MA53978A - Formes cristallines de modulateurs des canaux potassiques - Google Patents

Formes cristallines de modulateurs des canaux potassiques

Info

Publication number
MA53978A
MA53978A MA053978A MA53978A MA53978A MA 53978 A MA53978 A MA 53978A MA 053978 A MA053978 A MA 053978A MA 53978 A MA53978 A MA 53978A MA 53978 A MA53978 A MA 53978A
Authority
MA
Morocco
Prior art keywords
crystalline forms
potassium channel
channel modulators
modulators
potassium
Prior art date
Application number
MA053978A
Other languages
English (en)
Inventor
Gregg F Keaney
Jun Xu
Wenfeng Xue
Original Assignee
Cadent Therapeutics 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
Application filed by Cadent Therapeutics Inc filed Critical Cadent Therapeutics Inc
Publication of MA53978A publication Critical patent/MA53978A/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/10Drugs for disorders of the urinary system of the bladder
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • A61P9/00Drugs for disorders of the cardiovascular system
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Cardiology (AREA)
  • Epidemiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
MA053978A 2018-10-22 2019-10-21 Formes cristallines de modulateurs des canaux potassiques MA53978A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201862748632P 2018-10-22 2018-10-22

Publications (1)

Publication Number Publication Date
MA53978A true MA53978A (fr) 2021-09-01

Family

ID=68503217

Family Applications (1)

Application Number Title Priority Date Filing Date
MA053978A MA53978A (fr) 2018-10-22 2019-10-21 Formes cristallines de modulateurs des canaux potassiques

Country Status (12)

Country Link
US (1) US11993586B2 (fr)
EP (1) EP3870291A1 (fr)
JP (1) JP2022508945A (fr)
KR (1) KR20210080446A (fr)
CN (1) CN113226466A (fr)
AU (1) AU2019366312A1 (fr)
BR (1) BR112021007552A2 (fr)
CA (1) CA3116339A1 (fr)
IL (1) IL282348A (fr)
MA (1) MA53978A (fr)
MX (2) MX2021004647A (fr)
WO (1) WO2020086456A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3116339A1 (fr) 2018-10-22 2020-04-30 Cadent Therapeutics, Inc. Formes cristallines de modulateurs des canaux potassiques

Family Cites Families (202)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3040047A (en) 1960-04-04 1962-06-19 Takeda Pharmaceutical 2-(pyrazol-1-yl)-pyrimidine derivatives
JPS6059883B2 (ja) 1978-05-08 1985-12-27 北興化学工業株式会社 農園芸用殺菌剤
GB2183243B (en) 1985-10-09 1990-01-24 Nippon Oil Co Ltd Process for preparing oil-soluble nitrogen-containing compounds
AU3752589A (en) 1988-05-16 1989-12-12 Georgia State University Research Foundation, Inc. Nucleic acid interacting unfused heteropolycyclic compounds
LU87304A1 (fr) 1988-07-29 1990-02-07 Oreal Nouveaux derives d'ureylene triamino-2,4,6 pyrimidine oxyde-3,leur preparation et leur utilisation en cosmetique et dermopharmacie
JPH02282251A (ja) 1989-04-24 1990-11-19 Fuji Photo Film Co Ltd ハロゲン化銀カラー写真感光材料
DE3922735A1 (de) 1989-07-11 1991-01-24 Hoechst Ag Aminopyrimidin-derivate, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als fungizide
DE4034762A1 (de) 1990-11-02 1992-05-07 Hoechst Ag Pyridylpyrimidine, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als fungizide
GB2263639A (en) 1992-01-28 1993-08-04 Merck & Co Inc Substituted pyrimidinones as neurotensin antagonists
HU209678B (en) 1992-06-09 1994-10-28 Richter Gedeon Vegyeszet Process for producing biologically active eburnamenin-14-carbonyl-amino derivatives and pharmaceutical compositions containing them
DK72693D0 (da) 1993-06-18 1993-06-18 Lundbeck & Co As H Compounds
CA2133355A1 (fr) 1993-10-04 1995-04-05 Itaru Nitta Methode de preparation de polypeptide
WO1998006709A1 (fr) 1996-08-14 1998-02-19 Takeda Chemical Industries, Ltd. Composes d'urees cycliques, leur production et leur utilisation comme herbicides
DE19642863A1 (de) 1996-10-17 1998-04-23 Bayer Ag Amide
US6117973A (en) 1997-02-24 2000-09-12 Georgia Tech Research Corp. PNA monomers with electron donor or acceptor
JPH11158073A (ja) 1997-09-26 1999-06-15 Takeda Chem Ind Ltd アデノシンa3拮抗剤
JPH11282132A (ja) 1998-03-27 1999-10-15 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料の処理方法
JP2000072695A (ja) 1998-08-24 2000-03-07 Sumitomo Pharmaceut Co Ltd 環状化合物
JP2000075449A (ja) 1998-08-31 2000-03-14 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料の現像方法
US6878712B1 (en) 1999-09-04 2005-04-12 Astrazeneca Ab Amides as inhibitors for pyruvate dehydrogenase
WO2001032170A1 (fr) 1999-09-13 2001-05-10 Swope David M Composition et procede pour la reduction de la symptomatologie neurologique
US6906067B2 (en) 1999-12-28 2005-06-14 Bristol-Myers Squibb Company N-heterocyclic inhibitors of TNF-α expression
US20030181507A1 (en) 2000-06-29 2003-09-25 Jensen Bo Skaaning Use of 3-substituted oxindole derivatives as kcnq potassium channel modulators
CA2425259A1 (fr) 2000-10-11 2002-04-18 Tularik, Inc. Modulation de fonction de ccr4
EP1341773A2 (fr) 2000-12-07 2003-09-10 Cv Therapeutics, Inc. Composes d'augmentation d'abca-1
BR0206513A (pt) 2001-01-16 2004-01-06 Astrazeneca Ab Composição, métodos de tratamento de um ser humano ou animal que sofre de depressão, ansiedade generalizada, distúrbios da alimentação, demência, distúrbio do p nico, distúrbios do sono, distúrbios gastrointestinais, distúrbios motores, distúrbios endócrinos, vasoespasmo e disfunção sexual, uso de qualquer um dos compostos, composição farmacêutica, e, processo para preparar compostos
CA2434015A1 (fr) 2001-01-16 2002-07-18 Astrazeneca Ab Composes therapeutiques de chromane
KR100864356B1 (ko) 2001-01-16 2008-10-17 아스트라제네카 아베 치료용 헤테로시클릭 화합물
US20030130264A1 (en) 2001-02-16 2003-07-10 Tularik Inc. Methods of using pyrimidine-based antiviral agents
CN100540538C (zh) 2001-04-16 2009-09-16 田边三菱制药株式会社 高传导率钙-活化k通道开启剂
EP1270551A1 (fr) 2001-06-26 2003-01-02 Aventis Pharma Deutschland GmbH Dérivés d'urée avec une activité antiprotéolytique
US7378432B2 (en) 2001-09-14 2008-05-27 Tel Aviv University Future Technology Development L.P. Glycogen synthase kinase-3 inhibitors
US7012077B2 (en) 2001-12-20 2006-03-14 Hoffmann-La Roche Inc. Substituted cyclohexane derivatives
WO2003075828A2 (fr) 2002-03-11 2003-09-18 Zetiq Technologies Ltd. Composes utiles pour le traitement du cancer
MY141867A (en) 2002-06-20 2010-07-16 Vertex Pharma Substituted pyrimidines useful as protein kinase inhibitors
AU2003245669A1 (en) 2002-06-21 2004-01-06 Cellular Genomics, Inc. Certain aromatic monocycles as kinase modulators
US7235560B2 (en) 2002-08-19 2007-06-26 Glaxo Group Limited Pyrimidine derivative as selective COX-2 inhibitors
WO2004017920A2 (fr) 2002-08-23 2004-03-04 University Of Connecticut Nouveaux cannabinoides biphenyle et de type biphenyle
GB0311201D0 (en) 2003-05-15 2003-06-18 Merck Sharp & Dohme Therapeutic agents
US7589092B2 (en) 2003-06-20 2009-09-15 Koronis Pharmaceuticals, Incorporated Prodrugs of heteroaryl compounds
KR20060041309A (ko) 2003-08-13 2006-05-11 다케다 야쿠힌 고교 가부시키가이샤 4-피리미돈 유도체 및 펩티딜 펩티다제 저해제로서의 그의용도
US7582645B2 (en) 2003-10-10 2009-09-01 Bayer Pharmaceuticals Corporation Pyrimidine derivatives for treatment of hyperproliferative disorders
US7491724B2 (en) 2003-10-17 2009-02-17 Incyte Corporation Substituted cyclic hydroxamates as inhibitors of matrix metalloproteinases
AU2004295050A1 (en) 2003-11-24 2005-06-16 F.Hoffmann-La Roche Ag Pyrazolyl and imidazolyl pyrimidines
TW200528101A (en) 2004-02-03 2005-09-01 Astrazeneca Ab Chemical compounds
NZ549673A (en) 2004-03-30 2010-03-26 Taisho Pharmaceutical Co Ltd Pyrimidine derivatives and methods of treatment related to the use thereof
TWI380816B (zh) 2004-04-13 2013-01-01 Synta Pharmaceuticals Corp 抑制介白素-12(il-12)生成之二鹽抑制劑
SE0401971D0 (sv) 2004-08-02 2004-08-02 Astrazeneca Ab Piperidne derivatives
RU2007110731A (ru) 2004-09-23 2008-10-27 Редди Юс Терапевтикс Новые соединения пиримидина, способ их получения и содержащие их композиции
GB0422556D0 (en) 2004-10-11 2004-11-10 Syngenta Participations Ag Novel insecticides
EP1655283A1 (fr) 2004-11-08 2006-05-10 Evotec OAI AG Inhibiteurs de 11béta-HSD1
TW200628463A (en) 2004-11-10 2006-08-16 Synta Pharmaceuticals Corp Heteroaryl compounds
WO2006065590A2 (fr) 2004-12-16 2006-06-22 Xtl Biopharmaceuticals Inc. Compositions antivirales a base de pyridines et de pyrimidines
AU2005322855B2 (en) 2004-12-30 2012-09-20 Exelixis, Inc. Pyrimidine derivatives as kinase modulators and method of use
BRPI0519774A2 (pt) 2005-01-19 2009-02-10 Biolipox Ab composto ou um sal farmaceuticamente aceitÁvel do mesmo, formulaÇço farmacÊutica, uso de um composto ou um sal farmaceuticamente aceitÁvel do mesmo, mÉtodo de tratamento de uma doenÇa em que inibiÇço da atividade de um membro da famÍlia mapeg É desejada e/ou necessÁria, produto combinado, e, processo para a preparaÇço de um composto
CA2594878A1 (fr) 2005-01-19 2006-07-27 Biolipox Ab Indoles utiles dans le traitement de l'inflammation
JP2008527028A (ja) 2005-01-19 2008-07-24 バイオリポックス エービー 炎症の治療に有用なインドール類
JP2008527030A (ja) 2005-01-19 2008-07-24 バイオリポックス エービー 炎症の治療に有用なインドール類
US20090069384A1 (en) 2005-01-19 2009-03-12 Biolipox Ab Thienopyrroles useful in the treatment of inflammation
US20070135437A1 (en) 2005-03-04 2007-06-14 Alsgen, Inc. Modulation of neurodegenerative diseases
CN101115736A (zh) 2005-03-14 2008-01-30 神经研究公司 钾通道调节剂和它们的医药用途
EP1861388B1 (fr) 2005-03-14 2017-07-05 Saniona A/S Agents modulateurs du canal potassique et leur utilisation medicale
WO2006100212A1 (fr) 2005-03-22 2006-09-28 Neurosearch A/S Pyrazolyl-pyrimidines comme agents de modulation de la voie du potassium et leur utilisation medicale
US20060156481A1 (en) 2005-03-22 2006-07-20 The Procter & Gamble Company Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
US20090036475A1 (en) 2005-03-22 2009-02-05 Neurosearch A/S Pyrazolyl-Pyrimidines as Potassium Channel Modulating Agents and Their Medical Use
DE102005025315A1 (de) 2005-06-02 2006-12-14 Merck Patent Gmbh Ionische Flüssigkeiten mit niedriger Viskosität
CN101198597B (zh) 2005-06-14 2011-11-16 先灵公司 作为天冬氨酰基蛋白酶抑制剂的化合物的制备和用途
US8193206B2 (en) 2005-06-14 2012-06-05 Taigen Biotechnology Co., Ltd. Pyrimidine compounds
US7589197B2 (en) 2005-06-14 2009-09-15 Taigen Biotechnology Pyrimidine compounds
EP2301928A1 (fr) 2005-07-30 2011-03-30 AstraZeneca AB Composés d'imidazolyl-pyrimidine pour utilisation dans le traitement de dérèglements proliferatifs
DE102005043165A1 (de) 2005-09-12 2007-03-22 Merck Patent Gmbh Metallkomplexe
JP2007091649A (ja) 2005-09-29 2007-04-12 Taisho Pharmaceut Co Ltd ピリミジン誘導体及びその使用に関連する治療方法
GB0520657D0 (en) 2005-10-11 2005-11-16 Ludwig Inst Cancer Res Pharmaceutical compounds
FR2892859B1 (fr) 2005-10-27 2008-06-06 Commissariat Energie Atomique Procede de greffage de molecules d'interet sur des surfaces inorganiques, surfaces obtenues et applications
CA2630920A1 (fr) 2005-11-22 2007-05-31 University Of South Florida Inhibition of cell proliferation
CA2633541A1 (fr) 2005-12-12 2007-06-21 Genelabs Technologies, Inc. Composes antiviraux n-(noyau aromatique a 6 chainons) amido
TW200730476A (en) 2005-12-12 2007-08-16 Genelabs Tech Inc N-(5-membered aromatic ring)-amido anti-viral compounds
EP1966184B1 (fr) 2005-12-20 2010-08-25 NeuroSearch A/S Derives de pyridinyl-quinazoline et leur utilisation medicale
EP1993551A4 (fr) 2006-02-01 2011-10-19 Merck Sharp & Dohme Inhibiteurs du canal potassique
AU2007226582B2 (en) 2006-03-13 2012-07-05 Perkinelmer Health Sciences, Inc. Substrates and internal standards for mass spectroscopy detection
US20090318507A2 (en) 2006-05-02 2009-12-24 Chris Rundfeldt Potassium Channel Activators for the Prevention and Treatment of Dystonia and Dystonia Like Symptoms
US8222256B2 (en) 2006-07-05 2012-07-17 Exelixis, Inc. Methods of using IGFIR and ABL kinase modulators
FR2904316B1 (fr) 2006-07-31 2008-09-05 Sanofi Aventis Sa Derives de n-(amino-heteroaryl)-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique.
WO2008016300A2 (fr) 2006-08-03 2008-02-07 Prosensa Technologies B.V. Composition antibiotique
PT2061465E (pt) 2006-08-23 2013-07-15 Valeant Pharmaceuticals Int Derivados de 4-(n-azacicloalquil)anilidas como moduladores do canal de potássio
US20080070930A1 (en) 2006-08-24 2008-03-20 Huang Kenneth H Pyrimidine and Pyrazine Derivatives
EP2066655A2 (fr) 2006-09-07 2009-06-10 Neurosearch A/S Dérivés de pyridinyl-pyrimidine utiles comme agents modulateurs des canaux potassiques
JP2010505794A (ja) 2006-10-03 2010-02-25 ノイロサーチ アクティーゼルスカブ カリウムチャネル調節剤として有用なインダゾリル誘導体
WO2008052861A2 (fr) 2006-10-10 2008-05-08 Proionic Production Of Ionic Substances Gmbh & Co Keg Procédé de production de carbonates 1,3-hétéroaromatiques exempts de 4-carboxylate
TW200827368A (en) 2006-11-21 2008-07-01 Genelabs Tech Inc Amido anti-viral compounds
EP2121662A1 (fr) 2006-12-04 2009-11-25 Neurocrine Biosciences, Inc. Pyrimidines substituées en tant qu'antagonistes des récepteurs de l'adénosine
GB0701426D0 (en) 2007-01-25 2007-03-07 Univ Sheffield Compounds and their use
EA200901065A1 (ru) 2007-02-06 2010-02-26 Новартис Аг Ингибиторы pi 3-киназы и способы их применения
JP5491871B2 (ja) 2007-02-28 2014-05-14 アドビナス セラピュティックス プライベート リミテッド グルコキナーゼ活性化因子としての2,2,2−三置換アセトアミド誘導体、その方法及び薬学的応用
US20080221103A1 (en) 2007-03-09 2008-09-11 Orchid Research Laboratories Ltd. New heterocyclic compounds
US20120004246A1 (en) 2007-03-28 2012-01-05 Neurosearch A/S Purinyl derivatives and their use as potassium channel modulators
EP2132208A1 (fr) 2007-03-28 2009-12-16 NeuroSearch AS Dérivés de purinyle et leur utilisation en tant que modulateurs des canaux potassiques
WO2008125811A1 (fr) 2007-04-11 2008-10-23 Astrazeneca Ab DÉRIVÉS DE N-[HÉTÉROARYLCARBONYL]-S-THIÉNYL-L-ALANINE EN TANT QU'ANTAGONISTES DE L'INTÉGRINE α5β1
US8633186B2 (en) 2007-06-08 2014-01-21 Senomyx Inc. Modulation of chemosensory receptors and ligands associated therewith
US7928111B2 (en) 2007-06-08 2011-04-19 Senomyx, Inc. Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
WO2009017838A2 (fr) 2007-08-01 2009-02-05 Exelixis, Inc. Combinaisons d'inhibiteurs jak-2 et d'autres agents
JP5111039B2 (ja) 2007-09-27 2012-12-26 富士フイルム株式会社 重合性化合物、重合開始剤、および染料を含有する光硬化性組成物
US9089572B2 (en) 2008-01-17 2015-07-28 California Institute Of Technology Inhibitors of p97
ES2582228T3 (es) 2008-02-08 2016-09-09 Shiseido Company, Ltd. Agente de blanqueamiento cutáneo y preparación cutánea externa
WO2009105881A1 (fr) 2008-02-28 2009-09-03 Saint Mary's University Liquides ioniques comprenant des ligands qui contiennent des cycles hétérocycliques chargés positivement utiles en tant que catalyseurs et pour les extractions de métaux
JP2011515462A (ja) 2008-03-27 2011-05-19 アウククランド ウニセルビセス リミテッド 置換されたピリミジン、及びトリアジン、並びに癌療法におけるこれらの使用
US8575338B2 (en) 2008-04-09 2013-11-05 Mitsubishi Tanabe Pharma Corporation Pyrimidine, pyridine and triazine derivatives as maxi-K channel openers
EP2279192B1 (fr) 2008-05-28 2013-10-30 Merck Patent GmbH Liquides ioniques
EP2288602A1 (fr) 2008-06-11 2011-03-02 AstraZeneca AB Dérivés tricycliques de 2,4-diamino-l,3,5-triazine utiles pour le traitement du cancer et de troubles myéloprolifératifs
US9334242B2 (en) 2008-06-16 2016-05-10 Gtx, Inc. Compounds for treatment of cancer
US9447049B2 (en) 2010-03-01 2016-09-20 University Of Tennessee Research Foundation Compounds for treatment of cancer
US8822513B2 (en) 2010-03-01 2014-09-02 Gtx, Inc. Compounds for treatment of cancer
DE102008031480A1 (de) 2008-07-03 2010-01-07 Merck Patent Gmbh Salze enthaltend ein Pyrimidincarbonsäure-Derivat
WO2010015037A1 (fr) 2008-08-08 2010-02-11 Howard Florey Institute Procédés et compositions thérapeutiques
GB0815369D0 (en) 2008-08-22 2008-10-01 Summit Corp Plc Compounds for treatment of duchenne muscular dystrophy
CN102177154A (zh) 2008-09-02 2011-09-07 神经研究公司 吡唑基-嘧啶衍生物及其作为钾通道调节剂的应用
CN101684098A (zh) 2008-09-24 2010-03-31 中国科学院上海药物研究所 一类5-脂氧酶抑制剂及其制备方法、药物组合物和应用
WO2010034707A1 (fr) 2008-09-26 2010-04-01 Neurosearch A/S Dérivés de purinyl-pyrazole substitués et leur utilisation en tant que modulateurs des canaux potassiques
WO2010048149A2 (fr) 2008-10-20 2010-04-29 Kalypsys, Inc. Modulateurs hétérocycliques de gpr119 pour le traitement d'une maladie
GB2465405A (en) 2008-11-10 2010-05-19 Univ Basel Triazine, pyrimidine and pyridine analogues and their use in therapy
WO2010068863A2 (fr) 2008-12-12 2010-06-17 Cystic Fibrosis Foundation Therapeutics, Inc. Composés de pyrimidine et leurs procédés de fabrication et d'utilisation
AR074870A1 (es) 2008-12-24 2011-02-16 Palau Pharma Sa Derivados de pirazolo (1,5-a ) piridina
CA2755935A1 (fr) 2009-02-12 2010-08-19 Astellas Pharma Inc. Derive d'heterocycle
WO2010120994A2 (fr) 2009-04-17 2010-10-21 Wyeth Llc Composés d'uréido-aryl-pyrimidine et de carbamoylaryl-morpholino-pyrimidine, leur utilisation comme inhibiteurs de la kinase mtor et de la kinase pi-3, et leur synthèse
CA2760794C (fr) 2009-05-05 2017-07-25 Dana Farber Cancer Institute Inhibiteurs d'egfr et procedes de traitement de troubles
US8686009B2 (en) 2009-06-25 2014-04-01 Alkermes Pharma Ireland Limited Prodrugs of NH-acidic compounds
WO2010151797A2 (fr) 2009-06-26 2010-12-29 University Of Massachusetts Composés de modulation des protéines de liaison à l'arn et applications associées
AU2010270030B2 (en) 2009-07-08 2015-12-24 Baltic Bio Ab 1, 2, 4-thiazolidin-3-one derivatives and their use in the treatment of cancer
WO2011008931A2 (fr) 2009-07-15 2011-01-20 Cystic Fibrosis Foundation Therapeutics, Inc. Composés arylpyrimidines et thérapie de combinaison comprenant ceux-ci pour traiter une mucoviscidose et des troubles apparentés
WO2011018894A1 (fr) 2009-08-10 2011-02-17 Raqualia Pharma Inc. Dérivés de pyrrolopyrimidine comme modulateurs des canaux potassium
AR077999A1 (es) 2009-09-02 2011-10-05 Vifor Int Ag Antagonistas de pirimidin y triazin-hepcidina
US9340528B2 (en) 2009-09-04 2016-05-17 Bayer Pharma Aktiengesellschaft Substituted aminoquinoxalines as tyrosine threonine kinase inhibitors
AR078278A1 (es) 2009-09-09 2011-10-26 Vifor Int Ag Antagonistas de la tiazol y oxazol hepcidina, composiciones farmaceuticas que los contienen y uso de los mismos para el tratamiento de anemias y enfermedades asociadas a deficiencias de hierro.
WO2011060304A2 (fr) 2009-11-13 2011-05-19 Constar International, Inc. Laveurs d'oxygène, compositions comprenant les laveurs, et articles réalisés à partir des compositions
FR2954317B1 (fr) 2009-12-23 2012-01-27 Galderma Res & Dev Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique
AT509266B1 (de) 2009-12-28 2014-07-15 Tech Universität Wien Substituierte pyridine und pyrimidine
EP2569300A1 (fr) 2010-05-13 2013-03-20 Amgen Inc. Composés azotés hétérocycliques convenant comme inhibiteurs de la pde10
WO2012009258A2 (fr) 2010-07-13 2012-01-19 Edward Roberts Modulateurs des récepteurs à la galanine peptidomimétiques
KR20120018236A (ko) 2010-07-23 2012-03-02 현대약품 주식회사 치환된 피리미디닐 유도체 및 이의 제조방법
WO2012016133A2 (fr) 2010-07-29 2012-02-02 President And Fellows Of Harvard College Inhibiteurs de la ros1 kinase pour le traitement de glioblastome et d'autres cancers déficients en p53
EP2606033A1 (fr) 2010-08-20 2013-06-26 Grünenthal GmbH Dérivés de carboxamide et d'urée cycliques substitués en tant que ligands du récepteur vanilloïde
CN103189357B (zh) 2010-08-27 2015-11-25 格吕伦塔尔有限公司 作为kcnq2/3调节剂的取代的2-氧代-和2-硫代-二氢喹啉-3-甲酰胺
WO2012050884A2 (fr) 2010-09-28 2012-04-19 President And Fellows Of Harvard College Glycosides cardiaques qui sont de puissants inhibiteurs de l'expression du gène de l'interféron bêta
JP2013542562A (ja) 2010-09-30 2013-11-21 ビーエーエスエフ ソシエタス・ヨーロピア 電解質用添加剤
EP2630136A1 (fr) 2010-10-21 2013-08-28 Universität des Saarlandes Inhibiteurs sélectifs de cyp11b1 pour le traitement de maladies dépendantes du cortisol
WO2012080729A2 (fr) 2010-12-14 2012-06-21 Electrophoretics Limited Inhibiteurs de caséine kinase 1δ (ck1δ)
US8987271B2 (en) 2010-12-22 2015-03-24 Eutropics Pharmaceuticals, Inc. 2,2′-biphenazine compounds and methods useful for treating disease
US9290591B2 (en) 2011-02-08 2016-03-22 President And Fellows Of Harvard College Iron complexes and methods for polymerization
EP2683703B1 (fr) 2011-03-08 2015-05-27 Sanofi Nouveaux dérivés phényl-oxathiazine substitués, procédé pour leur préparation, agent pharmaceutique contenant ces composés et leur utilisation
WO2012129562A2 (fr) 2011-03-24 2012-09-27 The Scripps Research Institute Composés et procédés pour l'induction de la chondrogenèse
CN102731492B (zh) 2011-03-30 2016-06-29 江苏恒瑞医药股份有限公司 环己烷类衍生物、其制备方法及其在医药上的应用
WO2012154880A1 (fr) 2011-05-09 2012-11-15 Proteostasis Therapeutics, Inc. Régulateurs de protéostasie pour le traitement de la mucoviscidose et autres maladies de mauvais repliement des protéines
SI2707101T1 (sl) 2011-05-12 2019-06-28 Proteostasis Therapeutics, Inc. Regulatorji proteostaze
CN103582647A (zh) 2011-05-31 2014-02-12 默克专利股份有限公司 含有氢基-三氰基-硼酸根阴离子的化合物
WO2012167171A2 (fr) 2011-06-03 2012-12-06 Massachusetts Institute Of Technology Réactions de métathèse de fermeture de cycle z-sélective
US9321727B2 (en) 2011-06-10 2016-04-26 Hoffmann-La Roche Inc. Pyridine derivatives as agonists of the CB2 receptor
JP2013020223A (ja) 2011-06-17 2013-01-31 Fujifilm Corp 高分子フィルム、セルロースエステルフィルム、偏光板、及び液晶表示装置
BR112014004832A2 (pt) 2011-08-29 2017-04-04 Ptc Therapeutics Inc compostos antibacterianos e métodos para uso
JP5741850B2 (ja) 2011-09-13 2015-07-01 コニカミノルタ株式会社 光学フィルム、それを含む偏光板および液晶表示装置
JP5857713B2 (ja) 2011-12-15 2016-02-10 コニカミノルタ株式会社 光学フィルム、偏光板、及び液晶表示装置
WO2013120040A1 (fr) 2012-02-10 2013-08-15 Children's Medical Center Corporation Inhibition d'une voie ciblée pour améliorer la structure, le fonctionnement et l'activité musculaires dans la dystrophie musculaire
DE102012006896A1 (de) 2012-04-05 2013-10-10 Merck Patent Gmbh Silikate mit organischen Kationen
US9013997B2 (en) 2012-06-01 2015-04-21 Broadcom Corporation System for performing distributed data cut-through
FR2992317B1 (fr) 2012-06-22 2016-05-13 Diverchim Procede de preparation de peptides chiraux
US20150197503A1 (en) 2012-07-27 2015-07-16 Bial-Portela & Cª, S.A. Process for the synthesis of substituted urea compounds
WO2014031681A1 (fr) 2012-08-20 2014-02-27 The University Of Chicago Inhibition de bactéries à gram positif
WO2014031872A2 (fr) 2012-08-23 2014-02-27 The Broad Institute, Inc. Inhibiteurs à petites molécules pour le traitement d'infections parasitaires
JP6204476B2 (ja) 2012-09-18 2017-09-27 ヘプタレス セラピューティックス リミテッド ムスカリンm1受容体作動薬としての二環式アザ化合物
DE102012021452A1 (de) 2012-10-31 2014-04-30 Merck Patent Gmbh Salze mit Trihydroperfluoralkoxybutansulfonat- oder Trihydroperfluoralkoxypropansulfonat-Anion
CN104870423A (zh) 2012-11-16 2015-08-26 加利福尼亚大学董事会 用于蛋白质化学修饰的pictet-spengler连接反应
ES2469290B2 (es) 2012-12-17 2015-01-26 Ocupharm Diagnostics S.L. Mejora en la aplicación tópica de fármacos oculares mediante la administración de nucleótidos
US9499762B2 (en) 2012-12-21 2016-11-22 Afton Chemical Corporation Additive compositions with a friction modifier and a detergent
US9279094B2 (en) 2012-12-21 2016-03-08 Afton Chemical Corporation Friction modifiers for use in lubricating oil compositions
CA2914178C (fr) 2013-01-07 2023-06-13 University Of Southern California Inhibiteurs de la desoxyuridine triphosphatase
WO2014108487A1 (fr) 2013-01-10 2014-07-17 Universite D'aix-Marseille Précurseur chiral p-stéréogène de ligands chiraux et son utilisation
WO2014130756A1 (fr) 2013-02-22 2014-08-28 University Of Utah Research Foundation Modulation de canaux ioniques
WO2014134141A1 (fr) 2013-02-26 2014-09-04 President And Fellows Of Harvard College Synthèse d'amines acycliques et cycliques au moyen d'un transfert de groupe nitrène catalysé par le fer
HUE041544T2 (hu) 2013-03-12 2019-05-28 Vertex Pharma DNS-PK inhibitorok
CA2908695A1 (fr) 2013-04-05 2014-10-09 Salk Institute For Biological Studies Antagonistes de ppar
BR112015027055B1 (pt) 2013-05-01 2023-09-26 F. Hoffmann-La Roche Ag Bi-heteroarilas, usos das mesmas, e composição farmacêutica
WO2015000548A1 (fr) 2013-07-02 2015-01-08 Merck Patent Gmbh Dispositif électroluminescent organique
WO2015003360A2 (fr) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs et leurs méthodes d'utilisation
WO2015011284A2 (fr) 2013-07-25 2015-01-29 Fondazione Telethon Inhibiteurs de fapp2 et leurs utilisations
US9701635B2 (en) 2013-07-26 2017-07-11 The Regents Of The University Of California C-H fluorination of heterocycles with silver (II) fluoride
WO2015031725A1 (fr) 2013-08-30 2015-03-05 President And Fellows Of Harvard College Imidation d'arènes catalysée par des métaux de transition
DE102013016324A1 (de) 2013-10-04 2015-04-09 Merck Patent Gmbh Perfluoralkylfluor- oder Perfluoralkylchlorgermanate
ES2742305T3 (es) 2013-10-21 2020-02-13 Merck Patent Gmbh Compuestos de heteroarilo como inhibidores de BTK y sus usos
WO2015069752A1 (fr) 2013-11-05 2015-05-14 The Regents Of The University Of California Ligands de protéine de liaison à l'acétylcholine, modulateurs nachr coopérants et procédés de fabrication et d'utilisation
CN103626741A (zh) 2013-11-26 2014-03-12 苏州大学 具有腺苷受体拮抗剂活性的杂环氨基嘧啶化合物
EP3527639B1 (fr) 2013-11-29 2021-09-08 proionic GmbH Procédé de coupler un matériau thermoplastique au moyen d'une irradiation aux micro-ondes
US20160304466A1 (en) 2013-12-04 2016-10-20 The Scripps Research Institute Novel compounds as jnk kinase inhibitors
CN110229142A (zh) 2014-04-04 2019-09-13 希洛斯医药品股份有限公司 细胞周期蛋白依赖性激酶7(cdk7)的抑制剂
US10308648B2 (en) 2014-10-16 2019-06-04 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
US10227333B2 (en) 2015-02-11 2019-03-12 Curtana Pharmaceuticals, Inc. Inhibition of OLIG2 activity
GB201502412D0 (en) 2015-02-13 2015-04-01 Canbex Therapeutics Ltd Therapeutic use
US10980755B2 (en) 2015-09-10 2021-04-20 The Regents Of The University Of California LRH-1 modulators
US20170299609A1 (en) 2016-04-18 2017-10-19 Wright State University Treatment of amyotrophic lateral sclerosis with sk channel activators
CA3026149A1 (fr) * 2016-06-02 2017-12-07 Cadent Therapeutics, Inc. Modulateurs des canaux potassiques
US20170355708A1 (en) 2016-06-09 2017-12-14 Cadent Therapeutics, Inc. Potassium channel modulators
WO2018136918A1 (fr) 2017-01-23 2018-07-26 Cadent Therapeutics, Inc. Procédés de traitement de tremblements par modulation positive de canaux sk
ES2906078T3 (es) 2017-01-23 2022-04-13 Cadent Therapeutics Inc Moduladores del canal de potasio
CA3116339A1 (fr) 2018-10-22 2020-04-30 Cadent Therapeutics, Inc. Formes cristallines de modulateurs des canaux potassiques

Also Published As

Publication number Publication date
US11993586B2 (en) 2024-05-28
WO2020086456A1 (fr) 2020-04-30
IL282348A (en) 2021-05-31
MX2024003904A (es) 2024-04-23
CN113226466A (zh) 2021-08-06
BR112021007552A2 (pt) 2021-07-27
CA3116339A1 (fr) 2020-04-30
AU2019366312A1 (en) 2021-05-20
MX2021004647A (es) 2021-08-16
US20210395229A1 (en) 2021-12-23
JP2022508945A (ja) 2022-01-19
KR20210080446A (ko) 2021-06-30
EP3870291A1 (fr) 2021-09-01

Similar Documents

Publication Publication Date Title
MA54543A (fr) Inhibiteurs de kif18a
MA54550A (fr) Inhibiteurs de kif18a
MA47596A (fr) Formes cristallines du dérivé 4-pyrimidinesulfamide aprocitentan
MA50122A (fr) Conversion de contexte de session
MA51819A (fr) Nouvelles formes cristallines
MA53124A (fr) Agents de dégradation sélectifs des récepteurs des oestrogènes
MA52812A (fr) Inhibiteurs de sarm1
MA54386A (fr) Modulateurs de trex1
DK3749669T3 (da) Ahr-modulatorer
MA52813A (fr) Inhibiteurs de sarm1
AR120804A1 (es) Derivados de isoxazolina
MA52809A (fr) Inhibiteurs de sarm1
DK3636640T3 (da) Krystal af heterocyclidenacetamidderivat
MA46567A (fr) Formes cristallines de l'éravacycline
MA51611A (fr) Inhibiteurs de pi4kiiibêta
MA54542A (fr) Compositions de sparsentan amorphe
DK3830073T3 (da) Fremgangsmåde til monotopisk fremstilling af iodorganske mellemforbindelser til syntese af ioversol
DK3749673T3 (da) Krystallinsk form af bictegravir-natrium
DK3774751T3 (da) Co-krystaller
DK3571193T3 (da) Potassium Channel Modulators
MA53978A (fr) Formes cristallines de modulateurs des canaux potassiques
DK3841692T3 (da) Forbedringer til tilpasning af begrænset buffermængde
ES2977060T3 (es) Impresión de venda
GB201912411D0 (en) Crystalline forms of ivosidenib
DK3790870T3 (da) Cyclopentanforbindelser