MA39286A - Formes cristallines d'inhibiteurs de la tyrosine kinase et leurs sels - Google Patents

Formes cristallines d'inhibiteurs de la tyrosine kinase et leurs sels

Info

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
Application number
MA039286A
Other languages
English (en)
Inventor
Ling Wang
Jay Jie-Qiang Wu
Original Assignee
Mundipharma International Corporation Ltd
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
Application filed by Mundipharma International Corporation Ltd filed Critical Mundipharma International Corporation Ltd
Publication of MA39286A publication Critical patent/MA39286A/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/20Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • 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]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against 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.
MA039286A 2014-09-17 2015-09-02 Formes cristallines d'inhibiteurs de la tyrosine kinase et leurs sels MA39286A (fr)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

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

Similar Documents

Publication Publication Date Title
MA39286A (fr) Formes cristallines d'inhibiteurs de la tyrosine kinase et leurs sels
EP3434673A4 (fr) Forme polycristalline de base libre ou de sel d'acide d'inhibiteur d'egfr, procédé pour sa préparation et application
WO2015132799A3 (fr) Nouveaux composés hétérocycliques
PH12019501707A1 (en) N-[4-fluoro-5-[[(2s,4s)-2-methyl-4-[(5-methyl-1,2,4-oxadiazol-3-yl)methoxy]-1-piperidyl]methyl]thiazol-2-yl]acetamide as oga inhibitor
EP3552611A4 (fr) Composition pharmaceutique pour la prévention ou le traitement du cancer, comprenant un polymorphe cristallin d'hexoxyde de tétraarsenic
EP4616908A3 (fr) Oxystérols et leurs procédés d'utilisation
MA45130B1 (fr) Polymorphes du n-[(3-fluoro-4-methoxypyridin-2-yl)methyl]-3-(methoxymethyl)-1-((4-[2-oxopyridin-1-yl)methyl]phenyl)methyl)pyrazole-4-carboxamide en tant qu'inhibiteurs de kallikrein
SA519401322B1 (ar) مركبات أريل كربوكساميد غير متجانسة كمثطبات لكيناز بروتين سيرين/ ثريونين متداخل مع المستقبل 2
PH12015502110A1 (en) Crystalline forms of tyrosine kinase inhibitors and their salts
MA41633B1 (fr) Composés amide en tant qu'agonistes du récepteur 5-ht4
EA201791226A1 (ru) Композиции, содержащие 2-((1-(2-(4-фторфенил)-2-оксоэтил)пиперидин-4-ил)метил)изоиндолин-1-он для лечения шизофрении
MA55917A (fr) Procédé de cristallisation de dérivés d'aripiprazole dans des formulations à libération prolongée pour le traitement de la schizophrénie
JOP20190050A1 (ar) مثبطات دوبامين-b-هيدروكسيلاز تخترق حاجز المخ الدموي
EA202092146A1 (ru) Производные пиразотетрагидроизохинолина в качестве положительных модуляторов допаминового d1 рецептора
EA201890525A1 (ru) Кристаллическая форма 2-(2,6-дихлорфенил)-1-[(1s,3r)-3-(гидроксиметил)-5-(3-гидрокси-3-метилбутил)-1-метил-3,4-дигидроизохинолин-2(1h)-ил]этанона для лечения болезни паркинсона
PE20181003A1 (es) Compuestos terapeuticos y sus metodos de uso
PE20091617A1 (es) Tiazolil-dihidro-indazoles
EP4021920A4 (fr) Procédé amélioré pour la préparation de chlorhydrate d'ételcalcétide
EP3612167A4 (fr) Procédé de préparation d'une forme posologique à désintégration orale
EP3445763A4 (fr) Nouvelles formes de sel cristallin du 3-(1,2,4-triazolo[4,3-a]pyridin-3-yléthynyl)-4-méthyl-n-(4-((4-méthylpipérazin-1-yl)méthyl)-3-trifluorométhylphényl)benzamide pour une application médicale
EP3315135A4 (fr) Composition pour la prévention ou le traitement de l'entérite ischémique contenant un mélange de fragments d'adn isolés à partir de sperme ou de testicules de poisson
MA40345A (fr) Nouvelle forme polymorphe de chlorhydrate de n-[2-(6-fluoro-lh-indol-3-yl)éthyl]-3-(2,2,3,3-tétrafluoropropoxy) benzylamine pour le de traitement de la maladie d'alzheimer
EP4065559C0 (fr) Procédé amélioré pour la préparation de chlorure de 4-methylammonium-2,2,6,6-tetramethylpiperidine
TH128480A (th) สารประกอบที่เป็นประโยชน์เพื่อการยับยั้ง chk1
BR122018070836A8 (pt) Compostos de amidas heterocíclicas moduladoras de sting, composição contendo ditos compostos e uso dos mesmos para tratar uma doença mediada por sting