-12-21 | 2016-05-25 | 拜耳知识产权有限责任公司 | 取代的苄基吡唑 |
| US8906889B2 (en) | 2012-02-15 | 2014-12-09 | Bristol-Myers Squibb Company | C-3 cycloalkenyl triterpenoids with HIV maturation inhibitory activity |
| US9096579B2 (en) | 2012-04-20 | 2015-08-04 | Boehringer Ingelheim International Gmbh | Amino-indolyl-substituted imidazolyl-pyrimidines and their use as medicaments |
| US8889854B2 (en) | 2012-05-07 | 2014-11-18 | Bristol-Myers Squibb Company | C-17 bicyclic amines of triterpenoids with HIV maturation inhibitory activity |
| ES2984771T3 (es) | 2012-06-13 | 2024-10-31 | Incyte Holdings Corp | Compuestos tricíclicos sustituidos como inhibidores de FGFR |
| US9487504B2 (en) | 2012-06-20 | 2016-11-08 | Merck Sharp & Dohme Corp. | Imidazolyl analogs as syk inhibitors |
| WO2013192125A1 (fr) | 2012-06-20 | 2013-12-27 | Merck Sharp & Dohme Corp. | Dérivés de pyrazolyle en tant qu'inhibiteurs de syk |
| EP2863915B1 (fr) * | 2012-06-22 | 2017-12-06 | Merck Sharp & Dohme Corp. | Inhibiteurs de tyrosine kinase splénique (syk) diazines et triazines substituées |
| WO2013192098A1 (fr) * | 2012-06-22 | 2013-12-27 | Merck Sharp & Dohme Corp. | Inhibiteurs à pyridine substituée de la tyrosine kinase de la rate (syk) |
| WO2014026125A1 (fr) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Dérivés de pyrazine en tant qu'inhibiteurs de fgfr |
| US9353066B2 (en) | 2012-08-20 | 2016-05-31 | Merck Sharp & Dohme Corp. | Substituted phenyl-Spleen Tyrosine Kinase (Syk) inhibitors |
| EP2900665B1 (fr) | 2012-09-28 | 2018-01-03 | Merck Sharp & Dohme Corp. | Dérivés triazolyle en tant qu'inhibiteurs de la syk |
| LT2914296T (lt) | 2012-11-01 | 2018-09-25 | Infinity Pharmaceuticals, Inc. | Vėžio gydymas, panaudojant p13 kinazės izoformos moduliatorius |
| EP2916837A4 (fr) * | 2012-11-07 | 2016-07-20 | Merck Sharp & Dohme | Promédicament bipyridylaminopyridines en tant qu'inhibiteurs de syk |
| EP2916836A4 (fr) * | 2012-11-07 | 2016-08-03 | Merck Sharp & Dohme | Inhibiteurs de la tyrosine kinase de la rate (syk) contenant amino-pyridine |
| EP2931281B1 (fr) * | 2012-12-12 | 2018-01-17 | Merck Sharp & Dohme Corp. | Inhibiteurs de tyrosine kinase splénique contenant une aminopyridine |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| US9598405B2 (en) | 2012-12-21 | 2017-03-21 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminopyridines as spleen tyrosine kinase inhibitors |
| US20160024051A1 (en) | 2013-03-15 | 2016-01-28 | Infinity Pharmaceuticals, Inc. | Salts and solid forms of isoquinolinones and composition comprising and methods of using the same |
| EA035095B1 (ru) | 2013-04-19 | 2020-04-27 | Инсайт Холдингс Корпорейшн | Бициклические гетероциклы в качестве ингибиторов fgfr |
| WO2014176216A1 (fr) * | 2013-04-26 | 2014-10-30 | Merck Sharp & Dohme Corp. | Aminopyrimidines substituées par thiazole utilisées en tant qu'inhibiteurs de tyrosine kinase splénique |
| WO2014176210A1 (fr) * | 2013-04-26 | 2014-10-30 | Merck Sharp & Dohme Corp. | Composés aminohétéroaryle à substitution thiazole inhibiteurs de tyrosine kinase splénique |
| EP3003309B1 (fr) | 2013-05-30 | 2020-09-09 | Infinity Pharmaceuticals, Inc. | Traitement anticancer au moyen de modulateurs isoformes de la kinase p13 |
| US9751888B2 (en) | 2013-10-04 | 2017-09-05 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| WO2015051244A1 (fr) | 2013-10-04 | 2015-04-09 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
| US20160244452A1 (en) | 2013-10-21 | 2016-08-25 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| US9783531B2 (en) | 2013-12-20 | 2017-10-10 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminoheteroaryls as spleen tyrosine kinase inhibitors |
| EP3083560B1 (fr) * | 2013-12-20 | 2021-10-27 | Merck Sharp & Dohme Corp. | Composés aminohétéroaryle à substitution thiazole utilisés comme inhibiteurs de la tyrosine kinase splénique |
| US9822107B2 (en) * | 2013-12-20 | 2017-11-21 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminoheteroaryls as spleen tyrosine kinase inhibitors |
| WO2015138273A1 (fr) | 2014-03-13 | 2015-09-17 | Merck Sharp & Dohme Corp. | Composés 2-pyrazine carboxamide utiles comme inhibiteurs de la tyrosine kinase splénique |
| EP3119397B1 (fr) | 2014-03-19 | 2022-03-09 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques destinés à être utilisés dans le traitement de troubles médiés par pi3k-gamma |
| WO2015143712A1 (fr) | 2014-03-28 | 2015-10-01 | Merck Sharp & Dohme Corp. | Inhibiteurs nucléosidiques substitués en 4' de la transcriptase inverse |
| US20150320754A1 (en) | 2014-04-16 | 2015-11-12 | Infinity Pharmaceuticals, Inc. | Combination therapies |
| WO2016054491A1 (fr) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| EA038045B1 (ru) | 2015-02-20 | 2021-06-28 | Инсайт Корпорейшн | Бициклические гетероциклы в качестве ингибиторов fgfr |
| US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| RU2736732C2 (ru) | 2015-04-02 | 2020-11-19 | Интервет Интернэшнл Б.В. | Антитела к альфа-рецептору собачьего интерлейкина-4 |
| CA2988594C (fr) * | 2015-06-08 | 2023-08-15 | Acetylon Pharmaceuticals, Inc. | Procedes de fabrication d'inhibiteurs de proteine desacetylase |
| CN114230571B (zh) | 2015-09-14 | 2025-07-08 | 无限药品股份有限公司 | 异喹啉酮的固体形式、其制备方法、包含其的组合物及其使用方法 |
| US10919914B2 (en) | 2016-06-08 | 2021-02-16 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| UA125216C2 (uk) | 2016-06-24 | 2022-02-02 | Інфініті Фармасьютікалз, Інк. | Комбінована терапія |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| CN107235873B (zh) * | 2017-07-04 | 2018-11-06 | 中节能万润股份有限公司 | 一种美司钠的制备方法 |
| CN107573263B (zh) * | 2017-08-14 | 2020-04-07 | 大连理工大学 | 一种ω-取代缩二脲类化合物的合成方法 |
| CN111542521B (zh) * | 2017-09-11 | 2024-02-23 | 赛泰尔治疗公司 | Rad51抑制剂 |
| KR20200073216A (ko) | 2017-10-19 | 2020-06-23 | 바이엘 애니멀 헬스 게엠베하 | 동물에서의 질환의 치료 및 방지를 위한 융합된 헤테로방향족 피롤리돈의 용도 |
| US11040975B2 (en) | 2017-12-08 | 2021-06-22 | Merck Sharp & Dohme Corp. | Carbocyclic nucleoside reverse transcriptase inhibitors |
| US11174257B2 (en) | 2018-05-04 | 2021-11-16 | Incyte Corporation | Salts of an FGFR inhibitor |
| RS66310B1 (sr) | 2018-05-04 | 2025-01-31 | Incyte Corp | Čvrsti oblici inhibitora fgfr i procesi za njegovu pripremu |
| KR102328682B1 (ko) | 2018-08-27 | 2021-11-18 | 주식회사 대웅제약 | 신규한 헤테로사이클릭아민 유도체 및 이를 포함하는 약학 조성물 |
| WO2020185532A1 (fr) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Méthodes de traitement du cancer au moyen d'un inhibiteur de fgfr |
| KR20210142154A (ko) | 2019-03-21 | 2021-11-24 | 옹쎄오 | 암 치료를 위한 키나제 억제제와 조합된 dbait 분자 |
| PH12021552205A1 (en) | 2019-03-25 | 2022-06-13 | Cyteir Therapeutics Inc | Combinations of rad51 and parp inhibitors |
| PE20220597A1 (es) | 2019-05-10 | 2022-04-22 | Deciphera Pharmaceuticals Llc | Inhibidores de la autofagia de fenilaminopirimidina amida y metodos de uso de estos |
| EP4295846A3 (fr) | 2019-05-10 | 2024-02-28 | Deciphera Pharmaceuticals, LLC | Hétéroarylaminopyrimidine amides inhibiteurs d'autophagie et leurs procédés d'utilisation |
| CA3143489A1 (fr) | 2019-06-17 | 2020-12-24 | Deciphera Pharmaceuticals, Llc | Inhibiteurs de l'autophagie a base d'amide d'aminopyrimidine et leurs procedes d'utilisation |
| WO2021007269A1 (fr) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr |
| WO2021067374A1 (fr) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr |
| PH12022550892A1 (en) | 2019-10-14 | 2023-05-03 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| SMT202400273T1 (it) | 2019-11-29 | 2024-09-16 | Lupin Ltd | Composti triciclici sostituiti |
| AU2020395185A1 (en) | 2019-12-04 | 2022-06-02 | Incyte Corporation | Derivatives of an FGFR inhibitor |
| EP4069696A1 (fr) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr |
| BR112022011629A2 (pt) | 2019-12-20 | 2022-09-13 | Intervet Int Bv | Anticorpos biespecíficos caninizados para tratar dermatite atópica |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
| CN115003798B (zh) * | 2020-06-17 | 2025-08-01 | 兰迪·莱曼·阿伦 | 用于检测分析物的方法和试剂盒 |
| JP2023545183A (ja) | 2020-10-15 | 2023-10-26 | インターベット インターナショナル ベー. フェー. | イヌインターロイキン-31受容体アルファに対するイヌ化抗体 |
| MX2023011027A (es) | 2021-03-23 | 2023-09-27 | Halia Therapeutics Inc | Derivados de pirimidina utiles como inhibidores de la proteina cinasa de repeticion 2 rica en leucina (lrrk2). |
| JP2024513575A (ja) | 2021-04-12 | 2024-03-26 | インサイト・コーポレイション | Fgfr阻害剤及びネクチン-4標的化剤を含む併用療法 |
| WO2022261160A1 (fr) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr |
| TW202313610A (zh) | 2021-06-09 | 2023-04-01 | 美商英塞特公司 | 作為fgfr抑制劑之三環雜環 |
| US20250325630A1 (en) | 2021-08-20 | 2025-10-23 | Intervet Inc. | Homodimer fusion proteins for treating atopic dermatitis |
| CN114105958B (zh) * | 2021-12-03 | 2022-11-22 | 郑州大学第一附属医院 | 一组含羟肟酸的2-苯氨基嘧啶类衍生物及其应用 |
| CA3239826A1 (fr) | 2021-12-16 | 2023-06-22 | Mohamad Morsey | Anticorps caninises contre le recepteur alpha ii de l'interleukine-31 canine |
| EP4618755A1 (fr) * | 2022-11-15 | 2025-09-24 | Larkspur Biosciences, Inc. | Inhibiteurs et agents de dégradation de protéine pip4k |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1440973A3 (fr) | 1995-11-17 | 2004-10-20 | Gesellschaft für biotechnologische Forschung mbH (GBF) | Dérivés d'épothilone, procédé de production et utilisation |
| EP0977563B1 (fr) | 1996-12-03 | 2005-10-12 | Sloan-Kettering Institute For Cancer Research | Synthese d'epothilones, intermediaires utilises dans leur synthese, analogues et utilisations de celles-ci |
| GB9918035D0 (en) * | 1999-07-30 | 1999-09-29 | Novartis Ag | Organic compounds |
| WO2002083139A1 (fr) | 2001-04-10 | 2002-10-24 | Merck & Co., Inc. | Inhibiteurs de l'activite d'akt |
| WO2002083675A2 (fr) | 2001-04-10 | 2002-10-24 | Merck Sharp & Dohme Limited | Inhibiteurs de l'activite de l'akt |
| US6958334B2 (en) | 2001-04-10 | 2005-10-25 | Merck & Co., Inc. | Inhibitors of Akt activity |
| DE60227492D1 (de) | 2001-04-10 | 2008-08-21 | Merck & Co Inc | Hemmstoffe der akt aktivität |
| CA2446756C (fr) | 2001-06-01 | 2011-03-08 | Vertex Pharmaceuticals Incorporated | Composes de thiazole inhibiteurs des proteines kinase |
| HUP0402352A2 (hu) | 2001-06-19 | 2005-02-28 | Bristol-Myers Squibb Co. | Foszfodiészteráz (PDE) 7 inhibitorként alkalmazható pirimidinszármazékok és ezeket tartalmazó gyógyszerkészítmények |
| GB0123951D0 (en) | 2001-10-05 | 2001-11-28 | Glaxo Group Ltd | Therapies for treating respiratory diseases |
| TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| WO2003086394A1 (fr) | 2002-04-08 | 2003-10-23 | Merck & Co., Inc. | Inhibiteurs de l'activite akt |
| CA2480880C (fr) | 2002-04-08 | 2011-03-22 | Merck & Co., Inc. | Inhibiteurs de l'activite de akt |
| CA2481241C (fr) | 2002-04-08 | 2010-07-27 | Merck & Co., Inc. | Derives de quinolaxine fusionnee comme inhibiteurs de l'activite d'akt |
| JP4394959B2 (ja) | 2002-04-08 | 2010-01-06 | メルク エンド カムパニー インコーポレーテッド | Akt活性の阻害剤 |
| US7361665B2 (en) | 2002-07-09 | 2008-04-22 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-Jun N-terminal kinases (JNK) and other protein kinases |
| EP1605946B1 (fr) | 2003-03-25 | 2008-05-28 | Vertex Pharmaceuticals Incorporated | Thiazoles utiles en tant qu'inhibiteurs des proteines kinases |
| AU2004225965A1 (en) | 2003-03-25 | 2004-10-14 | Vertex Pharmaceuticals Incorporated | Thiazoles useful as inhibitors of protein kinases |
| ES2388434T3 (es) | 2003-11-03 | 2012-10-15 | Glaxo Group Limited | Dispositivo de administración de fluido |
| US7345043B2 (en) | 2004-04-01 | 2008-03-18 | Miikana Therapeutics | Inhibitors of histone deacetylase |
| EP2161275A1 (fr) | 2005-01-19 | 2010-03-10 | Rigel Pharmaceuticals, Inc. | Promédicaments de composés de 2,4-pyrimidinédiamine et leurs utilisations |
| ZA200707227B (en) * | 2005-02-28 | 2009-08-26 | Japan Tobacco Inc | Novel aminopyridine compound with syk inhibitory activity |
| AU2006219231B2 (en) * | 2005-02-28 | 2010-01-14 | Japan Tobacco Inc. | Novel aminopyridine compound with Syk inhibitory activity |
| WO2006129100A1 (fr) | 2005-06-03 | 2006-12-07 | Glaxo Group Limited | Nouveaux composes |
| GB0520838D0 (en) * | 2005-10-13 | 2005-11-23 | Glaxo Group Ltd | Novel compounds |
| CA2648923A1 (fr) | 2006-04-11 | 2007-10-18 | Vertex Pharmaceuticals Incorporated | Thiazoles, imidazoles, et pyrazoles utiles en tant qu'inhibiteurs de proteines kinases |
| WO2008024634A1 (fr) * | 2006-08-25 | 2008-02-28 | Smithkline Beecham Corporation | Composés de pyrimidine utilisés en tant qu'inhibiteurs de kinase |
| KR101149295B1 (ko) | 2006-12-08 | 2012-07-05 | 아이알엠 엘엘씨 | 단백질 키나제 억제제로서의 화합물 |
| TW200840581A (en) | 2007-02-28 | 2008-10-16 | Astrazeneca Ab | Novel pyrimidine derivatives |
| KR101122481B1 (ko) | 2007-05-04 | 2012-02-29 | 아이알엠 엘엘씨 | C-kit 및 pdgfr 키나제 억제제로서의 피리미딘 유도체 및 조성물 |
| WO2009012421A1 (fr) | 2007-07-17 | 2009-01-22 | Rigel Pharmaceuticals, Inc. | Pyrimidinediamines substituées par des amines cycliques utilisées en tant qu'inhibiteurs de la pkc |
| WO2009032861A1 (fr) | 2007-09-04 | 2009-03-12 | The Scripps Research Institute | Pyrimidinyl-amines substituées en tant qu'inhibiteurs de la protéine kinase |
| MX2010008926A (es) | 2008-02-15 | 2011-02-23 | Rigel Pharmaceuticals Inc | Compuestos de pirimidin-2-amina y su uso como inhibidores de jak cinasas. |
| WO2009122180A1 (fr) | 2008-04-02 | 2009-10-08 | Medical Research Council | Dérivés de pyrimidine capables d’inhiber une ou plusieurs kinases |
| CA2960692C (fr) | 2008-04-16 | 2019-09-24 | Portola Pharmaceuticals, Inc. | 2,6-diamino-pyrimidin-5-yl-carboxamides comme inhibiteurs d'activite de syk ou de jak kinase |
| US8551984B2 (en) | 2009-12-17 | 2013-10-08 | Merck Sharp & Dohme Corp. | Aminopyrimidines as SYK inhibitors |
| EA022188B1 (ru) * | 2010-01-12 | 2015-11-30 | Аб Сьянс | Оксазольные ингибиторы киназы, содержащие их композиции и их применение |
| DE102010000842A1 (de) * | 2010-01-13 | 2011-07-14 | Robert Bosch GmbH, 70469 | Batterie, Batteriesystem und Verfahren zur Verbindung einer Mehrzahl von Batterien |
-
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- 2014-04-17 US US14/255,480 patent/US20140243290A1/en not_active Abandoned
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