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AR057374A1 - Moduladres opioides triciclicos y composiciones farmaceuticas y veterinarias - Google Patents

Moduladres opioides triciclicos y composiciones farmaceuticas y veterinarias

Info

Publication number
AR057374A1
AR057374A1 ARP060102540A ARP060102540A AR057374A1 AR 057374 A1 AR057374 A1 AR 057374A1 AR P060102540 A ARP060102540 A AR P060102540A AR P060102540 A ARP060102540 A AR P060102540A AR 057374 A1 AR057374 A1 AR 057374A1
Authority
AR
Argentina
Prior art keywords
alkanyl
phenyl
amino
group
aminocarbonyl
Prior art date
Application number
ARP060102540A
Other languages
English (en)
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of AR057374A1 publication Critical patent/AR057374A1/es

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D451/00Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • AHUMAN NECESSITIES
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    • 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
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    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/10Drugs for disorders of the urinary system of the bladder
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D451/00Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/14Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing 9-azabicyclo [3.3.1] nonane ring systems, e.g. granatane, 2-aza-adamantane; Cyclic acetals thereof

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Addiction (AREA)
  • Urology & Nephrology (AREA)
  • Pulmonology (AREA)
  • Pain & Pain Management (AREA)
  • Dermatology (AREA)
  • Rheumatology (AREA)
  • Psychiatry (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Diabetes (AREA)
  • Otolaryngology (AREA)
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  • Gynecology & Obstetrics (AREA)
  • Vascular Medicine (AREA)
  • Obesity (AREA)
  • Immunology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
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Abstract

La presente se refiere un los compuestos de formula (1) utiles como moduladores de los receptores opioides delta y (mu). También se describen composiciones farmacéuticas y veterinarias y Kits. Estos compuestos son utiles para tratar el dolor leve un severo y diversas enfermedades utilizando los compuestos de la presente. Reivindicacion 1: Un compuesto de la formula (1), donde: R1 es hidroxi; mercapto; aminocarbonilo; alcanilC1-4-aminocarbonilo; di(alcanilC1-4)aminocarbonilo; (fenilmetílico)aminocarbonilo; (4-metoxi-fenilmetílico)aminocarbonilo; alcanilC1-4-oxicarbonilo; aminotiocarbonilo; amidino; hidroxiamidino; fenilcarbonilo; -C(=NOH)fenilo; amino; alcanilC1-4-amino; di(alcanilC1-4)amino; aminometilo; hidroximetilo; metansulfonilamino; arilC6-10-amino, donde arilo está opcionalmente sustituido con uno un tres sustituyentes seleccionados independientemente del grupo formado por alcanilo C1-6, alcoxi C1-6, halogeno, hidroxi; dihidroimidazolilo; formilamino; tioformilamino; o piridinilamino; u, opcionalmente, R1 es -S-C(NH2)=N- para formar una porcion fusionada en la cual el segundo punto de union es un átomo de carbono no puente adyacente; R2 es un sustituyente seleccionado del grupo formado por hidrogeno, alcanilo C1-8, halo1-3-alcanilo C1-8, alquenilo C2-8, alquinilo C2-8, cicloalcanilo C3-8, cicloalcanilalcanilo C1-8, alcanilC1-8-oxialcaniloC1-8, alcanilC1-8-tioalcaniloC1-8, hidroxialcanilo C1-8, alcanilC1-8-oxicarbonilo, halo1-3- alcanilC1-8-carbonilo, formilo, tioformilo, carbamimidoilo, feniliminoalcanilo C1-8, fenilalcanilo C1-8, fenilalquenilo C1-8, fenilalquinilo C1-8 naftilalcanilo C1-8 y heteroarilalcanilo C1-8, donde el heteroarilo se selecciona del grupo formado por benzo[1,3]dioxolilo, imidazolilo, furanilo, piridinilo, tienilo, indazolilo, indolilo, indolinilo, isoindolinilo, isoquinolinilo, isotiazolilo, isoxazolilo, oxazolilo, pirazinilo, pirazolilo, piridazinilo, pimidinilo, pirrolilo, quinolinilo, isoquinolinilo, tetrazolilo, tiazolilo; donde fenilo, naftilo y heteroarilo son opcionalmente sustituidos con fenilo, y de uno a tres sustituyentes seleccionados independientemente del grupo formado por alcanilo C1-6, alquenilo C2-6, alcanilC1-6oxi, amino, alcanilC1-6-amino, di(alcanilC1-6)amino, alcanilC1-6-carbonilo, alcanilC1-6-carboniloxi, alcanilC1-6-carboniloamino, alcanilC1-6-tio, alcanilC1-6-sulfonilo, halogeno, hidroxi, ciano, fluoralcanilo C1-6, tioureido, y fluoralcanilC1-6-oxi; alternativamente, cuando fenilo y heteroarilo son opcionalmente sustituidos con sustituyentes alcanilo o alcaniloxi unidos a átomos de carbono adyacentes, los dos sustituyentes pueden formar en conjunto un alcanilo o cicloheteroalcanilo cíclico fusionado seleccionado del grupo formado por -(CH2)3-5-, -O(CH2)2-4-, - (CH2)2-4O-, y -O(CH2)1-3O-; A es ausente o -(CH2)2-3-; Y es O o S; y enantiomeros, diastereomeros, tautomeros, o las sales farmacéuticamente aceptables de los mismos.
ARP060102540A 2005-06-16 2006-06-15 Moduladres opioides triciclicos y composiciones farmaceuticas y veterinarias AR057374A1 (es)

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US69110105P 2005-06-16 2005-06-16

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AR057374A1 true AR057374A1 (es) 2007-11-28

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US (2) US7582650B2 (es)
EP (1) EP1896467B1 (es)
JP (1) JP2008543866A (es)
CN (1) CN101243079A (es)
AR (1) AR057374A1 (es)
AT (1) ATE490251T1 (es)
AU (1) AU2006259273A1 (es)
BR (1) BRPI0611885A2 (es)
CA (1) CA2612491A1 (es)
DE (1) DE602006018604D1 (es)
RU (1) RU2008101667A (es)
TW (1) TW200716134A (es)
WO (1) WO2006138528A2 (es)

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CN110013476A (zh) * 2019-04-08 2019-07-16 南昌大学 6-羟基-1,2,3,7-四甲氧基呫吨酮在制备促海马神经发生的药物中的应用
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US20060287297A1 (en) 2006-12-21
EP1896467B1 (en) 2010-12-01
WO2006138528A2 (en) 2006-12-28
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JP2008543866A (ja) 2008-12-04
ATE490251T1 (de) 2010-12-15
RU2008101667A (ru) 2009-07-27
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