AR051089A1 - Compuestos de triazoloquinoleina y triazolonaftiridina sustituidas - Google Patents

Compuestos de triazoloquinoleina y triazolonaftiridina sustituidas

Info

Publication number
AR051089A1
AR051089A1 ARP050103899A ARP050103899A AR051089A1 AR 051089 A1 AR051089 A1 AR 051089A1 AR P050103899 A ARP050103899 A AR P050103899A AR P050103899 A ARP050103899 A AR P050103899A AR 051089 A1 AR051089 A1 AR 051089A1
Authority
AR
Argentina
Prior art keywords
alkyl
carbocyclyl
heterocyclyl
alkoxy
triazolo
Prior art date
Application number
ARP050103899A
Other languages
English (en)
Original Assignee
Smithkline Beecham Corp
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 Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of AR051089A1 publication Critical patent/AR051089A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • A61P25/16Anti-Parkinson drugs
    • 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
    • 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
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/14Ortho-condensed systems

Abstract

Composiciones farmacéuticas que los contienen, métodos de preparacion y usos en trastornos asociados con bajos niveles plasmáticos de apo-A1. Reivindicacion 1: Compuesto e triazoloquinoleína o su sal farmacéuticamente aceptable, o su solvato o su profármaco o una combinacion de éstos, caracterizado porque tiene la formula (1) en la que: X representa CH o N; Y representa CH o N; R1 representa H o alquilo C1-2; R2 representa H o alquilo C1-4; R3 representa alquilo C1-6, carbociclilo, carbociclil(alquilo C1-4), heterociclilo o heterociclil(alquilo C1-4), en el que cualquiera de los grupos carbociclilo o heterociclilo está opcionalmente sustituido con uno o dos grupos seleccionados de: halogeno, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, nitro, ciano, -COH, -COOH, (alcoxi C1-6)carbonilo, (alquil C1-6)carbonilo, -C(OH)R5R6 (en el que R5 y R6 representan independientemente H o alquilo C1-6), -(CH2)nNR3aR3b y -O(CH2)pNR3aR3b (en el que n representa 1, 2 o 3, p representa 2 o 3, y R3a y R3b representan independientemente H, alquilo C1-6 o carbociclil(alquilo C1-4), o R3a y R3b junto con los átomos interconectores forman un anillo de 5 o 6 miembros, conteniendo dicho anillo opcionalmente uno o dos heteroátomos seleccionados independientemente del grupo que consiste en O, S y N); R4 representa H, hidroxi, halogeno, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, alquenilo C2-6, alcoxi C1-6, haloalcoxi C1-6, carbociclilo o heterociclilo, en los que el grupo carbociclilo o heterociclilo está opcionalmente sustituido con uno o dos grupos seleccionados de: halogeno, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, nitro y ciano; con la condicion de que el compuesto no es: 7-cloro-5-fenil[1,2,4]triazolo[4,3-a]quinolin-4-amina; 7-cloro-1-metil-5-fenil[1,2,4]triazolo[4,3-a]quinolin-4-amina; o 7-cloro-5-(2-clorofenil)-1-metil-[1,2,4]triazolo[4,3-a]quinolin-4-amina.
ARP050103899A 2004-09-21 2005-09-20 Compuestos de triazoloquinoleina y triazolonaftiridina sustituidas AR051089A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB0420970A GB0420970D0 (en) 2004-09-21 2004-09-21 Novel triazoloquinoline compounds

Publications (1)

Publication Number Publication Date
AR051089A1 true AR051089A1 (es) 2006-12-20

Family

ID=33306953

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP050103899A AR051089A1 (es) 2004-09-21 2005-09-20 Compuestos de triazoloquinoleina y triazolonaftiridina sustituidas

Country Status (5)

Country Link
AR (1) AR051089A1 (es)
GB (1) GB0420970D0 (es)
PE (1) PE20060818A1 (es)
TW (1) TW200621772A (es)
WO (1) WO2006032470A1 (es)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
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WO2006044596A2 (en) 2004-10-15 2006-04-27 The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Multi-domain amphipathic helical peptides and methods of their use
EP2086975B1 (en) * 2006-11-20 2012-03-14 Bristol-Myers Squibb Company 7,8-dihydro-1,6-naphthyridin-5(6h)-ones and related bicyclic compounds as inhibitors of dipeptidyl peptidase iv and methods
WO2010049103A1 (en) * 2008-10-31 2010-05-06 Eth Zurich Soluble truncated apom proteins and medical uses thereof
US8680116B2 (en) 2009-07-22 2014-03-25 Merck Sharp & Dohme Corp. Quinolinone PDE2 inhibitors
ME02356B (me) 2009-11-05 2016-06-20 Glaxosmithkline Llc Inhibitor bromodomena benzodiazepina
GB0919432D0 (en) 2009-11-05 2009-12-23 Glaxosmithkline Llc Use
JP5524343B2 (ja) 2009-11-05 2014-06-18 グラクソスミスクライン エルエルシー ベンゾジアゼピンブロモドメイン阻害剤
RU2438672C1 (ru) 2010-04-30 2012-01-10 Общество с ограниченной ответственностью "Клевер Фарм" Агент, проявляющий свойства активатора когнитивных функций (варианты)
US9085582B2 (en) 2010-06-22 2015-07-21 Glaxosmithkline Llc Benzotriazolodiazepine compounds inhibitors of bromodomains
WO2013097052A1 (en) 2011-12-30 2013-07-04 Abbott Laboratories Bromodomain inhibitors
EP2838881B1 (en) 2012-04-20 2018-08-08 AbbVie Inc. Isoindolone derivatives
CN104718201A (zh) 2012-06-12 2015-06-17 艾伯维公司 吡啶酮和哒嗪酮衍生物
WO2014173241A1 (en) 2013-04-26 2014-10-30 Beigene, Ltd. Substituted5-(3,5-dimethylisoxazol-4-yl)indoline-2-ones
PL3442972T3 (pl) 2016-04-15 2020-07-27 Abbvie Inc. Inhibitory bromodomeny
WO2021048852A1 (en) 2019-09-11 2021-03-18 Yeda Research And Development Co. Ltd. Methods of treating breast cancer
US11753413B2 (en) 2020-06-19 2023-09-12 Incyte Corporation Substituted pyrrolo[2,1-f][1,2,4]triazine compounds as JAK2 V617F inhibitors
US11691971B2 (en) 2020-06-19 2023-07-04 Incyte Corporation Naphthyridinone compounds as JAK2 V617F inhibitors
MX2023000056A (es) 2020-07-02 2023-04-12 Incyte Corp Compuestos tricíclicos de urea como inhibidores de la variante v617f de la cinasa de janus 2 (jak2 v617f).
WO2022006456A1 (en) 2020-07-02 2022-01-06 Incyte Corporation Tricyclic pyridone compounds as jak2 v617f inhibitors
US11661422B2 (en) 2020-08-27 2023-05-30 Incyte Corporation Tricyclic urea compounds as JAK2 V617F inhibitors
WO2022140231A1 (en) 2020-12-21 2022-06-30 Incyte Corporation Deazaguaine compounds as jak2 v617f inhibitors
TW202302589A (zh) 2021-02-25 2023-01-16 美商英塞特公司 作為jak2 v617f抑制劑之螺環內醯胺
WO2023165528A1 (en) * 2022-03-01 2023-09-07 Insilico Medicine Ip Limited Diacylglycerol kinase (dgk) alpha inhibitors and uses thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50116498A (es) * 1974-02-27 1975-09-11
DE60134762D1 (de) * 2000-10-02 2008-08-21 Janssen Pharmaceutica Nv Metabotropische glutamatrezeptor-antagonisten
GB0108475D0 (en) * 2001-04-04 2001-05-23 Merck Sharp & Dohme New compounds

Also Published As

Publication number Publication date
WO2006032470A1 (en) 2006-03-30
PE20060818A1 (es) 2006-08-16
TW200621772A (en) 2006-07-01
GB0420970D0 (en) 2004-10-20

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