LU92327I9 - - Google Patents
Info
- Publication number
- LU92327I9 LU92327I9 LU92327C LU92327C LU92327I9 LU 92327 I9 LU92327 I9 LU 92327I9 LU 92327 C LU92327 C LU 92327C LU 92327 C LU92327 C LU 92327C LU 92327 I9 LU92327 I9 LU 92327I9
- Authority
- LU
- Luxembourg
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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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- 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
- A61K31/495—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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
-
- 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
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- 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
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physical Education & Sports Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
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 (fr) | 2005-12-23 | 2006-12-22 | Composes heteroaryles bicycliques |
Publications (2)
Publication Number | Publication Date |
---|---|
LU92327I2 LU92327I2 (fr) | 2014-02-05 |
LU92327I9 true LU92327I9 (fr) | 2019-01-16 |
Family
ID=38218600
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
LU92327C LU92327I2 (fr) | 2005-12-23 | 2013-12-05 | Ponatinib sous toutes ses formes telles que protégées par le brevet de base |
Country Status (20)
Country | Link |
---|---|
US (9) | US8114874B2 (fr) |
EP (4) | EP1973545B1 (fr) |
JP (3) | JP5200939B2 (fr) |
KR (1) | KR101436303B1 (fr) |
CN (1) | CN103044432B (fr) |
AU (1) | AU2006331673B2 (fr) |
CA (1) | CA2634923C (fr) |
CY (3) | CY1113907T1 (fr) |
DK (2) | DK2495016T3 (fr) |
EA (2) | EA027573B1 (fr) |
ES (2) | ES2403206T3 (fr) |
HU (2) | HUE047422T2 (fr) |
IL (2) | IL191938A (fr) |
LT (1) | LT2495016T (fr) |
LU (1) | LU92327I2 (fr) |
MX (2) | MX2008008152A (fr) |
PL (2) | PL1973545T3 (fr) |
PT (2) | PT2495016T (fr) |
SI (1) | SI2495016T1 (fr) |
WO (1) | WO2007075869A2 (fr) |
Families Citing this family (96)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8071609B2 (en) | 2005-08-11 | 2011-12-06 | Ariad Pharmaceuticals, Inc. | Unsaturated heterocyclic derivatives |
WO2007075869A2 (fr) * | 2005-12-23 | 2007-07-05 | Ariad Pharmaceuticals, Inc. | Composes heteroaryles bicycliques |
MX2008014290A (es) * | 2006-05-08 | 2008-11-26 | Ariad Pharma Inc | Compuestos heteroarilicos monociclicos. |
CN103435595A (zh) | 2006-05-08 | 2013-12-11 | 阿里亚德医药股份有限公司 | 炔类杂芳基化合物 |
CA2660836A1 (fr) | 2006-08-07 | 2008-02-21 | Incyte Corporation | Utilisation de triazolotriazines en tant qu'inhibiteurs des kinases |
US8143410B2 (en) | 2006-11-16 | 2012-03-27 | Allergan, Inc. | Kinase inhibitors |
US8558002B2 (en) | 2006-11-16 | 2013-10-15 | Allergan, Inc. | Sulfoximines as kinase inhibitors |
CA2669704A1 (fr) | 2006-11-16 | 2008-05-22 | Allergan, Inc. | Sulfoximines en tant qu'inhibiteurs de la kinase |
EA026126B1 (ru) | 2006-11-22 | 2017-03-31 | Инсайт Холдингс Корпорейшн | Имидазотриазины и имидазопиримидины в качестве ингибиторов киназы |
EP2070929A1 (fr) * | 2007-12-11 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | Composés d'alkynylaryle et sels correspondants, compositions pharmaceutiques contenant ceux-ci, procédés de préparation de ceux-ci et usage de ceux-ci |
WO2009143211A2 (fr) | 2008-05-21 | 2009-11-26 | Incyte Corporation | Sels de 2-fluoro-n-méthyl-4-[7-(quinoléin-6-yl-méthyl)- imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide et procédés associés à leur préparation |
FR2933981A1 (fr) * | 2008-07-18 | 2010-01-22 | Sanofi Aventis | NOUVEAUX DERIVES IMIDAZO°1,2-a!PYRIDINE, LEUR PROCEDE DE PREPARATION, LEUR APPLICATION A TITRE DE MEDICAMENTS, COMPOSITIONS PHARMACEUTIQUES ET NOUVELLE UTILISATION NOTAMMENT COMME INHIBITEURS DE MET |
US8455477B2 (en) * | 2008-08-05 | 2013-06-04 | Merck Sharp & Dohme Corp. | Therapeutic compounds |
CA2743449C (fr) | 2008-11-12 | 2016-10-18 | Ariad Pharmaceuticals, Inc. | Pyrazinopyrazines et derives utiles comme inhibiteurs de kinases |
JP2013509444A (ja) * | 2009-10-30 | 2013-03-14 | アリアド・ファーマシューティカルズ・インコーポレイテッド | がんの治療方法及び治療用組成物 |
AU2010343102B2 (en) | 2009-12-29 | 2016-03-24 | Dana-Farber Cancer Institute, Inc. | Type II Raf kinase inhibitors |
BR112012019302B1 (pt) | 2010-02-03 | 2022-06-21 | Incyte Holdings Corporation | Imidazo[1,2-b] [1,2,4]triazinas como inibidores de c-met, composição que as compreende e métodos in vitro de inibir a atividade de c-met cinase, de inibir a via de sinalização da hgf/c-met cinase em uma célula e de inibir a atividade proliferativa de uma célula |
CN101885722B (zh) * | 2010-07-01 | 2013-07-24 | 中国科学院广州生物医药与健康研究院 | 杂环炔苯类化合物及其药用组合物和应用 |
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 |
US9024021B2 (en) | 2011-01-21 | 2015-05-05 | Sun Pharma Advanced Research Company Ltd. | Diarylacetylene hydrazide containing tyrosine kinase inhibitors |
WO2012127030A1 (fr) * | 2011-03-23 | 2012-09-27 | Proteosys Ag | Arylpipérazines en tant qu'agents neuroprotecteurs |
KR20140022062A (ko) * | 2011-04-07 | 2014-02-21 | 어리어드 파마슈티칼스, 인코포레이티드 | 파킨슨병을 치료하기 위한 방법 및 조성물 |
WO2012139027A1 (fr) * | 2011-04-07 | 2012-10-11 | Ariad Pharmaceuticals, Inc. | Procédés et compositions pour le traitement de maladies neurodégénératives |
RU2477723C2 (ru) * | 2011-06-16 | 2013-03-20 | Общество С Ограниченной Ответственностью "Фьюжн Фарма" | Ингибиторы протеинкиназ (варианты), их применение для лечения онкологических заболеваний и фармацевтическая композиция на их основе |
AU2012340200B2 (en) | 2011-11-17 | 2017-10-12 | Dana-Farber Cancer Institute, Inc. | Inhibitors of c-Jun-N-Terminal Kinase (JNK) |
WO2013162727A1 (fr) * | 2012-04-25 | 2013-10-31 | Ariad Pharmaceuticals, Inc. | Procédés et compositions pour le traitement de maladies médiées par la kinase raf |
US9254288B2 (en) * | 2012-05-07 | 2016-02-09 | The Translational Genomics Research Institute | Susceptibility of tumors to tyrosine kinase inhibitors and treatment thereof |
WO2013170770A1 (fr) * | 2012-05-16 | 2013-11-21 | 上海医药集团股份有限公司 | Dérivés d'acétylène ayant une activité antitumorale |
US8859553B2 (en) * | 2012-07-30 | 2014-10-14 | Astar Biotech Llc | Protein kinase inhibitors |
WO2014028595A1 (fr) * | 2012-08-14 | 2014-02-20 | Concert Pharmaceuticals, Inc. | Ponatinib deutéré |
CN103664787B (zh) * | 2012-09-17 | 2015-09-09 | 南京圣和药业股份有限公司 | 炔杂芳环化合物及其应用 |
US10112927B2 (en) | 2012-10-18 | 2018-10-30 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (CDK7) |
WO2014063061A1 (fr) | 2012-10-19 | 2014-04-24 | Dana-Farber Cancer Institute, Inc. | Petites molécules marquées de façon hydrophobe en tant qu'inducteurs de la dégradation de protéine |
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 (zh) * | 2012-11-14 | 2017-03-21 | 加拓科學公司 | 作爲pi3激酶調節劑的芳雜環化合物及其使用方法和用途 |
CN103848829B (zh) | 2012-11-28 | 2017-04-12 | 南京圣和药业股份有限公司 | 杂芳基炔烃化合物及其应用 |
CA3022250A1 (fr) * | 2012-12-12 | 2014-06-12 | Ariad Pharmaceuticals, Inc. | Formes cristallines de 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-n-{4-[(4-methylpiperaz in-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 |
US9725454B2 (en) | 2013-07-04 | 2017-08-08 | Sandoz Ag | Crystalline forms of ponatinib hydrochloride |
CN104341416B (zh) * | 2013-07-31 | 2017-03-29 | 南京圣和药业股份有限公司 | 蛋白酪氨酸激酶抑制剂及其应用 |
GB2518873A (en) * | 2013-10-03 | 2015-04-08 | Agency Science Tech & Res | Bicyclic alkyne derivatives and uses thereof |
CA2927917C (fr) | 2013-10-18 | 2022-08-09 | Syros Pharmaceuticals, Inc. | Composes heteroaromatiques utiles pour le traitement des maladies proliferatives |
US10047070B2 (en) | 2013-10-18 | 2018-08-14 | Dana-Farber Cancer Institute, Inc. | Polycyclic inhibitors of cyclin-dependent kinase 7 (CDK7) |
US9636340B2 (en) | 2013-11-12 | 2017-05-02 | Ayyappan K. Rajasekaran | Kinase inhibitors |
CN104650086A (zh) * | 2013-11-22 | 2015-05-27 | 天津市汉康医药生物技术有限公司 | 盐酸帕纳替尼化合物 |
WO2015085971A1 (fr) | 2013-12-09 | 2015-06-18 | Zentiva, K.S. | Sel bromhydrate de 3-(2-imidazo[1,2-b]pyridazin-3-yl-éthynyl)-4-méthyl-n-[4-[(4-méthyl-1-pipérazinyl)méthyl]-3-(trifluorométhyl)phényl]benzamide |
WO2015085972A1 (fr) | 2013-12-09 | 2015-06-18 | Zentiva, K.S. | Nouveaux sels de 3-(2-imidazo[1,2-b]pyridazin-3-yl-éthynyl)-4-méthyl-n-[4-[(4-méthyl-1-pipérazinyl)méthyl]-3-(trifluorométhyl)phényl]benzamide |
WO2015085973A1 (fr) | 2013-12-09 | 2015-06-18 | Zentiva, K.S. | Modifications de sel de chlorhydrate de 3-(2-imidazo[1,2-b]pyridazine-3-yléthynyl)-4-méthyl-n-[4-[(4-méthyl-1-pipérazinyl)méthyl]-3-(trifluorométhyl)phényl] benzamide |
CN104496995A (zh) * | 2014-01-06 | 2015-04-08 | 广东东阳光药业有限公司 | 制备3-乙炔基咪唑并[1,2-b]哒嗪的方法 |
GB2522226A (en) * | 2014-01-17 | 2015-07-22 | Agency Science Tech & Res | Heteroaryl alkyne derivatives and uses thereof |
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WO2015164614A1 (fr) | 2014-04-23 | 2015-10-29 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de janus kinase et leurs utilisations |
BR112016028674A2 (pt) | 2014-06-06 | 2017-08-22 | Natco Pharma Ltd | ?1h-1, 8-naftiridin-2-onas como compostos antiproliferativos? |
CA2952083C (fr) | 2014-07-17 | 2023-01-24 | Sunshine Lake Pharma Co., Ltd. | Derives d'uree substitues et utilisations pharmaceutiques de ceux-ci |
WO2016059220A1 (fr) | 2014-10-16 | 2016-04-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Agents d'activation du tcr à utiliser dans le traitement de la lla-t |
JP6854762B2 (ja) | 2014-12-23 | 2021-04-07 | 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 | サイクリン依存性キナーゼ7(cdk7)の阻害剤 |
CN105837575B (zh) * | 2015-01-13 | 2019-01-15 | 四川大学 | 3-乙炔基吡唑并嘧啶衍生物及其制备方法和用途 |
EP3273966B1 (fr) | 2015-03-27 | 2023-05-03 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinases cycline-dépendantes |
CN106167491A (zh) * | 2015-05-19 | 2016-11-30 | 重庆大学 | 一种有效抑制肺癌转移的化合物及其应用 |
WO2016201203A1 (fr) * | 2015-06-11 | 2016-12-15 | Apicore Us Llc | Procédés de fabrication de ponatinib et de ses intermédiaires |
EP3307728A4 (fr) | 2015-06-12 | 2019-07-17 | Dana Farber Cancer Institute, Inc. | Thérapie d'association utilisant des inhibiteurs de transcription et des inhibiteurs de kinases |
WO2017044623A1 (fr) * | 2015-09-09 | 2017-03-16 | Lau Warren C | Méthodes, compositions et utilisations de nouveaux inhibiteurs de la kinase fyn |
JP7028766B2 (ja) | 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 | サイクリン依存性キナーゼの阻害剤 |
WO2017152126A1 (fr) | 2016-03-03 | 2017-09-08 | Cornell University | Inhibiteurs ire1-alpha à petites molécules |
US10722484B2 (en) | 2016-03-09 | 2020-07-28 | K-Gen, Inc. | Methods of cancer treatment |
WO2017222287A1 (fr) * | 2016-06-20 | 2017-12-28 | 재단법인 대구경북첨단의료산업진흥재단 | Nouveau dérivé d'imidazopyridine, son procédé de préparation, et composition pharmaceutique contenant celui-ci comme principe actif pour la prévention ou le traitement du cancer |
WO2018002958A1 (fr) | 2016-06-30 | 2018-01-04 | Sun Pharma Advanced Research Company Limited | Nouveaux composés contenant de l'hydrazide utilisés comme inhibiteurs de btk |
US10221184B2 (en) | 2017-01-20 | 2019-03-05 | Apicore Us Llc | Polymorphs of ponatinib hydrochloride |
MA47793A (fr) * | 2017-03-15 | 2020-01-22 | Sun Pharma Advanced Res Co Ltd | Nouvelle dispersion amorphe d'hydrazide n'- (2-chloro-6-méthyl-benzoyl) d'acide 4-méthyl-3-quinoline-3-yléthynyle-benzoïque |
CA3056356A1 (fr) | 2017-03-15 | 2018-09-20 | Sun Pharma Advanced Research Company Limited | Nouvelle dispersion amorphe d'acide cyclopropanecarboxylique (5-{5-[ n'-(2-chloro-6-methylbenzoyl) hydrazinocarbonyl] -2-methyl-phenylethynyl}-pyridin-2-yl) amide |
US11072620B2 (en) | 2017-06-20 | 2021-07-27 | Apotex Inc. | Crystalline forms of Ponatinib hydrochloride |
JP7024960B2 (ja) * | 2017-10-04 | 2022-02-24 | 国立大学法人京都大学 | Bcr-Ablタンパク質イメージング用分子プローブ |
WO2019246479A1 (fr) | 2018-06-22 | 2019-12-26 | Johnson Matthey Public Limited Company | Forme de ponatinib |
US11840535B2 (en) | 2018-07-02 | 2023-12-12 | Shenzhen Targetrx, Inc. | Alkynyl(hetero)aromatic compound for inhibiting protein kinase activity |
EP3808746B1 (fr) * | 2018-07-17 | 2023-08-02 | Shenzhen TargetRx, Inc. | Dérivés de n-[3-[2-[8-[(1h-pyrazol-4-yl)amino]imidazo[1,2-a]pyrazin-3-yl]éthynyl]phényl]-benzamide et composés similaires en tant qu'inhibiteurs de protéine kinase pour le traitement du cancer |
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