[go: up one dir, main page]

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)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Diabetes (AREA)
  • Hospice & Palliative Care (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Psychiatry (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 (2) CN113226466A (fr)
AU (2) AU2019366312B2 (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 (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3870291A1 (fr) 2018-10-22 2021-09-01 Cadent Therapeutics, Inc. Formes cristallines de modulateurs des canaux potassiques
CN118985622B (zh) * 2024-07-05 2025-12-02 云南大学 一种吡唑类化合物在防治植物根结线虫中的应用

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
WO1989011279A1 (fr) 1988-05-16 1989-11-30 Georgia State University Foundation, Inc. Compose heteropolycyclique non fusionne ayant une interaction avec des acides nucleiques
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
ES2307528T3 (es) 1999-09-04 2008-12-01 Astrazeneca Ab Amidas como inhibidores para la piruvato deshidrogenasa.
EP1218003A4 (fr) 1999-09-13 2004-02-11 David M Swope 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
EP1303269B1 (fr) 2000-06-29 2005-12-07 NeuroSearch A/S Utilisation de derives d'oxindole 3-substitue comme modulateurs du canal potassique kcnq
AU2002213467A1 (en) 2000-10-11 2002-04-22 Chemocentryx, Inc. Modulation of ccr4 function
AU2002239508B9 (en) 2000-12-07 2005-09-08 Gilead Palo Alto, Inc. Substituted 1, 3, 5-triazines and pyrimidines as ABCA-1 elevating compounds against coronary artery disease or atherosclerosis
WO2002055013A2 (fr) 2001-01-16 2002-07-18 Astrazeneca Ab Composes de chromone therapeutiques
IL156595A0 (en) 2001-01-16 2004-01-04 Astrazeneca Ab Therapeutic heterocyclic compounds
WO2002055014A2 (fr) 2001-01-16 2002-07-18 Astrazeneca Ab Composes therapeutiques de chromane
US20030130264A1 (en) 2001-02-16 2003-07-10 Tularik Inc. Methods of using pyrimidine-based antiviral agents
IL158168A0 (en) 2001-04-16 2004-03-28 Tanabe Seiyaku Co 5-membered, nitrogen-containing heterocyclic compounds and pharmaceutical compositions containing the same
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
AU2003212634A1 (en) 2002-03-11 2003-09-22 Zetiq Technologies Ltd. Compounds useful in the treatment of 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
DE60305053T2 (de) 2002-08-19 2006-08-31 Glaxo Group Ltd., Greenford Pyrimidinderivate als selektive cox-2-inhibitoren
JP2005536554A (ja) 2002-08-23 2005-12-02 ユニバーシティ オブ コネチカット 新規なビフェニル及びビフェニル様カンナビノイド
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
US7790736B2 (en) 2003-08-13 2010-09-07 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
JP4948173B2 (ja) 2003-10-10 2012-06-06 ニツポネツクス・インコーポレーテツド 過剰増殖性疾患治療用ピリミジン誘導体
CA2541509C (fr) 2003-10-17 2014-06-10 Incyte Corporation Inhibiteurs de metalloproteases matrices a base d'hydroxamates cycliques substitues
MXPA06005735A (es) 2003-11-24 2006-08-17 Hoffmann La Roche Pirazolil e imidazolil pirimidinas.
TW200528101A (en) 2004-02-03 2005-09-01 Astrazeneca Ab Chemical compounds
CN1976905A (zh) 2004-03-30 2007-06-06 大正制药株式会社 嘧啶衍生物以及与其应用有关的治疗方法
WO2005112938A2 (fr) 2004-04-13 2005-12-01 Synta Pharmaceuticals Corp. Inhibiteurs disel de production d'il-12
SE0401971D0 (sv) 2004-08-02 2004-08-02 Astrazeneca Ab Piperidne derivatives
EP1805142A4 (fr) 2004-09-23 2009-06-10 Reddy Us Therapeutics Inc Composes a base de pyridine, leur procede de preparation et compositions les contenant
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
US8211929B2 (en) 2004-12-30 2012-07-03 Exelixis, Inc. Pyrimidine derivatives as kinase modulators and method of use
EP1841736A1 (fr) 2005-01-19 2007-10-10 Biolipox AB Indoles utiles dans le traitement de l'inflammation
JP2008527027A (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
US20090042949A1 (en) 2005-01-19 2009-02-12 Benjamin Pelcman Indoles Useful in the Treatment of Inflammation
WO2006077366A1 (fr) 2005-01-19 2006-07-27 Biolipox Ab Indoles utiles dans le traitement de l'inflammation
CA2594665A1 (fr) 2005-01-19 2006-07-27 Biolipox Ab Thienopyrroles utiles dans le traitement de l'inflammation
US20070135437A1 (en) 2005-03-04 2007-06-14 Alsgen, Inc. Modulation of neurodegenerative diseases
MX2007010991A (es) 2005-03-14 2007-11-07 Neurosearch As Agentes que modulan el canal de potasio y su uso medico.
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
US20060156481A1 (en) 2005-03-22 2006-07-20 The Procter & Gamble Company Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
JP2008534472A (ja) 2005-03-22 2008-08-28 ノイロサーチ アクティーゼルスカブ カリウムチャンネル調節剤としてのピラゾリル−ピリミジン及びその医学的使用
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
US8193206B2 (en) 2005-06-14 2012-06-05 Taigen Biotechnology Co., Ltd. Pyrimidine compounds
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
EA015890B1 (ru) 2005-06-14 2011-12-30 Тайджен Байотекнолоджи Ко. Лтд. Производные пиримидина
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
US8642278B2 (en) 2005-11-22 2014-02-04 University Of South Florida Inhibition of cell proliferation
JP2009519346A (ja) 2005-12-12 2009-05-14 ジェネラブズ テクノロジーズ インコーポレーティッド N−(5員芳香族環)−アミド抗ウイルス化合物
AU2006326494A1 (en) 2005-12-12 2007-06-21 Genelabs Technologies, Inc. N-(6-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
WO2007089735A2 (fr) 2006-02-01 2007-08-09 Merck & Co., Inc. Inhibiteurs du canal potassique
WO2007106816A2 (fr) 2006-03-13 2007-09-20 Perkinelmer Las, Inc. Substrats et étalons internes pour détection par spectroscopie de masse
EP2012769A1 (fr) 2006-05-02 2009-01-14 Rundfeldt, Chris Activateurs de canaux potassiques pour la prévention et le traitement de la dystonie et des systèmes assimilés à la dystonie
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.
CA2659391A1 (fr) 2006-08-03 2008-02-07 Prosensa Technologies B.V. Composition antibiotique
AU2007288253B2 (en) 2006-08-23 2013-05-02 Xenon Pharmaceuticals Inc. Derivatives of 4-(N-azacycloalkyl) anilides as potassium channel modulators
WO2008024974A1 (fr) 2006-08-24 2008-02-28 Serenex, Inc. Dérivés de pyrimidine et de pyrazine
WO2008028935A2 (fr) 2006-09-07 2008-03-13 Neurosearch A/S Dérivés de pyridinyl-pyrimidine utiles comme agents modulateurs des canaux potassiques
WO2008040753A1 (fr) 2006-10-03 2008-04-10 Neurosearch A/S Dérivés d'indazolyle utiles en tant qu'agents modulant les canaux potassiques
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
JP2010510246A (ja) 2006-11-21 2010-04-02 スミスクライン ビーチャム コーポレーション アミド抗ウイルス化合物
CN101679371A (zh) 2006-12-04 2010-03-24 艾美罗股份公司 作为腺苷受体拮抗剂的取代的嘧啶
GB0701426D0 (en) 2007-01-25 2007-03-07 Univ Sheffield Compounds and their use
US8173647B2 (en) 2007-02-06 2012-05-08 Gordana Atallah PI 3-kinase inhibitors and methods of their use
CA2679185A1 (fr) 2007-02-28 2008-09-04 Advinus Therapeutics Private Limited Derives d'acetamide 2,2,2-tri-substitue en tant qu'activateurs de la glucokinase, leur procede de preparation et leur application pharmaceutique
US20080221103A1 (en) 2007-03-09 2008-09-11 Orchid Research Laboratories Ltd. New heterocyclic compounds
US20100105705A1 (en) 2007-03-28 2010-04-29 Neurosearch A/S Purinyl derivatives and their use as potassium channel modulators
WO2008116911A1 (fr) 2007-03-28 2008-10-02 Neurosearch A/S 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
EP2251001A4 (fr) 2008-02-08 2013-01-09 Shiseido Co Ltd Agent blanchissant pour la peau et préparation externe pour la peau
AU2009219070A1 (en) 2008-02-28 2009-09-03 Saint Mary's University Ionic liquids comprising ligands containing positively charged heterocyclic ring useful as catalyst and for metal extractions
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
EP2280948A1 (fr) 2008-04-09 2011-02-09 Mitsubishi Tanabe Pharma Corporation Dérivés de pyrimidine, pyridine et triazine en tant qu ouvreurs de canaux maxi-k
WO2009152902A2 (fr) 2008-05-28 2009-12-23 Merck Patent Gmbh, Liquides ioniques
KR20110017445A (ko) 2008-06-11 2011-02-21 아스트라제네카 아베 암 및 골수증식성 장애의 치료에 유용한 트리시클릭 2,4-디아미노-l,3,5-트리아진 유도체
US8822513B2 (en) 2010-03-01 2014-09-02 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
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
WO2010026087A1 (fr) 2008-09-02 2010-03-11 Neurosearch A/S Dérivés de pyrazolyl-pyrimidine et leur utilisation en tant que modulateurs de canal potassique
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
US20120165309A1 (en) 2009-02-12 2012-06-28 Astellas Pharma Inc. Hetero ring derivative
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
JP5918693B2 (ja) 2009-05-05 2016-05-18 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 Egfr阻害剤及び疾患の治療方法
NZ597108A (en) 2009-06-25 2014-04-30 Alkermes Pharma Ireland Ltd Prodrugs of nh-acidic compounds
US8377639B2 (en) 2009-06-26 2013-02-19 University Of Massachusetts Compounds for modulating RNA binding proteins and uses therefor
EA026674B1 (ru) 2009-07-08 2017-05-31 Балтик Био Аб Соединения, применимые в качестве лекарственных средств
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
TW201111379A (en) 2009-09-09 2011-04-01 Vifor Int Ag Novel thiazole-and oxazole-hepcidine-antagonists
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 Univ Wien Tech Substituierte pyridine und pyrimidine
WO2011109059A1 (fr) 2010-03-01 2011-09-09 Gtx, Inc. Composés destinés au traitement du cancer
CN103221404B (zh) 2010-05-13 2015-12-16 安姆根有限公司 可用作pde10抑制剂的不饱和氮杂环化合物
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
MX2013002011A (es) 2010-08-20 2013-03-25 Gruenenthal Gmbh Derivados ciclicos de carboxamida y urea sustituidos como ligandos del receptor vainiloide.
PE20140214A1 (es) 2010-08-27 2014-02-19 Gruenenthal Chemie 2-oxo- y 2-tioxo-dihidroquinolina-3-carboxamidas sustituidos como moduladores kcnq2/3
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
EP2622676A1 (fr) 2010-09-30 2013-08-07 Basf Se Additif pour électrolytes
JP2013540145A (ja) 2010-10-21 2013-10-31 ウニベルシテート デス ザールランデス コルチゾール依存性疾患の治療用の選択的cyp11b1阻害剤
ES2650744T3 (es) 2010-12-14 2018-01-22 Electrophoretics Limited Inhibidores de la caseína quinasa 1 delta (CK1delta)
EP2655334B1 (fr) 2010-12-22 2018-10-03 Eutropics Pharmaceuticals, Inc. Compositions et méthodes utilisables en vue du traitement de maladies
US9290591B2 (en) 2011-02-08 2016-03-22 President And Fellows Of Harvard College Iron complexes and methods for polymerization
US8895547B2 (en) 2011-03-08 2014-11-25 Sanofi Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof
US9464065B2 (en) 2011-03-24 2016-10-11 The Scripps Research Institute Compounds and methods for inducing chondrogenesis
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
PT2707101T (pt) 2011-05-12 2019-05-30 Proteostasis Therapeutics Inc Reguladores da proteostase
JP5990262B2 (ja) 2011-05-31 2016-09-07 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung ヒドリド−トリシアノ−ボラートアニオンを含む化合物
EP2721027B1 (fr) 2011-06-03 2017-05-31 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
KR20140085437A (ko) 2011-08-29 2014-07-07 피티씨 테라퓨틱스, 인크. 항균 화합물 및 이의 사용 방법
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
JP2015528013A (ja) 2012-07-27 2015-09-24 ビアル−ポルテラ エ コンパニア,ソシエダッド アノニマ 置換ウレア化合物の合成方法
US20150246024A1 (en) 2012-08-20 2015-09-03 The University Of Chicago Methods and compositions for inhibiting gram positive bacteria
WO2014031872A2 (fr) 2012-08-23 2014-02-27 The Broad Institute, Inc. Inhibiteurs à petites molécules pour le traitement d'infections parasitaires
EP2897948B1 (fr) 2012-09-18 2016-08-31 Heptares Therapeutics Limited Composés aza bicycliques utilisés comme agonistes du récepteur muscarinique m1
DE102012021452A1 (de) 2012-10-31 2014-04-30 Merck Patent Gmbh Salze mit Trihydroperfluoralkoxybutansulfonat- oder Trihydroperfluoralkoxypropansulfonat-Anion
US9605078B2 (en) 2012-11-16 2017-03-28 The Regents Of The University Of California Pictet-Spengler ligation for protein chemical modification
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
WO2014107622A1 (fr) 2013-01-07 2014-07-10 University Of Southern California Inhibiteurs de la désoxyuridine 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
US9487472B2 (en) 2013-02-26 2016-11-08 President And Fellows Of Harvard College Synthesis of acyclic and cyclic amines using iron-catalyzed nitrene group transfer
JP6360878B2 (ja) 2013-03-12 2018-07-18 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated Dna−pk阻害剤
CA2908695A1 (fr) 2013-04-05 2014-10-09 Salk Institute For Biological Studies Antagonistes de ppar
MA42164B1 (fr) 2013-05-01 2019-12-31 Hoffmann La Roche Composes biheteroaryle et leurs utilisations
KR102167199B1 (ko) 2013-07-02 2020-10-19 메르크 파텐트 게엠베하 유기 전계발광 소자
WO2015003360A2 (fr) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs et leurs méthodes d'utilisation
EP3024453A2 (fr) 2013-07-25 2016-06-01 Fondazione Telethon Inhibiteurs de fapp2 et leurs utilisations
WO2015013715A2 (fr) 2013-07-26 2015-01-29 Thr Regents Of The University Of California Fluoration c-h d'hétérocycles à l'aide de fluorure d'argent (ii)
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
EP3060550B1 (fr) 2013-10-21 2019-05-15 Merck Patent GmbH Composés hétéroaryle servant d'inhibiteurs de la btk et leurs utilisations
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
ES2906062T3 (es) 2013-11-29 2022-04-13 Proionic Gmbh Procedimiento para la unión de un material termoplástico por medio de radiación de microondas
EP3076789A4 (fr) 2013-12-04 2017-11-22 The Scripps Research Institute Nouveaux composés utilisables en tant qu'inhibiteurs des janus kinases
RS58175B1 (sr) 2014-04-04 2019-03-29 Syros Pharmaceuticals Inc Inhibitori ciklin-zavisne kinaze 7 (cdk7)
WO2016058544A1 (fr) 2014-10-16 2016-04-21 Syros Pharmaceuticals, Inc. Inhibiteurs de la kinase cycline-dépendante 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
AU2017275657B2 (en) 2016-06-02 2021-08-19 Novartis Ag Potassium channel modulators
US20170355708A1 (en) 2016-06-09 2017-12-14 Cadent Therapeutics, Inc. Potassium channel modulators
EP3571193B1 (fr) 2017-01-23 2021-12-01 Cadent Therapeutics, Inc. Modulateurs de canaux potassiques
US20180207138A1 (en) 2017-01-23 2018-07-26 Cadent Therapeutics, Inc. Methods for the treatment of tremors by positive modulation of sk channels
EP3870291A1 (fr) 2018-10-22 2021-09-01 Cadent Therapeutics, Inc. Formes cristallines de modulateurs des canaux potassiques

Also Published As

Publication number Publication date
BR112021007552A2 (pt) 2021-07-27
KR20210080446A (ko) 2021-06-30
CA3116339A1 (fr) 2020-04-30
CN120794960A (zh) 2025-10-17
MX2024003904A (es) 2024-04-23
US20210395229A1 (en) 2021-12-23
CN113226466A (zh) 2021-08-06
AU2019366312A1 (en) 2021-05-20
WO2020086456A1 (fr) 2020-04-30
EP3870291A1 (fr) 2021-09-01
AU2025208446A1 (en) 2025-08-07
AU2019366312B2 (en) 2025-04-24
JP2022508945A (ja) 2022-01-19
IL282348A (en) 2021-05-31
MX2021004647A (es) 2021-08-16
US11993586B2 (en) 2024-05-28

Similar Documents

Publication Publication Date Title
LT4069691T (lt) Pakeistieji tetrahidrofuranai kaip natrio kanalų moduliatoriai
EP3897522A4 (fr) Compositions de microcapsules
IL286218A (en) Solid state forms of ripretinib
MA47596A (fr) Formes cristallines du dérivé 4-pyrimidinesulfamide aprocitentan
MA50122A (fr) Conversion de contexte de session
MA53124A (fr) Agents de dégradation sélectifs des récepteurs des oestrogènes
EP3856193A4 (fr) Modulateurs de canal ionique
EP3877519A4 (fr) Biosynthèse de mogrosides
SI3743406T1 (sl) Modulatorji TMEM16A
EP3870178A4 (fr) Formes cristallines d'inhibiteurs de mnk
EP3934408A4 (fr) Détermination de conditions agricoles
LT4041713T (lt) Selektyvaus kalio kanalų moduliatoriaus kietos kristalinės formos
EP3900329A4 (fr) Optimisation de combinaison de fragments de vidéo
EP3668876A4 (fr) Forme polymorphe de tg02
EP3390422A4 (fr) Formes cristallines de lnt
IL269792B (en) Crystalline forms of (s)-afoxolaner
DK3636640T3 (da) Krystal af heterocyclidenacetamidderivat
DK3830073T3 (da) Fremgangsmåde til monotopisk fremstilling af iodorganske mellemforbindelser til syntese af ioversol
EP4082457A4 (fr) Instrument de néostomie
EP3825303A4 (fr) Inhibiteur du canal calcique de type t
SI3749673T1 (sl) Kristalinična oblika biktegravir natrija
MA53978A (fr) Formes cristallines de modulateurs des canaux potassiques
DK3571193T3 (da) Potassium Channel Modulators
EP3790652A4 (fr) Composition de mouillage améliorée
EP3404021A4 (fr) Inhibiteur du canal calcique de type t tension-dépendant