MX2012012614A - Compuestos de 7-(1h-pirazol-4-il)-1, 6-naftiridina como inhibidores de syk. - Google Patents
Compuestos de 7-(1h-pirazol-4-il)-1, 6-naftiridina como inhibidores de syk.Info
- Publication number
- MX2012012614A MX2012012614A MX2012012614A MX2012012614A MX2012012614A MX 2012012614 A MX2012012614 A MX 2012012614A MX 2012012614 A MX2012012614 A MX 2012012614A MX 2012012614 A MX2012012614 A MX 2012012614A MX 2012012614 A MX2012012614 A MX 2012012614A
- Authority
- MX
- Mexico
- Prior art keywords
- pyrazol
- syk inhibitors
- cells
- naphthyridine compounds
- syk
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- VSSWBQMHXZBTCH-UHFFFAOYSA-N 7-(1h-pyrazol-4-yl)-1,6-naphthyridine Chemical class C1=NNC=C1C1=CC2=NC=CC=C2C=N1 VSSWBQMHXZBTCH-UHFFFAOYSA-N 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 102000000551 Syk Kinase Human genes 0.000 abstract 1
- 108010016672 Syk Kinase Proteins 0.000 abstract 1
- 230000004913 activation Effects 0.000 abstract 1
- 230000000172 allergic effect Effects 0.000 abstract 1
- 208000010668 atopic eczema Diseases 0.000 abstract 1
- 230000001363 autoimmune Effects 0.000 abstract 1
- 210000003719 b-lymphocyte Anatomy 0.000 abstract 1
- 210000003651 basophil Anatomy 0.000 abstract 1
- 206010072757 chronic spontaneous urticaria Diseases 0.000 abstract 1
- 208000024376 chronic urticaria Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 150000003278 haem Chemical class 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 230000028709 inflammatory response Effects 0.000 abstract 1
- 210000002540 macrophage Anatomy 0.000 abstract 1
- 230000036210 malignancy Effects 0.000 abstract 1
- 238000011275 oncology therapy Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000000451 tissue damage Effects 0.000 abstract 1
- 231100000827 tissue damage Toxicity 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P35/02—Antineoplastic agents specific for leukemia
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P37/02—Immunomodulators
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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
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- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Transplantation (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Ophthalmology & Optometry (AREA)
- Oncology (AREA)
- Otolaryngology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Un compuesto de fórmula (I) o una sal del mismo: que es un inhibidor de la tirosina cinasa de bazo (Syk) y, por tanto, potencialmente útil en el tratamiento de enfermedades resultantes de la activación inadecuada de mastocitos y/o basófilos, macrófagos y linfocitos B, y respuestas inflamatorias y daños tisulares relacionados, por ejemplo enfermedad inflamatoria y/o trastornos alérgicos y en la terapia del cáncer, específicamente neoplasias malignas hematológicas, urticaria espontánea crónica y afecciones autoinmunes. (Ver Formula).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1007203.1A GB201007203D0 (en) | 2010-04-29 | 2010-04-29 | Novel compounds |
PCT/EP2011/056600 WO2011134971A1 (en) | 2010-04-29 | 2011-04-27 | 7-(1h-pyrazol-4-yl)-1,6-naphthyridine compounds as syk inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2012012614A true MX2012012614A (es) | 2012-12-17 |
Family
ID=42289852
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2012012614A MX2012012614A (es) | 2010-04-29 | 2011-04-27 | Compuestos de 7-(1h-pirazol-4-il)-1, 6-naftiridina como inhibidores de syk. |
Country Status (17)
Country | Link |
---|---|
US (1) | US8633319B2 (es) |
EP (1) | EP2563789B1 (es) |
JP (1) | JP2013525405A (es) |
KR (1) | KR20130069653A (es) |
CN (1) | CN102947306A (es) |
AR (1) | AR081138A1 (es) |
BR (1) | BR112012027198A2 (es) |
CA (1) | CA2796954A1 (es) |
EA (1) | EA201290910A1 (es) |
ES (1) | ES2543426T3 (es) |
GB (1) | GB201007203D0 (es) |
MX (1) | MX2012012614A (es) |
SG (1) | SG184513A1 (es) |
TW (1) | TW201206925A (es) |
UY (1) | UY33359A (es) |
WO (1) | WO2011134971A1 (es) |
ZA (1) | ZA201207859B (es) |
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PH12012501311A1 (en) | 2009-12-23 | 2016-07-22 | Takeda Pharmaceuticals Co | Fused heteroaromatic pyrrolidinones as syk inhibitors |
WO2012167423A1 (en) | 2011-06-08 | 2012-12-13 | Hutchison Medipharma Limited | Substituted pyridopyrazines as novel syk inhibitors |
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 |
NZ708563A (en) | 2012-11-01 | 2019-02-22 | Infinity Pharmaceuticals Inc | Treatment of cancers using pi3 kinase isoform modulators |
WO2014081616A1 (en) * | 2012-11-21 | 2014-05-30 | Merck Sharp & Dohme Corp. | Preparation of precursors for leukotriene antagonists |
NZ629037A (en) | 2013-03-15 | 2017-04-28 | Infinity Pharmaceuticals Inc | Salts and solid forms of isoquinolinones and composition comprising and methods of using the same |
WO2014194254A1 (en) | 2013-05-30 | 2014-12-04 | Infinity Pharmaceuticals, Inc. | Treatment of cancers using pi3 kinase isoform modulators |
MX2016001427A (es) | 2013-07-31 | 2016-08-03 | Gilead Sciences Inc | Inhibidores de syk. |
EP3964507A1 (en) | 2013-10-04 | 2022-03-09 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
WO2015051241A1 (en) | 2013-10-04 | 2015-04-09 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
JP6434506B2 (ja) | 2013-10-21 | 2018-12-05 | ジェノスコ | 置換ピリミジン化合物およびsyk阻害剤としてのそれらの使用 |
US20160244452A1 (en) | 2013-10-21 | 2016-08-25 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
JP6701088B2 (ja) | 2014-03-19 | 2020-05-27 | インフィニティー ファーマシューティカルズ, インコーポレイテッド | Pi3k−ガンマ媒介障害の治療で使用するための複素環式化合物 |
WO2015160986A2 (en) | 2014-04-16 | 2015-10-22 | Infinity Pharmaceuticals, Inc. | Combination therapies |
WO2016054491A1 (en) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
EP3303348B1 (en) | 2015-05-28 | 2019-08-07 | Theravance Biopharma R&D IP, LLC | Naphthyridine compounds as jak kinase inhibitors |
WO2017214269A1 (en) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
BR112018077021A2 (pt) | 2016-06-24 | 2019-04-02 | Infinity Pharmaceuticals, Inc. | terapias de combinação |
AU2019373221B2 (en) | 2018-10-31 | 2022-05-26 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds having HPK1 inhibitory activity |
PE20211655A1 (es) | 2018-10-31 | 2021-08-24 | Gilead Sciences Inc | Compuestos de 6-azabencimidazol sustituidos como inhibidores de hpk1 |
CN113316453A (zh) * | 2019-01-03 | 2021-08-27 | 匹兹堡大学联邦系统高等教育 | 用于提高转录因子eb多肽水平的方法和材料 |
CA3129665A1 (en) | 2019-03-21 | 2020-09-24 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
US11453681B2 (en) | 2019-05-23 | 2022-09-27 | Gilead Sciences, Inc. | Substituted eneoxindoles and uses thereof |
JP2023500906A (ja) | 2019-11-08 | 2023-01-11 | インサーム(インスティテュ ナシオナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシェ メディカル) | キナーゼ阻害剤に対する獲得抵抗性を有するがんの処置方法 |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
CN115003798A (zh) * | 2020-06-17 | 2022-09-02 | 兰迪·莱曼·阿伦 | 用于检测分析物的方法和试剂盒 |
AR122928A1 (es) * | 2020-07-10 | 2022-10-19 | Goldfinch Bio Inc | 1,6-naftiridinas sustituidas inhibidoras de cdk5 |
WO2023102800A1 (en) * | 2021-12-09 | 2023-06-15 | Theravance Biopharma R&D Ip, Llc | Synthesis of 5, 7-dichloro-1, 6-naphthyridine |
KR20250007541A (ko) * | 2022-04-07 | 2025-01-14 | 유니퀘스트 피티와이 리미티드 | 비장 티로신 키나제 억제제 |
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-
2010
- 2010-04-29 GB GBGB1007203.1A patent/GB201007203D0/en not_active Ceased
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2011
- 2011-04-27 EP EP20110719781 patent/EP2563789B1/en active Active
- 2011-04-27 BR BR112012027198A patent/BR112012027198A2/pt not_active IP Right Cessation
- 2011-04-27 SG SG2012074845A patent/SG184513A1/en unknown
- 2011-04-27 JP JP2013506640A patent/JP2013525405A/ja active Pending
- 2011-04-27 AR ARP110101455A patent/AR081138A1/es unknown
- 2011-04-27 TW TW100114711A patent/TW201206925A/zh unknown
- 2011-04-27 US US13/642,338 patent/US8633319B2/en not_active Expired - Fee Related
- 2011-04-27 UY UY0001033359A patent/UY33359A/es not_active Application Discontinuation
- 2011-04-27 WO PCT/EP2011/056600 patent/WO2011134971A1/en active Application Filing
- 2011-04-27 EA EA201290910A patent/EA201290910A1/ru unknown
- 2011-04-27 CN CN2011800318413A patent/CN102947306A/zh active Pending
- 2011-04-27 CA CA2796954A patent/CA2796954A1/en not_active Abandoned
- 2011-04-27 MX MX2012012614A patent/MX2012012614A/es not_active Application Discontinuation
- 2011-04-27 ES ES11719781.4T patent/ES2543426T3/es active Active
- 2011-04-27 KR KR1020127031384A patent/KR20130069653A/ko not_active Application Discontinuation
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2012
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ZA201207859B (en) | 2014-03-26 |
WO2011134971A1 (en) | 2011-11-03 |
CN102947306A (zh) | 2013-02-27 |
TW201206925A (en) | 2012-02-16 |
EP2563789B1 (en) | 2015-05-20 |
JP2013525405A (ja) | 2013-06-20 |
ES2543426T3 (es) | 2015-08-19 |
GB201007203D0 (en) | 2010-06-16 |
CA2796954A1 (en) | 2011-11-03 |
AR081138A1 (es) | 2012-06-27 |
UY33359A (es) | 2011-12-01 |
KR20130069653A (ko) | 2013-06-26 |
US8633319B2 (en) | 2014-01-21 |
SG184513A1 (en) | 2012-11-29 |
BR112012027198A2 (pt) | 2016-07-19 |
EP2563789A1 (en) | 2013-03-06 |
US20130040984A1 (en) | 2013-02-14 |
EA201290910A1 (ru) | 2013-05-30 |
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