ECSP11010801A - Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de crf1 - Google Patents

Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de crf1

Info

Publication number
ECSP11010801A
ECSP11010801A EC2011010801A ECSP11010801A ECSP11010801A EC SP11010801 A ECSP11010801 A EC SP11010801A EC 2011010801 A EC2011010801 A EC 2011010801A EC SP11010801 A ECSP11010801 A EC SP11010801A EC SP11010801 A ECSP11010801 A EC SP11010801A
Authority
EC
Ecuador
Prior art keywords
crf1
derivatives
antigonist
pirazolo
oxazol
Prior art date
Application number
EC2011010801A
Other languages
English (en)
Inventor
Ian Bruce
Nicholas James Devereux
Andrew James Culshaw
Francois Gessier
Jeffrey Mickenna
James Neff
Helen Elizabeth Oakman
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of ECSP11010801A publication Critical patent/ECSP11010801A/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-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
    • A61K31/41Heterocyclic 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
    • A61K31/42Oxazoles
    • A61K31/424Oxazoles condensed with heterocyclic ring systems, e.g. clavulanic acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12Antidiarrhoeals
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  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
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Abstract

Se describen derivados de pirazolo-[5.1-b]-oxazol de la estructura I útiles como antagonistas del receptor del factor de liberación de corticotropina (CRF1).
EC2011010801A 2008-08-06 2011-02-02 Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de crf1 ECSP11010801A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP08161930 2008-08-06
US20509609P 2009-01-14 2009-01-14
EP09150553 2009-01-14

Publications (1)

Publication Number Publication Date
ECSP11010801A true ECSP11010801A (es) 2011-03-31

Family

ID=41653505

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2011010801A ECSP11010801A (es) 2008-08-06 2011-02-02 Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de crf1

Country Status (18)

Country Link
US (1) US7994203B2 (es)
EP (1) EP2328902A1 (es)
JP (1) JP2011529943A (es)
KR (1) KR20110051226A (es)
CN (1) CN102171220A (es)
AR (1) AR073262A1 (es)
AU (1) AU2009279137A1 (es)
BR (1) BRPI0917565A2 (es)
CA (1) CA2733176A1 (es)
CO (1) CO6351723A2 (es)
EA (1) EA201100303A1 (es)
EC (1) ECSP11010801A (es)
IL (1) IL211030A0 (es)
MA (1) MA32537B1 (es)
MX (1) MX2011001392A (es)
TW (1) TW201011039A (es)
UY (1) UY32029A (es)
WO (1) WO2010015628A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2266990B1 (en) 2008-04-15 2012-09-26 Eisai R&D Management Co., Ltd. 3-PHENYLPYRAZOLO[5,1-b]THIAZOLE COMPOUND
US8273900B2 (en) 2008-08-07 2012-09-25 Novartis Ag Organic compounds
EP2487177A1 (en) 2009-10-08 2012-08-15 Eisai R&D Management Co., Ltd. Pyrazoloxazole compound
AR078521A1 (es) 2009-10-08 2011-11-16 Eisai R&D Man Co Ltd Compuesto pirazolotiazol
JP2013518085A (ja) * 2010-02-01 2013-05-20 ノバルティス アーゲー CRF−1受容体アンタゴニストとしてのピラゾロ[5,1b]オキサゾール誘導体
UY34094A (es) 2011-05-27 2013-01-03 Novartis Ag Derivados de la piperidina 3-espirocíclica como agonistas de receptores de la ghrelina
EP2567959B1 (en) 2011-09-12 2014-04-16 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
CA2867043A1 (en) 2012-05-03 2013-11-07 Novartis Ag L-malate salt of 2,7-diaza-spiro[4.5]dec-7-yle derivatives and crystalline forms thereof as ghrelin receptor agonists
RS65839B1 (sr) 2014-01-21 2024-09-30 Neurocrine Biosciences Inc Crf1 receptor antagonisti za tretman kongenitalne adrenalne hiperplazije
EP3661500B1 (en) 2017-07-31 2026-01-07 Novartis AG Use of mavoglurant in the reduction of cocaine use or in preventing relapse into cocaine use
US20220023266A1 (en) 2018-12-07 2022-01-27 Neurocrine Biosciences, Inc. Crf1 receptor antagonist, pharmaceutical formulations and solid forms thereof for the treatment of congenital adrenal hyperplasia
JP7623365B2 (ja) 2019-09-27 2025-01-28 ニューロクライン バイオサイエンシーズ,インコーポレイテッド Crf受容体アンタゴニストおよび使用方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996031517A1 (en) * 1995-04-04 1996-10-10 E.I. Du Pont De Nemours And Company Herbicidal heteroaryl-substituted anilides
KR20040034594A (ko) * 2001-01-26 2004-04-28 브리스톨-마이어스스퀴브컴파니 코르티코트로핀 방출 인자 억제제로서의 이미다졸릴 유도체

Also Published As

Publication number Publication date
CA2733176A1 (en) 2010-02-11
IL211030A0 (en) 2011-04-28
CN102171220A (zh) 2011-08-31
TW201011039A (en) 2010-03-16
BRPI0917565A2 (pt) 2015-11-17
US7994203B2 (en) 2011-08-09
MX2011001392A (es) 2011-03-25
CO6351723A2 (es) 2011-12-20
WO2010015628A1 (en) 2010-02-11
AU2009279137A8 (en) 2011-03-03
JP2011529943A (ja) 2011-12-15
EP2328902A1 (en) 2011-06-08
US20100035874A1 (en) 2010-02-11
KR20110051226A (ko) 2011-05-17
AU2009279137A1 (en) 2010-02-11
AR073262A1 (es) 2010-10-28
UY32029A (es) 2010-03-26
EA201100303A1 (ru) 2011-10-31
MA32537B1 (fr) 2011-08-01

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