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FR13C0069I2 - BICYCLIC HETEROARYL COMPOUNDS - Google Patents

BICYCLIC HETEROARYL COMPOUNDS

Info

Publication number
FR13C0069I2
FR13C0069I2 FR13C0069C FR13C0069C FR13C0069I2 FR 13C0069 I2 FR13C0069 I2 FR 13C0069I2 FR 13C0069 C FR13C0069 C FR 13C0069C FR 13C0069 C FR13C0069 C FR 13C0069C FR 13C0069 I2 FR13C0069 I2 FR 13C0069I2
Authority
FR
France
Prior art keywords
bicyclic heteroaryl
heteroaryl compounds
compounds
bicyclic
heteroaryl
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.)
Active
Application number
FR13C0069C
Other languages
French (fr)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ariad Pharmaceuticals Inc
Original Assignee
Ariad Pharmaceuticals Inc
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=38218600&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=FR13C0069(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Ariad Pharmaceuticals Inc filed Critical Ariad Pharmaceuticals Inc
Publication of FR13C0069I1 publication Critical patent/FR13C0069I1/en
Application granted granted Critical
Publication of FR13C0069I2 publication Critical patent/FR13C0069I2/en
Active legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32Nitrogen atom
    • C07D473/34Nitrogen atom attached in position 6, e.g. adenine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Immunology (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
FR13C0069C 2005-12-23 2013-12-12 BICYCLIC HETEROARYL COMPOUNDS Active FR13C0069I2 (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US75400005P 2005-12-23 2005-12-23
US75396205P 2005-12-23 2005-12-23
US75608906P 2006-01-03 2006-01-03
US79847206P 2006-05-08 2006-05-08
US83319106P 2006-07-25 2006-07-25
PCT/US2006/048758 WO2007075869A2 (en) 2005-12-23 2006-12-22 Bicyclic heteroaryl compounds

Publications (2)

Publication Number Publication Date
FR13C0069I1 FR13C0069I1 (en) 2014-01-17
FR13C0069I2 true FR13C0069I2 (en) 2014-04-18

Family

ID=38218600

Family Applications (1)

Application Number Title Priority Date Filing Date
FR13C0069C Active FR13C0069I2 (en) 2005-12-23 2013-12-12 BICYCLIC HETEROARYL COMPOUNDS

Country Status (21)

Country Link
US (9) US8114874B2 (en)
EP (4) EP1973545B1 (en)
JP (3) JP5200939B2 (en)
KR (1) KR101436303B1 (en)
CN (1) CN103044432B (en)
AU (1) AU2006331673B2 (en)
CA (1) CA2634923C (en)
CY (3) CY1113907T1 (en)
DK (2) DK2495016T3 (en)
EA (2) EA027573B1 (en)
ES (2) ES2761180T3 (en)
FR (1) FR13C0069I2 (en)
HU (2) HUE047422T2 (en)
IL (2) IL191938A (en)
LT (1) LT2495016T (en)
LU (1) LU92327I2 (en)
MX (2) MX343042B (en)
PL (2) PL2495016T3 (en)
PT (2) PT2495016T (en)
SI (1) SI2495016T1 (en)
WO (1) WO2007075869A2 (en)

Families Citing this family (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1940843A4 (en) 2005-08-11 2010-09-15 Ariad Pharma Inc Unsaturated heterocyclic derivatives
HUE047422T2 (en) * 2005-12-23 2020-04-28 Ariad Pharma Inc Bicyclic Heteroaryl Compounds
EP2024366B1 (en) * 2006-05-08 2015-09-16 Ariad Pharmaceuticals, Inc. Monocyclic heteroaryl compounds
MX2008014289A (en) 2006-05-08 2008-11-26 Ariad Pharma Inc Acetylenic heteroaryl compounds.
JP2010500365A (en) * 2006-08-07 2010-01-07 インサイト・コーポレイション Triazolotriazines as kinase inhibitors
CA2669704A1 (en) 2006-11-16 2008-05-22 Allergan, Inc. Sulfoximines as kinase inhibitors
US8558002B2 (en) 2006-11-16 2013-10-15 Allergan, Inc. Sulfoximines as kinase inhibitors
US8143410B2 (en) 2006-11-16 2012-03-27 Allergan, Inc. Kinase inhibitors
EP3443958A1 (en) * 2006-11-22 2019-02-20 Incyte Holdings Corporation Imidazotriazines and imidazopyrimidines as kinase inhibitors
EP2070929A1 (en) * 2007-12-11 2009-06-17 Bayer Schering Pharma Aktiengesellschaft Alkynylaryl compounds and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same
NZ602791A (en) 2008-05-21 2014-04-30 Incyte Corp Salts of 2-fluoro-n-methyl-4-[7-(quinolin-6-yl-methyl)- imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide and processes related to preparing the same
FR2933981A1 (en) * 2008-07-18 2010-01-22 Sanofi Aventis New imidazo(1,2-a)pyridine derivatives are mesenchymal-epithelial transition protein kinase inhibitors useful in a pharmaceutical composition for preparing a medicament to treat/prevent e.g. fibrotic disorders, allergies and asthma
AU2009279936A1 (en) * 2008-08-05 2010-02-11 Banyu Pharmaceutical Co., Ltd. Therapeutic compounds
EP2365809B8 (en) 2008-11-12 2018-10-10 Ariad Pharmaceuticals, Inc. Pyrazinopyrazines and derivatives as kinase inhibitors
CN102770129A (en) * 2009-10-30 2012-11-07 阿里亚德医药股份有限公司 Methods and compositions for treating cancer
US9180127B2 (en) * 2009-12-29 2015-11-10 Dana-Farber Cancer Institute, Inc. Type II Raf kinase inhibitors
ES2608329T3 (en) 2010-02-03 2017-04-07 Incyte Holdings Corporation Imidazo [1,2-b] [1,2,4] triazines as c-Met inhibitors
US8846671B2 (en) 2010-07-01 2014-09-30 Guangzhou Institute Of Biomedicine And Health, Chinese Academy Of Sciences Heterocyclic alkynyl benzene compounds and medical compositions and uses thereof
CN101885722B (en) * 2010-07-01 2013-07-24 中国科学院广州生物医药与健康研究院 Heterocycle alkyne and benzene compound, medicinal composition and application thereof
WO2012098416A1 (en) 2011-01-21 2012-07-26 Sun Pharma Advanced Research Company Ltd Diarylacetylene hydrazide containing tyrosine kinase inhibitors
WO2012127030A1 (en) * 2011-03-23 2012-09-27 Proteosys Ag Arylpiperazines as neuroprotective agents
EP2694064A1 (en) * 2011-04-07 2014-02-12 Ariad Pharmaceuticals, Incorporated Methods and compositions for treating neurodegenerative diseases
EP2694066A1 (en) * 2011-04-07 2014-02-12 ARIAD Pharmaceuticals, Inc Methods and compositions for treating parkinson's disease
RU2477723C2 (en) * 2011-06-16 2013-03-20 Общество С Ограниченной Ответственностью "Фьюжн Фарма" Protein kinase inhibitor (versions), use thereof for treating oncological diseases and based pharmaceutical composition
EP2822935B1 (en) 2011-11-17 2019-05-15 Dana-Farber Cancer Institute, Inc. Inhibitors of c-jun-n-terminal kinase (jnk)
US20150105377A1 (en) * 2012-04-25 2015-04-16 Ariad Pharmaceuticals, Inc. Methods and Compositions for RAF Kinase Mediated Diseases
US9254288B2 (en) * 2012-05-07 2016-02-09 The Translational Genomics Research Institute Susceptibility of tumors to tyrosine kinase inhibitors and treatment thereof
WO2013170774A1 (en) * 2012-05-16 2013-11-21 上海医药集团股份有限公司 Acetylene derivative having antineoplastic activity
US8859553B2 (en) * 2012-07-30 2014-10-14 Astar Biotech Llc Protein kinase inhibitors
WO2014028595A1 (en) * 2012-08-14 2014-02-20 Concert Pharmaceuticals, Inc. Deuterated ponatinib
CN103664787B (en) * 2012-09-17 2015-09-09 南京圣和药业股份有限公司 Alkynes heteroaromatic ring compounds and application thereof
WO2014063068A1 (en) 2012-10-18 2014-04-24 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
US9758522B2 (en) 2012-10-19 2017-09-12 Dana-Farber Cancer Institute, Inc. Hydrophobically tagged small molecules as inducers of protein degradation
US10000483B2 (en) 2012-10-19 2018-06-19 Dana-Farber Cancer Institute, Inc. Bone marrow on X chromosome kinase (BMX) inhibitors and uses thereof
TWI574962B (en) 2012-11-14 2017-03-21 加拓科學公司 Heteroaromatic compounds as pi3 kinase modulators and methods of use
CN103848829B (en) 2012-11-28 2017-04-12 南京圣和药业股份有限公司 Heteroaryl alkyne compounds and application thereof
CA2815506C (en) 2012-12-12 2018-12-11 Ariad Pharmaceuticals, Inc. Crystalline forms of 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-n-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide mono hydrochloride
US9725452B2 (en) 2013-03-15 2017-08-08 Presidents And Fellows Of Harvard College Substituted indoles and pyrroles as RIP kinase inhibitors
US20140343282A1 (en) 2013-05-16 2014-11-20 Apicore, Llc Processes for making ponatinib and intermediates thereof
AU2014286047B2 (en) 2013-07-04 2018-02-08 Sandoz Ag Crystalline forms of ponatinib hydrochloride
CN104341416B (en) * 2013-07-31 2017-03-29 南京圣和药业股份有限公司 Protein tyrosine kinase inhibitor and its application
GB2518873A (en) * 2013-10-03 2015-04-08 Agency Science Tech & Res Bicyclic alkyne derivatives and uses thereof
AU2014337044A1 (en) 2013-10-18 2016-05-05 Dana-Farber Cancer Institute, Inc. Polycyclic inhibitors of cyclin-dependent kinase 7 (CDK7)
EP3057955B1 (en) 2013-10-18 2018-04-11 Syros Pharmaceuticals, Inc. Heteroaromatic compounds useful for the treatment of prolferative diseases
US9636340B2 (en) 2013-11-12 2017-05-02 Ayyappan K. Rajasekaran Kinase inhibitors
CN104650086A (en) * 2013-11-22 2015-05-27 天津市汉康医药生物技术有限公司 Ponatinib hydrochloride compound
WO2015085973A1 (en) 2013-12-09 2015-06-18 Zentiva, K.S. Modifications of 3-(2-imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-n-[4-[(4-methyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl] benzamide hydrochloride salt
WO2015085972A1 (en) 2013-12-09 2015-06-18 Zentiva, K.S. NOVEL SALTS OF 3-(2-IMIDAZO[1,2-b]PYRIDAZIN-3-YLETHYNYL)-4-METHYL-N-[4-[(4-METHYL- 1-PIPERAZINYL)METHYL]-3-(TRIFLUOROMETHYL)PHENYL] BENZAMIDE
WO2015085971A1 (en) 2013-12-09 2015-06-18 Zentiva, K.S. Hydrobromide salt of 3-(2-imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-n-[4-[(4-methyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl] benzamide
CN104496995A (en) * 2014-01-06 2015-04-08 广东东阳光药业有限公司 Method for preparing 3-ethynyl imidazo[1,2-b]pyridazine
GB2522226A (en) * 2014-01-17 2015-07-22 Agency Science Tech & Res Heteroaryl alkyne derivatives and uses thereof
US9862688B2 (en) 2014-04-23 2018-01-09 Dana-Farber Cancer Institute, Inc. Hydrophobically tagged janus kinase inhibitors and uses thereof
WO2015164614A1 (en) 2014-04-23 2015-10-29 Dana-Farber Cancer Institute, Inc. Janus kinase inhibitors and uses thereof
CN106573929A (en) 2014-06-06 2017-04-19 纳科法尔马有限公司 1h-1,8- naphthyridin-2ones as anti proliferative compounds
EP3169671B1 (en) 2014-07-17 2019-08-21 Sunshine Lake Pharma Co., Ltd. 1-(5-(tert.-butyl)isoxazol-3-yl)-3-(4-((phenyl)ethynyl)phenyl)urea derivatives and related compounds as flt3 inhibitors for treating cancer
WO2016059220A1 (en) 2014-10-16 2016-04-21 INSERM (Institut National de la Santé et de la Recherche Médicale) Tcr-activating agents for use in the treatment of t-all
CA2972239A1 (en) 2014-12-23 2016-06-30 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
CN105837575B (en) * 2015-01-13 2019-01-15 四川大学 3- acetenyl Pyrazolopyrimidine derivative and its preparation method and application
WO2016160617A2 (en) 2015-03-27 2016-10-06 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinases
CN106167491A (en) * 2015-05-19 2016-11-30 重庆大学 The compound of a kind of effective suppression lung cancer metastasis and application thereof
WO2016201203A1 (en) * 2015-06-11 2016-12-15 Apicore Us Llc Processes for making ponatinib and intermediates thereof
US10702527B2 (en) 2015-06-12 2020-07-07 Dana-Farber Cancer Institute, Inc. Combination therapy of transcription inhibitors and kinase inhibitors
EP3347462A4 (en) * 2015-09-09 2019-08-14 Warren C. Lau Methods, compositions, and uses of novel fyn kinase inhibitors
JP7028766B2 (en) 2015-09-09 2022-03-02 ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド Inhibitor of cyclin-dependent kinase
AU2017228398A1 (en) 2016-03-03 2018-10-18 Cornell University Small molecule IRE1-alpha inhibitors
WO2017156350A1 (en) 2016-03-09 2017-09-14 K-Gen, Inc. Methods of cancer treatment
WO2017222287A1 (en) * 2016-06-20 2017-12-28 재단법인 대구경북첨단의료산업진흥재단 Novel imidazopyridine derivative, method for preparing same, and pharmaceutical composition containing same as active ingredient for preventing or treating cancer
WO2018002958A1 (en) 2016-06-30 2018-01-04 Sun Pharma Advanced Research Company Limited Novel hydrazide containing compounds as btk inhibitors
US20210006178A1 (en) * 2016-09-29 2021-01-07 Transportation Ip Holdings, Llc Harmonic distortion reduction system for converters connected to a common bus
US10221184B2 (en) 2017-01-20 2019-03-05 Apicore Us Llc Polymorphs of ponatinib hydrochloride
US11351123B2 (en) 2017-03-15 2022-06-07 Sun Pharma Advanced Research Company Limited Amorphous dispersion of 4-methyl-3-quinolin-3-ylethynyl-benzoic acid n'-(2-chloro-6-methyl-benzoyl) hydrazide
CN110506036A (en) * 2017-03-15 2019-11-26 太阳制药先进研究有限公司 The novel amorphous dispersions of cyclopropane-carboxylic acid (5- { 5- [N '-(the chloro- 6- methyl benzoyl of 2-) Hydrazinocarbonyl] -2- methylphenyl acetenyl }-pyridine -2- base) amide
US11072620B2 (en) 2017-06-20 2021-07-27 Apotex Inc. Crystalline forms of Ponatinib hydrochloride
JP7024960B2 (en) * 2017-10-04 2022-02-24 国立大学法人京都大学 Molecular probe for Bcr-Abl protein imaging
EP3781568A1 (en) 2018-06-22 2021-02-24 Johnson Matthey Public Limited Company Form of ponatinib
EP3810132A4 (en) 2018-06-25 2022-06-22 Dana-Farber Cancer Institute, Inc. TAIRE KINA INHIBITORS AND THEIR USES
WO2020007234A1 (en) 2018-07-02 2020-01-09 深圳市塔吉瑞生物医药有限公司 Alkynyl(hetero)aromatic compound for inhibiting protein kinase activity
EP3808746B1 (en) * 2018-07-17 2023-08-02 Shenzhen TargetRx, Inc. N-[3-[2-[8-[(1h-pyrazol-4-yl)amino]imidazo[1,2-a]pyrazin-3-yl]ethynyl]phenyl]-benzamide derivatives and related compounds as protein kinase inhibitors for the treatment of cancer
WO2020053812A1 (en) * 2018-09-12 2020-03-19 Purdue Research Foundation Alkynyl nicotinamide compounds as kinase inhibitors
WO2020079652A1 (en) 2018-10-17 2020-04-23 Insilico Medicine Hong Kong Limited Kinase inhibitors
SG11202104438VA (en) 2018-11-01 2021-05-28 Syros Pharmaceuticals Inc Inhibitors of cyclin-dependent kinase 7 (cdk7)
CA3124330A1 (en) 2018-12-21 2020-06-25 Daiichi Sankyo Company, Limited Combination of antibody-drug conjugate and kinase inhibitor
WO2020214999A1 (en) * 2019-04-17 2020-10-22 Emory University Abelson non-tyrosine kinase compounds for the treatment of neurodegenerative diseases
WO2020223235A1 (en) 2019-04-29 2020-11-05 Incyte Corporation Mini-tablet dosage forms of ponatinib
KR102205619B1 (en) 2019-06-12 2021-01-21 한국과학기술연구원 Novel indazole derivatives and pharmaceutical composition for preventing, improving or treating cancer containing the same
CN111004240B (en) * 2019-12-13 2020-12-01 山东铂源药业有限公司 Synthetic method of ponatinib intermediate 3-ethynylimidazo [1,2-b ] pyridazine
CN115996917A (en) 2020-05-06 2023-04-21 艾捷斯治疗公司 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors
WO2021228983A1 (en) 2020-05-13 2021-11-18 INSERM (Institut National de la Santé et de la Recherche Médicale) A pharmaceutical composition comprising an arsenic compound, an inductor of type-1 ifn and a protein kinase inhibitor for treating cancer
CA3188108A1 (en) * 2020-06-24 2021-12-30 Purdue Research Foundation 2,3-disubstituted pyrido[3,4-b]pyrazine-containing compounds as kinase inhibitors
WO2022053130A1 (en) 2020-09-09 2022-03-17 Sid Alex Group, S.R.O. Antago-mir-155 for treatment of v-src, c-src-tyrosine kinase-induced cancers
TW202241889A (en) 2020-12-23 2022-11-01 美商雅捷可斯治療公司 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors
US20220289756A1 (en) * 2021-03-11 2022-09-15 Wai Kit Pang Compounds and compositions as inhibitors of protein kinases
CN112778207A (en) * 2021-03-19 2021-05-11 海南鑫开源医药科技有限公司 Nilotinib hydrochloride raw material medicine impurity and preparation method thereof
WO2022217821A1 (en) * 2021-04-13 2022-10-20 深圳市新樾生物科技有限公司 Alkynylphenylbenzamide compound and use thereof
US20240199626A1 (en) * 2021-04-19 2024-06-20 Oregon Health & Science University Compounds with improved cardiac safety for the treatment of cancer and neurodegenerative disorders
EP4430047A1 (en) 2021-11-08 2024-09-18 Progentos Therapeutics, Inc. Platelet-derived growth factor receptor (pdgfr) alpha inhibitors and uses thereof
US12162881B2 (en) 2021-11-09 2024-12-10 Ajax Therapeutics, Inc. Forms and compositions of inhibitors of JAK2
US11970494B2 (en) 2021-11-09 2024-04-30 Ajax Therapeutics, Inc. 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors
TW202434233A (en) * 2023-01-13 2024-09-01 大陸商深圳市新樾生物科技有限公司 Salts and crystalline forms of compound a, methods of preparation, and uses thereof

Family Cites Families (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4736866A (en) 1984-06-22 1988-04-12 President And Fellows Of Harvard College Transgenic non-human mammals
US5099057A (en) 1987-10-19 1992-03-24 The Dow Chemical Company Process for the preparation of ar-amino-para-arenediols
US5099067A (en) 1988-08-05 1992-03-24 Northwestern University Use of ammonium formate as a hydrogen transfer reagent for reduction of chiral nitro compounds with retention of configuration
US5175383A (en) 1989-02-17 1992-12-29 President And Fellows Of Harvard College Animal model for benign prostatic disease
DE69106902T2 (en) 1990-03-01 1995-07-06 Takeda Chemical Industries Ltd Imidazopyridazines, their production and use.
KR19990008451A (en) 1995-05-09 1999-01-25 페라스타르크 Pyrazolo- (1,5a) -pyrimidine, its preparation method and its use
GB9823871D0 (en) * 1998-10-30 1998-12-23 Pharmacia & Upjohn Spa 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents
DE19948434A1 (en) 1999-10-08 2001-06-07 Gruenenthal Gmbh Substance library containing bicyclic imidazo-5-amines and / or bicyclic imidazo-3-amines
ATE298325T1 (en) 1999-11-08 2005-07-15 Schering Corp METHOD FOR PRODUCING N-(4-HYDROXYPHENYL)-N'-(4'-AMINOPHENYL)-PIPERAZ NE
US6420365B1 (en) 2000-01-18 2002-07-16 Neurogen Corporation Imidazopyridines and related derivatives as selective modulators of bradykinin B2 receptors
HN2001000008A (en) * 2000-01-21 2003-12-11 Inc Agouron Pharmaceuticals AMIDA COMPOSITE AND PHARMACEUTICAL COMPOSITIONS TO INHIBIT PROTEINKINASES, AND THE INSTRUCTIONS FOR USE
DE10019714A1 (en) 2000-04-20 2002-01-10 Gruenenthal Gmbh Salts of bicyclic, N-acylated imidazo-3-amines and imidazo-5-amines
DE10021246A1 (en) 2000-04-25 2001-10-31 Schering Ag New N-substituted benzamide derivatives are tyrosine kinase KDR and FLT inhibitors useful e.g. for treating tumors, psoriasis, rheumatoid arthritis, diabetic retinopathy or liver sclerosis
EP1301511A2 (en) 2000-07-14 2003-04-16 Bristol-Myers Squibb Pharma Company IMIDAZO 1,2-a]PYRAZINES FOR THE TREATMENT OF NEUROLOGICAL DISORDERS
DE10050663A1 (en) 2000-10-13 2002-04-18 Gruenenthal Gmbh Use of substituted imidazo [1,2-a] pyridine, pyrimidine and pyrazin-3-yl amine derivatives for the production of medicaments for NOS inhibition
SE0100568D0 (en) 2001-02-20 2001-02-20 Astrazeneca Ab Compounds
DE10117184A1 (en) 2001-04-05 2002-10-17 Gruenenthal Gmbh Substituted imidazole [1,2-a] pyridin-3-yl amide and amine compounds
DE10117183A1 (en) 2001-04-05 2002-10-10 Gruenenthal Gmbh Use of substituted imidazo [1,2-a] pyridine compounds as medicaments
WO2002096933A1 (en) 2001-05-30 2002-12-05 Novartis Ag 2-{[n-(2-amino-3-(heteroaryl or aryl)propionyl)-aminoacyl]-amino}-alkylboronic acid derivatives
WO2003000188A2 (en) 2001-06-21 2003-01-03 Ariad Pharmaceuticals, Inc. Novel quinazolines and uses thereof
IL159811A0 (en) * 2001-07-13 2004-06-20 Neurogen Corp Heteroaryl substituted fused bicyclic heteroaryl compounds as gabaa receptor ligands
DE60220296T2 (en) 2001-09-04 2008-01-17 Sumitomo Chemical Co., Ltd. IMIDAZO (1,2-a) PYRIMIDINE AND FUNGICIDAL COMPOSITIONS CONTAINING THEREOF
EP2407473A3 (en) 2002-02-01 2012-03-21 ARIAD Pharmaceuticals, Inc Method for producing phosphorus-containing compounds
KR20050008691A (en) 2002-04-19 2005-01-21 셀룰러 지노믹스 아이엔씨 Imidazo[1,2-a]Pyrazin-8-ylamines Method Of Making And Method Of Use Thereof
CA2487900A1 (en) * 2002-06-05 2003-12-18 Institute Of Medicinal Molecular Design, Inc. Immunity-related protein kinase inhibitors
EP1541575B1 (en) 2002-07-29 2010-03-03 Sumitomo Chemical Company, Limited Novel process for producing imidazo(1,2-b)pyridazine derivative
CA2466772C (en) 2002-09-11 2012-08-28 Becton, Dickinson And Company Apparatus and method for monitoring blood glucose levels including convenient display of blood glucose value average and constituent values
DE10246890A1 (en) 2002-10-08 2004-04-22 Grünenthal GmbH New C-(imidazo-(1,2-a)-pyridin-3-yl)-methylamines, are nitrogen monoxide synthase inhibitors useful e.g. for treating migraine, septic shock, neurodegenerative diseases, inflammatory pain or cancer
DE10247269A1 (en) 2002-10-10 2004-04-22 Grünenthal GmbH New C-(imidazo-(1,2-a)-pyridin-3-yl)-methylamines, are nitrogen monoxide synthase inhibitors useful e.g. for treating migraine, septic shock, neurodegenerative diseases, inflammatory pain or cancer
AR041992A1 (en) * 2002-11-06 2005-06-08 Smithkline Beecham Corp PIRIDINIL BENZOHETEROCICLIC COMPOSITE, PHARMACEUTICAL COMPOSITION THAT INCLUDES IT AND ITS USE TO PREPARE IT
GB0230089D0 (en) * 2002-12-24 2003-01-29 Astrazeneca Ab Therapeutic agents
EP1615697A2 (en) 2003-04-11 2006-01-18 Novo Nordisk A/S New pyrazolo[1,5-a] pyrimidine derivatives and pharmaceutical use thereof
ES2308256T3 (en) 2003-09-24 2008-12-01 Wyeth Holdings Corporation 6-ARIL-7-HALO-IMIDAZO (1,2-A) PYRIMIDINS AS ANTI-TARGET AGENTS.
US20050288295A1 (en) 2003-11-11 2005-12-29 Currie Kevin S Certain imidazo[1,2-a]pyrazin-8-ylamines, method of making, and method of use thereof
BRPI0416935A (en) 2003-11-28 2007-01-16 Novartis Ag diaryl urea derivatives in the treatment of protein kinase dependent diseases
JP2007513134A (en) 2003-12-05 2007-05-24 ビオヴィトルム・アクチボラゲット Improved synthesis of 2-substituted adenosine
JP2007517006A (en) * 2003-12-24 2007-06-28 アストラゼネカ アクチボラグ Pyrimidine with TIE2 (TEK) activity
DE602004018193D1 (en) * 2003-12-24 2009-01-15 Astrazeneca Ab PYRIMIDINES WITH TIE2 (TEK) ACTIVITY
PE20051089A1 (en) 2004-01-22 2006-01-25 Novartis Ag PYRAZOLE [1,5-A] PYRIMIDIN-7-IL-AMINE DERIVATIVES AS PROTEIN KINASE INHIBITORS
EA011930B1 (en) * 2004-04-07 2009-06-30 Лаборатуар Сероно Са Carboxylic acids
DE102004021716A1 (en) 2004-04-30 2005-12-01 Grünenthal GmbH Substituted imidazo [1,2-a] pyridine compounds and drugs containing substituted imidazo [1,2-a] pyridine compounds
EA200700243A1 (en) * 2004-07-14 2007-08-31 ПиТиСи ТЕРАПЬЮТИКС, ИНК. METHODS OF TREATMENT OF HEPATITIS C
US7776869B2 (en) * 2004-10-18 2010-08-17 Amgen Inc. Heteroaryl-substituted alkyne compounds and method of use
GB0502418D0 (en) 2005-02-05 2005-03-16 Astrazeneca Ab Compounds
PL1863818T3 (en) * 2005-03-23 2010-08-31 Hoffmann La Roche Acetylenyl-pyrazolo-pvrimidine derivatives as mglur2 antagonists
EP1893605A2 (en) 2005-03-31 2008-03-05 AstraZeneca AB Saminopyrimidine derivates with tie2 inhibiting activity
US20100216798A1 (en) 2005-07-29 2010-08-26 Astellas Pharma Inc Fused heterocycles as lck inhibitors
EP1940843A4 (en) 2005-08-11 2010-09-15 Ariad Pharma Inc Unsaturated heterocyclic derivatives
CN101389338B (en) * 2005-12-23 2013-06-26 阿里亚德医药股份有限公司 bicyclic heteroaryl compound
HUE047422T2 (en) 2005-12-23 2020-04-28 Ariad Pharma Inc Bicyclic Heteroaryl Compounds
MX2008014289A (en) 2006-05-08 2008-11-26 Ariad Pharma Inc Acetylenic heteroaryl compounds.
EP2024366B1 (en) * 2006-05-08 2015-09-16 Ariad Pharmaceuticals, Inc. Monocyclic heteroaryl compounds
EP2107054A1 (en) 2008-04-01 2009-10-07 Università Degli Studi Di Milano - Bicocca Antiproliferative compounds and therapeutic uses thereof
US20100273772A1 (en) 2009-04-23 2010-10-28 Wyeth Llc Bisaryl Alkynylamides as Negative Allosteric Modulators of Metabotropic Glutamate Receptor 5 (MGLUR5)
US8461851B2 (en) 2009-06-08 2013-06-11 University Of Hawaii Systems for transverse electromagnetic mode in-situ soil testing
US8329724B2 (en) 2009-08-03 2012-12-11 Hoffmann-La Roche Inc. Process for the manufacture of pharmaceutically active compounds
CN102770129A (en) 2009-10-30 2012-11-07 阿里亚德医药股份有限公司 Methods and compositions for treating cancer
EP2694064A1 (en) 2011-04-07 2014-02-12 Ariad Pharmaceuticals, Incorporated Methods and compositions for treating neurodegenerative diseases
JP5300939B2 (en) * 2011-08-25 2013-09-25 安田工業株式会社 Machining method using finishing tools
CA2815506C (en) 2012-12-12 2018-12-11 Ariad Pharmaceuticals, Inc. Crystalline forms of 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-n-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide mono hydrochloride

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