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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- 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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- 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
- C07D471/08—Bridged systems
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- 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
- C07D495/04—Ortho-condensed systems
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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)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
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- Diabetes (AREA)
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- Oncology (AREA)
- Virology (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
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- Endocrinology (AREA)
- Rheumatology (AREA)
- Biochemistry (AREA)
- Tropical Medicine & Parasitology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (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) | US8759366B2 (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 (92)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8735417B2 (en) | 2009-12-17 | 2014-05-27 | Merck Sharp & Dohme Corp. | Aminopyrimidines as Syk inhibitors |
| WO2011075517A1 (fr) | 2009-12-17 | 2011-06-23 | Merck Sharp & Dohme Corp. | Aminopyrimidines en tant qu'inhibiteurs de la syk |
| SG181857A1 (en) | 2009-12-23 | 2012-07-30 | Takeda Pharmaceutical | Fused heteroaromatic pyrrolidinones as syk inhibitors |
| MX2012008083A (es) | 2010-01-12 | 2012-08-15 | Ab Science | Inhibidores de triazol y oxazol quinaza. |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| BR112013028430A2 (pt) * | 2011-05-04 | 2017-08-01 | Merck Sharp & Dohme | composto, composição farmacêutica, método para tratar uma doença ou condição mediada por tirosina quinase do baço (syk), e, uso de uma quantidade terapeuticamente eficiente do composto |
| EP2707357B1 (fr) | 2011-05-10 | 2017-01-18 | Merck Sharp & Dohme Corp. | Pyridylaminopyridines en tant qu'inhibiteurs de syk |
| US9145391B2 (en) | 2011-05-10 | 2015-09-29 | Merck Sharp & Dohme Corp. | Bipyridylaminopyridines as Syk inhibitors |
| MX2013013090A (es) | 2011-05-10 | 2013-12-16 | Merck Sharp & Dohme | Aminopirimidinas como inhibidores de tirosina cinaza del bazo. |
| JP2014159375A (ja) * | 2011-06-15 | 2014-09-04 | Takeda Chem Ind Ltd | アゼパン化合物 |
| JP6026525B2 (ja) | 2011-06-22 | 2016-11-16 | 武田薬品工業株式会社 | 置換6−アザ−イソインドリン−1−オン誘導体 |
| WO2013092512A1 (fr) * | 2011-12-21 | 2013-06-27 | Bayer Intellectual Property Gmbh | Benzylpyrazoles substitués |
| 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 |
| ES2704744T3 (es) | 2012-06-13 | 2019-03-19 | Incyte Holdings Corp | Compuestos tricíclicos sustituidos como inhibidores de FGFR |
| EP2863914B1 (fr) | 2012-06-20 | 2018-10-03 | Merck Sharp & Dohme Corp. | Dérivés de pyrazolyle en tant qu'inhibiteurs de syk |
| US9487504B2 (en) | 2012-06-20 | 2016-11-08 | Merck Sharp & Dohme Corp. | Imidazolyl analogs as syk inhibitors |
| EP2863915B1 (fr) * | 2012-06-22 | 2017-12-06 | Merck Sharp & Dohme Corp. | Inhibiteurs de tyrosine kinase splénique (syk) diazines et triazines substituées |
| EP2863916B1 (fr) * | 2012-06-22 | 2018-07-18 | Merck Sharp & Dohme Corp. | Inhibiteurs à pyridine substituée de la tyrosine kinase de la rate (syk) |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| EP2884982B1 (fr) * | 2012-08-20 | 2017-09-20 | Merck Sharp & Dohme Corp. | Inhibiteurs de la phényle tyrosine kinase de la rate (syk) substitués |
| EP2900665B1 (fr) | 2012-09-28 | 2018-01-03 | Merck Sharp & Dohme Corp. | Dérivés triazolyle en tant qu'inhibiteurs de la syk |
| EP2914296B2 (fr) | 2012-11-01 | 2021-09-29 | Infinity Pharmaceuticals, Inc. | Traitement de cancers à l'aide de modulateurs d'isoforme de pi3 kinase |
| WO2014074422A1 (fr) * | 2012-11-07 | 2014-05-15 | Merck Sharp & Dohme Corp. | Inhibiteurs de la tyrosine kinase de la rate (syk) contenant amino-pyridine |
| EP2916837A4 (fr) * | 2012-11-07 | 2016-07-20 | Merck Sharp & Dohme | Promédicament bipyridylaminopyridines en tant qu'inhibiteurs de syk |
| WO2014093191A1 (fr) * | 2012-12-12 | 2014-06-19 | 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 |
| EP2934525B1 (fr) * | 2012-12-21 | 2019-05-08 | Merck Sharp & Dohme Corp. | Aminopyridines substituées par thiazole en tant qu'inhibiteurs de la tyrosine kinase de la rate |
| 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 |
| EP2988744A4 (fr) * | 2013-04-26 | 2016-11-02 | Merck Sharp & Dohme | Composés aminohétéroaryle à substitution thiazole inhibiteurs de tyrosine kinase splénique |
| EP2988749B1 (fr) * | 2013-04-26 | 2019-08-14 | Merck Sharp & Dohme Corp. | Aminopyrimidines substituées par thiazole utilisées en tant qu'inhibiteurs de tyrosine kinase splénique |
| SG11201509842SA (en) | 2013-05-30 | 2015-12-30 | Infinity Pharmaceuticals Inc | Treatment of cancers using pi3 kinase isoform modulators |
| WO2015051241A1 (fr) | 2013-10-04 | 2015-04-09 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
| MX2021012208A (es) | 2013-10-04 | 2023-01-19 | Infinity Pharmaceuticals Inc | Compuestos heterocíclicos y usos de los mismos. |
| WO2015061204A1 (fr) | 2013-10-21 | 2015-04-30 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
| 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 |
| US9783531B2 (en) | 2013-12-20 | 2017-10-10 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminoheteroaryls as spleen tyrosine kinase inhibitors |
| 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 |
| NZ724368A (en) | 2014-03-19 | 2023-07-28 | Infinity Pharmaceuticals Inc | Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders |
| 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 |
| WO2016134294A1 (fr) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| MX373169B (es) | 2015-02-20 | 2020-04-24 | Incyte Holdings Corp | Heterociclos bicíclicos como inhibidores de receptores del factor de crecimiento fibroblástico (fgfr). |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| AU2016239858B2 (en) | 2015-04-02 | 2021-07-01 | Intervet International B.V. | Antibodies to canine interleukin-4 receptor alpha |
| AR105812A1 (es) * | 2015-06-08 | 2017-11-15 | Acetylon Pharmaceuticals Inc | Métodos para la preparación de inhibidores de proteína deacetilasa |
| EP4585268A3 (fr) | 2015-09-14 | 2025-10-15 | Twelve Therapeutics, Inc. | Formes solides de dérivés d'isoquinolinone, procédé de fabrication, compositions comprenant celles-ci et leurs procédés d'utilisation |
| WO2017214269A1 (fr) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
| RU2754507C2 (ru) | 2016-06-24 | 2021-09-02 | Инфинити Фармасьютикалз, Инк. | Комбинированная терапия |
| 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 |
| SG10202107087YA (en) * | 2017-09-11 | 2021-07-29 | Cyteir Therapeutics Inc | Rad51 inhibitors |
| CA3079292A1 (fr) | 2017-10-19 | 2019-04-25 | Bayer Animal Health Gmbh | Utilisation de pyrrolidones heteroaromatiques fusionnees pour le traitement et la prevention de maladies chez des animaux |
| US11040975B2 (en) | 2017-12-08 | 2021-06-22 | Merck Sharp & Dohme Corp. | Carbocyclic nucleoside reverse transcriptase inhibitors |
| MA52493A (fr) | 2018-05-04 | 2021-03-10 | Incyte Corp | Sels d'un inhibiteur de fgfr |
| CR20200590A (es) | 2018-05-04 | 2021-04-26 | Incyte Corp | Formas sólidas de un inhibidor de fgfr y procesos para prepararlas |
| 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 |
| US20220143049A1 (en) | 2019-03-21 | 2022-05-12 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
| PH12021552205A1 (en) | 2019-03-25 | 2022-06-13 | Cyteir Therapeutics Inc | Combinations of rad51 and parp inhibitors |
| MX2021013662A (es) | 2019-05-10 | 2022-03-11 | Deciphera Pharmaceuticals Llc | Inhibidores de la autofagia de heteroarilaminopirimidina amida y metodos de uso de estos. |
| EP3966207B1 (fr) | 2019-05-10 | 2023-11-01 | Deciphera Pharmaceuticals, LLC | Phénylaminopyrimidine amides inhibiteurs d'autophagie et leurs procédés d'utilisation |
| IL325201A (en) | 2019-06-17 | 2026-02-01 | Deciphera Pharmaceuticals Llc | Aminopyrimidine amide autophagy inhibitors and methods of using them |
| 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 |
| TWI891666B (zh) | 2019-10-14 | 2025-08-01 | 美商英塞特公司 | 作為fgfr抑制劑之雙環雜環 |
| WO2021076728A1 (fr) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr |
| EP4054579A1 (fr) | 2019-11-08 | 2022-09-14 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Méthodes pour le traitement de cancers qui ont acquis une résistance aux inhibiteurs de kinase |
| CA3154914A1 (fr) | 2019-11-29 | 2021-06-03 | Lupin Limited | Composes tricycliques substitues |
| BR112022010664A2 (pt) | 2019-12-04 | 2022-08-16 | Incyte Corp | Derivados de um inibidor de fgfr |
| EP4069696A1 (fr) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr |
| MX2022007636A (es) | 2019-12-20 | 2022-07-19 | Intervet Int Bv | Anticuerpos biespecificos caninizados y pares de union biespecificos para el tratamiento contra dermatitis atopica. |
| WO2021146424A1 (fr) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr |
| 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 |
| US12605387B2 (en) | 2020-07-24 | 2026-04-21 | Secura Bio, Inc. | Treatment of cancers using PI3 kinase isoform modulators |
| AU2021359068A1 (en) | 2020-10-15 | 2023-06-15 | Intervet International B.V. | Caninized antibodies to canine interleukin-31 receptor alpha |
| WO2022094668A1 (fr) * | 2020-11-06 | 2022-05-12 | Actinogen Medical Limited | Procédé de préparation de composés de méthanone hétérocycliques et de leurs intermédiaires aza-bicyclo |
| CA3214360A1 (fr) | 2021-03-23 | 2022-09-29 | Halia Therapeutics, Inc. | Derives de pyrimidine utiles en tant qu'inhibiteurs de la lrrk2 kinase |
| TW202304459A (zh) | 2021-04-12 | 2023-02-01 | 美商英塞特公司 | 包含fgfr抑制劑及nectin-4靶向劑之組合療法 |
| EP4352059A1 (fr) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr |
| WO2022261159A1 (fr) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Hétérocycles tricycliques utiles en tant qu'inhibiteurs de fgfr |
| MX2024002149A (es) | 2021-08-20 | 2024-03-08 | Intervet Int Bv | Proteinas de fusion para tratar la dermatitis atopica. |
| 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 |
| EP4448571A1 (fr) | 2021-12-16 | 2024-10-23 | Intervet International B.V. | Anticorps caninisés contre le récepteur 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 |
|---|---|---|---|---|
| DK1186606T4 (da) | 1995-11-17 | 2011-12-05 | Biotechnolog Forschung Gmbh | Epothilonderivater, deres fremstilling og anvendelse |
| WO1999001124A1 (fr) | 1996-12-03 | 1999-01-14 | 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 |
| WO2002083675A2 (fr) | 2001-04-10 | 2002-10-24 | Merck Sharp & Dohme Limited | Inhibiteurs de l'activite de l'akt |
| WO2002083140A1 (fr) | 2001-04-10 | 2002-10-24 | Merck & Co., Inc. | Inhibiteurs de l'activite d'akt |
| WO2002083139A1 (fr) | 2001-04-10 | 2002-10-24 | Merck & Co., Inc. | Inhibiteurs de l'activite d'akt |
| US7034026B2 (en) | 2001-04-10 | 2006-04-25 | Merck & Co., Inc. | Inhibitors of Akt activity |
| CA2446756C (fr) | 2001-06-01 | 2011-03-08 | Vertex Pharmaceuticals Incorporated | Composes de thiazole inhibiteurs des proteines kinase |
| JP2005500294A (ja) | 2001-06-19 | 2005-01-06 | ブリストル−マイヤーズ スクイブ カンパニー | ホスホジエステラーゼ7に対するピリミジン阻害剤 |
| 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 |
| CA2480880C (fr) | 2002-04-08 | 2011-03-22 | Merck & Co., Inc. | Inhibiteurs de l'activite de akt |
| EP1494675A4 (fr) | 2002-04-08 | 2006-07-19 | Merck & Co Inc | Inhibiteurs de l'activite de akt |
| US7223738B2 (en) | 2002-04-08 | 2007-05-29 | Merck & Co., Inc. | Inhibitors of Akt activity |
| CA2481241C (fr) | 2002-04-08 | 2010-07-27 | Merck & Co., Inc. | Derives de quinolaxine fusionnee comme inhibiteurs de l'activite d'akt |
| CA2491895C (fr) | 2002-07-09 | 2011-01-18 | Vertex Pharmaceuticals Incorporated | Imidazoles, oxazoles et thiazoles presentant des activites d'inhibition des proteines kinases |
| US20040235834A1 (en) | 2003-03-25 | 2004-11-25 | Farmer Luc J. | Thiazoles useful as inhibitors of protein kinases |
| ATE396731T1 (de) | 2003-03-25 | 2008-06-15 | Vertex Pharma | Thiazole zur verwendung als inhibitoren von protein-kinasen |
| 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 |
| DE602006010979D1 (de) | 2005-01-19 | 2010-01-21 | Rigel Pharmaceuticals Inc | Prodrugs aus 2,4-pyrimidindiamin-verbindungen und ihre verwendungen |
| CN101166734A (zh) * | 2005-02-28 | 2008-04-23 | 日本烟草产业株式会社 | 具有Syk抑制活性的新型的氨基吡啶化合物 |
| WO2006093247A1 (fr) * | 2005-02-28 | 2006-09-08 | Japan Tobacco Inc. | NOUVEAU COMPOSÉ AMINOPYRIDINE AYANT UNE ACTIVITÉ D'INHIBITION DE LA Syk |
| 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 |
| WO2007117692A2 (fr) | 2006-04-11 | 2007-10-18 | Vertex Pharmaceuticals Incorporated | Thiazoles, imidazoles, et pyrazoles utiles en tant qu'inhibiteurs de protéines kinases |
| WO2008024634A1 (fr) * | 2006-08-25 | 2008-02-28 | Smithkline Beecham Corporation | Composés de pyrimidine utilisés en tant qu'inhibiteurs de kinase |
| BRPI0720264B1 (pt) | 2006-12-08 | 2022-03-03 | Novartis Ag | Compostos e composições como inibidores de proteína cinase |
| TW200840581A (en) | 2007-02-28 | 2008-10-16 | Astrazeneca Ab | Novel pyrimidine derivatives |
| EP2148874B1 (fr) | 2007-05-04 | 2012-02-08 | Irm Llc | Dérivés de pyrimidine et compositions utiles en tant qu'inhibiteurs des kinases c-kit et pdgfr |
| CA2693594A1 (fr) | 2007-07-17 | 2009-01-22 | Rigel Pharmaceuticals, Inc. | Pyrimidinediamines substituees par des amines cycliques utilisees en tant qu'inhibiteurs de la pkc |
| US8530480B2 (en) | 2007-09-04 | 2013-09-10 | The Scripps Research Institute | Substituted pyrimidinyl-amines as protein kinase inhibitors |
| US8309566B2 (en) | 2008-02-15 | 2012-11-13 | Rigel Pharmaceuticals, Inc. | Pyrimidine-2-amine compounds and their use as inhibitors of JAK kinases |
| WO2009122180A1 (fr) | 2008-04-02 | 2009-10-08 | Medical Research Council | Dérivés de pyrimidine capables d’inhiber une ou plusieurs kinases |
| EA024109B1 (ru) | 2008-04-16 | 2016-08-31 | Портола Фармасьютиклз, Инк. | Ингибиторы протеинкиназ |
| WO2011075517A1 (fr) | 2009-12-17 | 2011-06-23 | Merck Sharp & Dohme Corp. | Aminopyrimidines en tant qu'inhibiteurs de la syk |
| MX2012008083A (es) * | 2010-01-12 | 2012-08-15 | Ab Science | Inhibidores de triazol y oxazol quinaza. |
| 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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-
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- 2013-04-02 JP JP2013076543A patent/JP5829644B2/ja not_active Expired - Fee Related
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