PE20150666A1 - Inhibidores de serina/treonina cinasa - Google Patents
Inhibidores de serina/treonina cinasaInfo
- Publication number
- PE20150666A1 PE20150666A1 PE2014001344A PE2014001344A PE20150666A1 PE 20150666 A1 PE20150666 A1 PE 20150666A1 PE 2014001344 A PE2014001344 A PE 2014001344A PE 2014001344 A PE2014001344 A PE 2014001344A PE 20150666 A1 PE20150666 A1 PE 20150666A1
- Authority
- PE
- Peru
- Prior art keywords
- serine
- kinase inhibitors
- threonine kinase
- compounds
- hyperproliferative
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
- A61K31/495—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- 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
- C07F9/65586—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 at least one of the hetero rings does not contain nitrogen as ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—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
- A61K31/495—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Abstract
La invencion describe compuestos de formula l: o estereoisomeros, tautomeros, profarmacos o sales farmaceuticamente aceptables de los mismos, en la que R1, R2, R3, R4, X1, X2, Y1 y Y2 se definen en la presente solicitud. Estos compuestos son activos como inhibidores de serina/treonina cinasa, por lo que son utiles en el tratamiento de enfermedades hiperproliferativas e inflamatorias.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261605523P | 2012-03-01 | 2012-03-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20150666A1 true PE20150666A1 (es) | 2015-05-06 |
Family
ID=47892024
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2014001344A PE20150666A1 (es) | 2012-03-01 | 2013-03-01 | Inhibidores de serina/treonina cinasa |
Country Status (36)
Country | Link |
---|---|
US (4) | US8697715B2 (es) |
EP (2) | EP2820009B1 (es) |
JP (2) | JP6068515B2 (es) |
KR (1) | KR102093526B1 (es) |
CN (2) | CN104507926B (es) |
AR (2) | AR090220A1 (es) |
AU (1) | AU2013225737B2 (es) |
BR (1) | BR112014021634B1 (es) |
CA (1) | CA2866086C (es) |
CL (1) | CL2014002301A1 (es) |
CO (1) | CO7081155A2 (es) |
CR (1) | CR20140413A (es) |
CY (1) | CY1120172T1 (es) |
DK (2) | DK2820009T3 (es) |
ES (2) | ES2857649T3 (es) |
HK (3) | HK1204323A1 (es) |
HR (2) | HRP20180591T1 (es) |
HU (2) | HUE053994T2 (es) |
IL (2) | IL234376A (es) |
LT (2) | LT2820009T (es) |
MX (1) | MX354675B (es) |
MY (1) | MY191936A (es) |
NO (1) | NO2945854T3 (es) |
NZ (1) | NZ700314A (es) |
PE (1) | PE20150666A1 (es) |
PH (3) | PH12014501947B1 (es) |
PL (2) | PL2820009T3 (es) |
PT (2) | PT2820009T (es) |
RS (2) | RS57097B1 (es) |
RU (1) | RU2650501C2 (es) |
SG (1) | SG11201405356QA (es) |
SI (2) | SI2820009T1 (es) |
TW (1) | TWI589569B (es) |
UA (1) | UA116774C2 (es) |
WO (1) | WO2013130976A1 (es) |
ZA (2) | ZA201406688B (es) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2543050T3 (es) | 2011-02-28 | 2015-08-14 | Array Biopharma, Inc. | Inhibidores de serina/treonina quinasa |
US9187462B2 (en) | 2011-08-04 | 2015-11-17 | Array Biopharma Inc. | Substituted quinazolines as serine/threonine kinase inhibitors |
KR102093526B1 (ko) * | 2012-03-01 | 2020-03-25 | 어레이 바이오파마 인크. | 세린/트레오닌 키나제 억제제 |
EP2844652B1 (en) * | 2012-05-03 | 2019-03-13 | Genentech, Inc. | Pyrazole aminopyrimidine derivatives as lrrk2 modulators |
WO2014036015A1 (en) | 2012-08-27 | 2014-03-06 | Array Biopharma Inc. | Serine/threonine kinase inhibitors for the treatment of hyperproliferative|diseases |
AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
MX2015004615A (es) | 2012-10-16 | 2015-07-17 | Hoffmann La Roche | Inhibidores de serina/treonina cinasa. |
US9532987B2 (en) | 2013-09-05 | 2017-01-03 | Genentech, Inc. | Use of a combination of a MEK inhibitor and an ERK inhibitor for treatment of hyperproliferative diseases |
DK3063143T3 (en) | 2013-11-01 | 2018-08-20 | Novartis Ag | Amino heteroaryl benzamides as kinase inhibitors |
MX368443B (es) * | 2013-12-06 | 2019-10-02 | Genentech Inc | Inhibidores de serina/treonina cinasa. |
CA2934709C (en) | 2013-12-30 | 2022-08-30 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
KR102379517B1 (ko) * | 2013-12-30 | 2022-03-25 | 제넨테크, 인크. | 세린/트레오닌 키나아제 억제제 |
MX2016012808A (es) | 2014-04-02 | 2017-01-05 | Intermune Inc | Piridinonas anti-fibroticas. |
MX2016013162A (es) * | 2014-04-09 | 2017-04-27 | Genentech Inc | Proceso para la fabricacion de medicamentos. |
TWI704151B (zh) * | 2014-12-22 | 2020-09-11 | 美商美國禮來大藥廠 | Erk抑制劑 |
ES2700200T3 (es) * | 2014-12-22 | 2019-02-14 | Lilly Co Eli | Inhibidores de ERK |
US10238657B2 (en) * | 2015-06-03 | 2019-03-26 | Js Innopharm (Shanhai) Ltd. | Heterocyclic compounds for treating psoriasis |
WO2016192063A1 (en) * | 2015-06-03 | 2016-12-08 | Changzhou Jiekai Pharmatech Co. Ltd | Heterocyclic compounds as erk inhibitors |
AU2016341520C1 (en) | 2015-10-21 | 2021-07-22 | Otsuka Pharmaceutical Co., Ltd. | Benzolactam compounds as protein kinase inhibitors |
WO2017070708A1 (en) * | 2015-10-23 | 2017-04-27 | Array Biopharma, Inc. | 2-aryl- and 2-heteroaryl-substituted 2-pyridazin-3(2h)-one compounds as inhibitors of fgfr tyrosine kinases |
RS60155B1 (sr) | 2015-11-09 | 2020-05-29 | Astrazeneca Ab | Derivati dihidroimidazopirazinona korisni za upotrebu u tretmanu raka |
US11214565B2 (en) | 2015-11-20 | 2022-01-04 | Denali Therapeutics Inc. | Compound, compositions, and methods |
US11028080B2 (en) | 2016-03-11 | 2021-06-08 | Denali Therapeutics Inc. | Substituted pyrimidines as LRKK2 inhibitors |
WO2017180581A1 (en) | 2016-04-15 | 2017-10-19 | Genentech, Inc. | Diagnostic and therapeutic methods for cancer |
EP3998261A1 (en) | 2016-06-16 | 2022-05-18 | Denali Therapeutics Inc. | Pyrimidin-2-ylamino-1h-pyrazols as lrrk2 inhibitors for use in the treatment of neurodegenerative disorders |
GB201706327D0 (en) | 2017-04-20 | 2017-06-07 | Otsuka Pharma Co Ltd | A pharmaceutical compound |
EP3672973A4 (en) * | 2017-08-22 | 2021-05-26 | JS Innopharm (Shanghai) Ltd. | HETEROCYCLIC COMPOUNDS USED AS KINASE INHIBITORS, COMPOSITIONS INCLUDING THE HETEROCYCLIC COMPOUND, AND METHODS OF USE THEREOF |
EP3679159A1 (en) | 2017-09-08 | 2020-07-15 | H. Hoffnabb-La Roche Ag | Diagnostic and therapeutic methods for cancer |
EP3713927B1 (en) | 2017-11-24 | 2021-12-15 | Novartis AG | Pyridinone derivatives and their use as selective alk-2 inhibitors |
CN111683928B (zh) * | 2018-02-08 | 2021-12-10 | 漳州片仔癀药业股份有限公司 | 作为fgfr抑制剂的吡嗪-2(1h)-酮类化合物 |
EP3752200A1 (en) | 2018-02-13 | 2020-12-23 | Vib Vzw | Targeting minimal residual disease in cancer with rxr antagonists |
SG11202011513RA (en) * | 2018-05-22 | 2020-12-30 | Js Innomed Holdings Ltd | Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof |
US20220213119A1 (en) * | 2019-03-28 | 2022-07-07 | Jiangsu Hengrui Medicine Ca, Lid. | Thienoheterocyclic derivative, preparation method therefor and medical use thereof |
CN113784970B (zh) * | 2019-05-15 | 2022-11-29 | 南京明德新药研发有限公司 | Erk抑制剂及其应用 |
WO2021025407A1 (ko) | 2019-08-02 | 2021-02-11 | 웰마커바이오 주식회사 | 옥소-피리딘 융합고리 유도체 및 이를 포함하는 약학적 조성물 |
WO2022100586A1 (zh) * | 2020-11-11 | 2022-05-19 | 南京明德新药研发有限公司 | 一种含氧杂环丁烷的螺环类化合物的晶型、制备方法及其应用 |
CN115413669B (zh) * | 2022-06-14 | 2024-03-15 | 湖南大学 | 激酶抑制剂及其组合剂在提高植物青枯病抗性中的应用 |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0672035A1 (en) | 1993-10-01 | 1995-09-20 | Novartis AG | Pyrimidineamine derivatives and processes for the preparation thereof |
WO1995009851A1 (en) | 1993-10-01 | 1995-04-13 | Ciba-Geigy Ag | Pharmacologically active pyrimidineamine derivatives and processes for the preparation thereof |
US5543523A (en) | 1994-11-15 | 1996-08-06 | Regents Of The University Of Minnesota | Method and intermediates for the synthesis of korupensamines |
WO1998024780A2 (en) | 1996-12-05 | 1998-06-11 | Amgen Inc. | Substituted pyrimidinone and pyridinone compounds and their use |
US6602872B1 (en) * | 1999-12-13 | 2003-08-05 | Merck & Co., Inc. | Substituted pyridazines having cytokine inhibitory activity |
PL203805B1 (pl) | 2000-02-25 | 2009-11-30 | Hoffmann La Roche | Zastosowanie cyklicznych związków heteroaromatycznych, lek i cykliczne związki heteroaromatyczne |
KR20070058022A (ko) | 2000-04-26 | 2007-06-07 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 배변을 촉진하는 의약 조성물 |
EP1280771B1 (de) | 2000-05-02 | 2004-10-13 | Tietze, Lutz F., Prof. Dr. | Neue prodrugs von 6-hydroxy-2,3-dihydro-1h-indolen, 5-hydroxy-1,2-dihydro-3h-pyrrolo 3,2-e]indolen und 5-hydroxy-1,2-dihydro-3h-benzo e]indolen sowie von 6-hydroxy-1,2,3,4-tetrahydro-benzo f]chinolin-derivaten für eine selektive krebstherapie |
WO2002088079A2 (en) | 2001-05-01 | 2002-11-07 | Bristol-Myers Squibb Company | Dual inhibitors of pde 7 and pde 4 |
WO2003030909A1 (en) | 2001-09-25 | 2003-04-17 | Bayer Pharmaceuticals Corporation | 2- and 4-aminopyrimidines n-substtituded by a bicyclic ring for use as kinase inhibitors in the treatment of cancer |
TWI330183B (es) * | 2001-10-22 | 2010-09-11 | Eisai R&D Man Co Ltd | |
WO2003057689A1 (en) * | 2002-01-02 | 2003-07-17 | Fujisawa Pharmaceutical Co., Ltd. | Aminopyrimidine compounds, processes for their preparation and pharmaceutical compositions containing them |
CN100486576C (zh) * | 2002-02-14 | 2009-05-13 | 法玛西雅公司 | 作为p38map激酶调节剂的取代吡啶酮类 |
WO2003099808A1 (en) | 2002-05-21 | 2003-12-04 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
GB0215676D0 (en) * | 2002-07-05 | 2002-08-14 | Novartis Ag | Organic compounds |
DE60330485D1 (de) | 2002-07-15 | 2010-01-21 | Merck & Co Inc | Zur behandlung von diabetes |
US20050014753A1 (en) | 2003-04-04 | 2005-01-20 | Irm Llc | Novel compounds and compositions as protein kinase inhibitors |
NL1026826C2 (nl) * | 2003-08-13 | 2007-01-04 | Pharmacia Corp | Gesubstitueerde pyridinonen. |
TW200533357A (en) | 2004-01-08 | 2005-10-16 | Millennium Pharm Inc | 2-(amino-substituted)-4-aryl pyrimidines and related compounds useful for treating inflammatory diseases |
ATE485824T1 (de) | 2004-04-13 | 2010-11-15 | Icagen Inc | Polycyclische pyrimidine als kaliumionenkanal- modulatoren |
US7429604B2 (en) * | 2004-06-15 | 2008-09-30 | Bristol Myers Squibb Company | Six-membered heterocycles useful as serine protease inhibitors |
EP1786781A2 (en) | 2004-08-27 | 2007-05-23 | GPC Biotech AG | Pyrimidine derivatives |
GB0420722D0 (en) * | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
GB0428514D0 (en) | 2004-12-31 | 2005-02-09 | Prosidion Ltd | Compounds |
AR053712A1 (es) | 2005-04-18 | 2007-05-16 | Neurogen Corp | Heteroarilos sustituidos, antagonistas de cb1 (receptor 1 canabinoide) |
GT200600381A (es) | 2005-08-25 | 2007-03-28 | Compuestos organicos | |
US7572809B2 (en) | 2005-12-19 | 2009-08-11 | Hoffmann-La Roche Inc. | Isoquinoline aminopyrazole derivatives |
ATE485268T1 (de) | 2006-02-16 | 2010-11-15 | Schering Corp | Pyrrolidin-derivate als erk-hemmer |
US7998978B2 (en) | 2006-05-01 | 2011-08-16 | Pfizer Inc. | Substituted 2-amino-fused heterocyclic compounds |
DE102006035202A1 (de) | 2006-07-29 | 2008-01-31 | Lanxess Deutschland Gmbh | Konservierungsmittel auf Basis von Carbonsäureanhydriden |
CA2661334C (en) | 2006-08-23 | 2011-11-29 | Pfizer Products Inc. | Pyrimidone compounds as gsk-3 inhibitors |
WO2008039882A1 (en) | 2006-09-30 | 2008-04-03 | Sanofi-Aventis U.S. Llc | A combination of niacin and a prostaglandin d2 receptor antagonist |
JO2985B1 (ar) | 2006-12-20 | 2016-09-05 | Takeda Pharmaceuticals Co | مثبطات كينازmapk/erk |
JP2010514689A (ja) | 2006-12-22 | 2010-05-06 | ノバルティス アーゲー | 癌、炎症およびウイルス感染症の処置のためのcdk阻害剤としてのヘテロアリール−ヘテロアリール化合物 |
MX2009008271A (es) | 2007-02-01 | 2009-08-12 | Tibotec Pharm Ltd | Procesos e intermediarios para la preparacion de un inhibidor de proteasa macrocilico del vhc. |
KR20100020454A (ko) | 2007-06-08 | 2010-02-22 | 바이엘 크롭사이언스 소시에떼아노님 | 살진균제 헤테로사이클릴-피리미디닐-아미노 유도체 |
US8530480B2 (en) | 2007-09-04 | 2013-09-10 | The Scripps Research Institute | Substituted pyrimidinyl-amines as protein kinase inhibitors |
KR20100088150A (ko) | 2007-11-06 | 2010-08-06 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 살진균성 복소환식 아민 |
JP5276676B2 (ja) | 2008-02-21 | 2013-08-28 | メルク・シャープ・アンド・ドーム・コーポレーション | Erk阻害剤である化合物 |
WO2009146034A2 (en) | 2008-03-31 | 2009-12-03 | Takeda Pharmaceutical Company Limited | Mapk/erk kinase inhibitors and methods of use thereof |
KR20110025224A (ko) | 2008-06-27 | 2011-03-09 | 아빌라 테라퓨틱스, 인크. | 헤테로아릴 화합물 및 이의 용도 |
PE20110136A1 (es) | 2008-06-27 | 2011-03-17 | Novartis Ag | Compuestos organicos |
PT2370413E (pt) * | 2008-12-08 | 2015-10-23 | Arena Pharm Inc | Moduladores do recetor da prostaciclina (pgi2) úteis para o tratamento de distúrbios relacionados com o mesmo |
DE102009051799B4 (de) | 2009-11-03 | 2021-07-01 | Georg-August-Universität Göttingen Stiftung Öffentlichen Rechts | Bifunktionale Prodrugs und Drugs |
DE102009060175A1 (de) | 2009-12-23 | 2011-06-30 | Merck Patent GmbH, 64293 | Pyrrolo[2,3-d] pyrazin-7-yl-pyrimidin-Verbindungen |
JPWO2012020786A1 (ja) * | 2010-08-11 | 2013-10-28 | 日本新薬株式会社 | 医薬組成物 |
ES2543050T3 (es) | 2011-02-28 | 2015-08-14 | Array Biopharma, Inc. | Inhibidores de serina/treonina quinasa |
CN102250065B (zh) * | 2011-05-20 | 2015-05-13 | 浙江海正药业股份有限公司 | 取代的三嗪苯脲衍生物及其用途 |
US9187462B2 (en) | 2011-08-04 | 2015-11-17 | Array Biopharma Inc. | Substituted quinazolines as serine/threonine kinase inhibitors |
KR102093526B1 (ko) * | 2012-03-01 | 2020-03-25 | 어레이 바이오파마 인크. | 세린/트레오닌 키나제 억제제 |
WO2014036015A1 (en) | 2012-08-27 | 2014-03-06 | Array Biopharma Inc. | Serine/threonine kinase inhibitors for the treatment of hyperproliferative|diseases |
KR102244553B1 (ko) | 2013-08-23 | 2021-04-23 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 용량 소자 및 반도체 장치 |
US9532987B2 (en) * | 2013-09-05 | 2017-01-03 | Genentech, Inc. | Use of a combination of a MEK inhibitor and an ERK inhibitor for treatment of hyperproliferative diseases |
KR102379517B1 (ko) * | 2013-12-30 | 2022-03-25 | 제넨테크, 인크. | 세린/트레오닌 키나아제 억제제 |
CA2934709C (en) * | 2013-12-30 | 2022-08-30 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
MX2016013162A (es) * | 2014-04-09 | 2017-04-27 | Genentech Inc | Proceso para la fabricacion de medicamentos. |
-
2013
- 2013-03-01 KR KR1020147027516A patent/KR102093526B1/ko active IP Right Grant
- 2013-03-01 BR BR112014021634-7A patent/BR112014021634B1/pt active IP Right Grant
- 2013-03-01 ES ES17207123T patent/ES2857649T3/es active Active
- 2013-03-01 AR ARP130100671A patent/AR090220A1/es active IP Right Grant
- 2013-03-01 PT PT137102224T patent/PT2820009T/pt unknown
- 2013-03-01 HU HUE17207123A patent/HUE053994T2/hu unknown
- 2013-03-01 EP EP13710222.4A patent/EP2820009B1/en active Active
- 2013-03-01 CN CN201380022620.9A patent/CN104507926B/zh active Active
- 2013-03-01 ES ES13710222.4T patent/ES2665073T3/es active Active
- 2013-03-01 PL PL13710222T patent/PL2820009T3/pl unknown
- 2013-03-01 PE PE2014001344A patent/PE20150666A1/es active IP Right Grant
- 2013-03-01 TW TW102107403A patent/TWI589569B/zh active
- 2013-03-01 LT LTEP13710222.4T patent/LT2820009T/lt unknown
- 2013-03-01 SG SG11201405356QA patent/SG11201405356QA/en unknown
- 2013-03-01 CN CN201610625941.3A patent/CN106349217B/zh active Active
- 2013-03-01 SI SI201331002T patent/SI2820009T1/en unknown
- 2013-03-01 MY MYPI2014702447A patent/MY191936A/en unknown
- 2013-03-01 PT PT172071235T patent/PT3321262T/pt unknown
- 2013-03-01 JP JP2014560091A patent/JP6068515B2/ja active Active
- 2013-03-01 US US13/782,513 patent/US8697715B2/en active Active
- 2013-03-01 PL PL17207123T patent/PL3321262T3/pl unknown
- 2013-03-01 WO PCT/US2013/028622 patent/WO2013130976A1/en active Application Filing
- 2013-03-01 AU AU2013225737A patent/AU2013225737B2/en active Active
- 2013-03-01 EP EP17207123.5A patent/EP3321262B1/en active Active
- 2013-03-01 DK DK13710222.4T patent/DK2820009T3/en active
- 2013-03-01 RS RS20180399A patent/RS57097B1/sr unknown
- 2013-03-01 UA UAA201410688A patent/UA116774C2/uk unknown
- 2013-03-01 DK DK17207123.5T patent/DK3321262T3/da active
- 2013-03-01 MX MX2014010432A patent/MX354675B/es active IP Right Grant
- 2013-03-01 LT LTEP17207123.5T patent/LT3321262T/lt unknown
- 2013-03-01 HU HUE13710222A patent/HUE037423T2/hu unknown
- 2013-03-01 RU RU2014139601A patent/RU2650501C2/ru active
- 2013-03-01 SI SI201331857T patent/SI3321262T1/sl unknown
- 2013-03-01 CA CA2866086A patent/CA2866086C/en active Active
- 2013-03-01 RS RS20210252A patent/RS61500B1/sr unknown
- 2013-03-01 NZ NZ700314A patent/NZ700314A/en unknown
- 2013-12-23 NO NO13811985A patent/NO2945854T3/no unknown
-
2014
- 2014-02-14 US US14/181,418 patent/US9259470B2/en active Active
- 2014-08-29 CL CL2014002301A patent/CL2014002301A1/es unknown
- 2014-08-29 PH PH12014501947A patent/PH12014501947B1/en unknown
- 2014-08-31 IL IL234376A patent/IL234376A/en active IP Right Grant
- 2014-09-08 CR CR20140413A patent/CR20140413A/es unknown
- 2014-09-11 ZA ZA2014/06688A patent/ZA201406688B/en unknown
- 2014-09-18 CO CO14207777A patent/CO7081155A2/es unknown
-
2015
- 2015-05-21 HK HK15104843.4A patent/HK1204323A1/xx unknown
- 2015-07-06 HK HK15106441.5A patent/HK1206011A1/xx unknown
- 2015-07-24 PH PH12015501653A patent/PH12015501653B1/en unknown
- 2015-07-24 PH PH12015501654A patent/PH12015501654B1/en unknown
- 2015-09-11 JP JP2015179810A patent/JP2016027053A/ja not_active Withdrawn
- 2015-12-03 ZA ZA2015/08847A patent/ZA201508847B/en unknown
-
2016
- 2016-01-12 US US14/993,985 patent/US9708290B2/en active Active
- 2016-02-24 IL IL244276A patent/IL244276B/en active IP Right Grant
-
2017
- 2017-06-16 US US15/625,297 patent/US10519126B2/en active Active
-
2018
- 2018-04-13 HR HRP20180591TT patent/HRP20180591T1/hr unknown
- 2018-04-18 CY CY20181100417T patent/CY1120172T1/el unknown
- 2018-10-22 HK HK18113513.1A patent/HK1254429A1/zh unknown
-
2021
- 2021-03-24 HR HRP20210482TT patent/HRP20210482T1/hr unknown
- 2021-04-19 AR ARP210101043A patent/AR121879A2/es unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20150666A1 (es) | Inhibidores de serina/treonina cinasa | |
UY39630A (es) | Inhibidores de bromodominios | |
ECSP18083519A (es) | Inhibidores de bromodominios | |
UY35898A (es) | ?compuestos inhibidores de syk y composiciones que los comprenden?. | |
CL2017002483A1 (es) | Compuestos heterocíclicos como inhibidores de lsd1 | |
CR20150474A (es) | Inhibidores de bromodominios tetracíclicos | |
PE20150669A1 (es) | Derivados de benzamida para la inhibicion de la actividad de abl1, abl2 y bcr-abl1 | |
UY34451A (es) | Derivados de uracilo como inhibidores de la quinasa axl y c-met | |
CR20160035A (es) | Inhibidores de bromodominios | |
CO7180199A2 (es) | Imidazotriazincarbonitrilos útiles como inhibidores de cinasa | |
DOP2014000062A (es) | Benzilindazoles sustituidos para uso como inhibidores de la quinasa bub1 en el tratamiento de enfermedades hiperproliferativas | |
ECSP12012083A (es) | Pirrolidina-2-carboxamidas sustituidas | |
CU24397B1 (es) | Derivados de piperidinil-indol como inhibidores del factor de complemento b | |
UY34960A (es) | Dihidropiridona p1 como inhibidores del factor xia | |
UY36170A (es) | Compuestos de dihidroisoquinolinona sustituida | |
CR20140468A (es) | Inhibidores de diacilglicerol aciltransferasa 2 | |
IN2015DN00185A (es) | ||
IN2015DN00598A (es) | ||
UY33557A (es) | Inhibidores de oxadiazol de la produccion de leucotrieno | |
CR20130024A (es) | Compuestos heterocíclicos fusionados | |
MX368178B (es) | Compuestos de ácido dimetilbenzoico. | |
UY33549A (es) | Quinolil aminas como agentes inhibidores de las quinasas | |
CO2019001181A2 (es) | Compuestos de heteroarilcarboxamida como inhibidores de ripk2 | |
GB201209587D0 (en) | Therapeutic compounds | |
CU24608B1 (es) | Compuestos de dihidrooxadiazinonas sustituidas útiles en el tratamiento de enfermedades hiperproliferativas y métodos para preparar dichos compuestos |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant, registration |