CA2696609C - Therapeutic isoxazole compounds - Google Patents

Therapeutic isoxazole compounds Download PDF

Info

Publication number
CA2696609C
CA2696609C CA2696609A CA2696609A CA2696609C CA 2696609 C CA2696609 C CA 2696609C CA 2696609 A CA2696609 A CA 2696609A CA 2696609 A CA2696609 A CA 2696609A CA 2696609 C CA2696609 C CA 2696609C
Authority
CA
Canada
Prior art keywords
compound
pharmaceutically acceptable
acceptable salt
alkyl
aryl
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Fee Related
Application number
CA2696609A
Other languages
English (en)
French (fr)
Other versions
CA2696609A1 (en
Inventor
Alan P. Kaplan
Terence P. Keenan
Andrew J. Mcriner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dart Neuroscience Cayman Ltd
Original Assignee
Dart Neuroscience Cayman Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dart Neuroscience Cayman Ltd filed Critical Dart Neuroscience Cayman Ltd
Priority to CA2974477A priority Critical patent/CA2974477C/en
Publication of CA2696609A1 publication Critical patent/CA2696609A1/en
Application granted granted Critical
Publication of CA2696609C publication Critical patent/CA2696609C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4525—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4535—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom, e.g. pizotifen
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems
    • C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
CA2696609A 2007-08-27 2008-08-26 Therapeutic isoxazole compounds Expired - Fee Related CA2696609C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA2974477A CA2974477C (en) 2007-08-27 2008-08-26 Therapeutic isoxazole compounds

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US96820507P 2007-08-27 2007-08-27
US60/968,205 2007-08-27
PCT/US2008/074353 WO2009029632A1 (en) 2007-08-27 2008-08-26 Therapeutic isoxazole compounds

Related Child Applications (1)

Application Number Title Priority Date Filing Date
CA2974477A Division CA2974477C (en) 2007-08-27 2008-08-26 Therapeutic isoxazole compounds

Publications (2)

Publication Number Publication Date
CA2696609A1 CA2696609A1 (en) 2009-03-05
CA2696609C true CA2696609C (en) 2017-09-05

Family

ID=40387754

Family Applications (2)

Application Number Title Priority Date Filing Date
CA2696609A Expired - Fee Related CA2696609C (en) 2007-08-27 2008-08-26 Therapeutic isoxazole compounds
CA2974477A Expired - Fee Related CA2974477C (en) 2007-08-27 2008-08-26 Therapeutic isoxazole compounds

Family Applications After (1)

Application Number Title Priority Date Filing Date
CA2974477A Expired - Fee Related CA2974477C (en) 2007-08-27 2008-08-26 Therapeutic isoxazole compounds

Country Status (11)

Country Link
US (5) US8222243B2 (enExample)
EP (2) EP2182809B1 (enExample)
JP (3) JP5718053B2 (enExample)
KR (2) KR101669432B1 (enExample)
CN (2) CN101820764B (enExample)
AU (2) AU2008293542B9 (enExample)
CA (2) CA2696609C (enExample)
ES (2) ES2663517T3 (enExample)
IL (3) IL203910A (enExample)
MX (1) MX2010002258A (enExample)
WO (1) WO2009029632A1 (enExample)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR058439A1 (es) 2005-07-26 2008-02-06 Portela & Ca Sa Derivados de nitrocatecol como inhibidores de comt. procesos de obtencion y composiciones farmaceuticas.
EP1845097A1 (en) 2006-04-10 2007-10-17 Portela & Ca., S.A. Oxadiazole derivatives as COMT inhibitors
JP5517629B2 (ja) 2007-01-31 2014-06-11 ノヴィファーマ，エス．アー． Ｃｏｍｔ阻害剤用の投薬計画
CN101820764B (zh) * 2007-08-27 2014-06-04 海利空医疗公司 治疗用异噁唑化合物
ES2565080T3 (es) 2008-03-17 2016-03-31 Bial-Portela & Ca, S.A. Formas cristalinas de 5-[3-(2,5-dicloro-4,6-dimetil-1-oxi-piridin-3-il)-[1,2,4]oxadiazol-5-il]-3-nitrobenceno-1,2-diol
DE102009041242A1 (de) 2009-09-11 2011-12-15 Bayer Schering Pharma Aktiengesellschaft Heterocyclisch substituierte Aryl-Verbindungen und ihre Verwendung
DE102009041241A1 (de) 2009-09-11 2011-08-04 Bayer Schering Pharma Aktiengesellschaft, 13353 Substituierte Aryl-Verbindungen und ihre Verwendung
CA2757411C (en) 2009-04-01 2017-06-27 Teofilo Cardoso De Vasconcelos Pharmaceutical formulations comprising nitrocatechol derivatives and methods of making thereof
AR079545A1 (es) * 2009-12-21 2012-02-01 Bayer Cropscience Ag Tienilpiri(mi)dinilazol
US20140045900A1 (en) 2011-02-11 2014-02-13 Bial-Portela & Ca, S.A. Administration regime for nitrocatechols
CN102229606B (zh) * 2011-06-03 2014-07-02 浙江工业大学 含异噁唑杂环的2-甲基苯并呋喃类衍生物及制备与应用
CN102229603B (zh) * 2011-06-03 2014-07-02 浙江工业大学 含三唑杂环的2-甲基苯并呋喃类化合物及其制备与应用
CA2841113A1 (en) 2011-07-08 2013-01-17 Novartis Ag Novel trifluoromethyl-oxadiazole derivatives and their use in the treatment of disease
WO2013066839A2 (en) * 2011-10-31 2013-05-10 Glaxosmithkline Llc Compounds and methods
BR112014012815A8 (pt) 2011-11-28 2017-06-20 Novartis Ag derivados de trifluormetil-oxadiazol e uso dos mesmos no tratamento de doença
CA2858025C (en) 2011-12-13 2020-09-22 Bial-Portela & Ca., S.A. 5-[3-(2,5-dichloro-4,6-dimethyl-1-oxy-pyridin-3-yl)-[1,2,4]oxadiazol-5-yl]-2-hydroxy-3-methoxy-1-nitrobenzene as an intermediate to prepare a catechol-o-methyltransferase inhibitor
CN105143207B (zh) 2013-03-14 2018-04-24 达特神经科学(开曼)有限公司 作为pde4抑制剂的取代的吡啶和取代的吡嗪化合物
AU2014241759B2 (en) 2013-03-14 2017-10-19 Dart Neuroscience (Cayman) Ltd. Substituted naphthyridine and quinoline compounds as MAO inhibitors
CN104016938B (zh) * 2014-05-28 2016-08-17 浙江工业大学 一种含苯硒基的噁二唑类化合物及其制备与应用
CN104016939B (zh) * 2014-05-28 2016-06-15 浙江工业大学 一种2-亚乙基-3-乙酰基-1,3,4-噁二唑类化合物及其制备与应用
KR20170048589A (ko) * 2014-09-17 2017-05-08 다트 뉴로사이언스 (케이만) 엘티디. Mao-b 억제제 및 재활
JP2018500300A (ja) 2014-11-28 2018-01-11 ノヴィファーマ，エス．アー． パーキンソン病を遅延させるための医薬
WO2016179432A2 (en) 2015-05-05 2016-11-10 Dart Neuroscience, Llc Systems and methods for cognitive testing
UY37623A (es) * 2017-03-03 2018-09-28 Syngenta Participations Ag Derivados de oxadiazol tiofeno fungicidas
WO2018177993A1 (de) 2017-03-31 2018-10-04 Bayer Cropscience Aktiengesellschaft Pyrazole zur bekämpfung von arthropoden
JP7160487B2 (ja) 2017-05-04 2022-10-25 ビーエーエスエフ ソシエタス・ヨーロピア 植物病原菌を駆除するための置換５－（ハロアルキル）－５－ヒドロキシ－イソオキサゾール
TW201930276A (zh) * 2017-12-22 2019-08-01 德商拜耳廠股份有限公司 羥基異㗁唑啉及其衍生物
US10902558B2 (en) * 2018-05-18 2021-01-26 Gopro, Inc. Multiscale denoising of raw images with noise estimation
US10853215B2 (en) * 2018-09-10 2020-12-01 Microsoft Technology Licensing, Llc Intelligent configuration management of user devices
AU2024233204A1 (en) * 2023-03-09 2025-09-25 Aquinnah Pharmaceuticals, Inc. Inhibitors of tdp-43 and tau aggregation

Family Cites Families (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB935523A (en) * 1961-06-17 1963-08-28 Acraf New sulphamido-oxadiazoles
GB1051322A (enExample) * 1967-08-09
US3995048A (en) * 1975-10-20 1976-11-30 Sandoz, Inc. Isoxazolyl benzamides useful as tranquilizers and sleep-inducers
JPS6183181A (ja) * 1984-06-11 1986-04-26 イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− 除草剤性チオフエンスルホンアミド類およびピリジンスルホンアミド類
AU576868B2 (en) 1984-06-11 1988-09-08 E.I. Du Pont De Nemours And Company Thiophene and pyridine sulfonamides
DD265317A5 (de) * 1985-12-05 1989-03-01 Bayer Ag,De Herbizide und pflanzenwuchsregulierende mittel
DE3602016A1 (de) 1985-12-05 1987-06-11 Bayer Ag Pyri(mi)dyl-oxy- und thio-benzoesaeure-derivate
US5204482A (en) 1988-07-28 1993-04-20 Hoffman-Laroche Inc. Compounds for treating and preventing cognitive diseases and depression and methods of making same
US4938949A (en) 1988-09-12 1990-07-03 University Of New York Treatment of damaged bone marrow and dosage units therefor
US5047554A (en) 1989-04-18 1991-09-10 Pfizer Inc. 3-substituted-2-oxindole derivatives
DE3929233A1 (de) * 1989-09-02 1991-03-07 Bayer Ag 5-heterocyclyl-pyridin-3-carbon-benzylamide und -anilide
DE4126937A1 (de) 1991-08-10 1993-02-11 Basf Ag Salicyl(thio)etherderivate, verfahren und zwischenprodukte zu ihrer herstellung
GB2265371A (en) * 1992-03-06 1993-09-29 Shell Int Research Isoxazole compounds
US5246914A (en) * 1992-08-07 1993-09-21 Basf Aktiengesellschaft Salicyloyl (thio)ether derivatives, their preparation and intermediates for their preparation
ATE223390T1 (de) * 1995-02-13 2002-09-15 Searle & Co Substituierte isoxazole zur behandlung von entzündung
US5935966A (en) * 1995-09-01 1999-08-10 Signal Pharmaceuticals, Inc. Pyrimidine carboxylates and related compounds and methods for treating inflammatory conditions
CA2257196A1 (en) * 1996-06-06 1997-12-11 Morris Padgett Rorer Herbicidal pyridinyl and pyrazolylphenyl ketones
WO1998037068A1 (en) * 1997-02-21 1998-08-27 Bristol-Myers Squibb Company Benzoic acid derivatives and related compounds as antiarrhythmic agents
CN1252070A (zh) 1997-04-16 2000-05-03 艾博特公司 5,7－二取代4－氨基吡啶并[2,3－d]嘧啶化合物及其作为腺苷激酶抑制剂的用途
JPH11139975A (ja) * 1997-08-26 1999-05-25 Sankyo Co Ltd Ａ型モノアミンオキシダーゼ阻害薬
DE19743435A1 (de) * 1997-10-01 1999-04-08 Merck Patent Gmbh Benzamidinderivate
DE19744026A1 (de) 1997-10-06 1999-04-08 Hoechst Marion Roussel De Gmbh Pyrazol-Derivate, ihre Herstellung und ihre Verwendung in Arzneimitteln
AU751139B2 (en) 1997-10-13 2002-08-08 Astellas Pharma Inc. Amide derivative
JP4385414B2 (ja) 1997-10-13 2009-12-16 アステラス製薬株式会社 アミド若しくはアミン誘導体
DE19904389A1 (de) * 1999-02-04 2000-08-10 Bayer Ag Verwendung von substituierten Isoxazolcarbonsäuren und Derivate und neue Stoffe
KR20010113820A (ko) 1999-04-19 2001-12-28 시오노 요시히코 옥사디아졸 고리를 갖는 술폰아미드 유도체
PE20010628A1 (es) 1999-10-01 2001-06-18 Takeda Chemical Industries Ltd Compuestos de amina ciclica, su produccion y su uso
US7291641B2 (en) * 1999-10-11 2007-11-06 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) Derivatives of heterocycles with 5 members, their preparation and their use as medicaments
JP2003528107A (ja) 2000-03-22 2003-09-24 メルク フロスト カナダ アンド カンパニー Ｐｔｐ−１ｂ阻害薬としての硫黄置換アリールジフルオロメチルホスホン酸類
PL203161B1 (pl) 2000-04-21 2009-08-31 Shionogi & Co Pochodne oksadiazolu, kompozycja farmaceutyczna je zawierająca oraz zastosowanie pochodnej oksadiazolu do wytwarzania leku do leczenia raka
JP2001316378A (ja) * 2000-04-28 2001-11-13 Takeda Chem Ind Ltd ベンズアミド誘導体およびその用途
US6579880B2 (en) * 2000-06-06 2003-06-17 Ortho-Mcneil Pharmaceutical, Inc. Isoxazoles and oxadiazoles as anti-inflammatory inhibitors of IL-8
AU2001282910A1 (en) 2000-08-21 2002-03-04 Pharmacia And Upjohn Company Quinuclidine-substituted heteroaryl moieties for treatment of disease (nicotinic) acetylcholine receptor ligands
US6500840B2 (en) 2000-08-21 2002-12-31 Pharmacia & Upjohn Company Quinuclidine-substituted heteroaryl moieties for treatment of disease
US6599916B2 (en) 2000-08-21 2003-07-29 Pharmacia & Upjohn Company Quinuclidine-substituted heteroaryl moieties for treatment of disease
ZA200301696B (en) * 2000-09-15 2004-04-28 Vertex Pharma Isoxazoles and their use as inhibitors of erk.
ES2292830T3 (es) 2001-02-21 2008-03-16 Astrazeneca Ab Compuestos heteropoliciclicos y su uso como antagonistas del receptor metabotropico de glutamato.
EP1405636A4 (en) 2001-06-26 2009-04-15 Takeda Pharmaceutical FUNCTIONAL REGULATOR FOR RETINOID RELATIVE RECEPTOR
US6727264B1 (en) 2001-07-05 2004-04-27 Synaptic Pharmaceutical Corporation Substituted anilinic piperidines as MCH selective antagonists
HUP0401880A2 (hu) 2001-07-05 2005-01-28 Synaptic Pharmaceutical Corporation Helyettesített anilin-piperidinek mint MCH-szelektív antagonisták, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk
WO2003018585A1 (en) 2001-08-24 2003-03-06 Pharmacia & Upjohn Company Substituted-heteroaryl-7-aza[2.2.1]bicycloheptanes for the treatment of disease
US6660736B2 (en) * 2002-03-27 2003-12-09 Hoffmann-La Roche Inc. Phthalimido derivatives and a process for their preparation
TW200400035A (en) * 2002-03-28 2004-01-01 Glaxo Group Ltd Novel compounds
US7329401B2 (en) * 2002-04-15 2008-02-12 The Regents Of The University Of California Cyclooxygenase-2 selective agents useful as imaging probes and related methods
WO2003097047A1 (en) 2002-05-13 2003-11-27 Eli Lilly And Company Multicyclic compounds for use as melanin concentrating hormone antagonists in the treatment of obesity and diabetes
CA2494114A1 (en) * 2002-08-02 2004-02-12 Argenta Discovery Limited Substituted thienyl-hydroxamic acids as histone deacetylase inhibitors
US8124330B2 (en) 2002-08-19 2012-02-28 Helicon Therapeutics, Inc. Screening methods for cognitive enhancers
AR043048A1 (es) * 2002-08-30 2005-07-13 Syngenta Participations Ag Derivados de 4-(3,3-dihalo- aliloxi) fenol con propiedades pesticidas
SE0300010D0 (sv) 2003-01-07 2003-01-07 Astrazeneca Ab Novel Compounds
NZ541479A (en) 2003-02-11 2008-11-28 Vernalis Cambridge Liimited Isoxazole compounds as inhibitors of heat shock proteins
GB0303503D0 (en) * 2003-02-14 2003-03-19 Novartis Ag Organic compounds
EP1599447A1 (en) 2003-02-28 2005-11-30 Galderma Research & Development, S.N.C. Ligands that modulate lxr-type receptors
MXPA05010456A (es) * 2003-03-28 2006-03-21 Pfizer Prod Inc Compuestos de quinolina y quinoxalina.
DE10315571A1 (de) 2003-04-05 2004-10-14 Merck Patent Gmbh Pyrazolverbindungen
WO2004089367A1 (en) * 2003-04-11 2004-10-21 Novo Nordisk A/S Pharmaceutical use of substituted 1,2,4-triazoles
WO2005004021A1 (ja) 2003-07-07 2005-01-13 Fujitsu Limited サービス提供装置、方法及びプログラム
US7199149B2 (en) 2003-10-01 2007-04-03 Bristol Myers Squibb Company Monocyclic and bicyclic lactams as factor Xa inhibitors
GB0324159D0 (en) * 2003-10-15 2003-11-19 Glaxo Group Ltd Novel compounds
US7037927B2 (en) * 2003-10-16 2006-05-02 Abbott Laboratories Amides that inhibit vanilloid receptor subtype 1 (VR1) receptor
KR20060109937A (ko) * 2003-12-15 2006-10-23 니뽄 다바코 산교 가부시키가이샤 Ｎ-치환-ｎ-술포닐아미노시클로프로판 화합물 및 그의약제학적 용도
EP1732920B1 (en) 2004-01-05 2011-03-09 AstraZeneca AB Thiophene derivatives as chk 1 inhibitors
SI1731512T1 (sl) * 2004-03-05 2015-01-30 Nissan Chemical Industries, Ltd. Z izoksazolinom substituirana benzamidna spojina in sredstvo za uravnavanje škodljivih organizmov
TW200538098A (en) 2004-03-22 2005-12-01 Astrazeneca Ab Therapeutic agents
JP2008503446A (ja) * 2004-05-06 2008-02-07 プレキシコン，インコーポレーテッド Ｐｄｅ４ｂ阻害剤及びその使用
US20050256118A1 (en) * 2004-05-12 2005-11-17 Altenbach Robert J Bicyclic-substituted amines having cyclic-substituted monocyclic substituents
WO2005120584A2 (en) * 2004-06-03 2005-12-22 The Trustees Of Columbia University In The City Of New York Radiolabeled arylsulfonyl compounds and uses thereof
MX2007000669A (es) * 2004-07-20 2007-05-23 Siena Biotech Spa Moduladores de receptores acetilcolina nicotinicos alfa 7 y sus usos terapeuticos.
GB0418267D0 (en) * 2004-08-16 2004-09-15 Glaxo Group Ltd Novel compounds
US7338967B2 (en) 2004-09-10 2008-03-04 Syngenta Limited Substituted isoxazoles as fungicides
CA2584413A1 (en) 2004-10-29 2006-05-04 Astrazeneca Ab Novel sulphonamide derivatives as glucocorticoid receptor modulators for the treatment of inflammatory diseases
KR100924610B1 (ko) * 2004-12-07 2009-11-02 이난타 파마슈티칼스, 인코포레이티드 3,6-비시클롤리드
US8338614B2 (en) * 2005-01-19 2012-12-25 Merck, Sharp & Dohme Corp. Tertiary carbinamines having substituted heterocycles which are active as β-secretase inhibitors for the treatment of alzheimer's disease
GB0504103D0 (en) * 2005-02-28 2005-04-06 Syngenta Ltd Novel method
JP2006316054A (ja) * 2005-04-15 2006-11-24 Tanabe Seiyaku Co Ltd 高コンダクタンス型カルシウム感受性ｋチャネル開口薬
WO2006134481A1 (en) * 2005-06-16 2006-12-21 Pfizer Inc. Inhibitors of 11-beta hydroxysteroid dehydrogenase type 1
US7452892B2 (en) * 2005-06-17 2008-11-18 Bristol-Myers Squibb Company Triazolopyrimidine cannabinoid receptor 1 antagonists
JP5244589B2 (ja) 2005-06-27 2013-07-24 エグゼリクシス パテント カンパニー エルエルシー イミダゾールに基づくｌｘｒモジュレーター
JP5114395B2 (ja) * 2005-06-30 2013-01-09 プロシディオン・リミテッド Ｇｐｃｒアゴニスト
AU2006287528A1 (en) 2005-09-07 2007-03-15 Plexxikon, Inc. 1 , 4 and 1 , 5-disubstituted indole derivatives for use as PPAR active compounds
AR056871A1 (es) * 2005-10-04 2007-10-31 Aventis Pharma Inc Compuestos de pirimidina amida como inhibidores de pgds
WO2007043401A1 (ja) * 2005-10-07 2007-04-19 Kissei Pharmaceutical Co., Ltd. 含窒素複素環化合物およびそれを含有する医薬組成物
GB0603041D0 (en) * 2006-02-15 2006-03-29 Angeletti P Ist Richerche Bio Therapeutic compounds
NZ570847A (en) 2006-02-28 2011-10-28 Helicon Therapeutics Inc Therapeutic compounds
WO2007103456A2 (en) * 2006-03-06 2007-09-13 Trimeris, Inc. Piperazine and piperidine biaryl derivatives
WO2008023248A2 (en) 2006-08-24 2008-02-28 Wockhardt Research Centre Novel macrolides and ketolides having antimicrobial activity
US20080167286A1 (en) * 2006-12-12 2008-07-10 Abbott Laboratories Pharmaceutical compositions and their methods of use
EP2142516B1 (en) 2007-03-30 2012-12-26 Sanofi Pyrimidine hydrazide compounds as pgds inhibitors
CN101820764B (zh) 2007-08-27 2014-06-04 海利空医疗公司 治疗用异噁唑化合物
US8389550B2 (en) 2009-02-25 2013-03-05 Hoffmann-La Roche Inc. Isoxazoles / O-pyridines with ethyl and ethenyl linker

Also Published As

Publication number Publication date
US9029397B2 (en) 2015-05-12
AU2008293542A1 (en) 2009-03-05
ES2663517T3 (es) 2018-04-13
EP2182809A4 (en) 2012-02-15
US20090062252A1 (en) 2009-03-05
IL226702A0 (en) 2013-07-31
ES2748599T3 (es) 2020-03-17
US8921399B2 (en) 2014-12-30
KR20100046060A (ko) 2010-05-04
IL232406A (en) 2017-03-30
CA2974477C (en) 2019-12-31
AU2008293542B9 (en) 2014-08-07
JP2010538001A (ja) 2010-12-09
IL232406A0 (en) 2014-06-30
US20170204111A1 (en) 2017-07-20
CN101820764A (zh) 2010-09-01
EP2182809B1 (en) 2018-01-17
IL226702A (en) 2015-09-24
JP2015110666A (ja) 2015-06-18
CN104072489B (zh) 2017-07-07
AU2014202864A1 (en) 2014-06-19
CA2974477A1 (en) 2009-03-05
EP3311813A1 (en) 2018-04-25
HK1147938A1 (en) 2011-08-26
US20130053361A1 (en) 2013-02-28
KR101567454B1 (ko) 2015-11-09
CN101820764B (zh) 2014-06-04
US20150336941A1 (en) 2015-11-26
AU2008293542B2 (en) 2014-06-05
AU2014202864B2 (en) 2016-05-12
CN104072489A (zh) 2014-10-01
EP2182809A1 (en) 2010-05-12
JP6250746B2 (ja) 2017-12-20
KR20150059810A (ko) 2015-06-02
JP5718053B2 (ja) 2015-05-13
WO2009029632A1 (en) 2009-03-05
IL203910A (en) 2014-06-30
CA2696609A1 (en) 2009-03-05
US20120202786A1 (en) 2012-08-09
MX2010002258A (es) 2010-04-22
EP3311813B1 (en) 2019-08-07
US10053467B2 (en) 2018-08-21
KR101669432B1 (ko) 2016-10-26
US9650349B2 (en) 2017-05-16
US8222243B2 (en) 2012-07-17
JP2017002062A (ja) 2017-01-05

Similar Documents

Publication Publication Date Title
CA2696609C (en) Therapeutic isoxazole compounds
EP2465850A1 (en) Therapeutic compounds
US20060205743A1 (en) Protein kinase inhibitors
CN110573497A (zh) 组蛋白脱乙酰基酶抑制剂
MX2012005637A (es) COMPUESTOS BICICLICOS COMO LIGANDOS DEL RECEPTOR NICOTINICO DE ACETILCOLINA A4 ß2.
CA2290392C (en) Salts of optically active sulfoxide derivative
HK1147938B (en) Therapeutic isoxazole compounds
HK1025321B (en) Salts of optically active sulfoxide derivative
HK1172615A (en) Therapeutic compounds
WO2007067904A2 (en) Peptide deformylase inhibitors

Legal Events

Date Code Title Description
EEER Examination request

Effective date: 20130820

MKLA Lapsed

Effective date: 20210826