HK1206011A1 - Serine threonine kinase inhibitors - Google Patents
Serine threonine kinase inhibitorsInfo
- Publication number
- HK1206011A1 HK1206011A1 HK15106441.5A HK15106441A HK1206011A1 HK 1206011 A1 HK1206011 A1 HK 1206011A1 HK 15106441 A HK15106441 A HK 15106441A HK 1206011 A1 HK1206011 A1 HK 1206011A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- kinase inhibitors
- threonine kinase
- serine threonine
- serine
- inhibitors
- 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
- C07D401/14—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
-
- 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
- C07D401/02—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
-
- 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
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261605523P | 2012-03-01 | 2012-03-01 | |
PCT/US2013/028622 WO2013130976A1 (en) | 2012-03-01 | 2013-03-01 | Serine/threonine kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1206011A1 true HK1206011A1 (en) | 2015-12-31 |
Family
ID=47892024
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK15104843.4A HK1204323A1 (en) | 2012-03-01 | 2015-05-21 | Serine threonine kinase inhibitors |
HK15106441.5A HK1206011A1 (en) | 2012-03-01 | 2015-07-06 | Serine threonine kinase inhibitors |
HK18113513.1A HK1254429A1 (zh) | 2012-03-01 | 2018-10-22 | 絲氨酸/蘇氨酸激酶抑制劑 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK15104843.4A HK1204323A1 (en) | 2012-03-01 | 2015-05-21 | Serine threonine kinase inhibitors |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK18113513.1A HK1254429A1 (zh) | 2012-03-01 | 2018-10-22 | 絲氨酸/蘇氨酸激酶抑制劑 |
Country Status (36)
Country | Link |
---|---|
US (4) | US8697715B2 (xx) |
EP (2) | EP3321262B1 (xx) |
JP (2) | JP6068515B2 (xx) |
KR (1) | KR102093526B1 (xx) |
CN (2) | CN104507926B (xx) |
AR (2) | AR090220A1 (xx) |
AU (1) | AU2013225737B2 (xx) |
BR (1) | BR112014021634B1 (xx) |
CA (1) | CA2866086C (xx) |
CL (1) | CL2014002301A1 (xx) |
CO (1) | CO7081155A2 (xx) |
CR (1) | CR20140413A (xx) |
CY (1) | CY1120172T1 (xx) |
DK (2) | DK3321262T3 (xx) |
ES (2) | ES2857649T3 (xx) |
HK (3) | HK1204323A1 (xx) |
HR (2) | HRP20180591T1 (xx) |
HU (2) | HUE053994T2 (xx) |
IL (2) | IL234376A (xx) |
LT (2) | LT3321262T (xx) |
MX (1) | MX354675B (xx) |
MY (1) | MY191936A (xx) |
NO (1) | NO2945854T3 (xx) |
NZ (1) | NZ700314A (xx) |
PE (1) | PE20150666A1 (xx) |
PH (3) | PH12015501653A1 (xx) |
PL (2) | PL3321262T3 (xx) |
PT (2) | PT3321262T (xx) |
RS (2) | RS61500B1 (xx) |
RU (1) | RU2650501C2 (xx) |
SG (1) | SG11201405356QA (xx) |
SI (2) | SI2820009T1 (xx) |
TW (1) | TWI589569B (xx) |
UA (1) | UA116774C2 (xx) |
WO (1) | WO2013130976A1 (xx) |
ZA (2) | ZA201406688B (xx) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX339873B (es) | 2011-02-28 | 2016-06-15 | Genentech Inc | Inhibidores de serina/treonina cinasa. |
CN103958502B (zh) | 2011-08-04 | 2016-02-10 | 阵列生物制药公司 | 作为丝氨酸/苏氨酸激酶抑制剂的喹唑啉化合物 |
ES2857649T3 (es) * | 2012-03-01 | 2021-09-29 | Array Biopharma Inc | Inhibidores de serina/treonina cinasa |
MX363118B (es) * | 2012-05-03 | 2019-03-11 | Genentech Inc | Derivados de pirazol aminopirimidina como moduladores de cinasa 2 de repeticion rica en leucina (lrrk2). |
AR092253A1 (es) | 2012-08-27 | 2015-04-08 | Array Biopharma Inc | Inhibidores de serina/treonina cinasa |
AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
EP2909206A1 (en) | 2012-10-16 | 2015-08-26 | F. Hoffmann-La Roche AG | Serine/threonine kinase inhibitors |
WO2017156493A1 (en) | 2016-03-11 | 2017-09-14 | Denali Therapeutics Inc. | Compounds, compositions, and methods |
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 |
CU24425B1 (es) | 2013-11-01 | 2019-06-04 | Novartis Ag | Amino-heteroaril-benzamidas como inhibidores de cinasa |
KR102359759B1 (ko) * | 2013-12-06 | 2022-02-09 | 제넨테크, 인크. | 세린/트레오닌 키나제 저해제 |
JP6642942B2 (ja) * | 2013-12-30 | 2020-02-12 | アレイ バイオファーマ、インコーポレイテッド | セリン/トレオニンキナーゼ阻害剤 |
WO2015103133A1 (en) * | 2013-12-30 | 2015-07-09 | Genentech, Inc. | Serine/threonine kinase inhibitors |
CN110452216B (zh) | 2014-04-02 | 2022-08-26 | 英特穆恩公司 | 抗纤维化吡啶酮类 |
EP3129025B1 (en) * | 2014-04-09 | 2019-05-15 | Genentech, Inc. | Process for the manufacturing of medicaments |
US9879029B2 (en) | 2014-12-22 | 2018-01-30 | Eli Lilly And Company | ERK inhibitors |
TWI704151B (zh) * | 2014-12-22 | 2020-09-11 | 美商美國禮來大藥廠 | Erk抑制劑 |
AU2015396809B2 (en) * | 2015-06-03 | 2019-07-11 | Js Innopharm (Shanghai) Ltd. | Heterocyclic compounds for treating psoriasis |
WO2016192063A1 (en) * | 2015-06-03 | 2016-12-08 | Changzhou Jiekai Pharmatech Co. Ltd | Heterocyclic compounds as erk inhibitors |
IL291017B2 (en) | 2015-10-21 | 2023-11-01 | Otsuka Pharma 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 |
EA038028B1 (ru) | 2015-11-09 | 2021-06-24 | Астразенека Аб | Производные дигидроимидазопиразинона, применимые в лечении рака |
US11214565B2 (en) | 2015-11-20 | 2022-01-04 | Denali Therapeutics Inc. | Compound, compositions, and methods |
CN109072311A (zh) | 2016-04-15 | 2018-12-21 | 豪夫迈·罗氏有限公司 | 用于癌症的诊断和治疗方法 |
RS62868B1 (sr) | 2016-06-16 | 2022-02-28 | Denali Therapeutics Inc | Pirimidin-2-ilamino-1h-pirazoli kao inhibitori lrrk2 za upotrebu u lečenju neurodegenerativnih poremećaja |
GB201706327D0 (en) | 2017-04-20 | 2017-06-07 | Otsuka Pharma Co Ltd | A pharmaceutical compound |
WO2019037640A1 (en) * | 2017-08-22 | 2019-02-28 | Js Innopharm (Shanghai) Ltd | HETEROCYCLIC COMPOUNDS AS KINASE INHIBITORS, COMPOSITIONS COMPRISING THE HETEROCYCLIC COMPOUND, AND METHODS OF USING THE SAME |
AU2018329925A1 (en) | 2017-09-08 | 2020-03-05 | F. Hoffmann-La Roche Ag | Diagnostic and therapeutic methods for cancer |
EA202091293A1 (ru) | 2017-11-24 | 2020-11-23 | Новартис Аг | Производные пиридинона и их применение в качестве селективных ингибиторов alk-2 |
US11286248B2 (en) * | 2018-02-08 | 2022-03-29 | Zhangzhou Pien Tze Huang Pharmaceutical Co., Ltd. | Pyrazine-2(1H)-ketone compound acting as FGFR inhibitor |
WO2019158579A1 (en) | 2018-02-13 | 2019-08-22 | Vib Vzw | Targeting minimal residual disease in cancer with rxr antagonists |
WO2019223632A1 (en) * | 2018-05-22 | 2019-11-28 | Js Innomed Holdings Ltd. | Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof |
TW202102511A (zh) * | 2019-03-28 | 2021-01-16 | 大陸商江蘇恆瑞醫藥股份有限公司 | 噻吩并雜環類衍生物、其製備方法及其在醫藥上的應用 |
WO2020228817A1 (zh) * | 2019-05-15 | 2020-11-19 | 南京明德新药研发有限公司 | Erk抑制剂及其应用 |
CN114206883A (zh) | 2019-08-02 | 2022-03-18 | 伟迈可生物有限公司 | 氧代吡啶稠环衍生物及包含该衍生物的药物组合物 |
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 |
---|---|---|---|---|
US5612340A (en) | 1993-10-01 | 1997-03-18 | Ciba-Geigy Corporation | Pyrimidineamine derivatives and processes for the preparation thereof |
ATE325113T1 (de) * | 1993-10-01 | 2006-06-15 | Novartis Pharma Gmbh | Pharmacologisch wirksame pyrimidinderivate und verfahren zu deren herstellung |
US5543523A (en) | 1994-11-15 | 1996-08-06 | Regents Of The University Of Minnesota | Method and intermediates for the synthesis of korupensamines |
HUP0001140A3 (en) | 1996-12-05 | 2002-05-28 | Amgen Inc Thousand Oaks | Substituted pyrimidinone and pyridone compounds and methods of use |
US6602872B1 (en) * | 1999-12-13 | 2003-08-05 | Merck & Co., Inc. | Substituted pyridazines having cytokine inhibitory activity |
EP1261327B1 (en) | 2000-02-25 | 2005-04-27 | F.Hoffmann-La Roche Ag | Adenosine receptor modulators |
ATE284712T1 (de) | 2000-04-26 | 2005-01-15 | Eisai Co Ltd | Medizinische zusammensetzungen zur förderung der aktivierung der eingeweide |
WO2001083448A2 (de) | 2000-05-02 | 2001-11-08 | Tietze Lutz F | 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 (xx) * | 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 |
DE60330126D1 (de) * | 2002-02-14 | 2009-12-31 | Pharmacia Corp | Substituierte pyridinone als modulatoren für p38 map kinase |
CA2485166A1 (en) * | 2002-05-21 | 2003-12-04 | Amgen Inc. | Substituted pyrimidinone and pyridinone compounds |
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 |
CL2004002050A1 (es) * | 2003-08-13 | 2005-06-03 | Pharmacia Corp Sa Organizada B | Compuestos derivados de piridinonas sustituidas; su uso en el tratamiento de afecciones causadas o exacerbadas por actividad p38 map kinasa y/o tnf no regulada, tales como inflamaciones, tumores, sida y otros. |
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 |
CA2578122A1 (en) | 2004-08-27 | 2006-03-02 | 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 |
CA2606288A1 (en) | 2005-04-18 | 2006-10-26 | Neurogen Corporation | Subtituted heteroaryl cb1 antagonists |
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 |
ES2353437T3 (es) | 2006-02-16 | 2011-03-02 | Schering Corporation | Derivados de pirrolidina como inhibidores de erk. |
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 |
ES2373587T3 (es) | 2006-08-23 | 2012-02-06 | Pfizer Products Inc. | Compuestos de pirimidona como inhibidores de gsk-3. |
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 |
AU2007336933A1 (en) | 2006-12-22 | 2008-07-03 | Novartis Ag | Heteroaryl-heteroaryl compounds as CDK inhibitors for the treatment of cancer, inflammation and viral infections |
BRPI0806853B1 (pt) | 2007-02-01 | 2018-03-20 | Janssen Sciences Ireland Uc | Processos e intermediários para preparar um inibidor de protease macrocíclico de hcv |
US8273759B2 (en) | 2007-06-08 | 2012-09-25 | Bayer Cropscience Ag | Fungicide heterocyclyl-pyrimidinyl-amino derivatives |
CA2698511C (en) | 2007-09-04 | 2016-10-11 | The Scripps Research Institute | Substituted pyrimidinyl-amines as protein kinase inhibitors |
WO2009061761A2 (en) | 2007-11-06 | 2009-05-14 | E. I. Du Pont De Nemours And Company | Fungicidal heterocyclic amines |
NZ587504A (en) | 2008-02-21 | 2012-09-28 | Merck Sharp & Dohme | Benzopyrazole derivatives as ERK inhibitors |
US20090246198A1 (en) | 2008-03-31 | 2009-10-01 | Takeda Pharmaceutical Company Limited | Mapk/erk kinase inhibitors and methods of use thereof |
AU2009264242A1 (en) | 2008-06-27 | 2009-12-30 | Novartis Ag | Organic compounds |
KR20110025224A (ko) | 2008-06-27 | 2011-03-09 | 아빌라 테라퓨틱스, 인크. | 헤테로아릴 화합물 및 이의 용도 |
EP2370413B1 (en) * | 2008-12-08 | 2015-08-05 | Arena Pharmaceuticals, Inc. | Modulators of the prostacyclin (pgi2) receptor useful for the treatment of disorders related thereto |
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 |
WO2012020786A1 (ja) * | 2010-08-11 | 2012-02-16 | 日本新薬株式会社 | 医薬組成物 |
MX339873B (es) | 2011-02-28 | 2016-06-15 | Genentech Inc | Inhibidores de serina/treonina cinasa. |
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 |
CN103958502B (zh) | 2011-08-04 | 2016-02-10 | 阵列生物制药公司 | 作为丝氨酸/苏氨酸激酶抑制剂的喹唑啉化合物 |
ES2857649T3 (es) * | 2012-03-01 | 2021-09-29 | Array Biopharma Inc | Inhibidores de serina/treonina cinasa |
AR092253A1 (es) | 2012-08-27 | 2015-04-08 | Array Biopharma Inc | Inhibidores de serina/treonina cinasa |
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 |
JP6642942B2 (ja) * | 2013-12-30 | 2020-02-12 | アレイ バイオファーマ、インコーポレイテッド | セリン/トレオニンキナーゼ阻害剤 |
WO2015103133A1 (en) * | 2013-12-30 | 2015-07-09 | Genentech, Inc. | Serine/threonine kinase inhibitors |
EP3129025B1 (en) * | 2014-04-09 | 2019-05-15 | Genentech, Inc. | Process for the manufacturing of medicaments |
-
2013
- 2013-03-01 ES ES17207123T patent/ES2857649T3/es active Active
- 2013-03-01 LT LTEP17207123.5T patent/LT3321262T/lt unknown
- 2013-03-01 PL PL17207123T patent/PL3321262T3/pl unknown
- 2013-03-01 PE PE2014001344A patent/PE20150666A1/es active IP Right Grant
- 2013-03-01 DK DK17207123.5T patent/DK3321262T3/da active
- 2013-03-01 PT PT172071235T patent/PT3321262T/pt unknown
- 2013-03-01 MX MX2014010432A patent/MX354675B/es active IP Right Grant
- 2013-03-01 TW TW102107403A patent/TWI589569B/zh not_active IP Right Cessation
- 2013-03-01 NZ NZ700314A patent/NZ700314A/en unknown
- 2013-03-01 UA UAA201410688A patent/UA116774C2/uk unknown
- 2013-03-01 JP JP2014560091A patent/JP6068515B2/ja active Active
- 2013-03-01 PL PL13710222T patent/PL2820009T3/pl unknown
- 2013-03-01 CN CN201380022620.9A patent/CN104507926B/zh active Active
- 2013-03-01 KR KR1020147027516A patent/KR102093526B1/ko active IP Right Grant
- 2013-03-01 SI SI201331002T patent/SI2820009T1/en unknown
- 2013-03-01 PH PH12015501653A patent/PH12015501653A1/en unknown
- 2013-03-01 DK DK13710222.4T patent/DK2820009T3/en active
- 2013-03-01 CN CN201610625941.3A patent/CN106349217B/zh active Active
- 2013-03-01 SG SG11201405356QA patent/SG11201405356QA/en unknown
- 2013-03-01 LT LTEP13710222.4T patent/LT2820009T/lt unknown
- 2013-03-01 RS RS20210252A patent/RS61500B1/sr unknown
- 2013-03-01 BR BR112014021634-7A patent/BR112014021634B1/pt active IP Right Grant
- 2013-03-01 MY MYPI2014702447A patent/MY191936A/en unknown
- 2013-03-01 AU AU2013225737A patent/AU2013225737B2/en active Active
- 2013-03-01 PH PH12015501654A patent/PH12015501654A1/en unknown
- 2013-03-01 HU HUE17207123A patent/HUE053994T2/hu unknown
- 2013-03-01 EP EP17207123.5A patent/EP3321262B1/en active Active
- 2013-03-01 HU HUE13710222A patent/HUE037423T2/hu unknown
- 2013-03-01 RU RU2014139601A patent/RU2650501C2/ru active
- 2013-03-01 CA CA2866086A patent/CA2866086C/en active Active
- 2013-03-01 ES ES13710222.4T patent/ES2665073T3/es active Active
- 2013-03-01 AR ARP130100671A patent/AR090220A1/es active IP Right Grant
- 2013-03-01 RS RS20180399A patent/RS57097B1/sr unknown
- 2013-03-01 US US13/782,513 patent/US8697715B2/en active Active
- 2013-03-01 SI SI201331857T patent/SI3321262T1/sl unknown
- 2013-03-01 PT PT137102224T patent/PT2820009T/pt unknown
- 2013-03-01 EP EP13710222.4A patent/EP2820009B1/en active Active
- 2013-03-01 WO PCT/US2013/028622 patent/WO2013130976A1/en active Application Filing
- 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/PH12014501947A1/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
- 2015-09-11 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 |
---|---|---|
HK1254429A1 (zh) | 絲氨酸/蘇氨酸激酶抑制劑 | |
IL261282A (en) | Furinone compounds as kinase inhibitors | |
HK1210775A1 (en) | Imidazotriazinecarbonitriles useful as kinase inhibitors | |
HK1225735A1 (zh) | 絲氨酸/蘇氨酸激酶抑制劑 | |
HK1208442A1 (en) | Substituted pyrrolopyrimidinylamino-benzothiazolones as mknk kinase inhibitors mknk | |
HK1223877A1 (zh) | 絲氨酸/蘇氨酸激酶抑制劑 | |
HK1210174A1 (en) | Serine threonine kinase inhibitors for the treatment of hyperproliferativediseases | |
HK1200828A1 (en) | Kinase inhibitors | |
IL227399A0 (en) | Novel azaindolylphenyl sulfonamides as serine/threonine kinase inhibitors | |
EP2710007A4 (en) | Kinase Inhibitors | |
HK1211574A1 (en) | Serine threonine kinase inhibitors | |
HK1211578A1 (en) | Amidoimidazopyridazines as mknk-1 kinase inhibitors mknk-1 | |
GB201211310D0 (en) | CSF-1R kinase inhibitors | |
EP2702064A4 (en) | Kinase Inhibitors | |
ZA201604461B (en) | Serine/threonine kinase inhibitors | |
PL2634185T3 (pl) | Inhibitory kinazy TYK2 | |
HK1199873A1 (en) | Kinase inhibitors | |
HK1213252A1 (zh) | 雙環二氫吡啶酮激酶抑制劑 | |
SG11201500973WA (en) | Amino-quinolines as kinase inhibitors | |
HK1213181A1 (zh) | 雙環氧雜內酰胺激酶抑制劑 |