JP2006501277A5 - - Google Patents

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Publication number
JP2006501277A5
JP2006501277A5 JP2004537412A JP2004537412A JP2006501277A5 JP 2006501277 A5 JP2006501277 A5 JP 2006501277A5 JP 2004537412 A JP2004537412 A JP 2004537412A JP 2004537412 A JP2004537412 A JP 2004537412A JP 2006501277 A5 JP2006501277 A5 JP 2006501277A5
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JP
Japan
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alkyl
substituted
formula
compound
group
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.)
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Application number
JP2004537412A
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English (en)
Japanese (ja)
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JP2006501277A (ja
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Publication date
Priority claimed from EP20020292275 external-priority patent/EP1400244A1/en
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Publication of JP2006501277A publication Critical patent/JP2006501277A/ja
Publication of JP2006501277A5 publication Critical patent/JP2006501277A5/ja
Withdrawn legal-status Critical Current

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JP2004537412A 2002-09-17 2003-09-08 新規なスピロ縮合キナゾリノンおよびそれらのホスホジエステラーゼ阻害剤としての使用 Withdrawn JP2006501277A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP20020292275 EP1400244A1 (en) 2002-09-17 2002-09-17 New spirocondensed quinazolinones and their use as phosphodiesterase inhibitors
PCT/IB2003/003965 WO2004026818A1 (en) 2002-09-17 2003-09-08 New spirocondensed quinazolinones and their use as phosphodiesterase inhibitors

Publications (2)

Publication Number Publication Date
JP2006501277A JP2006501277A (ja) 2006-01-12
JP2006501277A5 true JP2006501277A5 (enExample) 2006-10-19

Family

ID=31896987

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004537412A Withdrawn JP2006501277A (ja) 2002-09-17 2003-09-08 新規なスピロ縮合キナゾリノンおよびそれらのホスホジエステラーゼ阻害剤としての使用

Country Status (30)

Country Link
US (1) US7429598B2 (enExample)
EP (2) EP1400244A1 (enExample)
JP (1) JP2006501277A (enExample)
KR (1) KR20050057371A (enExample)
CN (1) CN1681507A (enExample)
AP (1) AP2005003251A0 (enExample)
AR (1) AR041271A1 (enExample)
AU (1) AU2003259496A1 (enExample)
BR (1) BR0314379A (enExample)
CA (1) CA2499330C (enExample)
CO (1) CO5540391A2 (enExample)
CR (1) CR7728A (enExample)
EA (1) EA200500312A1 (enExample)
EC (1) ECSP055671A (enExample)
GT (1) GT200300201A (enExample)
HN (1) HN2003000285A (enExample)
HR (1) HRP20050223A2 (enExample)
IS (1) IS7700A (enExample)
MA (1) MA27439A1 (enExample)
MX (1) MXPA05002913A (enExample)
NO (1) NO20051695L (enExample)
OA (1) OA12924A (enExample)
PA (1) PA8582801A1 (enExample)
PE (1) PE20050073A1 (enExample)
PL (1) PL375977A1 (enExample)
TN (1) TNSN05073A1 (enExample)
TW (1) TWI251590B (enExample)
UY (1) UY27986A1 (enExample)
WO (1) WO2004026818A1 (enExample)
ZA (1) ZA200501381B (enExample)

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ES2425013T3 (es) 2002-06-12 2013-10-10 Symphony Evolution, Inc. Inhibidores de ADAM-10 humana
GB0504209D0 (en) * 2005-03-01 2005-04-06 Pfizer Ltd New use of PDE7 inhibitors
WO2006092692A1 (en) * 2005-03-01 2006-09-08 Pfizer Limited Use of combinations of pde7 inhibitors and alpha-2-delty ligands for the treatment of neuropathic pain
CA2599662A1 (en) * 2005-03-01 2006-09-08 Pfizer Limited Use of pde7 inhibitors for the treatment of neuropathic pain
EP2258358A3 (en) 2005-08-26 2011-09-07 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
JP2009506069A (ja) 2005-08-26 2009-02-12 ブレインセルス,インコーポレイティド ムスカリン性受容体調節による神経発生
CA2625153A1 (en) 2005-10-21 2007-04-26 Braincells, Inc. Modulation of neurogenesis by pde inhibition
CA2625210A1 (en) 2005-10-31 2007-05-10 Braincells, Inc. Gaba receptor mediated modulation of neurogenesis
JP2009517453A (ja) 2005-12-02 2009-04-30 ファイザー・リミテッド Pde7阻害剤としてのスピロ環式キナゾリン誘導体
WO2007087684A1 (en) 2006-02-03 2007-08-09 Bionomics Limited Substituted benzofurans, benzothiophenes, benzoselenophenes and indoles and their use as tubulin polymerisation inhibitors
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
MX2008014320A (es) 2006-05-09 2009-03-25 Braincells Inc Neurogenesis mediada por el receptor de 5-hidroxitriptamina.
EP2382975A3 (en) 2006-05-09 2012-02-29 Braincells, Inc. Neurogenesis by modulating angiotensin
JP2010502722A (ja) 2006-09-08 2010-01-28 ブレインセルス,インコーポレイティド 4−アシルアミノピリジン誘導体を含む組み合わせ
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
AU2008230710B2 (en) * 2007-03-27 2014-04-10 Omeros Corporation The use of PDE7 inhibitors for the treatment of movement disorders
US8637528B2 (en) 2007-03-27 2014-01-28 Omeros Corporation Use of PDE7 inhibitors for the treatment of movement disorders
US20100216823A1 (en) * 2007-05-24 2010-08-26 Pfizer Inc. Spirocyclic Derivatives
CL2008001933A1 (es) 2007-06-29 2009-09-25 Millennium Pharm Inc Compuestos derivados de pirimidina, inhibidores de la raf quinasa; compuestos intermediarios; procedimiento de preparacion; composicion farmaceutica; y su uso para tratar trastornos proliferativos, cardiacos, neurodegenerativos, inflamatorios, oseos, inmunologicos enfermedad viral, entre otros.
CA2694284A1 (en) * 2007-06-29 2009-01-08 Jennifer Cossrow Heterocyclic compounds useful as raf kinase inhibitors
SG193842A1 (en) 2008-08-06 2013-10-30 Biomarin Pharm Inc Dihydropyridophthalazinone inhibitors of poly(adp-ribose)polymerase (parp)
WO2010099217A1 (en) 2009-02-25 2010-09-02 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
CN106943406A (zh) 2010-02-03 2017-07-14 麦迪韦逊科技有限公司 用于pten基因缺失相关疾病的治疗的聚(adp‑核糖)聚合酶(parp)的二氢吡啶并酞嗪酮抑制剂
US20110190266A1 (en) * 2010-02-04 2011-08-04 Daniel Chu 5,6,6a,7,8,9-HEXAHYDRO-2H-PYRIDOPHTHALAZINONE INHIBITORS OF POLY(ADP-RIBOSE)POLYMERASE (PARP)
SI2533640T1 (sl) * 2010-02-08 2017-02-28 Medivation Technologies, Inc. Postopki sinteze derivatov dihidropiridoftalazinona
PL2630146T3 (pl) 2010-10-21 2020-11-02 Medivation Technologies Llc Krystaliczna sól tosylanowa (8S,9R)-5-fluoro-8-(4-fluorofenylo)-9-(1-metylo-1H-1,2,4-triazol-5-ilo)-8,9-dihydro-2H-pirydo[4,3,2-de]ftalazyno-3(7H)-onu
US9220715B2 (en) 2010-11-08 2015-12-29 Omeros Corporation Treatment of addiction and impulse-control disorders using PDE7 inhibitors
CN107375296A (zh) 2010-11-08 2017-11-24 奥默罗斯公司 使用pde7抑制剂治疗成瘾和冲动控制障碍
EP2804603A1 (en) 2012-01-10 2014-11-26 President and Fellows of Harvard College Beta-cell replication promoting compounds and methods of their use
EP3652180B1 (en) 2017-07-12 2023-11-29 Dart NeuroScience, LLC Substituted benzoxazole and benzofuran compounds as pde7 inhibitors
CN112574202B (zh) * 2020-12-11 2021-11-09 台州学院 一种螺喹唑啉-2-酮类衍生物及其制备方法和应用
CN119894518A (zh) 2022-08-18 2025-04-25 米托迪治愈有限责任公司 取代的苯并噁唑和苯并呋喃化合物用于治疗和预防与慢性疲劳、筋疲力尽和/或劳累不耐受相关的疾病的用途

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JPS5959685A (ja) * 1982-09-28 1984-04-05 Kyowa Hakko Kogyo Co Ltd 新規なピペリジン誘導体
JPS5959865A (ja) * 1982-09-30 1984-04-05 Ube Ind Ltd 耐熱鋳鋼
US4906630A (en) * 1985-11-22 1990-03-06 Rorer Pharmaceutical Corporation Method of increasing cardiac contractility using pharmaceutical compositions comprising benzodiazinone- pyridazinone or hydroxy-pyrazolyl compounds
US4666913A (en) * 1985-11-22 1987-05-19 William H. Rorer, Inc. Hydroxy and aminothiazolyl-benzodiazinone compounds, cardiotonic compositions including the same, and their uses
US4764512A (en) 1986-08-27 1988-08-16 Rorer Pharmaceutical Corporation Benzodiazinone-pyridone compounds, cardiotonic compositions including the same, and their uses
US5102886A (en) 1990-10-12 1992-04-07 American Home Products Corporation 1'-aminospiro[isoquinoline-4(1H),3'-pyrrolidine]-1,2',3,5'(2H)-tetrones and analogs thereof useful as aldose reductase inhibitors
IL102764A0 (en) * 1991-08-16 1993-01-31 Merck & Co Inc Quinazoline derivatives,and pharmaceutical compositions containing them
WO2000066560A1 (en) 1999-05-04 2000-11-09 American Home Products Corporation Quinazolinone and benzoxazine derivatives as progesterone receptor modulators
WO2002076953A1 (en) * 2001-03-21 2002-10-03 Warner-Lambert Company Llc New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors
US6596167B2 (en) 2001-03-26 2003-07-22 Koch Membrane Systems, Inc. Hydrophilic hollow fiber ultrafiltration membranes that include a hydrophobic polymer and a method of making these membranes

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