MA29850B1 - Composes de type pyrazolo [1.5 -alpha] pyrimidinyle pouvant etre employes en tant qu'antagonistes du recepteur du facteur de liberation de la corticotropine (crf) - Google Patents

Composes de type pyrazolo [1.5 -alpha] pyrimidinyle pouvant etre employes en tant qu'antagonistes du recepteur du facteur de liberation de la corticotropine (crf)

Info

Publication number
MA29850B1
MA29850B1 MA30813A MA30813A MA29850B1 MA 29850 B1 MA29850 B1 MA 29850B1 MA 30813 A MA30813 A MA 30813A MA 30813 A MA30813 A MA 30813A MA 29850 B1 MA29850 B1 MA 29850B1
Authority
MA
Morocco
Prior art keywords
crf
pyrazolo
alpha
factor receptor
release factor
Prior art date
Application number
MA30813A
Other languages
English (en)
Inventor
Frank Hossner
Original Assignee
Sb Pharmco Inc
Neurocrine Biosciences Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35395069&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA29850(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sb Pharmco Inc, Neurocrine Biosciences Inc filed Critical Sb Pharmco Inc
Publication of MA29850B1 publication Critical patent/MA29850B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • 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
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • 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
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • 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
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/32Alcohol-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/34Tobacco-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Psychiatry (AREA)
  • Addiction (AREA)
  • Diabetes (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pain & Pain Management (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Anesthesiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychology (AREA)
  • Nutrition Science (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Dérivés de pyrazolo[l,5-alpha]pyrimidinyle utiles comme antagonistes des récepeurs du facteur de libération de corticotrophine (CRF) La présente invention concerne de manière générale la forme polymorphe 2 de [3-(4-méthoxy-2-méthylphényl)-2, 5-diméthylpyrazolo [1, 5-a] pyrimidine-7-yl]-[(S)-l-(3-méthyl-[l, 2, 4] oxadiazole-5-yl) propyl] amine. La présente invention concerne également des compositions pharmaceutiques comprenant celle-ci et des méthodes pour leur utilisation.
MA30813A 2005-09-30 2008-04-04 Composes de type pyrazolo [1.5 -alpha] pyrimidinyle pouvant etre employes en tant qu'antagonistes du recepteur du facteur de liberation de la corticotropine (crf) MA29850B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0519957.5A GB0519957D0 (en) 2005-09-30 2005-09-30 Chemical compound
PCT/US2005/037576 WO2006044958A1 (fr) 2004-10-19 2005-10-19 Derives de pyrazolo[1,5-alpha]pyrimidinyle utiles comme antagonistes vis-a-vis du recepteur du facteur de liberation de la corticotropine (crf)

Publications (1)

Publication Number Publication Date
MA29850B1 true MA29850B1 (fr) 2008-10-03

Family

ID=35395069

Family Applications (1)

Application Number Title Priority Date Filing Date
MA30813A MA29850B1 (fr) 2005-09-30 2008-04-04 Composes de type pyrazolo [1.5 -alpha] pyrimidinyle pouvant etre employes en tant qu'antagonistes du recepteur du facteur de liberation de la corticotropine (crf)

Country Status (21)

Country Link
US (1) US7879862B2 (fr)
EP (2) EP1802627B1 (fr)
JP (2) JP4901744B2 (fr)
KR (2) KR20070088621A (fr)
CN (1) CN101273043B (fr)
AR (2) AR051461A1 (fr)
AU (2) AU2005295353B2 (fr)
BR (1) BRPI0616767A2 (fr)
CA (2) CA2584567C (fr)
CR (1) CR9918A (fr)
EA (1) EA200801000A1 (fr)
GB (1) GB0519957D0 (fr)
IL (1) IL190225A0 (fr)
MA (1) MA29850B1 (fr)
NO (2) NO20072541L (fr)
NZ (1) NZ554082A (fr)
PE (2) PE20060586A1 (fr)
RU (1) RU2007118683A (fr)
TW (2) TW200626599A (fr)
UA (1) UA92756C2 (fr)
WO (2) WO2006044958A1 (fr)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7196078B2 (en) 2002-09-04 2007-03-27 Schering Corpoartion Trisubstituted and tetrasubstituted pyrazolopyrimidines as cyclin dependent kinase inhibitors
MY143499A (en) * 2003-12-22 2011-05-31 Sb Pharmco Inc Crf receptor antagonist and methods relating thereto
GB0519957D0 (en) * 2005-09-30 2005-11-09 Sb Pharmco Inc Chemical compound
US7572807B2 (en) 2005-06-09 2009-08-11 Bristol-Myers Squibb Company Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors
US7579360B2 (en) 2005-06-09 2009-08-25 Bristol-Myers Squibb Company Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors
US8088779B2 (en) 2005-09-30 2012-01-03 Smithkline Beecham (Cork) Limited Pyrazolo [1,5-alpha] pyrimidinyl derivatives useful as corticotropin-releasing factor (CRF) receptor antagonists
GB0525068D0 (en) 2005-12-08 2006-01-18 Novartis Ag Organic compounds
US8119658B2 (en) 2007-10-01 2012-02-21 Bristol-Myers Squibb Company Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors
CN101932583A (zh) 2007-12-19 2010-12-29 沃泰克斯药物股份有限公司 用作JAK2抑制剂的吡唑并[1,5-a]嘧啶类
CA2721670C (fr) 2008-04-15 2013-09-10 Eisai R&D Management Co., Ltd. Compose de 3-phenylpyrazolo[5,1-b]thiazole
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
WO2011043387A1 (fr) * 2009-10-08 2011-04-14 エーザイ・アール・アンド・ディー・マネジメント株式会社 Composé de pyrazolooxazole
AR078521A1 (es) 2009-10-08 2011-11-16 Eisai R&D Man Co Ltd Compuesto pirazolotiazol
AR080055A1 (es) 2010-02-01 2012-03-07 Novartis Ag Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de los receptores de crf -1
AR080056A1 (es) 2010-02-01 2012-03-07 Novartis Ag Derivados de ciclohexil-amida como antagonistas de los receptores de crf
EP2531490B1 (fr) * 2010-02-02 2014-10-15 Novartis AG Dérivés de cyclohexylamide à titre d'antagonistes du récepteur crf
US8546416B2 (en) 2011-05-27 2013-10-01 Novartis Ag 3-spirocyclic piperidine derivatives as ghrelin receptor agonists
WO2013074641A1 (fr) 2011-11-16 2013-05-23 Array Biopharma Inc. Urées cycliques substituées par pipéridinyle en tant que modulateurs de gpr119
WO2013160317A2 (fr) * 2012-04-23 2013-10-31 Holsboermaschmeyer Neurochemie Gmbh Antagonistes de crhr1 pour une utilisation dans le traitement de patients présentant une hyperactivité de la crh
EP2852591A1 (fr) 2012-05-03 2015-04-01 Novartis AG Sel de l-malate de dérivés de 2,7-diaza-spiro[4.5]déc-7-yle et ses formes cristallines à titre d'agonistes des récepteurs de ghreline
GB201210686D0 (en) 2012-06-15 2012-08-01 Holsboermaschmeyer Neurochemie Gmbh V1B receptor antagonist for use in the treatment of patients having an elevated AVP level and/or an elevated copeptin level
GB201310782D0 (en) 2013-06-17 2013-07-31 Max Planck Innovation Gmbh Method for predicting a treatment response to a CRHR1 antagonist and/or V1B antagonist in a patient with depressive and/or anxiety symptoms
IL296683B2 (en) 2014-01-21 2023-12-01 Neurocrine Biosciences Inc Preparations for the treatment of congenital adrenal hyperplasia
JP6509238B2 (ja) * 2014-01-22 2019-05-08 キュロヴィル・アクチボラグ 治療に有用なピラゾロ[1,5−a]ピリミジン−7−アミン誘導体
CA3052479A1 (fr) 2017-02-17 2018-08-23 Trevena, Inc. Composes modulateurs du recepteur des opioides delta contenant des heterocycles aza a 7 chainons, et leurs procedes de preparation et d'utilisation
WO2018165520A1 (fr) 2017-03-10 2018-09-13 Vps-3, Inc. Composés inhibiteurs de métalloenzymes
JP2023508907A (ja) 2019-12-20 2023-03-06 テナヤ セラピューティクス, インコーポレイテッド フルオロアルキル-オキサジアゾールおよびその使用
WO2022093904A1 (fr) * 2020-10-27 2022-05-05 Trevena, Inc. Formes cristallines et amorphes d'un modulateur delta-opioïde

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4605642A (en) 1984-02-23 1986-08-12 The Salk Institute For Biological Studies CRF antagonists
US5707997A (en) 1994-06-21 1998-01-13 Otsuka Pharmaceutical Factory, Inc. Pyrazolo 1,5-a!pyrimidine derivative
US6664261B2 (en) 1996-02-07 2003-12-16 Neurocrine Biosciences, Inc. Pyrazolopyrimidines as CRF receptor antagonists
NZ330119A (en) 1996-02-07 2000-02-28 Janssen Pharmaceutica Nv Pyrazolopyrimidines as crf receptor antagonists
US6060478A (en) * 1996-07-24 2000-05-09 Dupont Pharmaceuticals Azolo triazines and pyrimidines
CA2259583C (fr) * 1996-07-24 2009-11-17 Du Pont Pharmaceuticals Company Azolo triazines et pyrimidines
US6313124B1 (en) 1997-07-23 2001-11-06 Dupont Pharmaceuticals Company Tetrazine bicyclic compounds
HU229024B1 (en) 1996-07-24 2013-07-29 Bristol Myers Squibb Pharma Co Azolo-pyridimidines, pharmaceutical compositions containing the same and use thereof
JPH10101672A (ja) 1996-08-06 1998-04-21 Otsuka Pharmaceut Factory Inc アデノシン増強剤
JPH10101671A (ja) 1996-08-08 1998-04-21 Otsuka Pharmaceut Factory Inc 一酸化窒素合成酵素阻害剤
CN1227554A (zh) 1996-08-28 1999-09-01 辉瑞大药厂 取代的6,5-杂二环衍生物
CA2314613C (fr) 1998-01-28 2009-12-08 Du Pont Pharmaceuticals Company Azolo triazines et pyrimidines
JP2000038350A (ja) 1998-05-18 2000-02-08 Yoshitomi Pharmaceut Ind Ltd 糖尿病治療薬
EP1149835A4 (fr) 1999-01-29 2002-08-21 Sumitomo Chemical Co Agents inhibiteurs d'accumulation de graisse
WO2000059908A2 (fr) * 1999-04-06 2000-10-12 Du Pont Pharmaceuticals Company Pyrazolopyrimidines antagonistes de corticoliberine (crf)
IL148905A0 (en) 1999-09-30 2002-09-12 Neurogen Corp Pfizer Inc Certain alkylene diamine-substituted pyrazolo{1,5,-a}-1,5-pyrimidines and pyrazolo{1,5,-a}-1,3,5-triazines
CN1377355A (zh) 1999-09-30 2002-10-30 纽罗杰有限公司 氨基取代的吡唑并[1,5-a]-1,5-嘧啶和吡唑并[1,5-a]-1,3,5-三嗪
IL139197A0 (en) * 1999-10-29 2001-11-25 Pfizer Prod Inc Use of corticotropin releasing factor antagonists and related compositions
AR033295A1 (es) * 2001-04-30 2003-12-10 Glaxo Group Ltd Compuestos biciclicos de pirimidina, proceso para su obtencion, uso de los mismos para la preparacion de una composicion farmaceutica y dicha composicion farmaceutica
EP1395591B1 (fr) * 2001-06-12 2008-06-04 Glaxo Group Limited Antagonistes du facteur de liberation de la corticotropine
GB0117396D0 (en) 2001-07-17 2001-09-05 Glaxo Group Ltd Chemical compounds
CA2487211C (fr) 2002-06-04 2010-09-14 Neogenesis Pharmaceuticals, Inc. Composes de pyrazolo(1,5a)pyrimidine servant d'agents antiviraux
ATE359782T1 (de) * 2003-01-16 2007-05-15 Sb Pharmco Inc Heteroaryl-substituierte pyrrol(2, 3- b)pyridin- derivate als crf-rezeptor-antagonisten
EP1608652A1 (fr) 2003-03-31 2005-12-28 Vernalis (Cambridge) Limited Composes pyrazolopyrimidines et leur utilisation en medecine
US20070021429A1 (en) * 2003-04-09 2007-01-25 Yves St-Denis Condensed n-heterocyclic compounds and their use as crf receptor antagonists
GB0308208D0 (en) * 2003-04-09 2003-05-14 Glaxo Group Ltd Chemical compounds
MY143499A (en) * 2003-12-22 2011-05-31 Sb Pharmco Inc Crf receptor antagonist and methods relating thereto
US20070293511A1 (en) * 2003-12-22 2007-12-20 Sb Pharmco Puerto Rico Inc. And Neurocrine Biosciences, Inc., A Corporation Crf Receptor Antagonists and Methods
DE102004008807A1 (de) * 2004-02-20 2005-09-08 Bayer Cropscience Ag Pyrazolopyrimidine
GB0519957D0 (en) * 2005-09-30 2005-11-09 Sb Pharmco Inc Chemical compound
ATE430746T1 (de) * 2004-10-19 2009-05-15 Smithkline Beecham Cork Ltd Crf-rezeptor-antagonisten und zugehörige verfahren
US8088779B2 (en) * 2005-09-30 2012-01-03 Smithkline Beecham (Cork) Limited Pyrazolo [1,5-alpha] pyrimidinyl derivatives useful as corticotropin-releasing factor (CRF) receptor antagonists

Also Published As

Publication number Publication date
KR20070088621A (ko) 2007-08-29
RU2007118683A (ru) 2008-11-27
AU2006298995A1 (en) 2007-04-12
EP1802627B1 (fr) 2012-08-29
NO20072541L (no) 2007-06-25
GB0519957D0 (en) 2005-11-09
CA2584567A1 (fr) 2006-04-27
CN101273043A (zh) 2008-09-24
US20080194589A1 (en) 2008-08-14
CA2584567C (fr) 2013-04-30
EP1934222B1 (fr) 2012-07-25
TW200745121A (en) 2007-12-16
WO2006044958A8 (fr) 2006-06-08
JP2009510004A (ja) 2009-03-12
JP4901744B2 (ja) 2012-03-21
CN101273043B (zh) 2011-08-03
KR20080063760A (ko) 2008-07-07
EP1934222A1 (fr) 2008-06-25
AR056104A1 (es) 2007-09-19
TW200626599A (en) 2006-08-01
EA200801000A1 (ru) 2009-02-27
PE20070845A1 (es) 2007-08-25
CA2624699A1 (fr) 2007-04-12
BRPI0616767A2 (pt) 2011-06-28
NZ554082A (en) 2010-12-24
JP2008517067A (ja) 2008-05-22
PE20060586A1 (es) 2006-09-20
WO2006044958A1 (fr) 2006-04-27
CR9918A (es) 2009-02-03
WO2007039264A1 (fr) 2007-04-12
EP1802627A1 (fr) 2007-07-04
AU2006298995B2 (en) 2012-06-14
UA92756C2 (ru) 2010-12-10
AR051461A1 (es) 2007-01-17
IL190225A0 (en) 2009-09-22
NO20081941L (no) 2008-04-23
AU2005295353A1 (en) 2006-04-27
US7879862B2 (en) 2011-02-01
AU2005295353B2 (en) 2012-01-12

Similar Documents

Publication Publication Date Title
MA29850B1 (fr) Composes de type pyrazolo [1.5 -alpha] pyrimidinyle pouvant etre employes en tant qu'antagonistes du recepteur du facteur de liberation de la corticotropine (crf)
PE20081377A1 (es) Compuestos de tiazol pirazolopirimidina
PE20150758A1 (es) Nuevos derivados biciclicos
IL210071A (en) Derivatives of {3– (pyrid – 2 – illmethyl) –3 h– [1, 2, 3] triazolo [4, 5 – d] pyrimidine-5-amine}, their pharmaceutical preparations and their use in drug preparation
ATE421967T1 (de) Nichtvernetzende pyrroloä2,1-cüä1, 4übenzodiazepine als potentielle antitumor- agentien und ihre herstellung
DE60132017D1 (de) Neue benzazepine und ähnliche heterocyclische derivate,die als orexin rezeptor antagonisten geeignet sind
WO2005040169A3 (fr) Composes heterocycliques fusionnes
IL207576A0 (en) Bridged, bicyclic heterocyclic or spiro bicyclic heterocyclic derivatives of pyrazolo[1,5-a]pyrimidines, methods for preparation and uses thereof
GEP20135780B (en) Novel pyrazolo [3,4-d] pyrimidine derivatives as anti-cancer agents
WO2009093210A3 (fr) Cyclo-alcano[e et d] pyrazolo[1,5-a]pyrimidines substituées fonctionnant comme des antagonistes des récepteurs 5-ht6 de sérotonine, procédés de fabrication et d'utilisation
WO2010124042A3 (fr) Modulateurs des récepteurs 5-ht et méthodes d'utilisation de ceux-ci
TW200630372A (en) Imidazo-benzodiazepine derivatives
ATE477255T1 (de) Imidazobenzdiazepinderivate
MA29623B1 (fr) Derives de pyrazolo [3, 4-d] azepine comme antagonistes d'histamine h3
GB2446080A (en) A novel Pyrrolo [2,1-C][1,4] benzodiazepine hybrid and a process for the preparation thereof
TW200626600A (en) Octahydropyrrolo[3, 4-c]pyrrole derivatives
EA201390921A1 (ru) НОВЫЕ ПРОТИВОГРИБКОВЫЕ 5,6-ДИГИДРО-4H-ПИРРОЛО[1,2-a][1,4]БЕНЗОДИАЗЕПИНЫ И 6H-ПИРРОЛО[1,2-a][1,4]БЕНЗОДИАЗЕПИНЫ, ЗАМЕЩЕННЫЕ БИЦИКЛИЧЕСКИМИ ПРОИЗВОДНЫМИ БЕНЗОЛА
MX339692B (es) Moduladores de los receptores 5-ht y metodos de uso de los mismos.
MA29910B1 (fr) Potentialisateurs des recepteurs ampa
DK1678182T3 (da) Fremgangsmåde til fremstilling af substituerede 5-amino-pyrazolo[4,3-E]-1,2,4-triazolo-[1,5-C]pyrimidiner
CA2520901A1 (fr) Derives de pyrrolo (2,1-c) (1,4) benzodiazepine lies au pyrene utiles en tant qu'agents anticancereux
BRPI0415966A (pt) combinações compreendendo antagonistas do receptor ampa para tratamento de esquizofrenia
TW200504074A (en) 7-substituted 3-nitro-pyrazolo[1,5-a]pyrimidines and compositions and methods related thereto
Peng et al. First synthesis of piperazine-derived [1, 2, 4] triazolo [1, 5-a] pyrazine as an adenosine A2a receptor antagonist
FI89487B (fi) Foerfarande foer framstaellning av terapeutiskt aktiva 4-/(substituerad)alkylkarbonyl/-4,5-dihydro- och -4,5,6,7-tetrahydro-7-/(substituerad)fenyl/pyrazolo-/1,5-a/pyrimidin-3-karbonitriler