MA39286A - Formes cristallines d'inhibiteurs de la tyrosine kinase et leurs sels - Google Patents
Formes cristallines d'inhibiteurs de la tyrosine kinase et leurs selsInfo
- Publication number
- MA39286A MA39286A MA039286A MA39286A MA39286A MA 39286 A MA39286 A MA 39286A MA 039286 A MA039286 A MA 039286A MA 39286 A MA39286 A MA 39286A MA 39286 A MA39286 A MA 39286A
- Authority
- MA
- Morocco
- Prior art keywords
- salts
- tyrosine kinase
- kinase inhibitors
- crystalline forms
- cyclohexylpiperazin
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title 1
- 229940121358 tyrosine kinase inhibitor Drugs 0.000 title 1
- 239000005483 tyrosine kinase inhibitor Substances 0.000 title 1
- -1 (3- (4-cyclohexylpiperazin-1-yl) -6-oxo-6h-anthra [1,9-cd] isoxazol-5-yl) amino Chemical group 0.000 abstract 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/20—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- 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]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicinal Preparation (AREA)
Abstract
L'invention concerne diverses formes polymorphes et la forme amorphe du 4 - ((3- (4-cyclohexylpipérazin-1-yl) -6-oxo-6h-anthra [1,9-cd] isoxazol-5-yl) amino) le benzoate, y compris la forme polymorphe a, les mélanges des polymorphes, le procédé pour la préparation de ceux-ci et leur utilisation dans une composition pharmaceutique la contenant.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462051698P | 2014-09-17 | 2014-09-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA39286A true MA39286A (fr) | 2016-03-24 |
Family
ID=55533687
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA039286A MA39286A (fr) | 2014-09-17 | 2015-09-02 | Formes cristallines d'inhibiteurs de la tyrosine kinase et leurs sels |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US10301271B2 (fr) |
| EP (1) | EP3193874A4 (fr) |
| JP (1) | JP2017529356A (fr) |
| AU (1) | AU2015318324A1 (fr) |
| CA (1) | CA2962206A1 (fr) |
| IL (1) | IL251197A0 (fr) |
| MA (1) | MA39286A (fr) |
| MX (1) | MX2017003439A (fr) |
| WO (1) | WO2016043975A1 (fr) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5752601B2 (ja) | 2008-12-08 | 2015-07-22 | ブイエム ファーマ エルエルシー | タンパク質受容体チロシンキナーゼ阻害薬の組成物 |
| US8999992B2 (en) | 2013-03-15 | 2015-04-07 | Vm Pharma Llc | Crystalline forms of tryosine kinase inhibitors and their salts |
| US20180370926A1 (en) * | 2015-08-07 | 2018-12-27 | Purdue Pharma L.P. | Process of preparing tyrosine kinase inhibitor |
| WO2017161235A1 (fr) | 2016-03-18 | 2017-09-21 | Purdue Pharma L. P. | Procédé pour préparer des 9,10-dioxo-9,10-dioxo-9,10-dihydroanthrécènes et des 6h-anthra(1,9-cd)isoxazol-6-ones substitués |
| US12240813B2 (en) | 2020-05-19 | 2025-03-04 | Cybin Irl Limited | Deuterated tryptamine derivatives and methods of use |
| WO2023168023A1 (fr) | 2022-03-04 | 2023-09-07 | Reset Pharmaceuticals, Inc. | Co-cristaux ou sels comprenant de la psilocine |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1062357A (en) | 1965-03-23 | 1967-03-22 | Pfizer & Co C | Quinazolone derivatives |
| US4337341A (en) | 1976-11-02 | 1982-06-29 | Eli Lilly And Company | 4a-Aryl-octahydro-1H-2-pyrindines |
| DE3815221C2 (de) | 1988-05-04 | 1995-06-29 | Gradinger F Hermes Pharma | Verwendung einer Retinol- und/oder Retinsäureester enthaltenden pharmazeutischen Zubereitung zur Inhalation zur Einwirkung auf die Schleimhäute des Tracheo-Bronchialtraktes einschließlich der Lungenalveolen |
| US5698155A (en) | 1991-05-31 | 1997-12-16 | Gs Technologies, Inc. | Method for the manufacture of pharmaceutical cellulose capsules |
| RU2065438C1 (ru) | 1993-12-22 | 1996-08-20 | Институт химии природного органического сырья СО РАН | Способ получения производных 3-фенилокси-5-гидроксиантра (1,9-cd)-изоксазол-6-она |
| US6635626B1 (en) | 1997-08-25 | 2003-10-21 | Bristol-Myers Squibb Co. | Imidazoquinoxaline protein tyrosine kinase inhibitors |
| US5998463A (en) | 1998-02-27 | 1999-12-07 | Pfizer Inc | Glycogen phosphorylase inhibitors |
| US6476032B2 (en) | 1998-12-17 | 2002-11-05 | Wyeth | 2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5(6H)one derivatives |
| AU5179000A (en) | 1999-06-03 | 2000-12-28 | Basf Aktiengesellschaft | Benzothiazinone and benzoxazinone compounds |
| FR2807660A1 (fr) | 2000-04-13 | 2001-10-19 | Warner Lambert Co | Utilisation d'antagonistes du ngf pour la prevention ou le traitement de douleurs viscerales chroniques |
| EP1430053B1 (fr) | 2001-09-27 | 2006-10-25 | SmithKline Beecham Corporation | DERIVES D'AZAOXOINDOLES EN TANT QU'INHIBITEURS DE PROTEINE KINASE Trk POUR LE TRAITEMENT DE CANCER ET DE LA DOULEUR CHRONIQUE |
| KR20030095729A (ko) | 2002-06-14 | 2003-12-24 | 크리스탈지노믹스(주) | 2-[5-(3-카복시-4-클로로-페닐)-푸란-2-일메틸렌]-3-옥소-2,3-디하이드로-5H-티아졸로[3,2-a]피리미딘-6-카복실산에틸 에스테르 유도체를 포함하는 단백질 티로신포스파타제 1B 활성 억제용 약학 조성물 |
| ZA200502612B (en) | 2002-10-08 | 2007-07-25 | Rinat Neuroscience Corp | Methods for treating post-surgical pain by administering a nerve crowth factor antagonist and compositions containing the same |
| UA80447C2 (en) | 2002-10-08 | 2007-09-25 | Methods for treating pain by administering nerve growth factor antagonist and opioid analgesic | |
| IL154370A0 (en) | 2003-02-10 | 2003-09-17 | Chemagis Ltd | Solid amorphous mixtures, processes for the preparation thereof and pharmaceutical compositions containing the same |
| JP4733023B2 (ja) | 2003-04-16 | 2011-07-27 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎ウイルスの大環状イソキノリンペプチド阻害剤 |
| EP1663962A4 (fr) | 2003-08-22 | 2007-08-22 | Dendreon Corp | Compositions et methodes permettant de traiter une maladie associee a l'expression de trp-p8 |
| WO2008021463A2 (fr) | 2006-08-15 | 2008-02-21 | Acadia Pharmaceuticals, Inc. | Analogues de diaryl[a,d]cycloheptène à substitution amino, utilisés comme agonistes muscariniques et méthodes de traitement de troubles neuropsychiatriques |
| EP3372614B1 (fr) | 2004-04-07 | 2022-06-08 | Rinat Neuroscience Corp. | Méthodes de traitement de la douleur associée au cancer des os par administration d'un antagoniste des facteurs de croissance neuronale |
| WO2006007864A1 (fr) | 2004-07-17 | 2006-01-26 | Max Planck Geselllschaft Zur Förderung Der Wissenschaft | Traitement d'etats neurodegeneratifs |
| US7671077B2 (en) | 2004-07-19 | 2010-03-02 | Leu-Fen Hou Lin | Neuroprotective small organic molecules, compositions and uses related thereto |
| US7718674B2 (en) * | 2004-09-27 | 2010-05-18 | Bridge Pharma, Inc. | Methods of relieving neuropathic pain with the S-isomer of 2-{2[N-(2-indanyl)-N-phenylamino]ethyl}piperidine |
| US7820668B2 (en) | 2005-01-19 | 2010-10-26 | Eisai Inc. | Diazabenzo[de]anthracen-3-one compounds and methods for inhibiting PARP |
| FR2881138B1 (fr) | 2005-01-27 | 2007-03-02 | Servier Lab | Nouveaux derives d'oximes heterocycliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| US20060257337A1 (en) | 2005-04-28 | 2006-11-16 | David Sherris | Compositions and methods to treat skin diseases characterized by cellular proliferation and angiogenesis |
| JP5191155B2 (ja) | 2006-03-27 | 2013-04-24 | 大塚製薬株式会社 | カルボスチリル化合物からなる医薬 |
| WO2008053863A1 (fr) | 2006-10-30 | 2008-05-08 | Santen Pharmaceutical Co., Ltd. | Nouveau composé ayant un squelette de 1,4-benzothiazin-3-one ou un squelette de 3,4-dihydroquinolin-2-one |
| CA2672860C (fr) | 2006-12-28 | 2013-01-29 | Abbott Laboratories | Inhibiteurs de poly(adp-ribose)polymerase |
| EP2218713A1 (fr) * | 2007-08-17 | 2010-08-18 | Hetero Drugs Limited | Forme A du polymorphe de chlorhydrate d'erlotinibe sensiblement dépourvue de la forme B du polymorphe |
| JP5662801B2 (ja) | 2007-11-16 | 2015-02-04 | ホリンワース ファンド,エル.エル.シー. | フィルタ設計方法およびメタマテリアル構造ベースのフィルタ |
| JP5752601B2 (ja) | 2008-12-08 | 2015-07-22 | ブイエム ファーマ エルエルシー | タンパク質受容体チロシンキナーゼ阻害薬の組成物 |
| EP2239256A1 (fr) | 2009-03-13 | 2010-10-13 | Almirall, S.A. | Sel de sodium de l'acide 5-cyclopropyl-2-{[2-(2,6-difluorophényl)pyrimidin-5-yl]amino}benzoïque en tant qu'inhibiteurs de la DHOD |
| US8853235B2 (en) | 2009-11-23 | 2014-10-07 | Senhwa Biosciences, Inc. | Polymorphs and salts of a kinase inhibitor |
| US20130158264A1 (en) * | 2010-06-23 | 2013-06-20 | Arlindo L. Castelhano | Polymorphs of OSI-906 |
| ES2637113T3 (es) | 2011-01-10 | 2017-10-10 | Infinity Pharmaceuticals, Inc. | Procedimientos para preparar isoquinolinonas y formas sólidas de isoquinolinonas |
| WO2012119079A1 (fr) | 2011-03-03 | 2012-09-07 | Indiana University Research And Technology Corporation | Inhibiteurs d'interaction upar-upa et procédés pour traiter le cancer |
| US8999992B2 (en) | 2013-03-15 | 2015-04-07 | Vm Pharma Llc | Crystalline forms of tryosine kinase inhibitors and their salts |
-
2015
- 2015-09-02 AU AU2015318324A patent/AU2015318324A1/en not_active Abandoned
- 2015-09-02 JP JP2017514882A patent/JP2017529356A/ja active Pending
- 2015-09-02 CA CA2962206A patent/CA2962206A1/fr not_active Abandoned
- 2015-09-02 WO PCT/US2015/048123 patent/WO2016043975A1/fr not_active Ceased
- 2015-09-02 US US15/511,946 patent/US10301271B2/en active Active
- 2015-09-02 EP EP15841380.7A patent/EP3193874A4/fr not_active Withdrawn
- 2015-09-02 MX MX2017003439A patent/MX2017003439A/es unknown
- 2015-09-02 MA MA039286A patent/MA39286A/fr unknown
-
2017
- 2017-03-15 IL IL251197A patent/IL251197A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US20170313666A1 (en) | 2017-11-02 |
| MX2017003439A (es) | 2017-12-04 |
| WO2016043975A1 (fr) | 2016-03-24 |
| IL251197A0 (en) | 2017-05-29 |
| JP2017529356A (ja) | 2017-10-05 |
| US10301271B2 (en) | 2019-05-28 |
| EP3193874A1 (fr) | 2017-07-26 |
| EP3193874A4 (fr) | 2018-04-25 |
| AU2015318324A1 (en) | 2017-04-06 |
| CA2962206A1 (fr) | 2016-03-24 |
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