WO2008120725A1 - 新規ピロリノン誘導体およびそれを含有する医薬組成物 - Google Patents

新規ピロリノン誘導体およびそれを含有する医薬組成物 Download PDF

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WO2008120725A1
WO2008120725A1 PCT/JP2008/056107 JP2008056107W WO2008120725A1 WO 2008120725 A1 WO2008120725 A1 WO 2008120725A1 JP 2008056107 W JP2008056107 W JP 2008056107W WO 2008120725 A1 WO2008120725 A1 WO 2008120725A1
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same
composition containing
medicinal composition
novel
derivative
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PCT/JP2008/056107
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English (en)
French (fr)
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Hiroyuki Kai
Shunji Shinohara
Takayuki Kameyama
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Shionogi & Co., Ltd.
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Priority to CA002682473A priority Critical patent/CA2682473A1/en
Priority to JP2009507522A priority patent/JP5624762B2/ja
Priority to EP08739225A priority patent/EP2143713A4/en
Priority to CN200880017760A priority patent/CN101679246A/zh
Priority to US12/450,548 priority patent/US8101644B2/en
Publication of WO2008120725A1 publication Critical patent/WO2008120725A1/ja
Priority to US13/242,518 priority patent/US8497263B2/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/36—Oxygen or sulfur atoms
    • C07D207/38—2-Pyrrolones
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    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A61K31/4162—1,2-Diazoles condensed with heterocyclic ring systems
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42—Oxazoles
    • A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • 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
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • A—HUMAN NECESSITIES
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    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
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    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D487/04—Ortho-condensed systems

Abstract

　本発明は、Ｐ２Ｘ3および／またはＰ２Ｘ2/3アンタゴニストとして有用な、式（Ｉ）： ［式中、Ｒ1、Ｒ2、Ｒ3、Ｚ1、Ｚ2、Ｒa、Ｒb、ｑ、Ａおよびｎは、明細書において定義するとおりである］で表される化合物、製薬上許容される塩またはそれらの溶媒和物を提供する。
PCT/JP2008/056107 2007-03-30 2008-03-28 新規ピロリノン誘導体およびそれを含有する医薬組成物 WO2008120725A1 (ja)

Priority Applications (6)

Application Number Priority Date Filing Date Title
CA002682473A CA2682473A1 (en) 2007-03-30 2008-03-28 Novel pyrrolinone derivative and pharmaceutical composition comprising the same
JP2009507522A JP5624762B2 (ja) 2007-03-30 2008-03-28 新規ピロリノン誘導体およびそれを含有する医薬組成物
EP08739225A EP2143713A4 (en) 2007-03-30 2008-03-28 NEW PYRROLINONE DERIVATIVE AND MEDICAL COMPOSITION CONTAINING THIS
CN200880017760A CN101679246A (zh) 2007-03-30 2008-03-28 新型吡咯啉酮衍生物以及包含其的药物组合物
US12/450,548 US8101644B2 (en) 2007-03-30 2008-03-28 Pyrrolinone derivative and pharmaceutical composition comprising the same
US13/242,518 US8497263B2 (en) 2007-03-30 2011-09-23 Pyrrolinone derivative and pharmaceutical composition comprising the same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007091624 2007-03-30
JP2007-091624 2007-03-30

Related Child Applications (2)

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US12/450,548 A-371-Of-International US8101644B2 (en) 2007-03-30 2008-03-28 Pyrrolinone derivative and pharmaceutical composition comprising the same
US13/242,518 Division US8497263B2 (en) 2007-03-30 2011-09-23 Pyrrolinone derivative and pharmaceutical composition comprising the same

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WO2008120725A1 true WO2008120725A1 (ja) 2008-10-09

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US (2) US8101644B2 (ja)
EP (1) EP2143713A4 (ja)
JP (1) JP5624762B2 (ja)
KR (1) KR20100016076A (ja)
CN (1) CN101679246A (ja)
CA (1) CA2682473A1 (ja)
TW (1) TW200843739A (ja)
WO (1) WO2008120725A1 (ja)

Cited By (19)

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WO2010035727A1 (ja) * 2008-09-25 2010-04-01 塩野義製薬株式会社 新規ピロリノン誘導体およびそれを含有する医薬組成物
WO2011004018A1 (en) * 2009-07-10 2011-01-13 Vivalis Substituted pyrrolidinone as inhibitors of hepatitis c ns5b polymerase, the pharmaceutical composition thereof and their therapeutic use
WO2011004017A1 (en) * 2009-07-10 2011-01-13 Vivalis 1-(6 members azo-heterocyclic)-pyrrolin-2-one compounds as inhibitors of hepatitis c ns5b polymerase, the pharmaceutical composition thereof and their therapeutic use
JP2011518133A (ja) * 2008-04-09 2011-06-23 サントル・ナショナル・ドゥ・ラ・レシェルシュ・サイエンティフィーク−セ・エン・エール・エス− Ｓｙｋチロシンキナーゼタンパク質が関与している代謝経路を阻害する分子および前記分子を同定するための方法
JP2013237688A (ja) * 2006-11-09 2013-11-28 Probiodrug Ag 潰瘍、癌及び他の疾患の治療のためのグルタミニルシクラーゼの阻害薬としての３−ヒドロキシ−１，５−ジヒドロ−ピロール−２−オン誘導体
US8815926B2 (en) 2012-01-26 2014-08-26 Novartis Ag Substituted pyrrolo[3,4-D]imidazoles for the treatment of MDM2/4 mediated diseases
JP2014533745A (ja) * 2011-11-29 2014-12-15 ノバルティス アーゲー ピラゾロピロリジン化合物
WO2015004610A1 (en) 2013-07-11 2015-01-15 Adamed Sp. Z O.O. 1,5-dihydropyrrol-2-one derivatives as inhibitors of p53-mdm2/mdm4 protein-protein interaction
US8975417B2 (en) 2013-05-27 2015-03-10 Novartis Ag Pyrazolopyrrolidine derivatives and their use in the treatment of disease
US9051279B2 (en) 2009-12-22 2015-06-09 Novartis Ag Substituted isoquinolinones and quinazolinones
US9365576B2 (en) 2012-05-24 2016-06-14 Novartis Ag Pyrrolopyrrolidinone compounds
JP2016520118A (ja) * 2013-05-28 2016-07-11 ノバルティス アーゲー Ｂｅｔ阻害剤としてのピラゾロ−ピロリジン−４−オン誘導体および疾患の処置におけるその使用
US9403827B2 (en) 2013-01-22 2016-08-02 Novartis Ag Substituted purinone compounds
US9550796B2 (en) 2013-11-21 2017-01-24 Novartis Ag Pyrrolopyrrolone derivatives and their use as BET inhibitors
US9556180B2 (en) 2013-01-22 2017-01-31 Novartis Ag Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the P53/MDM2 interaction
US9714249B2 (en) 2013-05-28 2017-07-25 Novartis Ag Pyrazolo-pyrrolidin-4-one derivatives and their use in the treatment of disease
US9737522B2 (en) 2012-08-09 2017-08-22 Emory University NMDA receptor modulators and uses related thereto
US9890166B2 (en) 2013-05-27 2018-02-13 Novartis Ag Imidazopyrrolidine derivatives and their use in the treatment of disease
WO2020179859A1 (ja) 2019-03-06 2020-09-10 第一三共株式会社 ピロロピラゾール誘導体

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Publication number Priority date Publication date Assignee Title
CA2682473A1 (en) * 2007-03-30 2008-10-09 Shionogi & Co., Ltd. Novel pyrrolinone derivative and pharmaceutical composition comprising the same
WO2012020742A1 (ja) * 2010-08-10 2012-02-16 塩野義製薬株式会社 新規複素環誘導体およびそれらを含有する医薬組成物
GB201016880D0 (en) * 2010-10-07 2010-11-17 Riotech Pharmaceuticals Ltd Phosphodiesterase inhibitors
WO2013118855A1 (ja) * 2012-02-09 2013-08-15 塩野義製薬株式会社 複素環および炭素環誘導体
CN103819476B (zh) * 2013-03-05 2016-08-17 中国人民解放军第二军医大学 吡咯酮并吡唑类化合物及其作为药物的用途
CN104447733B (zh) * 2015-01-05 2016-08-17 中国药科大学 1-苄基-2-吡咯啉酮-4-酰胺类化合物及其制备方法与应用
CN112142742B (zh) * 2019-06-26 2022-01-07 香港理工大学深圳研究院 Ctcf转录因子抑制剂及其应用
CN111138289B (zh) * 2020-02-27 2022-08-30 奥锐特药业(天津)有限公司 一种化合物及使用该化合物合成5-乙酰基-1h-吡唑-3-羧酸的工艺

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002094767A2 (en) 2001-05-18 2002-11-28 Abbott Laboratories Trisubstituted-n-[(1s)-1,2,3,4-tetrahydro-1-naphthalenyl] benzamides which inhibit p2x3 and p2x2/3 containing receptors
WO2005095359A1 (en) 2004-03-05 2005-10-13 F. Hoffmann-La Roche Ag Diaminopyrimidines as p2x3 and p2x2/3 antagonists
WO2006044000A1 (en) * 2004-10-12 2006-04-27 Decode Genetics Sulfonamide pert-substituted bicyclics for occlusive artery disease
US20070037974A1 (en) 2005-08-15 2007-02-15 Roche Palo Alto Llc Inhibitors of P2X3
US20070049609A1 (en) 2005-09-01 2007-03-01 Roche Palo Alto Llc Methods of using diaminopyrimidine P2X3 and P2X2/3 receptor modulators for treatment of respiratory and gastrointestinal diseases
US20070049534A1 (en) 2005-09-01 2007-03-01 Roche Palo Alto Llc Diaminopyrimidines as P2X3 and P2X2/3 modulators
US20070049610A1 (en) 2005-09-01 2007-03-01 Roche Palo Alto Llc Diaminopyrimidines as P2X3 and P2X2/3 modulators
US20070049758A1 (en) 2005-09-01 2007-03-01 Roche Palo Alto Llc Diaminopyrimidines as P2X3 and P2X2/3 modulators

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2097038A1 (en) 1970-07-29 1972-03-03 Bellon Labor Sa Roger 1-(substd phenyl)-2-oxo-4-piperazinocarbonyl pyrrolidines - analgesic
US5508300A (en) * 1994-01-14 1996-04-16 Pfizer Inc. Dihydro pyrazolopyrroles, compositions and use
RU2067575C1 (ru) 1994-07-27 1996-10-10 Пермский фармацевтический институт 4-ацетил-5-п-иодфенил-1-карбоксиметил-3-гидрокси-2,5-дигидропиррол-2-он, проявляющий анальгетическую активность
NZ532018A (en) * 2001-10-03 2004-12-24 Ucb S Pyrrolidinone derivatives
DE102006025318A1 (de) * 2006-05-31 2007-12-06 Bayer Healthcare Ag Dihydro-pyrrolopyridin-, Dihydro-pyrrolopyridazin- und Dihydro-pyrrolopyrimidin-Derivate und ihre Verwendung
CA2682473A1 (en) * 2007-03-30 2008-10-09 Shionogi & Co., Ltd. Novel pyrrolinone derivative and pharmaceutical composition comprising the same
EP2336109A4 (en) * 2008-09-25 2012-05-02 Shionogi & Co NOVEL PYRROLINONE DERIVATIVE AND DRUG COMPOSITION CONTAINING THE SAME

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002094767A2 (en) 2001-05-18 2002-11-28 Abbott Laboratories Trisubstituted-n-[(1s)-1,2,3,4-tetrahydro-1-naphthalenyl] benzamides which inhibit p2x3 and p2x2/3 containing receptors
WO2005095359A1 (en) 2004-03-05 2005-10-13 F. Hoffmann-La Roche Ag Diaminopyrimidines as p2x3 and p2x2/3 antagonists
WO2006044000A1 (en) * 2004-10-12 2006-04-27 Decode Genetics Sulfonamide pert-substituted bicyclics for occlusive artery disease
US20070037974A1 (en) 2005-08-15 2007-02-15 Roche Palo Alto Llc Inhibitors of P2X3
US20070049609A1 (en) 2005-09-01 2007-03-01 Roche Palo Alto Llc Methods of using diaminopyrimidine P2X3 and P2X2/3 receptor modulators for treatment of respiratory and gastrointestinal diseases
US20070049534A1 (en) 2005-09-01 2007-03-01 Roche Palo Alto Llc Diaminopyrimidines as P2X3 and P2X2/3 modulators
US20070049610A1 (en) 2005-09-01 2007-03-01 Roche Palo Alto Llc Diaminopyrimidines as P2X3 and P2X2/3 modulators
US20070049758A1 (en) 2005-09-01 2007-03-01 Roche Palo Alto Llc Diaminopyrimidines as P2X3 and P2X2/3 modulators

Non-Patent Citations (18)

* Cited by examiner, † Cited by third party
Title
DATABASE REGISTRY [online] 6 April 2004 (2004-04-06), XP008114737, accession no. STN Database accession no. (671764-08-2) *
EXPERT OPIN. THER. PATENS, vol. 16, no. 8, 2006, pages 113 - 1127
GEIN V.L. ET AL.: "Synthesis and antiinflammatory and analgesic activity of 1-(2-aminoethyl)-5-aryl-4-acyl-3-hydroxy-3-pyrrolin-2-ones", PHARMACEUTICAL CHEMISTRY JOURNAL, vol. 39, no. 9, 2005, pages 484 - 487, XP019223697 *
GEIN V.L. ET AL.: "Synthesis and biological activity of 5-aryl-4-acyl-3-hydroxy-1-morpholinoalkyl-3-pyrrolin-2-ones", PHARMACEUTICAL CHEMISTRY JOURNAL, vol. 41, no. 5, 18 November 2007 (2007-11-18), pages 256 - 263, XP019555868 *
GEIN V.L. ET AL.: "Synthesis and pharmacological activity of 5-aryl-4-acetyl-1-carboxylalkyltetrahydropyrrole-2,3-diones", KHIMIKO-FARMATSEVTICHESKII ZHURNAL, vol. 31, no. 5, 1997, pages 33 - 36, XP008136051 *
J. PHYSIOL., vol. 567.2, 2005, pages 621 - 639
J. PHYSIOLOGY, vol. 553, no. 3, 2003, pages 683 - 694
J. PHYSIOLOGY, vol. 554, no. 2, 2003, pages 301 - 308
KOZ'MINYCH E.N. ET AL.: "1,3,4,6-Tetracarbonyl compounds. Part 2. Preparation of biologically active 2-hydroxy-2,3-diyhdro-3-pyrrolones and aroylpyruvic acid-substituted amides", KHIMIKO-FARMATSEVTICHESKII ZHURNAL, vol. 30, no. 7, 1996, pages 31 - 35, XP008136318 *
NATURE, vol. 407, no. 26, 2000, pages 1011 - 1015
NATURE, vol. 407, no. 26, 2000, pages 1015 - 1017
NEUROSCIENTIST, vol. 11, 2005, pages 345 - 356
PFLUNGERS ARCH EUR J PHYSIOL, vol. 452, 2006, pages 513 - 537
PHARMACEUTICAL CHEMISTRY JOURNAL, vol. 31, no. 5, 1997, pages 251 - 254
PHARMACEUTICAL CHEMISTRY JOURNAL, vol. 39, no. 9, 2005, pages 484 - 487
PNAS, vol. 99, no. 26, 2002, pages 17179 - 17184
See also references of EP2143713A4
ZANKOWSKA-JASINSKA W. ET AL.: "the new synthesis of the pyrrolo[3,4-e][1,4]diazepine derivatives", ZESZYTY NAUKOWE UNIWERSYTETU JAGIELLONSKIEGO, PRACE CHEMICZNE, vol. 32, 1989, pages 75 - 82, XP008136400 *

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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US8575197B2 (en) 2008-09-25 2013-11-05 Shionogi & Co., Ltd. Pyrolinone derivative and pharmaceutical composition comprising the same
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