HK1125924A1 - Thieno-pyridine derivatives as mek inhibitors mek - - Google Patents
Thieno-pyridine derivatives as mek inhibitors mek -Info
- Publication number
- HK1125924A1 HK1125924A1 HK09103590.9A HK09103590A HK1125924A1 HK 1125924 A1 HK1125924 A1 HK 1125924A1 HK 09103590 A HK09103590 A HK 09103590A HK 1125924 A1 HK1125924 A1 HK 1125924A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- mek
- thieno
- pyridine derivatives
- inhibitors
- mek inhibitors
- Prior art date
Links
Classifications
-
- 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
- A61K31/4365—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 having sulfur as a ring hetero atom, e.g. ticlopidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- 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
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Transplantation (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0601962.4A GB0601962D0 (en) | 2006-01-31 | 2006-01-31 | Therapeutic agents |
PCT/GB2007/000310 WO2007088345A1 (en) | 2006-01-31 | 2007-01-30 | Thieno-pyridine derivatives as mek inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1125924A1 true HK1125924A1 (en) | 2009-08-21 |
Family
ID=36100789
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK09103590.9A HK1125924A1 (en) | 2006-01-31 | 2009-04-20 | Thieno-pyridine derivatives as mek inhibitors mek - |
Country Status (27)
Country | Link |
---|---|
US (3) | US8283359B2 (xx) |
EP (1) | EP1981892B1 (xx) |
JP (1) | JP5249787B2 (xx) |
KR (1) | KR101446919B1 (xx) |
CN (1) | CN101379067B (xx) |
AU (1) | AU2007211377B2 (xx) |
BR (1) | BRPI0708016B1 (xx) |
CA (1) | CA2640594C (xx) |
CY (1) | CY1115404T1 (xx) |
DK (1) | DK1981892T3 (xx) |
EA (1) | EA016128B1 (xx) |
EC (1) | ECSP088704A (xx) |
ES (1) | ES2471970T3 (xx) |
GB (1) | GB0601962D0 (xx) |
HK (1) | HK1125924A1 (xx) |
HR (1) | HRP20140503T1 (xx) |
IL (1) | IL192603A (xx) |
MY (1) | MY146387A (xx) |
NO (1) | NO341064B1 (xx) |
NZ (1) | NZ569638A (xx) |
PL (1) | PL1981892T3 (xx) |
PT (1) | PT1981892E (xx) |
RS (1) | RS53342B (xx) |
SI (1) | SI1981892T1 (xx) |
UA (1) | UA95939C2 (xx) |
WO (1) | WO2007088345A1 (xx) |
ZA (1) | ZA200807447B (xx) |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0601962D0 (en) | 2006-01-31 | 2006-03-15 | Ucb Sa | Therapeutic agents |
GB0616214D0 (en) * | 2006-08-15 | 2006-09-27 | Ucb Sa | Therapeutic Agents |
GB0714384D0 (en) | 2007-07-23 | 2007-09-05 | Ucb Pharma Sa | theraputic agents |
WO2009082687A1 (en) * | 2007-12-21 | 2009-07-02 | Genentech, Inc. | Azaindolizines and methods of use |
EP2240494B1 (en) | 2008-01-21 | 2016-03-30 | UCB Biopharma SPRL | Thieno-pyridine derivatives as mek inhibitors |
GB0811304D0 (en) * | 2008-06-19 | 2008-07-30 | Ucb Pharma Sa | Therapeutic agents |
JP5503930B2 (ja) * | 2009-09-18 | 2014-05-28 | 住友化学株式会社 | 3−アミノ−1−tert−ブトキシカルボニルピペリジンの精製方法およびそのクエン酸塩 |
CA2806734A1 (en) | 2010-07-26 | 2012-02-09 | Biomatrica, Inc. | Compositions for stabilizing dna, rna and proteins in saliva and other biological samples during shipping and storage at ambient temperatures |
JP5933544B2 (ja) | 2010-07-26 | 2016-06-08 | バイオマトリカ, インコーポレーテッド | 外界温度で出荷および貯蔵中の血中dna、rnaおよびタンパク質ならびに他の生体試料を安定化させるための組成物 |
EP2934572A4 (en) | 2012-12-20 | 2016-11-23 | Biomatrica Inc | FORMULATIONS AND METHODS FOR STABILIZING PCR REAGENTS |
US10011874B2 (en) | 2013-02-25 | 2018-07-03 | Novartis Ag | Androgen receptor mutation |
EA201690089A1 (ru) | 2013-06-11 | 2017-04-28 | Латвийский Институт Органического Синтеза | ТИЕНО[2,3-b]ПИРИДИНЫ КАК МОДУЛЯТОРЫ СОСТОЯНИЯ МНОЖЕСТВЕННОЙ ЛЕКАРСТВЕННОЙ УСТОЙЧИВОСТИ |
JP6604942B2 (ja) | 2013-06-13 | 2019-11-13 | バイオマトリカ,インク. | 細胞安定化 |
CN106572650B (zh) | 2014-06-10 | 2021-08-31 | 生物马特里卡公司 | 在环境温度下稳定凝血细胞 |
CN105384754B (zh) * | 2014-09-02 | 2018-04-20 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的杂环类化合物及其制备方法和用途 |
WO2017033113A1 (en) | 2015-08-21 | 2017-03-02 | Acerta Pharma B.V. | Therapeutic combinations of a mek inhibitor and a btk inhibitor |
KR20230145258A (ko) | 2015-12-08 | 2023-10-17 | 바이오매트리카 인코포레이티드 | 적혈구 침강 속도의 감소 |
MX2019013561A (es) | 2017-05-19 | 2022-02-09 | Nflection Therapeutics Inc | Compuestos de pirrolopiridina-anilina para el tratamiento de trastornos dermicos. |
CA3063535A1 (en) * | 2017-05-19 | 2018-11-22 | Nflection Therapeutics, Inc. | Fused heteroaromatic-aniline compounds for treatment of dermal disorders |
CN109836434B (zh) * | 2017-11-27 | 2020-09-25 | 上海宇耀生物科技有限公司 | 噻吩并环类化合物及其合成方法和应用 |
WO2020106303A1 (en) * | 2018-11-20 | 2020-05-28 | Nflection Therapeutics, Inc. | Aryl-aniline and heteroaryl-aniline compounds for treatment of skin cancers |
CA3120371A1 (en) | 2018-11-20 | 2020-05-28 | Nflection Therapeutics, Inc. | Cyanoaryl-aniline compounds for treatment of dermal disorders |
CN114364798A (zh) | 2019-03-21 | 2022-04-15 | 欧恩科斯欧公司 | 用于治疗癌症的Dbait分子与激酶抑制剂的组合 |
KR20220098759A (ko) | 2019-11-08 | 2022-07-12 | 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) | 키나제 억제제에 대해 내성을 획득한 암의 치료 방법 |
CN111138449B (zh) * | 2020-01-15 | 2022-11-29 | 四川大学华西医院 | 双靶向erk1和erk5抑制剂的制备及其抗肿瘤应用 |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
GB202205203D0 (en) | 2022-04-08 | 2022-05-25 | UCB Biopharma SRL | Combination with inhibitor |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ501277A (en) | 1997-07-01 | 2002-12-20 | Warner Lambert Co | -2(4-bromo or 4-iodo phenylamino) benzoic acid derivatives and their use as MEK inhibitors |
US6232320B1 (en) | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
CA2349180A1 (en) | 1999-01-13 | 2000-07-20 | Stephen Douglas Barrett | Anthranilic acid derivatives |
ID30439A (id) | 1999-01-13 | 2001-12-06 | Warner Lambert Co | Benzoheterosiklus dan penggunaannya sebagai penghambat mek |
ES2461854T3 (es) | 2000-07-19 | 2014-05-21 | Warner-Lambert Company Llc | Ésteres oxigenados de ácidos 4-yodofenilamino-benzhidroxámicos |
US7235537B2 (en) | 2002-03-13 | 2007-06-26 | Array Biopharma, Inc. | N3 alkylated benzimidazole derivatives as MEK inhibitors |
TWI338685B (en) | 2002-03-13 | 2011-03-11 | Array Biopharma Inc | N3 alkylated benzimid azole derivatives as mek inhibitors |
RU2300528C2 (ru) | 2002-03-13 | 2007-06-10 | Эррэй Биофарма, Инк. | N3-алкилированные бензимидазольные производные в качестве ингибиторов мек |
US20030225273A1 (en) * | 2002-03-21 | 2003-12-04 | Michaelides Michael R. | Thiopyrimidine and isothiazolopyrimidine kinase inhibitors |
GB0214268D0 (en) * | 2002-06-20 | 2002-07-31 | Celltech R&D Ltd | Chemical compounds |
CL2003002287A1 (es) * | 2002-11-25 | 2005-01-14 | Wyeth Corp | COMPUESTOS DERIVADOS DE TIENO[3,2-b]-PIRIDINA-6-CARBONITRILOS Y TIENEO[2,3-b]-PIRIDINA-5-CARBONITRILOS, COMPOSICION FARMACEUTICA, PROCEDIMIENTO DE PREPARACION Y COMPUESTOS INTERMEDIARIOS, Y SU USO EN EL TRATAMIENTO DEL CANCER, APOPLEJIA, OSTEOPOROSIS |
WO2004054505A2 (en) * | 2002-12-12 | 2004-07-01 | Pharmacia Corporation | Method of using aminocyanopyridine compounds as mitogen activated protein kinase-activated protein kinase-2 inhibitors |
WO2004113348A1 (en) * | 2003-06-20 | 2004-12-29 | Celltech R & D Limited | Thienopyridone derivatives as kinase inhibitors |
MXPA05013227A (es) | 2003-06-20 | 2006-03-09 | Celltech R&D Ltd | Derivados de tienopiridona como inhibidores de cinasa. |
US20050049276A1 (en) * | 2003-07-23 | 2005-03-03 | Warner-Lambert Company, Llc | Imidazopyridines and triazolopyridines |
ES2331246T3 (es) | 2003-07-24 | 2009-12-28 | Warner-Lambert Company Llc | Derivados de benzamidazol como inhibidores del mek. |
US7144907B2 (en) | 2003-09-03 | 2006-12-05 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
EP1670804A2 (en) * | 2003-09-10 | 2006-06-21 | GPC Biotech AG | Heterobicyclic compounds as pharmaceutically active agents |
WO2005051300A2 (en) | 2003-11-19 | 2005-06-09 | Array Biopharma Inc. | Bicyclic inhibitors of mek and methods of use thereof |
US7217723B2 (en) * | 2004-02-02 | 2007-05-15 | Eisai Co., Ltd. | Heterocyclic compound having oxime group |
CN101305010A (zh) * | 2005-09-01 | 2008-11-12 | 阿雷生物药品公司 | Raf抑制剂化合物及其用法 |
WO2007044515A1 (en) | 2005-10-07 | 2007-04-19 | Exelixis, Inc. | Azetidines as mek inhibitors for the treatment of proliferative diseases |
GB0601962D0 (en) | 2006-01-31 | 2006-03-15 | Ucb Sa | Therapeutic agents |
TW200808769A (en) | 2006-04-18 | 2008-02-16 | Astrazeneca Ab | Therapeutic compounds |
GB0616214D0 (en) | 2006-08-15 | 2006-09-27 | Ucb Sa | Therapeutic Agents |
AU2007284562B2 (en) | 2006-08-16 | 2013-05-02 | Exelixis, Inc. | Using PI3K and MEK modulators in treatments of cancer |
CA2671982C (en) | 2006-12-14 | 2016-01-26 | Exelixis, Inc. | Methods of using mek inhibitors |
GB0714384D0 (en) | 2007-07-23 | 2007-09-05 | Ucb Pharma Sa | theraputic agents |
EP2240494B1 (en) * | 2008-01-21 | 2016-03-30 | UCB Biopharma SPRL | Thieno-pyridine derivatives as mek inhibitors |
GB0811304D0 (en) * | 2008-06-19 | 2008-07-30 | Ucb Pharma Sa | Therapeutic agents |
-
2006
- 2006-01-31 GB GBGB0601962.4A patent/GB0601962D0/en not_active Ceased
-
2007
- 2007-01-30 DK DK07705076.3T patent/DK1981892T3/da active
- 2007-01-30 CN CN2007800040774A patent/CN101379067B/zh active Active
- 2007-01-30 JP JP2008552878A patent/JP5249787B2/ja active Active
- 2007-01-30 SI SI200731467T patent/SI1981892T1/sl unknown
- 2007-01-30 RS RS20140304A patent/RS53342B/en unknown
- 2007-01-30 BR BRPI0708016-6A patent/BRPI0708016B1/pt active IP Right Grant
- 2007-01-30 UA UAA200809945A patent/UA95939C2/ru unknown
- 2007-01-30 AU AU2007211377A patent/AU2007211377B2/en active Active
- 2007-01-30 PL PL07705076T patent/PL1981892T3/pl unknown
- 2007-01-30 WO PCT/GB2007/000310 patent/WO2007088345A1/en active Application Filing
- 2007-01-30 ZA ZA200807447A patent/ZA200807447B/xx unknown
- 2007-01-30 NZ NZ569638A patent/NZ569638A/en unknown
- 2007-01-30 CA CA2640594A patent/CA2640594C/en active Active
- 2007-01-30 EA EA200801684A patent/EA016128B1/ru not_active IP Right Cessation
- 2007-01-30 MY MYPI20082765A patent/MY146387A/en unknown
- 2007-01-30 KR KR1020087018972A patent/KR101446919B1/ko active IP Right Grant
- 2007-01-30 PT PT77050763T patent/PT1981892E/pt unknown
- 2007-01-30 ES ES07705076.3T patent/ES2471970T3/es active Active
- 2007-01-30 EP EP07705076.3A patent/EP1981892B1/en active Active
-
2008
- 2008-07-03 IL IL192603A patent/IL192603A/en active IP Right Grant
- 2008-07-30 US US12/182,931 patent/US8283359B2/en active Active
- 2008-08-28 EC EC2008008704A patent/ECSP088704A/es unknown
- 2008-08-29 NO NO20083739A patent/NO341064B1/no unknown
-
2009
- 2009-04-20 HK HK09103590.9A patent/HK1125924A1/xx unknown
-
2012
- 2012-09-05 US US13/604,282 patent/US8394822B2/en active Active
-
2013
- 2013-02-06 US US13/760,788 patent/US8604051B2/en active Active
-
2014
- 2014-06-02 HR HRP20140503TT patent/HRP20140503T1/hr unknown
- 2014-06-11 CY CY20141100415T patent/CY1115404T1/el unknown
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