PE20091324A1 - Compuestos espiro como antagonistas del receptor npy y5 - Google Patents

Compuestos espiro como antagonistas del receptor npy y5

Info

Publication number
PE20091324A1
PE20091324A1 PE2009000118A PE2009000118A PE20091324A1 PE 20091324 A1 PE20091324 A1 PE 20091324A1 PE 2009000118 A PE2009000118 A PE 2009000118A PE 2009000118 A PE2009000118 A PE 2009000118A PE 20091324 A1 PE20091324 A1 PE 20091324A1
Authority
PE
Peru
Prior art keywords
pyridinyl
alkyl
azaespiro
decan
ona
Prior art date
Application number
PE2009000118A
Other languages
English (en)
Inventor
Matteo Biagetti
Stefania Anne Contini
Thorsten Genski
Sebastien Guery
Colin Philip Leslie
Angelica Mazzali
Domenica Antonia Pizzi
Fabio Maria Sabbatini
Catia Seri
Original Assignee
Glaxo Group Ltd
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
Priority claimed from GB0801597A external-priority patent/GB0801597D0/en
Priority claimed from GB0819112A external-priority patent/GB0819112D0/en
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of PE20091324A1 publication Critical patent/PE20091324A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61P1/14Prodigestives, 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
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs 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
    • A61P3/00Drugs for disorders of the metabolism
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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
    • C07D417/14Heterocyclic 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 three or more hetero rings

Abstract

REFERIDA A COMPUESTOS ESPIRO DE FORMULA (I) DONDE R ES ARILO O HETEROARILO OPCIONALMENTE SUSTITUIDO CON UNO O MAS HALO, ALQUILO(C1-C4), ALCOXI(C1-C4), ENTRE OTROS; Z1 ES H, ALQUILO(C1-C4) O F; Z ES UN ENLACE, CH2, CH(ALQUILO C1-C4), ENTRE OTROS; A ES ARILO O HETEROARILO DE 5-6 MIEMBROS OPCIONALMENTES SUSTITUIDO CON HALO, ALQUILO(C1-C4), ALCOXI(C1-C4), ENTRE OTROS; B ES H, FENILO, HETEROARILO DE 5-6 MIEMBROS, ENTRE OTROS. SON COMPUESTOS SELECCIONADOS: (TRANS)-3-FENIL-8-({[5-(TRIFLUOROMETIL)-2-PIRIDINIL]AMINO}METIL)-1-OXA-3-AZAESPIRO[4.5]DECAN-2-ONA, (TRANS)-3-(2-PIRIDINIL)-8-({[5-(TRIFLUOROMETIL)-2-PIRIDINIL]AMINO}METIL)-1-OXA-3-AZAESPIRO[4.5]DECAN-2-ONA, (TRANS)-3-(2-PIRIDINIL)-8-({[5-(2-PIRIMIDINIL)-2-PIRIDINIL]AMINO}METIL)-1-OXA-3-AZAESPIRO[4.5]DECAN-2-ONA, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DEL RECEPTOR NPY Y5, SIENDO UTILES PARA EL TRATAMIENTO DE TRASTORNOS DE LA ALIMENTACION, TRASTORNOS DE LA BEBIDA, OBESIDAD O DEPRESION
PE2009000118A 2008-01-29 2009-01-28 Compuestos espiro como antagonistas del receptor npy y5 PE20091324A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0801597A GB0801597D0 (en) 2008-01-29 2008-01-29 Chemical compounds
GB0819112A GB0819112D0 (en) 2008-10-17 2008-10-17 Chemical compounds

Publications (1)

Publication Number Publication Date
PE20091324A1 true PE20091324A1 (es) 2009-09-25

Family

ID=40456386

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2009000118A PE20091324A1 (es) 2008-01-29 2009-01-28 Compuestos espiro como antagonistas del receptor npy y5

Country Status (7)

Country Link
US (1) US20090203705A1 (es)
AR (1) AR070268A1 (es)
CL (1) CL2009000171A1 (es)
PE (1) PE20091324A1 (es)
TW (1) TW200944520A (es)
UY (1) UY31619A1 (es)
WO (1) WO2009095377A1 (es)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005118586A1 (en) * 2004-06-02 2005-12-15 Sandoz Ag Meropenem intermediate in crystalline form
NZ566073A (en) * 2005-09-21 2011-08-26 4Sc Ag Sulphonylpyrrole hydrochloride salts as histone deacetylases inhibitors
EA201001799A1 (ru) * 2005-10-31 2011-06-30 Янссен Фармацевтика Н.В. Новые способы получения пиперазинильных и диазепанильных производных бензамида
MX2008016008A (es) * 2006-06-16 2009-01-16 Lundbeck & Co As H Formas cristalinas de 4-[2-(4-metilfenilsulfonil)-fenil] piperidina con inhibicion combinada de la recaptacion de serotonina y norepinefrina para el tratamiento del dolor neuropatico.
CA2667345C (en) * 2006-10-27 2016-03-22 Signal Pharmaceuticals, Llc Solid forms comprising 4-[9-(tetrahydro-furan-3-yl)-8-(2,4,6-trifluoro-phenylamino)-9h-purin-2-ylamino]-cyclohexan-1-ol, compositions thereof, and uses therewith
EP2085397A1 (en) * 2008-01-21 2009-08-05 Esteve Quimica, S.A. Crystalline form of abacavir
US7935817B2 (en) * 2008-03-31 2011-05-03 Apotex Pharmachem Inc. Salt form and cocrystals of adefovir dipivoxil and processes for preparation thereof
AR071318A1 (es) * 2008-04-15 2010-06-09 Basilea Pharmaceutica Ag Benzhidril ester del acido (6r,7r)-7-{2-(5-amino-[1,2,4]tiadiazol-3-il)-2-[(z)-tritiloxiimino]-acetilamino}-3-[(r)-1'-terc-butoxicarbonil-2-oxo-[1,3']bipirrolidinil-(3e)-ilidenometil]-8-oxo-5-tia-1-aza-biciclo[4.2.0]oct-2-eno-2-carboxilico cristalino; su elaboracion y uso
US8097719B2 (en) * 2008-07-15 2012-01-17 Genesen Labs Meropenem intermediate in novel crystalline form and a method of manufacture of meropenem
CN102762551A (zh) 2009-12-21 2012-10-31 拜尔农作物科学股份公司 噻吩基吡(嘧)啶基吡唑及其用于防治植物致病菌的用途
ES2742195T3 (es) 2010-03-12 2020-02-13 Omeros Corp Inhibidores de PDE10 y composiciones y métodos relacionados
CN103189360A (zh) * 2010-09-01 2013-07-03 艾尼纳制药公司 5-ht2c激动剂的非吸湿性盐
JO3154B1 (ar) * 2011-06-17 2017-09-20 Glaxosmithkline Llc عوامل مضادة لـ trpv4
WO2012174340A1 (en) * 2011-06-17 2012-12-20 Glaxosmithkline Llc Trpv4 antagonists
EP2720546B1 (en) * 2011-06-17 2016-04-06 Glaxosmithkline Intellectual Property (No. 2) Limited Spiro-cyclic trpv4 antagonists
WO2013044816A1 (en) * 2011-09-30 2013-04-04 Sunshine Lake Pharma Co., Ltd. Crystalline forms of azilsartan and preparation and uses thereof
NZ716494A (en) 2014-04-28 2017-07-28 Omeros Corp Processes and intermediates for the preparation of a pde10 inhibitor
NZ630803A (en) * 2014-04-28 2016-03-31 Omeros Corp Optically active pde10 inhibitor
BR112017021408B1 (pt) 2015-04-08 2022-05-17 Bayer Cropscience Aktiengesellschaft Derivados de heterociclo bicíclico condensado, método para controlar pragas animais, e formulação agroquímica
KR20170139074A (ko) 2015-04-24 2017-12-18 오메로스 코포레이션 Pde10 억제제 및 관련 조성물 및 방법
BR112018002571B1 (pt) 2015-08-07 2022-04-05 Bayer Cropscience Aktiengesellschaft Derivados heterocíclicos condensados substituídos por 2-(het)arila como agentes de controle de praga, seu uso, formulação agroquímica, e método para controlar pragas animais
BR112018008440B1 (pt) 2015-10-26 2021-12-21 Bayer Cropscience Aktiengesellschaft Derivados de heterociclo bicíclico fusionado como pesticidas
CA3003611C (en) 2015-11-04 2022-11-01 Omeros Corporation Solid state forms of a pde10 inhibitor
WO2017093180A1 (de) 2015-12-01 2017-06-08 Bayer Cropscience Aktiengesellschaft Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel
WO2017144341A1 (de) 2016-02-23 2017-08-31 Bayer Cropscience Aktiengesellschaft Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel
WO2017174414A1 (de) 2016-04-05 2017-10-12 Bayer Cropscience Aktiengesellschaft Naphthalin-derivate als schädlingsbekämpfungsmittel
EP3241830A1 (de) 2016-05-04 2017-11-08 Bayer CropScience Aktiengesellschaft Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel
BR112018073700A2 (pt) * 2016-05-19 2019-02-26 Glaxosmithkline Intellectual Property (No. antagonista trpv4
BR112019001135B1 (pt) 2016-07-19 2022-11-01 Bayer Cropscience Aktiengesellschaft Derivados de heterociclo bicíclico fundido como pesticidas, seu uso, formulação agroquímica, e método para controlar pragas animais
PE20190800A1 (es) 2016-08-15 2019-06-10 Bayer Cropscience Ag Derivados del heterociclo biciclico condensado como agentes de control de plagas
CA3035195A1 (en) * 2016-08-29 2018-03-08 Michael J. Soth Inhibitors of dual leucine zipper (dlk) kinase for the treatment of disease
EP3515921B1 (de) 2016-09-19 2021-10-27 Bayer CropScience Aktiengesellschaft Pyrazolo[1,5-a]pyridin- derivative und ihre verwendung als schädlingsbekämpfungsmittel
WO2018065288A1 (de) 2016-10-07 2018-04-12 Bayer Cropscience Aktiengesellschaft 2-[2-phenyl-1-(sulfonylmethyl)vinyl]-imidazo[4,5-b]pyridin-derivate und verwandte verbindungen als schädlingsbekämpfungsmittel im pflanzenschutz
EP3551610B1 (en) 2016-12-08 2021-08-11 Board of Regents, The University of Texas System Bicyclo[1.1.1]pentane inhibitors of dual leucine zipper (dlk) kinase for the treatment of disease
CN110382485B (zh) 2017-01-10 2022-05-10 拜耳公司 作为害虫防治剂的杂环烯衍生物
KR102628073B1 (ko) 2017-01-10 2024-01-22 바이엘 악티엔게젤샤프트 해충 방제제로서의 헤테로사이클 유도체
WO2018138050A1 (de) 2017-01-26 2018-08-02 Bayer Aktiengesellschaft Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel
ES2923376T3 (es) 2017-04-24 2022-09-27 Bayer Ag Derivados de heterociclos bicíclicos fusionados como plaguicidas
EP3305786A3 (de) 2018-01-22 2018-07-25 Bayer CropScience Aktiengesellschaft Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel
JP2021514949A (ja) 2018-02-21 2021-06-17 バイエル・アクチエンゲゼルシヤフト 有害生物防除剤としての縮合二環式ヘテロ環誘導体
BR112021010430A2 (pt) 2019-02-26 2021-08-24 Bayer Aktiengesellschaft Derivados de heterociclo bicíclico fundido como pesticidas
KR20210133984A (ko) 2019-02-26 2021-11-08 바이엘 악티엔게젤샤프트 해충 방제제로서의 축합된 비시클릭 헤테로시클릭 유도체
US11560366B2 (en) 2019-10-21 2023-01-24 Board Of Regents, The University Of Texas System Bicyclo[1.1.1]pentane inhibitors of dual leucine zipper (DLK) kinase for the treatment of disease
CN111303230B (zh) * 2020-03-09 2021-07-13 中国食品药品检定研究院 一种黄体酮共晶物及其制备方法和用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102005030051A1 (de) * 2005-06-27 2006-12-28 Grünenthal GmbH Substituierte 1-Oxa-3,8-diazaspiro[4,5]-decan-2-on-Verbindungen und deren Verwendung zur Herstellung von Arzneimitteln
JP2010502705A (ja) * 2006-09-07 2010-01-28 メルク エンド カムパニー インコーポレーテッド アルツハイマー病の治療用としてのスピロピペリジンベータセクレターゼ阻害剤
JP2010517966A (ja) * 2007-02-01 2010-05-27 グラクソ グループ リミテッド 摂食障害の処置のための1−オキサ−3−アザスピロ(4.5)デカン−2−オンおよび1−オキサ−3,8−ジアザスピロ(4.5)デカン−2−オン誘導体
WO2008092891A1 (en) * 2007-02-01 2008-08-07 Glaxo Group Limited 1-oxa-3-azaspiro(4.5)decan-2-one derivatives for the treatment of eating disorders
GB0707934D0 (en) * 2007-04-24 2007-05-30 Glaxo Group Ltd Chemical compounds
WO2009112033A1 (en) * 2008-03-12 2009-09-17 Københavns Universitet (University Of Copenhagen) Use of npy y5 receptor antagonists for the prevention of psychostimulant and opioid abuse

Also Published As

Publication number Publication date
CL2009000171A1 (es) 2009-11-27
UY31619A1 (es) 2009-08-31
TW200944520A (en) 2009-11-01
US20090203705A1 (en) 2009-08-13
WO2009095377A1 (en) 2009-08-06
AR070268A1 (es) 2010-03-25

Similar Documents

Publication Publication Date Title
PE20091324A1 (es) Compuestos espiro como antagonistas del receptor npy y5
PE20060079A1 (es) DERIVADOS DE PIRIDILO COMO ANTAGONISTAS DEL RECEPTOR mGlus5
EA200970967A1 (ru) Оксадиазол замещенные производные индазола для применения в качестве агонистов сфингозин 1-фосфата (sip)
PE20141421A1 (es) 4-fenil-piridinas sustituidas para el tratamiento de enfermedades relacionadas con el receptor de nk1
BR112013021675A2 (pt) compostos de triazolopiridina como inibidores de pim cinase
EA200601895A1 (ru) 3-(4-гетероарилциклогексиламино)циклопентанкарбоксамиды в качестве модуляторов хемокиновых рецепторов
PE20141685A1 (es) Novedosas dihidropirimidinoisoquinolinonas y composiciones farmaceuticas de las mismas para el tratamiento de transtornos inflamatorios
MX2009006304A (es) Nuevos compuestos de oxadiazol.
CO6382155A2 (es) Agonistas del receptor gpr120 de arilo y usos de los mismos
DE602005021696D1 (de) Indazolcarbonsäureamidverbindungen
PE20081735A1 (es) Derivados de 1-oxa-3[4,5]decan-2-ona en el tratamiento de trastornos alimenticios
EA201391662A1 (ru) Соединения с активностью антагонистов мускариновых рецепторов и агонистов адренергического рецептора бета2
NZ630124A (en) Estrogen receptor modulators and uses thereof
CL2008003847A1 (es) Compuestos derivados de 6-fenilpirazin-2-carboxamida y 6-fenilpirazin-2-carbotioamida, inhibidores de dgat-1; composicion farmaceutica; y su uso en el tratamiento de la diabetes mellitus y obesidad.
EA201170302A1 (ru) Процессированные аналоги глюкозозависимого инсулинотропного полипетида
MY155036A (en) Quinolinone-carboxamide compounds as 5-ht4 receptor agonists
PE20091724A1 (es) Derivados de indol como moduladores del receptor nicotinico de acetilcolina alfa 7
HN2010001563A (es) Compuestos
CL2009000873A1 (es) Compuestos derivados de ciclohepta[b]piridina, antagonistas del receptor de cgrp; composicion farmaceutica; y uso para el tratamiento de la migrana.b
DE602005014566D1 (de) Chinolinon-carboxamid-verbindungen
EA201590873A1 (ru) Соединения, обладающие активностью антагонистов мускариновых рецепторов и агонистов бета2 адренергических рецепторов
PH12015501955A1 (en) Heterocyclic compounds and use thereof as modulators of type iii receptor tyrosine kinases
DE602007005160D1 (de) Benzimidazol-cannabinoid-agonisten mit einer substituierten heterocyclischen gruppe
DE602006019595D1 (de) Benzimidazoloncarbonsäureamidverbindungen als agonisten des 5-ht4-rezeptors
EA201171074A1 (ru) Цитотоксические конъюгаты с соединением, связывающим рецептор нейропептида y

Legal Events

Date Code Title Description
FA Abandonment or withdrawal