JP2012517971A - キナーゼ阻害薬としての[1,2,4]トリアゾロ[1,5−a]ピリジン類 - Google Patents

キナーゼ阻害薬としての[1,2,4]トリアゾロ[1,5−a]ピリジン類 Download PDF

Info

Publication number
JP2012517971A
JP2012517971A JP2011549537A JP2011549537A JP2012517971A JP 2012517971 A JP2012517971 A JP 2012517971A JP 2011549537 A JP2011549537 A JP 2011549537A JP 2011549537 A JP2011549537 A JP 2011549537A JP 2012517971 A JP2012517971 A JP 2012517971A
Authority
JP
Japan
Prior art keywords
triazolo
pyridin
chloro
phenyl
phenylamino
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2011549537A
Other languages
English (en)
Japanese (ja)
Other versions
JP2012517971A5 (cg-RX-API-DMAC10.html
Inventor
レリシュ,カロリーヌ
オークレール,エリック
ルー,ジャック ル
ミドルミス,デーヴィッド
Original Assignee
フォーヴィア・ファーマシューティカルズ
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=42229029&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=JP2012517971(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by フォーヴィア・ファーマシューティカルズ filed Critical フォーヴィア・ファーマシューティカルズ
Publication of JP2012517971A publication Critical patent/JP2012517971A/ja
Publication of JP2012517971A5 publication Critical patent/JP2012517971A5/ja
Pending legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • A61K31/437—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 five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • 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
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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)
  • Diabetes (AREA)
  • Emergency Medicine (AREA)
  • Immunology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
JP2011549537A 2009-02-13 2010-02-09 キナーゼ阻害薬としての[1,2,4]トリアゾロ[1,5−a]ピリジン類 Pending JP2012517971A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP09360013 2009-02-13
EP09360013.8 2009-02-13
PCT/EP2010/051556 WO2010092041A1 (en) 2009-02-13 2010-02-09 [1, 2, 4] triazolo [1, 5 -a] pyridines as kinase inhibitors

Publications (2)

Publication Number Publication Date
JP2012517971A true JP2012517971A (ja) 2012-08-09
JP2012517971A5 JP2012517971A5 (cg-RX-API-DMAC10.html) 2013-05-02

Family

ID=42229029

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011549537A Pending JP2012517971A (ja) 2009-02-13 2010-02-09 キナーゼ阻害薬としての[1,2,4]トリアゾロ[1,5−a]ピリジン類

Country Status (24)

Country Link
US (1) US20120041195A1 (cg-RX-API-DMAC10.html)
EP (1) EP2396324A1 (cg-RX-API-DMAC10.html)
JP (1) JP2012517971A (cg-RX-API-DMAC10.html)
KR (1) KR20110116160A (cg-RX-API-DMAC10.html)
CN (1) CN102317288A (cg-RX-API-DMAC10.html)
AR (1) AR075411A1 (cg-RX-API-DMAC10.html)
BR (1) BRPI1008850A2 (cg-RX-API-DMAC10.html)
CA (1) CA2751517A1 (cg-RX-API-DMAC10.html)
CL (1) CL2011001947A1 (cg-RX-API-DMAC10.html)
CO (1) CO6420343A2 (cg-RX-API-DMAC10.html)
CR (1) CR20110386A (cg-RX-API-DMAC10.html)
DO (1) DOP2011000248A (cg-RX-API-DMAC10.html)
EA (1) EA201101188A1 (cg-RX-API-DMAC10.html)
EC (1) ECSP11011250A (cg-RX-API-DMAC10.html)
HN (1) HN2011002095A (cg-RX-API-DMAC10.html)
IL (1) IL214426A0 (cg-RX-API-DMAC10.html)
MX (1) MX2011008549A (cg-RX-API-DMAC10.html)
NI (1) NI201100151A (cg-RX-API-DMAC10.html)
NZ (1) NZ594508A (cg-RX-API-DMAC10.html)
PE (1) PE20120110A1 (cg-RX-API-DMAC10.html)
SG (1) SG173610A1 (cg-RX-API-DMAC10.html)
TN (1) TN2011000379A1 (cg-RX-API-DMAC10.html)
WO (1) WO2010092041A1 (cg-RX-API-DMAC10.html)
ZA (1) ZA201105896B (cg-RX-API-DMAC10.html)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013512268A (ja) * 2009-11-30 2013-04-11 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング トリアゾロピリジン誘導体
JP2013512264A (ja) * 2009-11-30 2013-04-11 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング トリアゾロピリジン
JP2013532147A (ja) * 2010-06-16 2013-08-15 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング 置換トリアゾロピリジン

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010141796A2 (en) 2009-06-05 2010-12-09 Cephalon, Inc. PREPARATION AND USES OF 1,2,4-TRIAZOLO [1,5a] PYRIDINE DERIVATIVES
EP2343294A1 (en) * 2009-11-30 2011-07-13 Bayer Schering Pharma AG Substituted triazolopyridines
TW201204723A (en) * 2010-06-22 2012-02-01 Fovea Pharmaceuticals Heterocyclic compounds, their preparation and their therapeutic application
US20140120087A1 (en) 2011-04-21 2014-05-01 Bayer Intellectual Property Gmbh Triazolopyridines
WO2012160029A1 (en) 2011-05-23 2012-11-29 Bayer Intellectual Property Gmbh Substituted triazolopyridines
UA112096C2 (uk) 2011-12-12 2016-07-25 Байєр Інтеллектуал Проперті Гмбх Заміщені триазолопіридини та їх застосування як інгібіторів ttk
KR20130091464A (ko) 2012-02-08 2013-08-19 한미약품 주식회사 타이로신 카이네이즈 억제 활성을 갖는 트리아졸로피리딘 유도체
JP6166289B2 (ja) 2012-03-14 2017-07-19 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH 置換イミダゾピリダジン
CN104603136B (zh) 2012-07-10 2017-06-27 拜耳医药股份有限公司 制备取代的三唑并吡啶的方法
WO2014020043A1 (en) 2012-08-02 2014-02-06 Bayer Pharma Aktiengesellschaft Combinations for the treatment of cancer
CA2914745A1 (en) 2013-06-11 2014-12-18 Bayer Pharma Aktiengesellschaft Prodrug derivatives of substituted triazolopyridines
WO2021098813A1 (zh) * 2019-11-22 2021-05-27 南京明德新药研发有限公司 作为dna-pk抑制剂的嘧啶并吡咯类螺环化合物及其衍生物

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004058769A2 (en) * 2002-12-18 2004-07-15 Vertex Pharmaceuticals Incorporated Triazolopyridazines as protein kinases inhibitors
WO2005037843A1 (en) * 2003-10-14 2005-04-28 Vertex Pharmaceuticals Incorporated Compositions useful as inhibitors of protein kinases
WO2007067537A1 (en) * 2005-12-07 2007-06-14 Osi Pharmaceuticals, Inc. Pyrrolopyridine kinase inhibiting compounds
WO2008025821A1 (en) * 2006-08-30 2008-03-06 Cellzome Limited Triazole derivatives as kinase inhibitors
WO2008051757A1 (en) * 2006-10-20 2008-05-02 Irm Llc Compositions and methods for modulating c-kit and pdgfr receptors
WO2010027500A1 (en) * 2008-09-08 2010-03-11 Signal Pharmaceuticals, Llc Aminotriazolopyridines and their use as kinase inhibitors

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6056684B2 (ja) 1977-11-07 1985-12-11 東興薬品工業株式会社 点眼剤
US4271143A (en) 1978-01-25 1981-06-02 Alcon Laboratories, Inc. Sustained release ophthalmic drug dosage
US4407792A (en) 1979-05-09 1983-10-04 Alcon Laboratories, Inc. Sustained release ophthalmic drug dosage
JPH0830004B2 (ja) 1983-11-14 1996-03-27 コロンビア ラボラトリーズ インコーポレイテッド 生物接着性組成物およびそれにより治療する方法
US5041434A (en) 1991-08-17 1991-08-20 Virginia Lubkin Drugs for topical application of sex steroids in the treatment of dry eye syndrome, and methods of preparation and application
CA2386955A1 (en) 1999-11-22 2001-05-31 Warner-Lambert Company Quinazolines and their use for inhibiting cyclin-dependent kinase enzymes
EP1590341B1 (en) 2003-01-17 2009-06-17 Warner-Lambert Company LLC 2-aminopyridine substituted heterocycles as inhibitors of cellular proliferation
WO2005037285A1 (en) 2003-10-16 2005-04-28 Chiron Corporation 2,6-disubstituted quinazolines, quinoxalines, quinolines and isoquinolines as inhibitors of raf kinase for treatment of cancer
AU2005231507B2 (en) 2004-04-08 2012-03-01 Targegen, Inc. Benzotriazine inhibitors of kinases
NZ588896A (en) 2004-08-25 2012-05-25 Targegen Inc Heterocyclic compounds and methods of use
US20070054916A1 (en) 2004-10-01 2007-03-08 Amgen Inc. Aryl nitrogen-containing bicyclic compounds and methods of use
WO2006101977A2 (en) 2005-03-16 2006-09-28 Targegen, Inc. Pyrimidine compounds and methods of use
EP1878727A4 (en) 2005-04-28 2013-11-13 Kyowa Hakko Kirin Co Ltd 2-AMINOQUINAZOLINE DERIVATIVES
WO2006133411A1 (en) 2005-06-08 2006-12-14 Targegen, Inc. Methods and compositions for the treatment of ocular disorders
PE20070978A1 (es) 2006-02-14 2007-11-15 Novartis Ag COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks)
TW200829566A (en) 2006-12-08 2008-07-16 Astrazeneca Ab Chemical compounds
CA2673003A1 (en) 2006-12-22 2008-07-03 Novartis Ag Quinazolines for pdk1 inhibition
GB0719803D0 (en) * 2007-10-10 2007-11-21 Cancer Rec Tech Ltd Therapeutic compounds and their use
AU2009259853A1 (en) * 2008-06-20 2009-12-23 Genentech, Inc. Triazolopyridine JAK inhibitor compounds and methods
PE20110063A1 (es) * 2008-06-20 2011-02-16 Genentech Inc DERIVADOS DE [1, 2, 4]TRIAZOLO[1, 5-a]PIRIDINA COMO INHIBIDORES DE JAK
WO2010010189A1 (en) * 2008-07-25 2010-01-28 Galapagos Nv Novel compounds useful for the treatment of degenerative and inflammatory diseases
WO2010010188A1 (en) * 2008-07-25 2010-01-28 Galapagos Nv Novel compounds useful for the treatment of degenerative and inflammatory diseases.
WO2010010184A1 (en) * 2008-07-25 2010-01-28 Galapagos Nv [1, 2, 4] triazolo [1, 5-a] pyridines as jak inhibitors
UY32045A (es) * 2008-08-12 2010-03-26 Takeda Pharmaceutical Compuesto amida

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004058769A2 (en) * 2002-12-18 2004-07-15 Vertex Pharmaceuticals Incorporated Triazolopyridazines as protein kinases inhibitors
WO2005037843A1 (en) * 2003-10-14 2005-04-28 Vertex Pharmaceuticals Incorporated Compositions useful as inhibitors of protein kinases
WO2007067537A1 (en) * 2005-12-07 2007-06-14 Osi Pharmaceuticals, Inc. Pyrrolopyridine kinase inhibiting compounds
WO2008025821A1 (en) * 2006-08-30 2008-03-06 Cellzome Limited Triazole derivatives as kinase inhibitors
WO2008051757A1 (en) * 2006-10-20 2008-05-02 Irm Llc Compositions and methods for modulating c-kit and pdgfr receptors
WO2010027500A1 (en) * 2008-09-08 2010-03-11 Signal Pharmaceuticals, Llc Aminotriazolopyridines and their use as kinase inhibitors

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013512268A (ja) * 2009-11-30 2013-04-11 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング トリアゾロピリジン誘導体
JP2013512264A (ja) * 2009-11-30 2013-04-11 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング トリアゾロピリジン
JP2013532147A (ja) * 2010-06-16 2013-08-15 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング 置換トリアゾロピリジン

Also Published As

Publication number Publication date
BRPI1008850A2 (pt) 2016-03-15
IL214426A0 (en) 2011-09-27
CR20110386A (es) 2011-12-02
ECSP11011250A (es) 2011-10-31
NI201100151A (es) 2012-10-03
AR075411A1 (es) 2011-03-30
SG173610A1 (en) 2011-09-29
US20120041195A1 (en) 2012-02-16
EA201101188A1 (ru) 2012-04-30
EP2396324A1 (en) 2011-12-21
MX2011008549A (es) 2011-12-06
WO2010092041A1 (en) 2010-08-19
HN2011002095A (es) 2014-01-06
CO6420343A2 (es) 2012-04-16
CA2751517A1 (en) 2010-08-19
DOP2011000248A (es) 2011-10-31
CL2011001947A1 (es) 2012-03-16
NZ594508A (en) 2013-12-20
ZA201105896B (en) 2012-03-28
TN2011000379A1 (en) 2013-03-27
KR20110116160A (ko) 2011-10-25
CN102317288A (zh) 2012-01-11
PE20120110A1 (es) 2012-02-20

Similar Documents

Publication Publication Date Title
US20120041195A1 (en) Heterocyclic compounds
DE602004010151T2 (de) Zusammensetzungen, die sich als inhibitoren von proteinkinasen eignen
US9718787B2 (en) Poly (ADP-ribose) polymerase inhibitor
RU2550821C2 (ru) Бициклические пиридины и аналоги в качестве модуляторов сиртуина
JP2012514020A (ja) 置換キナゾリン化合物
KR100736012B1 (ko) 벤즈아졸 유도체 및 이의 jnk 조절자로의 용도
JP2013533237A (ja) 複素環化合物、それらの調製およびそれらの療法的適用
KR102038462B1 (ko) Pi3k의 활성 또는 기능의 억제제의 용도
IL197015A (en) Benzotriazole Kinase Modulators, Methods for their Preparation, Pharmaceuticals Containing Them, and Their Use in the Preparation of Medicines for the Treatment of Diseases
US10849901B2 (en) Arf6 inhibitors and methods of synthesis and use thereof
WO2006100212A1 (en) Pyrazolyl-pyrimidines as potassium channel modulating agents and their medical use
US20090036475A1 (en) Pyrazolyl-Pyrimidines as Potassium Channel Modulating Agents and Their Medical Use
EP2066655A2 (en) Pyridinyl-pyrimidine derivatives useful as potassium channel modulating agents
AU2011211410B2 (en) [1,2,4] triazolo [1,5-A] pyridines as kinase inhibitors
TWI883217B (zh) 作為酪蛋白激酶1δ及/或類活化素受體激酶5之抑制劑之雜環化合物
KR101992356B1 (ko) 피리딘 유도체 또는 이의 약제학적 허용가능한 염 및 이를 유효성분으로 함유하는 약학 조성물
OA16290A (en) Heterocyclic compounds, their preparation and their therapeutic application.
DE102004022383A1 (de) Neue Pyridopyrazine und deren Verwendung als Modulatoren von Kinasen

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20130115

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20130313

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20140407

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20141105