[go: up one dir, main page]

MA49839B1 - Inhibiteurs bicycliques de la histone déacétylase - Google Patents

Inhibiteurs bicycliques de la histone déacétylase

Info

Publication number
MA49839B1
MA49839B1 MA49839A MA49839A MA49839B1 MA 49839 B1 MA49839 B1 MA 49839B1 MA 49839 A MA49839 A MA 49839A MA 49839 A MA49839 A MA 49839A MA 49839 B1 MA49839 B1 MA 49839B1
Authority
MA
Morocco
Prior art keywords
bicyclic
histone deacetylase
deacetylase inhibitors
hdac2
hdac
Prior art date
Application number
MA49839A
Other languages
English (en)
Other versions
MA49839A (fr
Inventor
Nathan Fuller
John Lowe
Original Assignee
Alkermes 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 Alkermes Inc filed Critical Alkermes 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)
  • Oncology (AREA)
  • Rheumatology (AREA)
  • Communicable Diseases (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

L'invention concerne des composés et des sels pharmaceutiquement acceptables de ceux-ci, ainsi que des compositions pharmaceutiques de ceux-ci, qui sont utiles dans le traitement de pathologies associées à l'inhibition de hdac (par exemple, hdac2).
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 MA49839A (fr) 2020-06-17
MA49839B1 true 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 (25)

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)
CY (1) CY1125199T1 (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)
SM (1) SMT202200232T1 (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
WO2017007756A1 (fr) 2015-07-06 2017-01-12 Rodin Therapeutics, Inc Inhibiteurs hétéro-halogéno d'histone désacétylase
WO2018132531A1 (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
AU699727B2 (en) 1995-02-02 1998-12-10 Smithkline Beecham Plc Indole derivatives as 5-HT receptor antagonist
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
US5872136A (en) 1996-04-03 1999-02-16 Merck & Co., Inc. Arylheteroaryl inhibitors of farnesyl-protein transferase
WO1997036901A1 (fr) 1996-04-03 1997-10-09 Merck & Co., Inc. Inhibiteurs de transferase de farnesyl-proteine
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
ATE274510T1 (de) 1998-06-19 2004-09-15 Chiron Corp Glycogen synthase kinase 3 inhibitoren
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
AU2001286454B2 (en) 2000-08-14 2006-09-14 Ortho-Mcneil Pharmaceutical, Inc. Substituted pyrazoles
PL365606A1 (en) 2000-09-06 2005-01-10 Ortho Mcneil Pharmaceutical, Inc. A method for treating allergies using substituted pyrazoles
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
AU3950802A (en) 2000-12-07 2002-06-18 Cv Therapeutics Inc Abca-1 elevating compounds
EP1353674A1 (fr) 2000-12-29 2003-10-22 Alteon, Inc. Methode de traitement du glaucome ivb
ATE375340T1 (de) 2001-02-21 2007-10-15 Nps Pharma Inc Heteropolycyclische verbindungen und deren verwendung als metabotrope glutamatrezeptorantagonisten
AU2002305450A1 (en) 2001-05-08 2002-11-18 Yale University Proteomimetic compounds and methods
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
EP1467986A1 (fr) 2002-01-17 2004-10-20 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
WO2004000318A2 (fr) 2002-06-21 2003-12-31 Cellular Genomics, Inc. Utilisation de certains monocycles a substitution amino en tant que modulateurs de l'activite des kinases
AU2003262642B2 (en) 2002-08-14 2010-06-17 Vertex Pharmaceuticals Incorporated Protein kinase inhibitors and uses thereof
US7632858B2 (en) 2002-11-15 2009-12-15 Bristol-Myers Squibb Company Open chain prolyl urea-related modulators of androgen receptor function
WO2004071426A2 (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
ATE431822T1 (de) 2003-07-24 2009-06-15 Euro Celtique Sa Zur behandlung oder vorbeugung von schmerzen geeignete heteroaryl-tetrahydropiperidyl- verbindungen
TWI287567B (en) 2003-07-30 2007-10-01 Chi Mei Optoelectronics Corp Light-emitting element and iridium complex
JP2007501805A (ja) 2003-08-08 2007-02-01 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ ピリジルピペラジニルウレア
MXPA06001739A (es) 2003-08-14 2006-05-12 Asahi Kasei Pharma Corp Derivado de acido arilalcanoico substituido y uso del mismo.
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
EP1715867A4 (fr) 2004-02-12 2009-04-15 Merck & Co Inc Amides bipyridyles en tant que modulateurs du r cepteur-5 metabotropique du glutamate
US7470701B2 (en) 2004-03-30 2008-12-30 Novartis Vaccines And Diagnostics, Inc. Substituted 2,5-heterocyclic derivatives
EP1735278B1 (fr) 2004-04-01 2010-01-06 Eli Lilly And Company Agents recepteurs de l'histamine h3, preparation et utilisations therapeutiques
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
MX2007001029A (es) 2004-07-26 2007-04-12 Lilly Co Eli Agentes del receptor de histamina h3, preparacion y usos terapeuticos.
ATE502025T1 (de) 2004-10-19 2011-04-15 Compass Pharmaceuticals Llc Arylcarboxamide und ihre verwendung als antitumormittel
WO2006051311A1 (fr) 2004-11-12 2006-05-18 Galapagos Nv Composés hétéroaromatiques de l'azote qui se lient au site actif d'enzymes de type protéines kinases
JP2008520742A (ja) 2004-11-23 2008-06-19 ピーティーシー セラピューティクス, インコーポレイテッド Vegf産生の阻害に有用なカルバゾール誘導体、カルボリン誘導体およびインドール誘導体
KR20070091675A (ko) 2004-12-22 2007-09-11 아스트라제네카 아베 항암제로서 사용하기 위한 피리딘 카르복사미드 유도체
WO2006067445A2 (fr) 2004-12-22 2006-06-29 Astrazeneca Ab Composes chimiques
US7622583B2 (en) 2005-01-14 2009-11-24 Chemocentryx, Inc. Heteroaryl sulfonamides and CCR2
CA2594726C (fr) 2005-01-14 2013-03-19 Chemocentryx, Inc. Sulfonamides d'heteroaryle et ccr2
EP1683796A1 (fr) 2005-01-24 2006-07-26 Schering Aktiengesellschaft Pyrazolopyridines, leur préparation et leur utilisation médicale
US20080146612A1 (en) 2005-01-27 2008-06-19 Astrazeneca Ab Novel Biaromatic Compounds, Inhibitors of the P2X7-Receptor
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
US20060235028A1 (en) 2005-04-14 2006-10-19 Li James J Inhibitors of 11-beta hydroxysteroid dehydrogenase type I
JP2008545624A (ja) 2005-05-13 2008-12-18 チバ ホールディング インコーポレーテッド 金属錯体を含むケラチン繊維を着色するための方法
US20070032493A1 (en) 2005-05-26 2007-02-08 Synta Pharmaceuticals Corp. Method for treating B cell regulated autoimmune disorders
WO2006128129A2 (fr) 2005-05-26 2006-11-30 Synta Pharmaceuticals Corp. Traitement anticancereux
JP2008545744A (ja) 2005-06-02 2008-12-18 バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト フェニルアルキル置換ヘテロアリール誘導体
CA2610884A1 (fr) 2005-06-09 2006-12-21 Merck & Co., Inc. Inhibiteurs de kinases checkpoint
AR053901A1 (es) 2005-06-20 2007-05-23 Astrazeneca Ab Formas fisicas de oxabispidinas n,n'- disustituidas
WO2007002313A2 (fr) 2005-06-24 2007-01-04 Bristol-Myers Squibb Company Derives de phenylglycinamide et pyridylglycinamide utiles en tant que anticoagulants
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
AU2006312083A1 (en) 2005-11-03 2007-05-18 Merck Sharp & Dohme Corp. Histone deacetylase inhibitors with aryl-pyrazolyl motifs
KR101561482B1 (ko) 2005-11-08 2015-10-20 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)
CA2630884A1 (fr) 2005-11-30 2007-06-07 Vertex Pharmaceuticals Incorporated Inhibiteurs de c-met et leurs utilisations
KR101121240B1 (ko) 2005-12-23 2012-06-12 에프. 호프만-라 로슈 아게 아릴-아이속사졸-4-일-옥사다이아졸 유도체
JP2009523726A (ja) 2006-01-12 2009-06-25 メルク エンド カムパニー インコーポレーテッド ヒドロキシアルキルアリールアミド誘導体
AU2007208494A1 (en) 2006-01-12 2007-08-02 Merck Sharp & Dohme Corp. 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
DK2004181T6 (da) 2006-03-27 2023-08-21 Univ California Androgen receptormodulator til behandling af prostatacancer og androgen receptor-associerede sygdomme
AU2007234843B2 (en) 2006-04-07 2013-07-11 Methylgene Inc. Inhibitors of histone deacetylase
JPWO2007125984A1 (ja) 2006-04-28 2009-09-10 日本農薬株式会社 イソキサゾリン誘導体及び有害生物防除剤並びにその使用方法
JP2009535388A (ja) 2006-05-03 2009-10-01 アストラゼネカ アクチボラグ ピラゾール誘導体、及びそのpi3k阻害薬としての使用
WO2007129044A1 (fr) 2006-05-03 2007-11-15 Astrazeneca Ab Dérivés de thiazole et leur utilisation comme agents anti-tumoraux
US20080064871A1 (en) 2006-05-26 2008-03-13 Japan Tobacco Inc. Production Method of Nitrogen-Containing Fused Ring Compounds
CA2653506A1 (fr) 2006-05-31 2007-12-06 Galapagos Nv. Composes de triazolopyrazine utilises dans le traitement des maladies degeneratives et inflammatoires
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
US7981874B2 (en) 2006-07-20 2011-07-19 Merck Sharp & Dohme Corp. Phosphorus derivatives as histone deacetylase inhibitors
KR20090029274A (ko) 2006-07-21 2009-03-20 아이알엠 엘엘씨 Itpkb 억제제로서의 화합물 및 조성물
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
WO2008013963A2 (fr) 2006-07-28 2008-01-31 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
US20080076813A1 (en) 2006-08-24 2008-03-27 Huang Kenneth H Benzene, Pyridine, and Pyridazine Derivatives
US20080119457A1 (en) 2006-08-24 2008-05-22 Serenex, Inc. Benzene, Pyridine, and Pyridazine Derivatives
US8481538B2 (en) 2006-09-18 2013-07-09 Vertex Pharmaceuticals Incorporated Heterocyclic inhibitors of c-Met and uses thereof
HRP20110158T1 (hr) 2006-10-18 2011-04-30 Pfizer Products Inc. Biaril eterski spojevi ureje
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
WO2008053913A1 (fr) 2006-11-02 2008-05-08 Shionogi & Co., Ltd. Dérivé de sulfonylurée capable d'inhiber sélectivement 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
JP5498796B2 (ja) 2006-12-21 2014-05-21 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ 置換ピラゾロ−キナゾリン誘導体、これらの調製方法及びキナーゼ阻害剤としてのこれらの使用
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
ES2702362T3 (es) 2007-01-31 2019-02-28 Ym Biosciences Australia Pty Compuestos a base de tiopirimidina y usos de los mismos
WO2008115262A2 (fr) 2007-03-20 2008-09-25 Curis, Inc. Inhibiteurs de hsp90 contenant une fraction de liaison de zinc
ES2430217T3 (es) 2007-03-20 2013-11-19 Curis, Inc. Aminopiridina condensada como inhibidores de HSP90
WO2008119015A2 (fr) 2007-03-27 2008-10-02 Sloan-Kettering Institute For Cancer Research Synthèse de dérivés de la thiohydantoïne
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
MX2009013169A (es) 2007-06-03 2010-04-30 Univ Vanderbilt Moduladores alostericos positivos del mglur5 benzamida y metodos de elaboracion y uso de los mismos.
CN101679346B (zh) 2007-06-05 2014-10-22 塞诺菲-安万特股份有限公司 取代的苯甲酰氨基茚满-2-羧酸及相关化合物
US7928111B2 (en) 2007-06-08 2011-04-19 Senomyx, Inc. Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
US8633186B2 (en) 2007-06-08 2014-01-21 Senomyx Inc. Modulation of chemosensory receptors and ligands associated therewith
JP2010531358A (ja) 2007-06-27 2010-09-24 メルク・シャープ・エンド・ドーム・コーポレイション ヒストン脱アセチル化酵素阻害剤としてのピリジル及びピリミジニル誘導体
WO2009022171A1 (fr) 2007-08-13 2009-02-19 Astrazeneca Ab Composés chimiques 1 - 821
ES2535166T3 (es) 2007-09-04 2015-05-06 The Scripps Research Institute Pirimidinil-aminas sustituidas como inhibidores de proteína-quinasas
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
WO2009037001A2 (fr) 2007-09-19 2009-03-26 4Sc Ag Nouvelles pyridines tétrahydrocondensées
CA2702946A1 (fr) 2007-10-16 2009-04-23 Northeastern University Inhibiteurs de la monoacylglycerol lipase de modulation de l'activite cannabinoide
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
US20110098267A1 (en) 2008-02-07 2011-04-28 Synta Pharmaceuticals Corporation Topical formulations for the treatment of 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
CA2727389A1 (fr) 2008-06-10 2009-12-17 Prabha N. Ibrahim Derives 5h-pyrrolo-[2,3-b]-pyrazine destines a la modulation de kinases, et des indications pour ceux-ci
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
PE20110136A1 (es) 2008-06-27 2011-03-17 Novartis Ag Compuestos organicos
KR101345941B1 (ko) 2008-07-11 2013-12-30 아이알엠 엘엘씨 Gpr119 활성의 조절제로서의 4-페녹시메틸피페리딘
WO2010007756A1 (fr) 2008-07-14 2010-01-21 塩野義製薬株式会社 Dérivé de pyridine ayant une activité d'inhibition de la ttk
NZ590285A (en) 2008-07-15 2012-10-26 Novartis Ag Heteroaryl derivatives as dgat1 inhibitors
US8722686B2 (en) 2008-09-19 2014-05-13 Pfizer Inc. Hydroxamic acid derivatives useful as antibacterial agents
BRPI0920608A2 (pt) 2008-09-29 2019-09-24 Boehringer Ingelheim Int compostos quimicos
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
EP2367824B1 (fr) 2008-12-23 2016-03-23 AbbVie Inc. Dérivés de pyrimidine antiviraux
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
JP2012522748A (ja) 2009-04-01 2012-09-27 ノバルティス アーゲー ステアロイル−coaデサチュラーゼ調節用スピロ誘導体
DK2427436T3 (da) 2009-05-07 2013-04-02 Gruenenthal Gmbh Substituerede aromatiske carboxamid og urea derivater som vanilloidreceptorligander.
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
JP5586692B2 (ja) 2009-06-08 2014-09-10 ギリアード サイエンシーズ, インコーポレイテッド アルカノイルアミノベンズアミドアニリンhdacインヒビター化合物
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
AU2010327936B2 (en) 2009-12-11 2015-08-20 Nono Inc. Agents and methods for treating ischemic and other diseases
AU2010338387B2 (en) 2009-12-16 2014-10-23 Novo Nordisk A/S Double-acylated GLP-1 derivatives
US20130022629A1 (en) 2010-01-04 2013-01-24 Sharpe Arlene H Modulators of Immunoinhibitory Receptor PD-1, and Methods of Use Thereof
WO2011119869A1 (fr) 2010-03-24 2011-09-29 Medical University Of South Carolina Compositions et méthodes destinées au traitement de maladies neurodégénératives
EP2842944B1 (fr) 2010-04-06 2017-03-15 Nippon Soda Co., Ltd. Procédé de production de composé hétérocyclique contenant de l'azote
US9133123B2 (en) 2010-04-23 2015-09-15 Cytokinetics, Inc. Certain amino-pyridines and amino-triazines, compositions thereof, and methods for their use
US8217044B2 (en) 2010-04-28 2012-07-10 Hoffmann-La Roche Inc. Spiroindolinone pyrrolidines
DK2588465T3 (en) 2010-06-30 2017-05-01 Ironwood Pharmaceuticals Inc SGC stimulators
US20130109682A1 (en) 2010-07-06 2013-05-02 Novartis Ag Cyclic ether compounds useful as kinase inhibitors
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
US8883839B2 (en) 2010-08-13 2014-11-11 Abbott Laboratories 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
EP2606056A4 (fr) 2010-08-20 2014-01-08 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
RU2582679C2 (ru) 2010-11-09 2016-04-27 Айронвуд Фармасьютикалз, Инк. СТИМУЛЯТОРЫ sGC
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
WO2012085789A1 (fr) 2010-12-21 2012-06-28 Koninklijke Philips Electronics N.V. Agents pour l'élimination de biomolécules hors de la circulation
CN103429571A (zh) 2010-12-22 2013-12-04 普渡制药公司 作为钠通道阻断剂的取代吡啶
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
EP2681205B1 (fr) 2011-03-03 2016-11-16 Universität des Saarlandes Derivés de biaryl en tant qu'inhibiteurs sélectifs de la 17-bêta-hydroxystéroïde déshydrogénase de type 2
GB201104267D0 (en) 2011-03-14 2011-04-27 Cancer Rec Tech Ltd Pyrrolopyridineamino derivatives
WO2012127385A1 (fr) 2011-03-18 2012-09-27 Lupin Limited Dérivés benzo[b][1,4]oxazine en tant que modulateurs de récepteurs de détection de calcium
WO2012147890A1 (fr) 2011-04-27 2012-11-01 持田製薬株式会社 Nouveau dérivé d'azole
CA2834548C (fr) * 2011-04-28 2021-06-01 The Broad Institute, Inc. Inhibiteurs de l'histone desacetylase
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
WO2012156920A1 (fr) 2011-05-16 2012-11-22 Koninklijke Philips Electronics N.V. Activation d'un médicament bio-orthogonal
EP2713722B1 (fr) 2011-05-31 2017-03-15 Receptos, LLC Nouveaux stabilisants et modulateurs du récepteur de glp-1
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
CA2842916A1 (fr) 2011-07-26 2013-01-31 Grunenthal Gmbh Derives de carboxamide et d'uree contenant un pyrazole heteroaromatique substitues en tant que ligands de recepteur de vanilloide
AR087302A1 (es) 2011-07-26 2014-03-12 Gruenenthal Gmbh Derivados aza heterociclicos sustituidos
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
EA201490279A1 (ru) 2011-08-30 2014-08-29 Схди Фаундейшн, Инк. Ингибиторы кинуренин-3-монооксигеназы, фармацевтические композиции и способы их применения
JP6165733B2 (ja) 2011-09-16 2017-07-19 ノバルティス アーゲー N−置換ヘテロシクリルカルボキサミド類
AR087971A1 (es) 2011-09-23 2014-04-30 Bayer Ip Gmbh Uso de derivados del acido 1-fenil-pirazol-3-carboxilico 4-sustituidos como principios activos contra estres abiotico de plantas
WO2013055984A1 (fr) 2011-10-14 2013-04-18 Bristol-Myers Squibb Company Composés tétrahydroisoquinolines substitués en tant qu'inhibiteurs du facteur xia
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
AU2012321111A1 (en) 2011-10-31 2013-05-16 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
WO2013152198A1 (fr) 2012-04-04 2013-10-10 Rigel Pharmaceuticals, Inc. Inhibiteurs de protéine kinase c et utilisations de ceux-ci
WO2013152727A1 (fr) 2012-04-12 2013-10-17 The University Of Hong Kong Complexes de platine (ii) pour applications oled
US20150105433A1 (en) 2012-04-27 2015-04-16 The Uab Research Foundation TREATING VIRAL INFECTIONS HAVING VIRAL RNAs TRANSLATED BY A NON-IRES MEDIATED MECHANISM
CN104334552B (zh) 2012-05-31 2016-08-31 住友化学株式会社 稠合杂环化合物
US9013997B2 (en) 2012-06-01 2015-04-21 Broadcom Corporation System for performing distributed data cut-through
HK1208681A1 (en) 2012-06-12 2016-03-11 Abbvie Inc. Pyridinone and pyridazinone derivatives
CN106905297A (zh) 2012-06-15 2017-06-30 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
US9682970B2 (en) 2012-06-29 2017-06-20 Biotium, Inc. Fluorescent compounds and uses thereof
AU2013292529A1 (en) 2012-07-18 2015-02-12 Marvin J. Miller 5,5-heteroaromatic anti-infective compounds
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
US9738623B2 (en) 2012-08-06 2017-08-22 The General Hospital Corporation Curcumin analogs
WO2014031928A2 (fr) 2012-08-24 2014-02-27 Philip Jones 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
AU2013326867B2 (en) 2012-10-05 2018-03-08 Rigel Pharmaceuticals, Inc. GDF-8 inhibitors
WO2014056620A1 (fr) 2012-10-11 2014-04-17 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
CA2889892A1 (fr) 2012-11-09 2014-05-15 Indiana University Research And Technology Corporation Nouvelles utilisations d'effecteurs d'assemblage du vhb
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
DK2922574T3 (da) 2012-11-22 2023-08-21 Tagworks Pharmaceuticals B V Kemisk spaltbar gruppe
US20150297741A1 (en) 2012-11-22 2015-10-22 Tagworks Pharmaceuticals B.V. Bio-orthogonal drug activation
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
WO2014164704A2 (fr) 2013-03-11 2014-10-09 The Broad Institute, Inc. Composés et compositions utilisables en vue du traitement du cancer
US9944644B2 (en) 2013-03-14 2018-04-17 The Trustees Of Columbia University In The City Of New York Octahydropyrrolopyrroles their preparation and use
WO2014153208A1 (fr) 2013-03-14 2014-09-25 Epizyme, Inc. Inhibiteurs d'arginine méthyltransférase et leurs utilisations
JP2016518316A (ja) 2013-03-15 2016-06-23 セルジーン アビロミクス リサーチ, インコーポレイテッド Mk2阻害剤およびそれらの使用
EA201591532A1 (ru) 2013-03-15 2016-03-31 Эпизим, Инк. Ингибиторы carm1 и их применение
RU2642454C2 (ru) 2013-03-20 2018-01-25 Ф. Хоффманн-Ля Рош Аг Производные мочевины и их применение в качестве ингибиторов белка, связывающего жирные кислоты
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
WO2014190199A1 (fr) 2013-05-24 2014-11-27 The California Institute For Biomedical Research Composés pour le traitement de la tuberculose résistante aux médicaments et persistante
WO2014194270A1 (fr) 2013-05-30 2014-12-04 Washington University Composés et méthodes de traitement d'infections bactériennes
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
MX2016002795A (es) 2013-09-06 2016-05-26 Inception 2 Inc Compuestos de triazolona y usos de los mismos.
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
EP3060550B1 (fr) 2013-10-21 2019-05-15 Merck Patent GmbH Composés hétéroaryle servant d'inhibiteurs de la btk et leurs utilisations
AU2014353150A1 (en) 2013-11-19 2016-07-07 Vanderbilt University Substituted imidazopyridine and triazolopyridine compounds as negative allosteric modulators of mGluR5
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
EP3129350B1 (fr) 2014-04-09 2021-10-27 Lumiphore, Inc. Macrocycles
WO2015170218A1 (fr) 2014-05-07 2015-11-12 Pfizer Inc. Inhibiteurs de kinases apparentées à la tropomyosine
AU2015270926A1 (en) * 2014-06-02 2017-01-05 Chdi Foundation, Inc. Histone deacetylase inhibitors and compositions and methods of use thereof
US20170349540A1 (en) 2014-07-28 2017-12-07 The General Hospital Corporation Histone deacetylase inhibitors
EP3177622A1 (fr) 2014-08-04 2017-06-14 Fundacion para la Investigacion Medica Aplicada Nouveaux composés à utiliser pour améliorer la cognition
US9701685B2 (en) 2014-08-18 2017-07-11 Hudson Biopharma Inc. Spiropyrrolidines as MDM2 inhibitors
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
EP3204006A4 (fr) 2014-10-08 2018-04-04 Regenacy Pharmaceuticals, LLC Induction de gata2 par des inhibiteurs de hdac1 et hdac2
WO2016058544A1 (fr) 2014-10-16 2016-04-21 Syros Pharmaceuticals, Inc. Inhibiteurs de la kinase cycline-dépendante 7 (cdk7)
KR102612943B1 (ko) 2014-10-16 2023-12-13 세이지 테라퓨틱스, 인크. Cns 장애의 치료를 위한 조성물 및 방법
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
EP3259264B1 (fr) 2015-02-20 2022-07-27 Rigel Pharmaceuticals, Inc. Inhibiteurs du gdf 8
WO2016176657A1 (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
WO2017007756A1 (fr) 2015-07-06 2017-01-12 Rodin Therapeutics, Inc Inhibiteurs hétéro-halogéno d'histone désacétylase
EP3319968A1 (fr) * 2015-07-06 2018-05-16 Rodin Therapeutics, Inc. N-aminophényl-amides hétérocycliques en tant qu'inhibiteurs de l'histone désacétylase
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
WO2017044889A1 (fr) 2015-09-10 2017-03-16 The Regents Of The University Of California Modulateurs lrh-1
EP3362436B1 (fr) 2015-09-14 2021-06-30 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
CN108697714B (zh) 2016-02-23 2022-04-26 大鹏药品工业株式会社 稠合嘧啶化合物或其盐
DK3426654T3 (en) 2016-03-09 2022-01-03 Harvard College Direct palladium-catalyzed aromatic fluorination
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
WO2018098296A1 (fr) 2016-11-23 2018-05-31 Regenacy Pharmaceuticals, Llc Dérivés pipérazine en tant qu'inhibiteurs sélectifs de hdac1,2
WO2018132531A1 (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
WO2020014602A1 (fr) 2018-07-13 2020-01-16 Rodin Therapeutics, Inc. Inhibiteurs bicycliques de l'histone désacétylase
SG11202012916WA (en) 2018-07-13 2021-01-28 Alkermes Inc Inhibitors of histone deacetylase

Also Published As

Publication number Publication date
MD3664802T2 (ro) 2022-07-31
PT3664802T (pt) 2022-05-24
SG11202000970WA (en) 2020-02-27
MX2020001484A (es) 2020-08-20
EA202090424A1 (ru) 2020-05-26
AU2018313094A1 (en) 2020-02-20
LT3664802T (lt) 2022-06-27
KR20200037286A (ko) 2020-04-08
CN111032040B (zh) 2023-08-29
IL272479B1 (en) 2023-04-01
ES2914355T3 (es) 2022-06-09
DK3664802T3 (en) 2022-05-30
WO2019032528A8 (fr) 2019-03-21
SI3664802T1 (sl) 2022-10-28
SMT202200232T1 (it) 2022-07-21
MA49839A (fr) 2020-06-17
US11225475B2 (en) 2022-01-18
WO2019032528A1 (fr) 2019-02-14
CY1125199T1 (el) 2024-12-13
IL272479A (en) 2020-03-31
US11912702B2 (en) 2024-02-27
HRP20220648T1 (hr) 2022-09-02
US20220340558A1 (en) 2022-10-27
US20210147410A1 (en) 2021-05-20
PL3664802T3 (pl) 2022-07-11
JP2020530019A (ja) 2020-10-15
CA3071861A1 (fr) 2019-02-14
HUE058799T2 (hu) 2022-09-28
CN111032040A (zh) 2020-04-17
RS63343B1 (sr) 2022-07-29
EA039417B1 (ru) 2022-01-25
EP3664802A1 (fr) 2020-06-17
JP7152471B2 (ja) 2022-10-12
IL272479B2 (en) 2023-08-01
EP3664802B1 (fr) 2022-02-23

Similar Documents

Publication Publication Date Title
SA522433000B1 (ar) مركبات فلورو ألكيل-أوكساديازول واستخداماتها
MA40111B1 (fr) Dérivés du tétrahydronaphtalène inhibant la protéine mcl-1
EA202090871A1 (ru) Ингибирование убиквитин-специфической пептидазы 30
ZA202004023B (en) 1,2,4-oxadiazole derivatives as histone deacetylase 6 inhibitors
MA37762B1 (fr) Composés n-aryltriazole utilisés comme antagonistes de lpar
MA37764A1 (fr) Composés n-alkyltriazole utilisés comme antagonistes de lpar
MA49839B1 (fr) Inhibiteurs bicycliques de la histone déacétylase
MA40290A1 (fr) Agents immunorégulateurs
MX2021006347A (es) Metodos de tratamiento de cánceres que sobreexpresan whsc1 mediante la inhibición de setd2.
EA201792028A1 (ru) Альфа-цинамидные соединения и композиции как ингибиторы hdac8
MA54386B1 (fr) Modulateurs de trex1
EP3616696A4 (fr) Composition pharmaceutique contenant de l'enzalutamide pouvant être administrée par voie orale
MX394242B (es) Inhibidores biciclicos de histona desacetilasa
EA202191955A1 (ru) Таблетированные составы с модифицированным высвобождением, содержащие ингибиторы фосфодиэстеразы
MX2021003643A (es) Derivados de terpenoides y usos de los mismos.
MX2020010552A (es) Derivados de bumetanida para el tratamiento de la hiperhidrosis.
MA42776B1 (fr) Composés utiles pour l'inhibition du ror-gamma-t
EA202190077A1 (ru) Ингибиторы гистондеацетилазы
MX2020005238A (es) Compuestos novedosos como inhibidores mpges-1.
MA39447A1 (fr) (s)-pirlindole ou ses sels pharmaceutiquement acceptables pour une utilisation en médecine
MA39448A1 (fr) (r)-pirlindole et ses sels pharmaceutiquement acceptables destinés à un usage médical
EA202192118A1 (ru) Фармацевтическая композиция, содержащая ацетаминофен и ибупрофен
EA202092190A1 (ru) Композиции и способы для лечения сильного запора
EA202192544A1 (ru) Новые ингибиторы калиевых каналов
JOP20200104A1 (ar) مركبات مثبطة لـ btk