MA49839A - Inhibiteurs bicycliques d'histone désacétylase - Google Patents

Inhibiteurs bicycliques d'histone désacétylase

Info

Publication number
MA49839A
MA49839A MA049839A MA49839A MA49839A MA 49839 A MA49839 A MA 49839A MA 049839 A MA049839 A MA 049839A MA 49839 A MA49839 A MA 49839A MA 49839 A MA49839 A MA 49839A
Authority
MA
Morocco
Prior art keywords
bicyclic
histone deacetylase
deacetylase inhibitors
inhibitors
histone
Prior art date
Application number
MA049839A
Other languages
English (en)
Other versions
MA49839B1 (fr
Inventor
Nathan Oliver Fuller
John A Lowe Iii
Original Assignee
Rodin 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 Rodin Therapeutics Inc filed Critical Rodin Therapeutics Inc
Publication of MA49839A publication Critical patent/MA49839A/fr
Publication of MA49839B1 publication Critical patent/MA49839B1/fr

Links

Classifications

    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Rheumatology (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Communicable Diseases (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
MA49839A 2017-08-07 2018-08-07 Inhibiteurs bicycliques de la histone déacétylase MA49839B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762541807P 2017-08-07 2017-08-07
PCT/US2018/045528 WO2019032528A1 (fr) 2017-08-07 2018-08-07 Inhibiteurs bicycliques d'histone désacétylase

Publications (2)

Publication Number Publication Date
MA49839A true MA49839A (fr) 2020-06-17
MA49839B1 MA49839B1 (fr) 2022-05-31

Family

ID=63364199

Family Applications (1)

Application Number Title Priority Date Filing Date
MA49839A MA49839B1 (fr) 2017-08-07 2018-08-07 Inhibiteurs bicycliques de la histone déacétylase

Country Status (23)

Country Link
US (2) US11225475B2 (fr)
EP (1) EP3664802B1 (fr)
JP (1) JP7152471B2 (fr)
KR (1) KR20200037286A (fr)
CN (1) CN111032040B (fr)
AU (1) AU2018313094A1 (fr)
CA (1) CA3071861A1 (fr)
DK (1) DK3664802T3 (fr)
EA (1) EA039417B1 (fr)
ES (1) ES2914355T3 (fr)
HR (1) HRP20220648T1 (fr)
HU (1) HUE058799T2 (fr)
IL (1) IL272479B2 (fr)
LT (1) LT3664802T (fr)
MA (1) MA49839B1 (fr)
MD (1) MD3664802T2 (fr)
MX (1) MX2020001484A (fr)
PL (1) PL3664802T3 (fr)
PT (1) PT3664802T (fr)
RS (1) RS63343B1 (fr)
SG (1) SG11202000970WA (fr)
SI (1) SI3664802T1 (fr)
WO (1) WO2019032528A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2899906T3 (es) 2015-07-06 2022-03-15 Alkermes Inc Inhibidores bicíclicos de histona desacetilasa
WO2018132533A1 (fr) 2017-01-11 2018-07-19 Rodin Therapeutics, Inc. Inhibiteurs bicycliques d'histone désacétylase
CA3071861A1 (fr) 2017-08-07 2019-02-14 Rodin Therapeutics, Inc. Inhibiteurs bicycliques d'histone desacetylase
EP4074700A4 (fr) * 2019-12-10 2024-02-07 Shionogi & Co., Ltd Inhibiteur d'histone désacétylase comprenant un groupe hétérocyclique aromatique contenant de l'azote

Family Cites Families (295)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5112824A (en) 1989-12-08 1992-05-12 Merck & Co., Inc. Benzofuran compounds as class III antiarrhythmic agents
FR2665159B1 (fr) 1990-07-24 1992-11-13 Rhone Poulenc Sante Nouveaux derives de la pyridine et de la quinoleine, leur preparation et les compositions pharmaceutiques qui les contiennent.
DE4212748A1 (de) 1992-04-16 1993-10-21 Thomae Gmbh Dr K Benzimidazole, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
GB9420521D0 (en) 1994-10-12 1994-11-30 Smithkline Beecham Plc Novel compounds
GB9420999D0 (en) 1994-10-18 1994-12-07 Smithkline Beecham Plc Novel compounds
WO1996018617A1 (fr) 1994-12-12 1996-06-20 Merck & Co., Inc. Pyridines 2-acylaminees substitutees utilisees comme inhibiteurs de synthase d'oxyde d'azote
GB9500580D0 (en) 1995-01-12 1995-03-01 Merck Sharp & Dohme Therapeutic agents
ATE197300T1 (de) 1995-02-02 2000-11-15 Smithkline Beecham Plc Indolderivate als 5-ht rezeptorantagoniste
US5668148A (en) 1995-04-20 1997-09-16 Merck & Co., Inc. Alpha1a adrenergic receptor antagonists
GB9517559D0 (en) 1995-08-26 1995-10-25 Smithkline Beecham Plc Novel compounds
US5886186A (en) 1995-10-25 1999-03-23 Versicor, Inc. Synthesis of substituted N-heteroaromatic compounds and methods of use thereof
AU706150B2 (en) 1996-04-03 1999-06-10 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
US5872136A (en) 1996-04-03 1999-02-16 Merck & Co., Inc. Arylheteroaryl inhibitors of farnesyl-protein transferase
FR2763944B1 (fr) 1997-06-03 2000-12-15 Centre Nat Rech Scient Nouveaux derives de coumarines, leurs procedes de preparation et leur application comme medicaments en tant qu'inhibiteurs de proteases
JPH1149676A (ja) 1997-07-31 1999-02-23 Geron Corp ピリジン系テロメラーゼ阻害剤
JPH11209366A (ja) 1998-01-23 1999-08-03 Nissan Chem Ind Ltd クロマン誘導体及び心不全治療薬
WO1999065897A1 (fr) 1998-06-19 1999-12-23 Chiron Corporation Inhibiteurs de glycogene synthase kinase 3
AR019190A1 (es) 1998-07-08 2001-12-26 Sod Conseils Rech Applic Derivados de 2-aminopiridinas, productos intermedios para su preparacion, medicamentos y composiciones farmaceuticas que los contienen y su uso para preparar medicamentos
EP1165490B1 (fr) 1999-03-16 2006-08-16 Cytovia, Inc. Inhibiteurs de caspases 2-aminobenzamidiques substitues et leur utilisation
GB9922171D0 (en) 1999-09-21 1999-11-17 Zeneca Ltd Chemical compounds
RU2317988C2 (ru) 2000-08-14 2008-02-27 Орто-Макнейл Фармасьютикал, Инк. Замещенные пиразолы, фармацевтическая композиция на их основе, применение фармацевтической композиции и способ ингибирования активности катепсина s
JP2004531456A (ja) 2000-09-06 2004-10-14 オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド 置換ピラゾールを用いてアレルギーを治療する方法
WO2002026708A1 (fr) 2000-09-27 2002-04-04 Toray Industries, Inc. Composes conenant de l'azote et inhibiteurs de ccr3 contenant ces composes en tant que principe actif
HN2001000224A (es) 2000-10-19 2002-06-13 Pfizer Compuestos de imidazol condensado con arilo o heteroarilo como agentes anti - inflamatorios y analgesicos.
US6710058B2 (en) 2000-11-06 2004-03-23 Bristol-Myers Squibb Pharma Company Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors
IL156315A0 (en) 2000-12-07 2004-01-04 Cv Therapeutics Inc Abca-1 elevating compounds
WO2002053160A1 (fr) 2000-12-29 2002-07-11 Alteon, Inc. Methode de traitement du glaucome ivb
PL369598A1 (en) 2001-02-21 2005-05-02 Nps Pharmaceuticals, Inc. Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists
ATE409181T1 (de) 2001-05-08 2008-10-15 Univ Yale Proteomimetische verbindungen und verfahren
WO2003042190A1 (fr) 2001-11-12 2003-05-22 Pfizer Products Inc. Derives de n-adamantylalkyle benzamide en tant qu'antagonistes du recepteur p2x7
US20030187026A1 (en) 2001-12-13 2003-10-02 Qun Li Kinase inhibitors
TW200301698A (en) 2001-12-21 2003-07-16 Bristol Myers Squibb Co Acridone inhibitors of IMPDH enzyme
JP2003192673A (ja) 2001-12-27 2003-07-09 Bayer Ag ピペラジンカルボキシアミド誘導体
WO2003062224A1 (fr) 2002-01-17 2003-07-31 Eli Lilly And Company Composes azacycliques en tant que modulateurs de recepteurs d'acetylcholine
JP4167848B2 (ja) 2002-04-10 2008-10-22 広栄化学工業株式会社 ビアリール化合物の製造法
CN1181065C (zh) 2002-05-08 2004-12-22 上海医药工业研究院 芳烷甲酰烷基哌嗪衍生物及其作为脑神经保护剂的应用
US20040082627A1 (en) 2002-06-21 2004-04-29 Darrow James W. Certain aromatic monocycles as kinase modulators
AU2003249369A1 (en) 2002-06-21 2004-01-06 Cellular Genomics, Inc. Certain amino-substituted monocycles as kinase modulators
NZ538715A (en) 2002-08-14 2007-07-27 Vertex Pharma Protein kinase inhibitors and uses thereof
AU2003302084A1 (en) 2002-11-15 2004-06-15 Bristol-Myers Squibb Company Open chain prolyl urea-related modulators of androgen receptor function
CA2515544A1 (fr) 2003-02-11 2004-08-26 Kemia Inc. Composes destines au traitement d'une infection virale
CL2004000234A1 (es) 2003-02-12 2005-04-15 Biogen Idec Inc Compuestos derivados 3-(piridin-2-il)-4-heteroaril-pirazol sustituidos, antagonistas de aik5 y/o aik4; composicion farmaceutica y uso del compuesto en el tratamiento de desordenes fibroticos como esclerodermia, lupus nefritico, cicatrizacion de herid
ES2327684T3 (es) 2003-07-24 2009-11-02 Euro-Celtique S.A. Compuestos heteroaril-tetrahidropiridilo utiles para el tratamiento o la prevencion del dolor.
TWI287567B (en) 2003-07-30 2007-10-01 Chi Mei Optoelectronics Corp Light-emitting element and iridium complex
WO2005014580A1 (fr) 2003-08-08 2005-02-17 Janssen Pharmaceutica, N.V. Urees pyridyle piperazinyle
WO2005016862A1 (fr) 2003-08-14 2005-02-24 Asahi Kasei Pharma Corporation Derive d'acide arylalcanoique substitue et son utilisation
US7504401B2 (en) 2003-08-29 2009-03-17 Locus Pharmaceuticals, Inc. Anti-cancer agents and uses thereof
CA2539117A1 (fr) * 2003-09-24 2005-04-07 Methylgene Inc. Inhibiteurs d'histone deacetylase
AU2005215379A1 (en) 2004-02-12 2005-09-01 Merck & Co., Inc. Bipyridyl amides as modulators of metabotropic glutamate receptor-5
WO2005095386A1 (fr) 2004-03-30 2005-10-13 Chiron Corporation Derives du thiophene substitues en tant qu'agents anticancereux
PT1735278E (pt) 2004-04-01 2010-03-09 Lilly Co Eli Agentes receptores h3 de histamina, sua preparação e utilizações terapêuticas
US7459562B2 (en) 2004-04-23 2008-12-02 Bristol-Myers Squibb Company Monocyclic heterocycles as kinase inhibitors
FR2869904B1 (fr) 2004-05-07 2006-07-28 Fournier S A Sa Lab Modulateurs des recepteurs lxr
CN1989115B (zh) 2004-07-26 2012-03-21 伊莱利利公司 作为组胺h3受体药物的噁唑衍生物及其制备和制药用途
ATE502025T1 (de) 2004-10-19 2011-04-15 Compass Pharmaceuticals Llc Arylcarboxamide und ihre verwendung als antitumormittel
JP2008519814A (ja) 2004-11-12 2008-06-12 ガラパゴス・ナムローゼ・フェンノートシャップ プロテインキナーゼ酵素の活性部位と結合する窒素複素環式芳香族化合物
CA2588607A1 (fr) 2004-11-23 2006-06-01 Ptc Therapeutics, Inc. Derives de carbazole, de carboline et d'indole utilises dans l'inhibition de la production de vegf
AR053992A1 (es) 2004-12-22 2007-05-30 Astrazeneca Ab Compuestos quimicos con actividad anticancerosa, un procedimiento para su preparacion, su uso en la preparacion de medicamentos y composicion farmaceutica.
CN101128454A (zh) 2004-12-22 2008-02-20 阿斯利康(瑞典)有限公司 用作抗癌药物的吡啶羧酰胺衍生物
US7622583B2 (en) 2005-01-14 2009-11-24 Chemocentryx, Inc. Heteroaryl sulfonamides and CCR2
WO2006076644A2 (fr) 2005-01-14 2006-07-20 Chemocentryx, Inc. Sulfonamides d'heteroaryle et ccr2
EP1683796A1 (fr) 2005-01-24 2006-07-26 Schering Aktiengesellschaft Pyrazolopyridines, leur préparation et leur utilisation médicale
EP1844003A4 (fr) 2005-01-27 2010-09-22 Astrazeneca Ab Nouveaux composes biaromatiques, inhibiteurs du recepteur p2x7
US7888374B2 (en) 2005-01-28 2011-02-15 Abbott Laboratories Inhibitors of c-jun N-terminal kinases
US20060178388A1 (en) 2005-02-04 2006-08-10 Wrobleski Stephen T Phenyl-substituted pyrimidine compounds useful as kinase inhibitors
US20070135437A1 (en) 2005-03-04 2007-06-14 Alsgen, Inc. Modulation of neurodegenerative diseases
EP2527337A1 (fr) 2005-04-14 2012-11-28 Bristol-Myers Squibb Company Inhibiteurs de la 11-bêta hydroxystéroïde déshydrogénase de type I
EP1879548A2 (fr) 2005-05-13 2008-01-23 Ciba Specialty Chemicals Holding Inc. Coloration de fibres de keratine avec des complexes metalliques
WO2006128129A2 (fr) 2005-05-26 2006-11-30 Synta Pharmaceuticals Corp. Traitement anticancereux
WO2006128172A2 (fr) 2005-05-26 2006-11-30 Synta Pharmaceuticals Corp. Procede pour traiter des troubles auto-immuns regules par des lymphocytes b
US8017635B2 (en) 2005-06-02 2011-09-13 Fmc Corporation Phenylalkyl substituted heteroaryl derivatives
WO2006135604A2 (fr) 2005-06-09 2006-12-21 Merck & Co., Inc. Inhibiteurs de kinases checkpoint
WO2006137772A1 (fr) 2005-06-20 2006-12-28 Astrazeneca Ab Nouvelle forme physique d'oxabispidines n,n-disubstituees
DE602006011752D1 (de) 2005-06-24 2010-03-04 Bristol Myers Squibb Co Als antikoagulationsmittel geeignete phenylglycinamid- und pyridylglycinamidderivate
PE20070099A1 (es) 2005-06-30 2007-02-06 Janssen Pharmaceutica Nv N-heteroarilpiperazinil ureas como moduladores de la amida hidrolasa del acido graso
WO2007008541A2 (fr) 2005-07-08 2007-01-18 Kalypsys, Inc. Modificateurs d'absorption de cholesterol cellulaire
FR2892412B1 (fr) 2005-10-26 2008-05-16 Galderma Res & Dev Composes biaromatiques modulateurs des ppars
TW200804307A (en) 2005-10-27 2008-01-16 Synta Pharmaceuticals Corp Process for preparing mesylate salts of IL-12 inhibitory compounds
US8026260B2 (en) 2005-11-03 2011-09-27 Merck Sharp & Dohme Corp. Histone deacetylase inhibitors with aryl-pyrazolyl-motifs
KR101331768B1 (ko) 2005-11-08 2013-11-22 버텍스 파마슈티칼스 인코포레이티드 Atp 결합 카세트 수송체의 헤테로사이클릭 조정제
WO2007055374A1 (fr) 2005-11-14 2007-05-18 Mitsubishi Tanabe Pharma Corporation Agent therapeutique pour l'osteoporose
AR057579A1 (es) 2005-11-23 2007-12-05 Merck & Co Inc Compuestos espirociclicos como inhibidores de histona de acetilasa (hdac)
AU2006320580B2 (en) 2005-11-30 2011-06-23 Vertex Pharmaceuticals Incorporated Inhibitors of c-Met and uses thereof
JP5015172B2 (ja) 2005-12-23 2012-08-29 エフ.ホフマン−ラ ロシュ アーゲー アリール−イソオキサゾロ−4−イル−オキサジアゾール誘導体
EP1973405A4 (fr) 2006-01-12 2011-06-01 Merck Sharp & Dohme Derives d'hydroxyalkymarylamide
US20090012075A1 (en) 2006-01-12 2009-01-08 Miller Thomas A Fluorinated Arylamide Derivatives
TW200813015A (en) 2006-03-15 2008-03-16 Mitsubishi Pharma Corp 2-(cyclic amino)-pyrimidone derivatives
JP2007283748A (ja) 2006-03-23 2007-11-01 Fujifilm Corp 光記録媒体および可視情報記録方法
DK2656841T3 (en) 2006-03-27 2016-12-05 Univ California Androgen receptor MODULATOR FOR THE TREATMENT OF PROSTATE CANCER AND androgen receptor-ASSOCIATED DISEASES
ES2452820T3 (es) 2006-04-07 2014-04-02 Methylgene, Inc. Derivados de benzamida como inhibidores de histona desacetilasa
WO2007125984A1 (fr) 2006-04-28 2007-11-08 Nihon Nohyaku Co., Ltd. Derive isoxazoline, agent insecticide et utilisation de l'agent insecticide
WO2007129052A1 (fr) 2006-05-03 2007-11-15 Astrazeneca Ab Dérivés de pyrazole et leur emploi en tant qu'inhibiteurs de pi3k
CN101484452A (zh) 2006-05-03 2009-07-15 阿斯利康(瑞典)有限公司 噻唑衍生物及其作为抗肿瘤药物的用途
US20080064871A1 (en) 2006-05-26 2008-03-13 Japan Tobacco Inc. Production Method of Nitrogen-Containing Fused Ring Compounds
EA200870592A1 (ru) 2006-05-31 2009-08-28 Галапагос Н.В. Триазолопиразиновые соединения, пригодные для лечения дегенеративных и воспалительных заболеваний
WO2007143557A2 (fr) 2006-06-02 2007-12-13 Brandeis University Composés et procédés de traitement des infections parasitaires gastro-intestinales des mammifères
US20080280891A1 (en) 2006-06-27 2008-11-13 Locus Pharmaceuticals, Inc. Anti-cancer agents and uses thereof
ES2431466T3 (es) 2006-06-30 2013-11-26 Sunesis Pharmaceuticals, Inc. Inhibidores de piridinonil pdk1
US8519135B2 (en) 2006-07-14 2013-08-27 Chemocentryx, Inc. Heteroaryl sulfonamides and CCR2/CCR9
AU2007275743A1 (en) 2006-07-20 2008-01-24 Merck Sharp & Dohme Corp. Phosphorus derivatives as histone deacetylase inhibitors
US20090306039A1 (en) 2006-07-21 2009-12-10 Shifeng Pan Compounds and compositions as itpkb inhibitors
GB0614579D0 (en) 2006-07-21 2006-08-30 Black James Foundation Pyrimidine derivatives
FR2903985B1 (fr) 2006-07-24 2008-09-05 Sanofi Aventis Sa Derives de n-(amino-heteroaryl)-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique
CA2658887C (fr) 2006-07-28 2016-08-23 University Of Connecticut Inhibiteurs d'hydrolase des amides d'acides gras
WO2008016643A2 (fr) 2006-08-01 2008-02-07 Cytokinetics, Incorporated Entités chimiques, compositions et méthodes
WO2008024970A2 (fr) 2006-08-24 2008-02-28 Serenex, Inc. Dérivés de benzène, de pyridine et de pyridazine
US20080119457A1 (en) 2006-08-24 2008-05-22 Serenex, Inc. Benzene, Pyridine, and Pyridazine Derivatives
CA2663528A1 (fr) 2006-09-18 2008-03-27 Vertex Pharmaceuticals Incorporated Inhibiteurs heterocycliques de c-met et leurs utilisations
CA2663984C (fr) 2006-10-18 2012-02-21 Pfizer Products Inc. Composes d'uree de bisaryle ether
DE102006050515A1 (de) 2006-10-26 2008-04-30 Bayer Healthcare Ag Substituierte Dipyridiyl-dihydropyrazolone und ihre Verwendung
US7858645B2 (en) 2006-11-01 2010-12-28 Hoffmann-La Roche Inc. Indazole derivatives
US20100099676A1 (en) 2006-11-02 2010-04-22 Shionogi & Co., Ltd. Sulfonylurea derivative capable of selectively inhibiting mmp-13
JP2009023986A (ja) 2006-11-08 2009-02-05 Pharma Ip 抗癌剤としてのビアリール誘導体
US20080145816A1 (en) 2006-12-15 2008-06-19 Hershey Adrienne A Yankauer suction device
SI2125822T1 (sl) 2006-12-21 2015-01-30 Nerviano Medical Sciences S.R.L. Substituirani pirazolo-kinazolinski derivati, postopek za njihovo pripravo in njihova uporaba kot inhibitorji kinaze
AR064660A1 (es) 2006-12-26 2009-04-15 Mitsubishi Tanabe Pharma Corp Derivados de pirimidinona 6-heterociclica 2-sustituida, medicamentos que los contienen y usos para prevenir y/o tratar enfermedades neurodegenerativas entre otras
FR2910473B1 (fr) 2006-12-26 2009-02-13 Sanofi Aventis Sa Derives de n-(amino-heteroaryl)-1h-pyrrolopyridine-2- carboxamides, leur preparation et leur application en therapeutique.
JP2008179067A (ja) 2007-01-25 2008-08-07 Fujifilm Corp 光記録媒体および可視情報記録方法
JP2008179068A (ja) 2007-01-25 2008-08-07 Fujifilm Corp 光記録媒体および可視情報記録方法
CA2702647C (fr) 2007-01-31 2016-03-22 Ym Biosciences Australia Pty Ltd Composes a base de thiopyrimidine et ses utilisations
BRPI0808301B1 (pt) 2007-03-20 2022-05-03 Curis, Inc Composto e composição farmacêutica
US20080234297A1 (en) 2007-03-20 2008-09-25 Changgeng Qian HSP90 Inhibitors Containing a Zinc Binding Moiety
US8461343B2 (en) 2007-03-27 2013-06-11 Sloan-Kettering Institute For Cancer Research Synthesis of thiohydantoins
FR2915198B1 (fr) 2007-04-18 2009-12-18 Sanofi Aventis Derives de triazolopyridine-carboxamides et triazolopyridine -carboxamides, leur preparation et leur application en therapeutique.
WO2008129280A1 (fr) 2007-04-20 2008-10-30 Biolipox Ab Pyrazoles utiles dans le traitement de l'inflammation
WO2008139152A1 (fr) 2007-05-11 2008-11-20 Sentinel Oncology Limited Composés pharmaceutiques contenant un n-oxyde
EA200971143A1 (ru) 2007-06-03 2010-06-30 Вандербилт Юниверсити Бензамидные mglur5 позитивные аллостерические модуляторы и способы их получения и применения
TWI446905B (zh) 2007-06-05 2014-08-01 Sanofi Aventis 經取代之苯甲醯基胺基-氫茚-2-羧酸及相關化合物
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
US8461189B2 (en) 2007-06-27 2013-06-11 Merck Sharp & Dohme Corp. Pyridyl derivatives as histone deacetylase inhibitors
WO2009022171A1 (fr) 2007-08-13 2009-02-19 Astrazeneca Ab Composés chimiques 1 - 821
PT2200436E (pt) 2007-09-04 2015-04-29 Scripps Research Inst Pirimidinilaminas substituídas como inibidoras da proteína quinase
US8354383B2 (en) 2007-09-17 2013-01-15 Enanta Pharmaceuticals, Inc. 6,11-bridged biaryl macrolides
JP5469604B2 (ja) 2007-09-19 2014-04-16 4エスツェー アクチェンゲゼルシャフト 新規テトラヒドロ融合ピリジン
US8440830B2 (en) 2007-09-19 2013-05-14 4Sc Ag Tetrahydro-fused pyridines as histone deacetylase inhibitors
EP2203058A4 (fr) 2007-10-16 2011-08-31 Univ Northeastern Procédés et composés permettant la modulation de l'activité cannabinoïde
US20090156825A1 (en) 2007-11-26 2009-06-18 Heidebrecht Jr Richard W Fluorescent compounds that bind to histone deacetylase
WO2009078992A1 (fr) 2007-12-17 2009-06-25 Amgen Inc. Composés tricycliques linéaires utilisés comme inhibiteurs de la kinase p38
FR2926553B1 (fr) 2008-01-23 2010-02-19 Sanofi Aventis Derives d'indole-2-carboxamides et d'azaindole-2- carboxamides substitues par un groupe silanyle, leur preparation et leur application en therapeutique
EP2244709A4 (fr) 2008-02-07 2012-02-29 Synta Pharmaceuticals Corp Formulations topiques pour le traitement du psoriasis
JP2009209090A (ja) 2008-03-04 2009-09-17 Mitsui Chemicals Inc 殺虫剤及び該殺虫剤に含まれる化合物、並びに該化合物の使用方法
CL2009000600A1 (es) 2008-03-20 2010-05-07 Bayer Cropscience Ag Uso de compuestos de diaminopirimidina como agentes fitosanitarios; compuestos de diaminopirimidina; su procedimiento de preparacion; agente que los contiene; procedimiento para la preparacion de dicho agente; y procedimiento para combatir plagas de animales y/u hongos dañinos patogenos de plantas.
US8158636B2 (en) 2008-05-19 2012-04-17 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
PE20091846A1 (es) 2008-05-19 2009-12-16 Plexxikon Inc DERIVADOS DE PIRROLO[2,3-d]-PIRIMIDINA COMO MODULADORES DE CINASAS
CN104530052A (zh) 2008-06-10 2015-04-22 普莱希科公司 用于激酶调节的5h-吡咯[2,3-b]吡嗪衍生物和其适应症
WO2009152087A1 (fr) 2008-06-10 2009-12-17 Plexxikon, Inc. Composés hétéroaryles bicycliques et procédés destinés à la modulation de kinases, et des indications pour celle-ci
KR20110026481A (ko) 2008-06-20 2011-03-15 메타볼렉스, 인코포레이티드 아릴 gpr119 작동약 및 이의 용도
BRPI0913966A2 (pt) 2008-06-27 2015-11-17 Novartis Ag compostos orgânicos
EP2331503B1 (fr) 2008-07-11 2013-08-21 Irm Llc 4-phénoxyméthylpipéridines comme modulateurs de l activité de gpr119
TW201028381A (en) 2008-07-14 2010-08-01 Shionogi & Co Pyridine derivative having ttk inhibition activity
JP5401544B2 (ja) 2008-07-15 2014-01-29 ノバルティス アーゲー Dgat1阻害剤としてのヘテロアリール誘導体
CA2735929C (fr) 2008-09-19 2013-12-17 Pfizer Inc. Derives d'acide hydroxamique utiles comme agents antibacteriens
PE20110294A1 (es) 2008-09-29 2011-05-26 Boehringer Ingelheim Int Compuestos heterociclicos como inhibidores de enzimas de senal especifica
WO2010046780A2 (fr) 2008-10-22 2010-04-29 Institut Pasteur Korea Composés antiviraux
WO2010068863A2 (fr) 2008-12-12 2010-06-17 Cystic Fibrosis Foundation Therapeutics, Inc. Composés de pyrimidine et leurs procédés de fabrication et d'utilisation
US8541424B2 (en) 2008-12-23 2013-09-24 Abbott Laboratories Anti-viral compounds
WO2010088574A1 (fr) 2009-01-30 2010-08-05 Sirtris Pharmaceuticals, Inc. Azabenzimidazoles et analogues apparentés en tant que modulateurs de la sirtuine
WO2010111527A1 (fr) 2009-03-26 2010-09-30 Plexxikon, Inc. Pyrazolo [ 3, 4 -b] pyridines en tant qu'inhibiteurs de la kinase et leur utilisation médicale
ES2552282T3 (es) 2009-03-27 2015-11-26 Nerviano Medical Sciences S.R.L. Derivados de N-aril-2-(2-arilaminopirimidin-4-il)pirrol-4-carboxamida como inhibidores de la cinasa MPS1
CN102388052A (zh) 2009-04-01 2012-03-21 诺瓦提斯公司 调节硬脂酰基-CoA去饱和酶的螺环衍生物
US8334315B2 (en) 2009-05-07 2012-12-18 Gruenenthal Gmbh Substituted aromatic carboxamide and urea derivatives as vanilloid receptor ligands
JP2011006408A (ja) 2009-05-29 2011-01-13 Sumitomo Chemical Co Ltd 神経栄養因子の活性が関与する疾患の治療または予防剤
WO2010144371A1 (fr) 2009-06-08 2010-12-16 Gilead Colorado, Inc. Composés inhibiteurs d'hdac à base d'alkanoylamino benzamide aniline
WO2010151747A1 (fr) 2009-06-26 2010-12-29 Cystic Fibrosis Foundation Therapeutics, Inc. Composés de pyramine ainsi que leurs procédés de fabrication et d'utilisation
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
US8415381B2 (en) 2009-07-30 2013-04-09 Novartis Ag Heteroaryl compounds and their uses
CA2781888C (fr) 2009-12-11 2019-06-18 Nono Inc. Agents et methodes de traitement de maladies ischemiques et d'autres maladies
PL2513140T3 (pl) 2009-12-16 2016-04-29 Novo Nordisk As Podwójnie acylowane pochodne glp-1
US20130022629A1 (en) 2010-01-04 2013-01-24 Sharpe Arlene H Modulators of Immunoinhibitory Receptor PD-1, and Methods of Use Thereof
EP2550260A1 (fr) 2010-03-24 2013-01-30 Medical University Of South Carolina Compositions et méthodes destinées au traitement de maladies neurodégénératives
CN102844302B (zh) 2010-04-06 2014-07-09 日本曹达株式会社 含氮杂环化合物及其制造方法
WO2011133920A1 (fr) 2010-04-23 2011-10-27 Cytokinetics, Inc. Aminopyridines et aminotriazines, leurs compositions et leurs procédés d'utilisation
US8217044B2 (en) 2010-04-28 2012-07-10 Hoffmann-La Roche Inc. Spiroindolinone pyrrolidines
BR112012033341B1 (pt) 2010-06-30 2022-08-23 Cyclerion Therapeutics, Inc Estimulantes de sgc
JP2013530199A (ja) 2010-07-06 2013-07-25 ノバルティス アーゲー キナーゼ阻害剤として有用な環状エーテル化合物
US8883839B2 (en) 2010-08-13 2014-11-11 Abbott Laboratories Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
US9051280B2 (en) 2010-08-13 2015-06-09 AbbVie Deutschland GmbH & Co. KG Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
US8846743B2 (en) 2010-08-13 2014-09-30 Abbott Laboratories Aminoindane derivatives, pharmaceutical compositions containing them, and their use in therapy
WO2012024604A2 (fr) 2010-08-20 2012-02-23 President And Fellows Of Harvard College Complexes de fluorure de palladium de valence élevée et leurs utilisations
JP2012107001A (ja) 2010-10-22 2012-06-07 Shionogi & Co Ltd インドールアミド化合物を含有する医薬
WO2012061337A1 (fr) 2010-11-02 2012-05-10 Exelixis, Inc. Modulateurs de fgfr2
US9061030B2 (en) 2010-11-09 2015-06-23 Ironwood Pharmaceuticals, Inc. sGC stimulators
WO2012074050A1 (fr) 2010-12-01 2012-06-07 富士フイルム株式会社 Film polymère, film de différence de phase, plaque de polarisation, dispositif d'affichage à cristaux liquides et composé
RU2013133813A (ru) 2010-12-21 2015-01-27 Конинклейке Филипс Электроникс Н.В. Средства для выведения биомолекул из кровотока
AU2011346751A1 (en) 2010-12-22 2013-05-02 Purdue Pharma L.P. Substituted pyridines as sodium channel blockers
US20120184572A1 (en) 2011-01-13 2012-07-19 Metabolex, Inc. Aryl gpr119 agonists and uses thereof
WO2012101062A1 (fr) 2011-01-28 2012-08-02 Novartis Ag Composés bi-hétéroaryles substitués en tant qu'inhibiteurs de cdk9 et leurs utilisations
US8957066B2 (en) * 2011-02-28 2015-02-17 Biomarin Pharmaceutical Inc. Histone deacetylase inhibitors
WO2012117097A1 (fr) 2011-03-03 2012-09-07 Universität des Saarlandes Dérivés biaryle en tant qu'inhibiteurs sélectifs de la 17bêta-hydroxystéroïde déshydrogénase de type 2
GB201104267D0 (en) 2011-03-14 2011-04-27 Cancer Rec Tech Ltd Pyrrolopyridineamino derivatives
US9464063B2 (en) 2011-03-18 2016-10-11 Lupin Atlantis Holdings Sa Benzo [B] [1,4] oxazin derivatives as calcium sensing receptor modulators
WO2012147890A1 (fr) 2011-04-27 2012-11-01 持田製薬株式会社 Nouveau dérivé d'azole
EP2712655B1 (fr) 2011-04-28 2019-12-18 The Broad Institute, Inc. Inhibiteurs de l'histone désacétylase
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
US9309200B2 (en) 2011-05-12 2016-04-12 AbbVie Deutschland GmbH & Co. KG Benzazepine derivatives, pharmaceutical compositions containing them, and their use in therapy
WO2012156918A1 (fr) 2011-05-16 2012-11-22 Koninklijke Philips Electronics N.V. Activation d'un médicament bio-orthogonal
DK2713722T3 (en) 2011-05-31 2017-07-03 Celgene Int Ii Sarl Newly known GLP-1 receptor stabilizers and modulators
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
EA201400161A1 (ru) 2011-07-26 2014-06-30 Грюненталь Гмбх Замещенные гетероароматические пиразолсодержащие карбоксамидные и мочевинные производные в качестве лигандов ваниллоидных рецепторов
AU2012289255A1 (en) 2011-07-26 2014-01-30 Grunenthal Gmbh Substituted heterocyclic aza derivatives
WO2013017480A1 (fr) 2011-07-29 2013-02-07 Cellzome Limited Dérivés de pyrazolo[4,3-c]pyridine en tant qu'inhibiteurs de jak
BR112014003112A2 (pt) 2011-08-12 2017-02-21 Basf Se composto da fórmula geral (i), métodos para preparar um composto da fórmula (i), composição agrícola ou veterinária, método para combater ou controlar pragas invertebradas, método para proteger o cultivo de plantas, método para a proteção de sementes, semente, usos de um composto e método para tratar um animal
AU2012300246A1 (en) 2011-08-30 2014-03-06 Chdi Foundation, Inc. Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
WO2013038390A1 (fr) 2011-09-16 2013-03-21 Novartis Ag Hétérocyclyle carboxamides n-substitués
JP2014527973A (ja) 2011-09-23 2014-10-23 バイエル・インテレクチユアル・プロパテイー・ゲー・エム・ベー・ハー 非生物的な植物ストレスに対する作用剤としての4−置換1−フェニルピラゾール−3−カルボン酸誘導体の使用
CN103987697B (zh) 2011-10-14 2017-04-26 百时美施贵宝公司 作为因子xia抑制剂的取代的四氢异喹啉化合物
WO2013059648A1 (fr) 2011-10-21 2013-04-25 Neurotherapeutics Pharma, Inc. Dérivés aminés d'hétéroaryle et d'aryle 2,3,5 trisubstitués, compositions et procédés d'utilisation associés
US9388137B2 (en) 2011-10-31 2016-07-12 Purdue Pharma L.P. Quaternized amines as sodium channel blockers
US9365512B2 (en) 2012-02-13 2016-06-14 AbbVie Deutschland GmbH & Co. KG Isoindoline derivatives, pharmaceutical compositions containing them, and their use in therapy
JP6113828B2 (ja) 2012-04-04 2017-04-12 ライジェル ファーマシューティカルズ, インコーポレイテッド プロテインキナーゼc阻害剤およびその使用
US9306178B2 (en) 2012-04-12 2016-04-05 The University Of Hong Kong Platinum(II) complexes for OLED applications
WO2013163404A1 (fr) 2012-04-27 2013-10-31 The Uab Research Foundation Traitement d'infections virales avec arn viraux traduits par un mécanisme non médié par l'ires
BR112014029501B1 (pt) 2012-05-31 2020-05-19 Sumitomo Chemical Co composto heterocíclico fundido, seu uso, agente de controle de pragas e método para o controle de pragas
US9013997B2 (en) 2012-06-01 2015-04-21 Broadcom Corporation System for performing distributed data cut-through
EP2858982A4 (fr) 2012-06-12 2015-11-11 Abbvie Inc Dérivés de pyridinone et de pyridazinone
CN104583206A (zh) 2012-06-15 2015-04-29 加利福尼亚大学董事会 用于脑癌的新颖治疗剂
CN103508961B (zh) 2012-06-26 2015-07-22 中美冠科生物技术(太仓)有限公司 抗肿瘤药物
WO2014005125A2 (fr) 2012-06-29 2014-01-03 Biotium, Inc. Composés fluorescents et utilisation de ceux-ci
BR112015001201B1 (pt) 2012-07-18 2022-02-22 University Of Notre Dame Du Lac Compostos anti-infecciosos 5,5-heteroaromáticos e composição
CN103570625A (zh) 2012-07-19 2014-02-12 南京英派药业有限公司 N-(3-杂芳基芳基)-4-芳基芳基甲酰胺和类似物作为Hedgehog通路抑制剂及其应用
WO2014025808A1 (fr) 2012-08-06 2014-02-13 The General Hospital Corporation Analogues de curcumine
EP2888256A4 (fr) 2012-08-24 2016-02-17 Univ Texas Modulateurs hétérocycliques de l'activité du facteur hif utilisés pour le traitement de maladies
US9309235B2 (en) 2012-09-18 2016-04-12 Ironwood Pharmaceuticals, Inc. SGC stimulators
MX2015004151A (es) 2012-10-05 2015-07-06 Rigel Pharmaceuticals Inc Inhibidores del factor de diferenciacion de crecimiento-8 (gdf-8).
EP2906217A1 (fr) 2012-10-11 2015-08-19 Grünenthal GmbH Prévention et/ou traitement des maladies et/ou troubles induits par tspo
JP2014101353A (ja) 2012-10-26 2014-06-05 Shionogi & Co Ltd オキサジン誘導体を含有するアルツハイマー症治療用または予防用医薬組成物
US9145412B2 (en) 2012-11-02 2015-09-29 Acetylon Pharmaceuticals, Inc. Selective HDAC1 and HDAC2 inhibitors
JP2016502519A (ja) 2012-11-09 2016-01-28 インディアナ・ユニバーシティ・リサーチ・アンド・テクノロジー・コーポレーション Hbv集合エフェクターの代替的使用
WO2014081300A1 (fr) 2012-11-22 2014-05-30 Tagworks Pharmaceuticals B.V. Liposomes activables par des protéines de canal
WO2014081299A1 (fr) 2012-11-22 2014-05-30 Tagworks Pharmaceuticals B.V. Liposome pouvant être actif
WO2014081301A1 (fr) 2012-11-22 2014-05-30 Tagworks Pharmaceuticals B.V. Activation de médicament bio-orthogonale
EP2922574B1 (fr) 2012-11-22 2023-05-17 Tagworks Pharmaceuticals B.V. Groupe clivable par voie chimique
EP2928891B1 (fr) 2012-12-04 2019-02-20 Rigel Pharmaceuticals, Inc. Inhibiteurs de la protéine kinase c et utilisations de ceux-ci
CN103864754B (zh) 2012-12-10 2016-12-21 中国科学院上海药物研究所 五元唑类杂环化合物及其制备方法、药物组合物和用途
US9890127B2 (en) 2013-03-11 2018-02-13 The Broad Institute, Inc. Compounds and compositions for the treatment of cancer
US9045455B2 (en) 2013-03-14 2015-06-02 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
WO2014151936A1 (fr) 2013-03-14 2014-09-25 The Trustees Of Columbia University In The City Of New York Octahydropyrrolopyrroles, leur préparation et leur utilisation
CN105163738A (zh) 2013-03-15 2015-12-16 西建阿维拉米斯研究公司 Mk2抑制剂和其用途
JP2016519078A (ja) 2013-03-15 2016-06-30 エピザイム,インコーポレイティド Carm1阻害剤およびその使用
EP2991967A1 (fr) 2013-03-20 2016-03-09 F. Hoffmann-La Roche AG Dérivés d'urée et leurs utilisations en tant qu'inhibiteurs de la protéine de liaison à un acide gras (fabp)
WO2014181287A1 (fr) 2013-05-09 2014-11-13 Piramal Enterprises Limited Composés hétérocyclyliques et leurs utilisations
CN104163792B (zh) 2013-05-20 2017-04-12 湖南化工研究院 N‑吡啶酰胺类化合物及其制备方法与应用
CN104163791B (zh) 2013-05-20 2017-05-03 湖南化工研究院 N‑吡啶(杂)芳酰胺类化合物及其制备方法与应用
CN105473578A (zh) 2013-05-24 2016-04-06 加州生物医学研究所 用于治疗抗药性和持续性结核病的化合物
CA2913622A1 (fr) 2013-05-30 2014-12-04 Washington University Composes et methodes de traitement d'infections bacteriennes
US9673409B2 (en) 2013-06-10 2017-06-06 Arizona Board Of Regents On Behalf Of Arizona State University Phosphorescent tetradentate metal complexes having modified emission spectra
GB2515785A (en) 2013-07-03 2015-01-07 Redx Pharma Ltd Compounds
GB2516303A (en) 2013-07-18 2015-01-21 Redx Pharma Ltd Compounds
US9359330B2 (en) 2013-08-26 2016-06-07 Purdue Pharma L.P. Substituted piperidines as sodium channel blockers
WO2015031725A1 (fr) 2013-08-30 2015-03-05 President And Fellows Of Harvard College Imidation d'arènes catalysée par des métaux de transition
CN105579440A (zh) 2013-09-06 2016-05-11 因森普深2公司 三唑酮化合物及其应用
WO2015051043A1 (fr) 2013-10-01 2015-04-09 Amgen Inc. Composés d'acylsulfonamide de biaryle en tant qu'inhibiteurs des canaux sodiques
CA2926571C (fr) 2013-10-08 2022-05-17 Qing-bin LU Composes anticancereux non a base de platine destines a etre utilises dans la chimiotherapie-cible
BR112016008632A8 (pt) 2013-10-21 2020-03-17 Merck Patent Gmbh compostos de heteroarila como inibidores de btk, seus usos, e composição farmacêutica
WO2015077246A1 (fr) 2013-11-19 2015-05-28 Vanderbilt University Composés imidazopyridine et triazolopyridine substitués utilisés comme modulateurs allostériques négatifs de mglur
CN103601718A (zh) 2013-12-05 2014-02-26 江西天人生态股份有限公司 一类基于鱼泥丁受体的邻甲酰氨基苯甲酰胺衍生物及其制备方法和用途
WO2015110999A1 (fr) 2014-01-24 2015-07-30 Piramal Enterprises Limited Inhibiteurs de ezh2 et leurs utilisations
CN103804312B (zh) 2014-02-17 2016-04-20 四川百利药业有限责任公司 一类氮杂环化合物及其制备方法和用途
WO2015142903A2 (fr) 2014-03-17 2015-09-24 Genentech, Inc. Procédé pour réguler la production de lactate à l'aide de dérivés de pipéridine-dione
US9533982B2 (en) 2014-03-20 2017-01-03 Vanderbilt University Substituted bicyclic heteroaryl carboxamide analogs as mGluR5 negative allosteric modulators
GB201405002D0 (en) 2014-03-20 2014-05-07 Isis Innovation Fluorination method
US11691997B2 (en) 2014-04-09 2023-07-04 Lumiphore, Inc. Macrocycles
WO2015170218A1 (fr) 2014-05-07 2015-11-12 Pfizer Inc. Inhibiteurs de kinases apparentées à la tropomyosine
WO2015187542A1 (fr) * 2014-06-02 2015-12-10 Chdi Foundation Inc. Inhibiteurs d'histone désacétylase, et compositions et méthodes d'utilisation de ceux-ci
WO2016018795A1 (fr) 2014-07-28 2016-02-04 The General Hospital Corporation Inhibiteurs d'histone désacétylase
CN107124882A (zh) 2014-08-04 2017-09-01 基础应用医学研究基金会 用于认知改善的新型化合物
WO2016028391A2 (fr) 2014-08-18 2016-02-25 Hudson Biopharma Inc. Spiropyrrolidines utiles en tant qu'inhibiteurs de mdm2
GB201416513D0 (en) 2014-09-18 2014-11-05 Astex Therapeutics Ltd And Cancer Res Technology Ltd Pharmaceutical compounds
US9550778B2 (en) 2014-10-03 2017-01-24 Vanderbilt University Substituted 6-aryl-imidazopyridine and 6-aryl-triazolopyridine carboxamide analogs as negative allosteric modulators of mGluR5
WO2016057779A2 (fr) 2014-10-08 2016-04-14 Acetylon Pharmaceuticals, Inc. Induction de gata2 par des inhibiteurs de hdac1 et hdac2
SG10202009859YA (en) 2014-10-16 2020-11-27 Sage Therapeutics Inc Compositions and methods for treating cns disorders
US10308648B2 (en) 2014-10-16 2019-06-04 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
WO2016100711A1 (fr) 2014-12-18 2016-06-23 The Broad Institute, Inc. Modulateurs de métabolisme des lipoprotéines hépatiques
CN105777632A (zh) 2015-01-09 2016-07-20 成都贝斯凯瑞生物科技有限公司 芳环并氮杂环衍生物及其应用
JP6800158B2 (ja) 2015-02-20 2020-12-16 ライジェル ファーマシューティカルズ, インコーポレイテッド Gdf−8阻害剤
CA3241654A1 (fr) 2015-04-30 2016-11-03 Memorial Sloan-Kettering Cancer Center Analogues de la mitragynine et leurs utilisations
CN106083823A (zh) 2015-04-30 2016-11-09 中国科学院上海药物研究所 一类具有激酶抑制活性的化合物、制备方法和用途
US10738035B2 (en) 2015-05-13 2020-08-11 Enanta Pharmaceuticals, Inc. Hepatitis B antiviral agents
EP3319968A1 (fr) 2015-07-06 2018-05-16 Rodin Therapeutics, Inc. N-aminophényl-amides hétérocycliques en tant qu'inhibiteurs de l'histone désacétylase
ES2899906T3 (es) 2015-07-06 2022-03-15 Alkermes Inc Inhibidores bicíclicos de histona desacetilasa
WO2017027984A1 (fr) 2015-08-20 2017-02-23 Simon Fraser University Composés et procédés de traitement anticancéreux par l'inhibition d'atg4b et le blocage de l'autophagie
US10980755B2 (en) 2015-09-10 2021-04-20 The Regents Of The University Of California LRH-1 modulators
WO2017046133A1 (fr) 2015-09-14 2017-03-23 Universiteit Antwerpen Procédé pour le clivage catalytique dirigé de composés contenant un amide
WO2017075694A1 (fr) 2015-11-04 2017-05-11 Simon Fraser University Composés antibiotiques, leurs formulations pharmaceutiques, ainsi que procédés associés et utilisations associées
TWI773657B (zh) 2015-12-18 2022-08-11 美商亞德利克斯公司 作爲非全身tgr5促效劑之經取代之4-苯基吡啶化合物
MD3269370T2 (ro) 2016-02-23 2020-05-31 Taiho Pharmaceutical Co Ltd Compus pirimidinic condensat nou sau sare a acestuia
WO2017156265A1 (fr) 2016-03-09 2017-09-14 President And Fellows Of Harvard College Fluoration aromatique directe catalysée par du palladium
TWI794171B (zh) 2016-05-11 2023-03-01 美商滬亞生物國際有限公司 Hdac抑制劑與pd-l1抑制劑之組合治療
CN110049978A (zh) 2016-11-23 2019-07-23 雷格南希制药有限责任公司 作为选择性hdac1,2抑制剂的哌嗪衍生物
WO2018132533A1 (fr) 2017-01-11 2018-07-19 Rodin Therapeutics, Inc. Inhibiteurs bicycliques d'histone désacétylase
CN106946890A (zh) 2017-04-26 2017-07-14 中国药科大学 吡啶类irak4抑制剂、其制备方法及应用
CA3071861A1 (fr) 2017-08-07 2019-02-14 Rodin Therapeutics, Inc. Inhibiteurs bicycliques d'histone desacetylase
CA3106355A1 (fr) 2018-07-13 2020-01-16 Alkermes, Inc. Derives d'(amino-pyridinyle)pyrrolidinyle-1-carboxyamide et compositions pharmaceutiques connexes utiles comme inhibiteurs d'histone-desacetylase
TW202019910A (zh) 2018-07-13 2020-06-01 美商羅登醫療公司 組蛋白去乙醯酶雙環抑制劑

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