EA200400616A1 - ПРОИЗВОДНЫЕ АМИНОБЕНЗАМИДОВ В КАЧЕСТВЕ ИНГИБИТОРОВ ГЛИКОГЕНСИНТАЗА-КИНАЗЫ 3β - Google Patents

ПРОИЗВОДНЫЕ АМИНОБЕНЗАМИДОВ В КАЧЕСТВЕ ИНГИБИТОРОВ ГЛИКОГЕНСИНТАЗА-КИНАЗЫ 3β

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Publication number
EA200400616A1
EA200400616A1 EA200400616A EA200400616A EA200400616A1 EA 200400616 A1 EA200400616 A1 EA 200400616A1 EA 200400616 A EA200400616 A EA 200400616A EA 200400616 A EA200400616 A EA 200400616A EA 200400616 A1 EA200400616 A1 EA 200400616A1
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EA
Eurasian Patent Office
Prior art keywords
hydrogen
alkyl
optionally substituted
6alkyloxy
nrr
Prior art date
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EA200400616A
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English (en)
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EA007063B1 (ru
Inventor
Эдди Жан Эдгар Фрейн
Петер Якобус Йоханнес Антониус Бейнстерс
Марк Виллемс
Вернер Констант Йохан Эмбрехтс
Поль Адриан Ян Жанссен
Паулус Йоаннес Леви
Ян Херес
Марк Рене Де Жонж
Люсьен Мария Хенрикус Койманс
Фредерик Франс Дезире Дайер
Майкл Джозеф Кукла
Юго Альфонс Габриель Гертс
Рони Мария Нюйденс
Марк Юбер Меркен
Дональд Вилльям Лудовики
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Янссен Фармацевтика Н.В.
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Publication of EA200400616A1 publication Critical patent/EA200400616A1/ru
Publication of EA007063B1 publication Critical patent/EA007063B1/ru

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    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Abstract

Данное изобретение относится к соединению формулы (I'), его N-оксиду, фармацевтически приемлемой аддитивной соли, четвертичному амину и стереохимически изомерной форме, где кольцо A является 6-членным гетероциклом; Rозначает водород; арил; формил; Cалкилкарбонил; необязательно замещенный Cалкил; Cалкилоксикарбонил; необязательно замещенный Cалкилокси-Cалкилкарбонил; X означает прямую связь, или линкерный атом, или линкерную группу; Z представляет O или S; Rозначает водород, Cалкил, Cалкенил, Cалкинил, карбоцикл или гетероцикл, причем каждая из указанных групп может быть необязательно замещена; Rозначает водород; гидрокси; галоген; необязательно замещенный Cалкил, или Cалкенил, или Cалкинил; Cалкилокси; Cалкилтио; Cалкилоксикарбонил; Cалкилкарбонилокси; карбоксил; циано; нитро; амино; моно- или ди(Cалкил)амино; полигалоген-Cалкил; полигалоген-Cалкилокси; полигалоген-Cалкилтио; R; R-Cалкил; R-O-; R-S-; R-C(=O)-; R-S(=O)-; R-S(=O)-; R-S(=O)-NH-; R-S(=O)-NH-; R-C(=O)-; -NHC(=O)H; -C(=O)NHNH; R-C(=O)-NH-; R-C(=O)-NH-; -C(=NH)R; -C(=NH)R; Rили R, каждый независимо, означает водород, R, -Y-NR-Y-NRR, -Y-NR-Y-R, -Y-NRR; при условии, что -X-Rи/или Rявляется другим, чем водород; их применению, содержащим их фармацевтическим композициям и способам их получения.Международная заявка была опубликована вместе с отчетом о международном поиске.
EA200400616A 2001-11-01 2002-10-29 ПРОИЗВОДНЫЕ АМИНОБЕНЗАМИДОВ В КАЧЕСТВЕ ИНГИБИТОРОВ ГЛИКОГЕНСИНТАЗА-КИНАЗЫ 3β; EA007063B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP01204192 2001-11-01
PCT/EP2002/012079 WO2003037877A1 (en) 2001-11-01 2002-10-29 AMINOBENZAMIDE DERIVATIVES AS GLYCOGEN SYNTHASE KINASE 3β INHIBITORS

Publications (2)

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EA200400616A1 true EA200400616A1 (ru) 2004-08-26
EA007063B1 EA007063B1 (ru) 2006-06-30

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EA200400616A EA007063B1 (ru) 2001-11-01 2002-10-29 ПРОИЗВОДНЫЕ АМИНОБЕНЗАМИДОВ В КАЧЕСТВЕ ИНГИБИТОРОВ ГЛИКОГЕНСИНТАЗА-КИНАЗЫ 3β;

Country Status (21)

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US (1) US20060063789A1 (ru)
EP (1) EP1442024B1 (ru)
JP (1) JP2005507420A (ru)
KR (1) KR20040062557A (ru)
CN (1) CN100436427C (ru)
AT (1) ATE389638T1 (ru)
AU (1) AU2002363177B2 (ru)
BR (1) BR0213790A (ru)
CA (1) CA2463823A1 (ru)
DE (1) DE60225709T2 (ru)
DK (1) DK1442024T3 (ru)
EA (1) EA007063B1 (ru)
ES (1) ES2303565T3 (ru)
HU (1) HUP0402245A3 (ru)
IL (1) IL161663A0 (ru)
MX (1) MXPA04004176A (ru)
NO (1) NO326889B1 (ru)
NZ (1) NZ531854A (ru)
PL (1) PL368920A1 (ru)
PT (1) PT1442024E (ru)
WO (1) WO2003037877A1 (ru)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003078448A1 (en) 2002-03-13 2003-09-25 Signum Biosciences, Inc. Modulation of protein methylation and phosphoprotein phosphate
NZ539823A (en) * 2002-11-28 2008-04-30 Schering Aktiengessellschaft Chk-, Pdk- and Akt-inhibitory pyrimidines, their production and use as pharmaceutical agents
DE10322911A1 (de) * 2003-05-21 2004-12-16 Bayer Materialscience Ag Verfestigungsstabile blockierte Polyisocyanate
NZ585188A (en) * 2003-08-15 2011-09-30 Novartis Ag 2,4-Pyrimidinediamines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders
WO2005097127A2 (en) 2004-04-02 2005-10-20 Merck & Co., Inc. Method of treating men with metabolic and anthropometric disorders
US8221804B2 (en) * 2005-02-03 2012-07-17 Signum Biosciences, Inc. Compositions and methods for enhancing cognitive function
US7923041B2 (en) 2005-02-03 2011-04-12 Signum Biosciences, Inc. Compositions and methods for enhancing cognitive function
US20080207594A1 (en) 2005-05-04 2008-08-28 Davelogen Aktiengesellschaft Use of Gsk-3 Inhibitors for Preventing and Treating Pancreatic Autoimmune Disorders
CA2620333A1 (en) 2005-08-26 2007-03-01 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
EP2258358A3 (en) 2005-08-26 2011-09-07 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
EP1940389A2 (en) 2005-10-21 2008-07-09 Braincells, Inc. Modulation of neurogenesis by pde inhibition
JP2009513672A (ja) 2005-10-31 2009-04-02 ブレインセルス，インコーポレイティド 神経発生のｇａｂａ受容体媒介調節
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
JP2009536669A (ja) 2006-05-09 2009-10-15 ブレインセルス，インコーポレイティド アンジオテンシン調節による神経新生
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
WO2008051547A1 (en) 2006-10-23 2008-05-02 Cephalon, Inc. Fused bicyclic derivatives of 2,4-diaminopyrimidine as alk and c-met inhibitors
TW200902010A (en) 2007-01-26 2009-01-16 Smithkline Beecham Corp Anthranilamide inhibitors of aurora kinase
US8969514B2 (en) 2007-06-04 2015-03-03 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
EP2152079A4 (en) 2007-06-04 2011-03-09 Avila Therapeutics Inc HETEROCYCLIC COMPOUNDS AND USES THEREOF
US7989465B2 (en) * 2007-10-19 2011-08-02 Avila Therapeutics, Inc. 4,6-disubstituted pyrimidines useful as kinase inhibitors
JP5600063B2 (ja) 2007-10-19 2014-10-01 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 ヘテロアリール化合物およびその使用
US8461147B2 (en) * 2007-12-03 2013-06-11 Boehringer Ingelheim International Gmbh Diaminopyridines for the treatment of diseases which are characterised by excessive or anomal cell proliferation
CN102014897B (zh) 2008-04-21 2015-08-05 西格纳姆生物科学公司 化合物、组合物和其制备方法
WO2010009319A2 (en) 2008-07-16 2010-01-21 Synergy Pharmaceuticals Inc. Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders
WO2010099217A1 (en) 2009-02-25 2010-09-02 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
US9334269B2 (en) * 2010-02-17 2016-05-10 Amgen Inc. Carboxamides as inhibitors of voltage-gated sodium channels
EP2571867B1 (en) 2010-05-21 2015-11-04 Noviga Research AB Novel pyrimidine derivatives
US20130156720A1 (en) 2010-08-27 2013-06-20 Ironwood Pharmaceuticals, Inc. Compositions and methods for treating or preventing metabolic syndrome and related diseases and disorders
US9616097B2 (en) 2010-09-15 2017-04-11 Synergy Pharmaceuticals, Inc. Formulations of guanylate cyclase C agonists and methods of use
BR112013020874A2 (pt) 2011-02-18 2019-05-21 Endo Pharmaceuticals Inc. composto, regime, método para a preparação do referido composto, e, uso de um composto
KR20140006048A (ko) 2011-03-24 2014-01-15 케밀리아 에이비 신규한 피리미딘 유도체
WO2014028675A1 (en) 2012-08-15 2014-02-20 Endo Pharmaceuticals Inc. Use of aminoindane compounds in treating overactive bladder and interstitial cystitis
EA201590197A1 (ru) 2012-08-23 2015-07-30 Алиос Биофарма, Инк. Соединения для лечения парамиксовирусных вирусных инфекций
KR102272746B1 (ko) 2013-06-05 2021-07-08 보슈 헬스 아일랜드 리미티드 구아닐레이트 사이클라제 c의 초순수 작용제, 및 이의 제조 및 사용 방법
UA118278C2 (uk) 2014-01-10 2018-12-26 Глаксосмітклайн Інтеллектьюел Проперті (№ 2) Лімітед Гідроксиформамідні похідні та їх застосування
WO2017156527A1 (en) * 2016-03-11 2017-09-14 H. Lee Moffitt Cancer Center And Research Institute, Inc. Aurora kinase and janus kinase inhibitors for prevention of graft versus host disease
CN106632021A (zh) * 2016-09-27 2017-05-10 中国药科大学 2‑取代异烟酸类化合物、其制备方法及其用途
WO2020163812A1 (en) 2019-02-08 2020-08-13 Frequency Therapeutics, Inc. Valproic acid compounds and wnt agonists for treating ear disorders
CN112876420B (zh) * 2019-11-29 2023-01-24 沈阳化工研究院有限公司 一种硫代苯甲酰衍生物及其应用
US20230090742A1 (en) * 2020-01-30 2023-03-23 Sumitomo Pharma Oncology, Inc. Aminopyrimidinylaminobenzonitrile derivatives as nek2 inhibitors
CN114105887B (zh) * 2021-09-16 2023-12-01 沈阳药科大学 一种氨基嘧啶衍生物及其制备方法和用途

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0164204A1 (en) * 1984-05-12 1985-12-11 FISONS plc Novel pharmaceutically useful pyrimidines
EP0162204A3 (de) * 1984-05-22 1988-07-06 Franz Grimme Landmaschinenfabrik GmbH & Co. KG. Riemenschloss für Riemen von Siebkettenförderbändern
EP0233461B2 (en) * 1986-01-13 2002-05-29 American Cyanamid Company 4,5,6-Substituted-2-pyrimidinamines
US4966622A (en) * 1988-04-12 1990-10-30 Ciba-Geigy Corporation N-phenyl-N-pyrimidin-2-ylureas
GB9012592D0 (en) * 1990-06-06 1990-07-25 Smithkline Beecham Intercredit Compounds
US5516775A (en) * 1992-08-31 1996-05-14 Ciba-Geigy Corporation Further use of pyrimidine derivatives
GB9705361D0 (en) * 1997-03-14 1997-04-30 Celltech Therapeutics Ltd Chemical compounds
EP0945443B9 (en) * 1998-03-27 2003-08-13 Janssen Pharmaceutica N.V. HIV inhibiting pyrimidine derivatives
WO1999065897A1 (en) * 1998-06-19 1999-12-23 Chiron Corporation Inhibitors of glycogen synthase kinase 3
GB9914258D0 (en) * 1999-06-18 1999-08-18 Celltech Therapeutics Ltd Chemical compounds
GB0004890D0 (en) * 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
ATE430742T1 (de) * 2000-12-21 2009-05-15 Smithkline Beecham Corp Pyrimidinamine als angiogenesemodulatoren
AU2002316421B2 (en) * 2001-06-26 2008-05-15 Bristol-Myers Squibb Company N-heterocyclic inhibitors of TNF-ALPHA expression
US6939874B2 (en) * 2001-08-22 2005-09-06 Amgen Inc. Substituted pyrimidinyl derivatives and methods of use
CA2463989C (en) * 2001-10-17 2012-01-31 Boehringer Ingelheim Pharma Gmbh & Co. Kg Pyrimidine derivatives, pharmaceutical compositions containing these compounds, the use thereof and process for the preparation thereof

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EP1442024B1 (en) 2008-03-19
NZ531854A (en) 2006-03-31
EA007063B1 (ru) 2006-06-30
AU2002363177B2 (en) 2008-09-18
NO326889B1 (no) 2009-03-16
EP1442024A1 (en) 2004-08-04
US20060063789A1 (en) 2006-03-23
DK1442024T3 (da) 2008-06-30
CN1703405A (zh) 2005-11-30
IL161663A0 (en) 2004-09-27
DE60225709D1 (de) 2008-04-30
DE60225709T2 (de) 2009-05-07
CA2463823A1 (en) 2003-05-08
BR0213790A (pt) 2004-12-07
HUP0402245A2 (hu) 2005-02-28
WO2003037877A1 (en) 2003-05-08
KR20040062557A (ko) 2004-07-07
HUP0402245A3 (en) 2010-03-29
ES2303565T3 (es) 2008-08-16
NO20042253L (no) 2004-06-01
JP2005507420A (ja) 2005-03-17
PL368920A1 (en) 2005-04-04
ATE389638T1 (de) 2008-04-15
PT1442024E (pt) 2008-06-12
MXPA04004176A (es) 2004-09-06

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