[go: up one dir, main page]

ATE299868T1 - Dihydro-benzo (b) (1,4) diazepin-2-on-derivate als mglur2 antagonisten - Google Patents

Dihydro-benzo (b) (1,4) diazepin-2-on-derivate als mglur2 antagonisten

Info

Publication number
ATE299868T1
ATE299868T1 AT02737911T AT02737911T ATE299868T1 AT E299868 T1 ATE299868 T1 AT E299868T1 AT 02737911 T AT02737911 T AT 02737911T AT 02737911 T AT02737911 T AT 02737911T AT E299868 T1 ATE299868 T1 AT E299868T1
Authority
AT
Austria
Prior art keywords
diazepine
benzo
dihydro
derivatives
mglur2 antagonists
Prior art date
Application number
AT02737911T
Other languages
English (en)
Inventor
Geo Adam
Erwin Goetschi
Vincent Mutel
Juergen Wichmann
Thomas Johannes Woltering
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Application granted granted Critical
Publication of ATE299868T1 publication Critical patent/ATE299868T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D243/00Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/10Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D243/141,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
    • C07D243/161,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
    • C07D243/181,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
    • C07D243/24Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/10Heterocyclic 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 carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/10Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
AT02737911T 2001-04-12 2002-04-02 Dihydro-benzo (b) (1,4) diazepin-2-on-derivate als mglur2 antagonisten ATE299868T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP01109125 2001-04-12
PCT/EP2002/003644 WO2002083652A1 (en) 2001-04-12 2002-04-02 DIHYDRO-BENZO [b] [1, 4] DIAZEPIN-2-ONE DERIVATIVES AS MGLUR2 ANTAGONISTS II

Publications (1)

Publication Number Publication Date
ATE299868T1 true ATE299868T1 (de) 2005-08-15

Family

ID=8177126

Family Applications (1)

Application Number Title Priority Date Filing Date
AT02737911T ATE299868T1 (de) 2001-04-12 2002-04-02 Dihydro-benzo (b) (1,4) diazepin-2-on-derivate als mglur2 antagonisten

Country Status (37)

Country Link
US (1) US6544985B2 (de)
EP (1) EP1379511B1 (de)
JP (1) JP4071115B2 (de)
KR (1) KR100566171B1 (de)
CN (1) CN1264825C (de)
AR (1) AR035816A1 (de)
AT (1) ATE299868T1 (de)
AU (1) AU2002312788B2 (de)
BG (1) BG108254A (de)
BR (1) BR0208891A (de)
CA (1) CA2442557C (de)
CZ (1) CZ20033003A3 (de)
DE (1) DE60205100T2 (de)
DK (1) DK1379511T3 (de)
EC (1) ECSP034797A (de)
ES (1) ES2246012T3 (de)
GT (1) GT200200073A (de)
HR (1) HRP20030792A2 (de)
HU (1) HUP0400851A3 (de)
IL (2) IL157873A0 (de)
JO (1) JO2285B1 (de)
MA (1) MA27012A1 (de)
MX (1) MXPA03009311A (de)
MY (1) MY140271A (de)
NO (1) NO20034576L (de)
NZ (1) NZ528315A (de)
PA (1) PA8543301A1 (de)
PE (1) PE20021041A1 (de)
PL (1) PL367064A1 (de)
PT (1) PT1379511E (de)
RU (1) RU2263112C2 (de)
SI (1) SI1379511T1 (de)
SK (1) SK13682003A3 (de)
UY (1) UY27258A1 (de)
WO (1) WO2002083652A1 (de)
YU (1) YU79003A (de)
ZA (1) ZA200307243B (de)

Families Citing this family (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE261945T1 (de) 1999-10-15 2004-04-15 Hoffmann La Roche Benzodiazepinderivate und deren verwendung als metabotrope glutamatrezeptor antagonisten
PT1459765E (pt) * 2001-12-27 2008-10-03 Taisho Pharmaceutical Co Ltd Derivados de 6-fluorobiciclo [3.1.0] hexano
EP1925614A1 (de) * 2002-03-28 2008-05-28 Wisys Technology Foundation, Inc. Anxiolytische Mittel mit reduzierter sedativer und ataxischer Wirkung
IL163958A0 (en) 2002-03-28 2005-12-18 Wisys Technology Foundation Anxiolytic agents with reduced sedative and ataxideffects
ATE374030T1 (de) * 2003-07-25 2007-10-15 Hoffmann La Roche Kombination eines mglur2 antagonists und eines ache inhibitors zur behandlung von akuten und/oder chronischen neurologischen krankheiten
US7329662B2 (en) 2003-10-03 2008-02-12 Hoffmann-La Roche Inc. Pyrazolo-pyridine
US20060160823A1 (en) * 2004-05-28 2006-07-20 Leonore Witchey-Lakshmanan Particulate-stabilized injectable pharmaceutical compositions of Posaconazole
JP4608542B2 (ja) * 2004-06-21 2011-01-12 エフ.ホフマン−ラ ロシュ アーゲー ピラゾロピリミジン誘導体
WO2006084634A1 (en) * 2005-02-11 2006-08-17 F.Hoffmann-La Roche Ag Pyrazolo-pyrimidine derivatives as mglur2 antagonists
DE602006012815D1 (de) 2005-03-23 2010-04-22 Hoffmann La Roche Acetylenylpyrazolopyrimidinderivate als mglur2-antagonsten
JP5237798B2 (ja) * 2005-06-23 2013-07-17 アレイ バイオファーマ、インコーポレイテッド ベンズイミダゾール化合物の調製方法
JP5048675B2 (ja) 2005-09-27 2012-10-17 エフ.ホフマン−ラ ロシュ アーゲー mGluR2アンタゴニストとしてのオキサジアゾリルピラゾロ−ピリミジン類
GB0600228D0 (en) * 2006-01-06 2006-02-15 Fermentas Uab Inactivation method
TWI417095B (zh) 2006-03-15 2013-12-01 Janssen Pharmaceuticals Inc 1,4-二取代之3-氰基-吡啶酮衍生物及其作為mGluR2-受體之正向異位性調節劑之用途
TW200808751A (en) * 2006-04-13 2008-02-16 Astrazeneca Ab New compounds
MX2009002538A (es) * 2006-09-20 2009-03-20 Hoffmann La Roche Derivados de 4-oxo-2,3,4,5-tetrahidro-benzo[b][1,4]diazepina.
TW200900065A (en) 2007-03-07 2009-01-01 Janssen Pharmaceutica Nv 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives
TW200845978A (en) 2007-03-07 2008-12-01 Janssen Pharmaceutica Nv 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives
AU2008240802B2 (en) 2007-04-19 2012-07-05 F. Hoffmann-La Roche Ag Dihydro-benzo[B][1,4]diazepin-2-one sulfonamide derivatives
NZ584148A (en) * 2007-09-14 2011-05-27 Ortho Mcneil Janssen Pharm 1,3-disubstituted-4-phenyl-1 h-pyridin-2-ones
CA2697399C (en) 2007-09-14 2016-01-19 Ortho-Mcneil-Janssen Pharmaceuticals, Inc. 1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones
MY152078A (en) 2007-09-14 2014-08-15 Ortho Mcneil Janssen Pharm 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-ones
RU2492170C9 (ru) 2007-11-14 2013-12-27 Орто-Макнейл-Янссен Фармасьютикалз, Инк. Имидазо[1,2-а]пиридиновые производные и их применение в качестве положительных аллостерических модуляторов рецепторов mglur2
AU2009289784B2 (en) 2008-09-02 2012-03-22 Addex Pharma S.A. 3-azabicyclo[3.1.0]hexyl derivatives as modulators of metabotropic glutamate receptors
ES2466341T3 (es) 2008-10-16 2014-06-10 Janssen Pharmaceuticals, Inc. Derivados de indol y benzomorfolina como moduladores de receptores de glutamato metabotrópicos
WO2010060589A1 (en) 2008-11-28 2010-06-03 Ortho-Mcneil-Janssen Pharmaceuticals, Inc. Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors
AU2010246609B2 (en) 2009-05-12 2013-09-05 Addex Pharma S.A. 1,2,4-triazolo [4,3-a] pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders
NZ596053A (en) 2009-05-12 2013-05-31 Janssen Pharmaceuticals Inc 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors
MY153913A (en) 2009-05-12 2015-04-15 Janssen Pharmaceuticals Inc 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors
EP2593447B1 (de) 2010-07-15 2016-08-17 Bayer Intellectual Property GmbH 3-pyridyl-heteroarylcarboxamidverbindungen als schädlingsbekämpfungsmittel
WO2012059432A1 (en) 2010-11-01 2012-05-10 Abbott Gmbh & Co. Kg N-phenyl-(homo)piperazinyl-benzenesulfonyl or benzenesulfonamide compounds suitable for treating disorders that respond to the modulation of the 5-ht6 receptor
WO2012059431A1 (en) 2010-11-01 2012-05-10 Abbott Gmbh & Co. Kg Benzenesulfonyl or sulfonamide compounds suitable for treating disorders that respond to the modulation of the serotonin 5-ht6 receptor
CN103298810B (zh) 2010-11-08 2016-03-16 杨森制药公司 1,2,4-三唑并[4,3-a]吡啶衍生物及其作为MGLUR2受体的正变构调节剂的用途
EP2643320B1 (de) 2010-11-08 2015-03-04 Janssen Pharmaceuticals, Inc. 1,2,4-triazolo[4,3-a]pyridinderivate und ihre verwendung als positiv allosterische modulatoren des mglur2 receptors
EP2661435B1 (de) 2010-11-08 2015-08-19 Janssen Pharmaceuticals, Inc. 1,2,4-triazol[4,3-a]pyridinderivate und ihre verwendung als positive allosterische mglur2-rezeptormodulatoren
WO2012149540A1 (en) 2011-04-28 2012-11-01 The Broad Institute Inc Inhibitors of histone deacetylase
JP5790195B2 (ja) * 2011-06-22 2015-10-07 セントラル硝子株式会社 ピラゾール化合物の製造方法
CA2847247C (en) * 2011-08-29 2019-10-15 Sanford-Burnham Medical Research Institute Benzodiazepinones as modulators of metabotropic glutamate receptor functions and neurological uses thereof
CA2880117C (en) 2012-07-27 2021-04-06 The Broad Institute, Inc. Inhibitors of histone deacetylase
EP2925292A1 (de) 2012-10-23 2015-10-07 F. Hoffmann-La Roche AG Mglu2/3-antagonisten zur behandlung von autistischen störungen
US9914717B2 (en) 2012-12-20 2018-03-13 The Broad Institute, Inc. Cycloalkenyl hydroxamic acid derivatives and their use as histone deacetylase inhibitors
EP2940014B1 (de) * 2012-12-28 2018-09-26 Crystalgenomics, Inc. 2,3-dihydro-isoindol-1-on derivat als btk-kinase-hemmer und pharmazeutische zusammensetzung damit
JO3368B1 (ar) 2013-06-04 2019-03-13 Janssen Pharmaceutica Nv مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2
JO3367B1 (ar) 2013-09-06 2019-03-13 Janssen Pharmaceutica Nv مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2
DK3096790T3 (da) 2014-01-21 2019-10-07 Janssen Pharmaceutica Nv Kombinationer omfattende positive allosteriske modulatorer eller orthosteriske agonister af metabotrop glutamaterg subtype 2-receptor og anvendelse af disse
KR20220038826A (ko) 2014-01-21 2022-03-29 얀센 파마슈티카 엔.브이. 대사 조절형 글루탐산 작동성 수용체 제2아형의 양성 알로스테릭 조절제 또는 오르토스테릭 작동제를 포함하는 조합 및 그 용도
HRP20221373T1 (hr) 2014-03-07 2023-01-06 Biocryst Pharmaceuticals, Inc. Supstituirani pirazoli kao inhibitori kalikreina u ljudskoj plazmi
RU2016144702A (ru) * 2014-04-23 2018-05-24 Ф. Хоффманн-Ля Рош Аг Антагонисты mglu2/3 для лечения интеллектуальной недостаточности
US9969726B2 (en) 2014-06-10 2018-05-15 Sanford-Burnham Medical Research Institute Metabotropic glutamate receptor negative allosteric modulators (NAMS) and uses thereof
CN108727345B (zh) * 2017-04-25 2023-06-27 广东东阳光药业有限公司 一种咪唑环中间体的制备方法
JP2021510733A (ja) 2018-01-12 2021-04-30 ケーディーエーシー セラピューティクス,インコーポレーテッドKdac Therapeutics, Inc. がんの処置のための選択的ヒストンデアセチラーゼ3(hdac3)インヒビターと免疫治療剤との組み合わせ
CN108586447B (zh) * 2018-01-19 2021-01-29 中国人民解放军第四军医大学 一种苯二氮杂卓化合物及其制备方法和应用
JP7581244B2 (ja) * 2019-06-06 2024-11-12 アーカス バイオサイエンシズ インコーポレイティド アミノピリミジン化合物の調製方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU224435B1 (hu) * 1995-02-09 2005-10-28 EGIS Gyógyszergyár Rt. Benzodiazepin-származékok, eljárás előállításukra, alkalmazásukra és ezeket tartalmazó gyógyászati készítmények
SK283859B6 (sk) * 1995-02-09 2004-03-02 Egis Gy�Gyszergy�R Rt. 1-[2'-(Substituovaný)vinyl]-5H-2,3-benzodiazepínové deriváty, spôsob ich prípravy a medziprodukty na ich prípravu, liečivá ich obsahujúce a ich použitie
EP1210338A2 (de) * 1999-08-05 2002-06-05 IGT Pharma Inc. 1,4-diazepin-derivate zur behandlung von krankheiten des zentralen nervensystems
ATE261945T1 (de) * 1999-10-15 2004-04-15 Hoffmann La Roche Benzodiazepinderivate und deren verwendung als metabotrope glutamatrezeptor antagonisten
WO2001029011A2 (en) * 1999-10-15 2001-04-26 F. Hoffmann-La Roche Ag Benzodiazepine derivatives as metabotropic glutamate receptor antagonists

Also Published As

Publication number Publication date
CA2442557C (en) 2008-12-23
DE60205100D1 (de) 2005-08-25
MA27012A1 (fr) 2004-12-20
HK1068888A1 (en) 2005-05-06
CZ20033003A3 (cs) 2004-05-12
PL367064A1 (en) 2005-02-21
YU79003A (sh) 2006-05-25
ES2246012T3 (es) 2006-02-01
CN1535266A (zh) 2004-10-06
SK13682003A3 (sk) 2004-07-07
NO20034576D0 (no) 2003-10-10
AR035816A1 (es) 2004-07-14
PT1379511E (pt) 2005-10-31
HUP0400851A3 (en) 2010-03-29
EP1379511B1 (de) 2005-07-20
HUP0400851A2 (hu) 2004-07-28
US6544985B2 (en) 2003-04-08
IL157873A (en) 2008-11-26
NZ528315A (en) 2005-04-29
RU2263112C2 (ru) 2005-10-27
HRP20030792A2 (en) 2005-10-31
KR20030087076A (ko) 2003-11-12
RU2003130637A (ru) 2005-04-10
DE60205100T2 (de) 2006-06-01
ZA200307243B (en) 2004-12-16
US20020193367A1 (en) 2002-12-19
PA8543301A1 (es) 2003-01-24
JP2004529925A (ja) 2004-09-30
MXPA03009311A (es) 2004-02-12
WO2002083652A1 (en) 2002-10-24
CA2442557A1 (en) 2002-10-24
IL157873A0 (en) 2004-03-28
JO2285B1 (en) 2005-09-12
UY27258A1 (es) 2002-10-31
DK1379511T3 (da) 2005-11-07
NO20034576L (no) 2003-11-12
GT200200073A (es) 2002-11-07
EP1379511A1 (de) 2004-01-14
BR0208891A (pt) 2004-04-20
MY140271A (en) 2009-12-31
AU2002312788B2 (en) 2005-11-10
ECSP034797A (es) 2003-12-01
KR100566171B1 (ko) 2006-03-29
BG108254A (bg) 2004-09-30
SI1379511T1 (en) 2005-10-31
PE20021041A1 (es) 2002-11-19
JP4071115B2 (ja) 2008-04-02
CN1264825C (zh) 2006-07-19

Similar Documents

Publication Publication Date Title
DE60205100D1 (de) DIHYDRO-BENZO (b) (1,4) DIAZEPIN-2-ON-DERIVATE ALS MGLUR2 ANTAGONISTEN
ATE287883T1 (de) Dihydro-benzo(b)(1,4)diazepin-2-on-derivate als mglur2 antagonisten
ATE354570T1 (de) 5,6-diaryl-pyrazineamidderivate als cb1 antagonisten
DE60131971D1 (de) 1,3,8-TRIAZA-SPIROi4,5 DECAN-4-ONDERIVATIVE ALS NEUROKININREZEPTORANTAGONISTEN
DE60216115D1 (de) BENZIMIDAZO 4,5-föISOCHINOLINON-DERIVATE
DE60019577D1 (de) 4, 5, 6, 7-tetrahydroindazolderivate als antitumormittel
DE602004006169D1 (de) Substituierte 8'-pyri(mi)dinyl-dihydrospiro-äcycloalkylaminü-pyrimidoä1,2aüpyrimidin-6-onderivate
ATE326467T1 (de) Imidazo 1,2-aöpyridine
DE60210598D1 (de) 3,7-DIAZABICYCLOc3.3.1Ü-FORMULIERUNGEN ALS ANTIARRHYTHMIKA
DE60017110D1 (de) Biphenylderivate als neurokinin-1 antagonisten
DE60214138D1 (de) Isoxazolin-derivate als antidepressiva
ATE418542T1 (de) Als ccr5-antagonisten verwendbare aryloxim- piperazine
DE50005743D1 (de) Substituierte benzoylcyclohexandione als herbizide
DE60210058D1 (de) Alkoxycarbonylamino-heteroaryl-carbonsäurederivate als ip-antagonisten
DE50206910D1 (de) Substituierte y-lactonverbindungen als nmda-antagonisten
DE60213084D1 (de) 3,7-DIAZABICYCLOc3.3.1Ü-FORMULIERUNGEN ALS ANTIARRHYTHMIKA
DK1261588T3 (da) Imidazolforbindelser som alfa2-adrenoceptorantagonister
DE60012953D1 (de) 3-amino-2-phenylpiperidinderivate als substanz p antagonisten
ITTO20020744A1 (it) Composizione.
DE50208676D1 (de) Builder-Zusammensetzung
ITTO20020745A1 (it) Composizione.
DE50214487D1 (de) Substituierte 1,5-diaminopentan-3-ol-verbindungen
IS7131A (is) Nýjar 2,4-díamínóþíasól afleiður
DE60017150D1 (de) 1,4,5,6 -tetrahydropyrimidine-derivative als vitronectin-hemmer
SE0100199D0 (sv) New formulation

Legal Events

Date Code Title Description
UEP Publication of translation of european patent specification

Ref document number: 1379511

Country of ref document: EP

REN Ceased due to non-payment of the annual fee