AR020276A1 - Compuestos derivados de aminoalcoholes de aplicacion como agonistas de receptores adrenergicos y sus sales, proceso para prepararlos composicionesfarmaceuticas formuladas con dichos compuestos, uso de los mismos en la preparacion de dichas composiciones y metodo para el tratamiento profilactico y/ot - Google Patents

Compuestos derivados de aminoalcoholes de aplicacion como agonistas de receptores adrenergicos y sus sales, proceso para prepararlos composicionesfarmaceuticas formuladas con dichos compuestos, uso de los mismos en la preparacion de dichas composiciones y metodo para el tratamiento profilactico y/ot

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AR020276A1
AR020276A1 ARP990104285A ARP990104285A AR020276A1 AR 020276 A1 AR020276 A1 AR 020276A1 AR P990104285 A ARP990104285 A AR P990104285A AR P990104285 A ARP990104285 A AR P990104285A AR 020276 A1 AR020276 A1 AR 020276A1
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Argentina
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lower alkyl
alkyl
hydrogen
alkoxy
hydroxy
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ARP990104285A
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English (en)
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Fujisawa Pharmaceutical Co
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    • C07C323/23Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C323/24Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C323/25Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
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Abstract

Compuestos derivados de aminoalcoholes de aplicacion como agonistas de receptores adrenérgicos beta, caracterizados porque tienen la formula 1 en la cualA es un grupo heterocíclico o arilo, cada uno de los cuales puede tener entre 1 y 3sustituyentes - que pueden ser los mismos o diferentes - seleccionados deun grupo que consiste en halogeno, hidroxi, amino, alquilo inferior, alquil-sulfonilamino inferior, fenil-alcoxi (inferior) y fenilalcoxicarbonilamino(inferior), -X- es unenlace, -CH2, -CH2 -CH2-, NH-CH2-, -O-CH2, -S-CH2-, -SO-CH2- o -SO2-CH2-, -Y< es -CR11< (en la cual R11 es hidrogeno, hidroxi, alcoxiinferior o aciloxi)y Z es formulas 3, 4, 5 y 6 -(CH2)n-CH=CH-(CH2)m - o -(CH2)n-C:::C-(CH2)m - donde -Q- es -O-,-S-, -SO-, -SO2-, -N-C( R10)O-, -CO-N-(R10),-C(R11)H-CO-N(R10), -C(R11)H-CH2-N(R10), SO2-N(R10), -N(R10)-CO2-, -CO- o - N-(R10) en la cual R10 es hidrogeno, o alquilo inferior y R11 es alquilo inferior.R6, R,7 R8 y R9, cada uno de ellos en formaindependiente, son hidrogeno , hidroxi, alquilo inferior, alquenilo inferior, alcoxi inferior, alcoxi inferior-alquilo (inferio) o arilo, el cual puede tener de 1 a 3 alcoxi inferior, n, m y k, cada uno de ellos en forma independiente es 0 a 6. p es0 a 4, q es 1 a 4 y,r es 2 a 4), y -Z-Y<es is-(CH2)i-CH=C< (en la cual i es 0 a 6), R1 es hidrogeno o grupo amino protector, y R2, R3, R4 y R5, cada uno de ellos en formaindependiente, es hidrogeno; alquilo inferior; alquiltio inferior;alquil-sulfonilo inferior; hidroxi; alcoxi inferior; amino; alquilamino inferior; acilamino;N-(alquilo inferior)-acilamino; carboxi; alcoxicarbonilo inferior; carbamoilo, sustituido de manera opcional con uno o dos alquilo inferior;hidroxi-alquilo(inferior); alcoxi inferior-alquilo (inferio r); N-acilamino-alquilo (inferior); N-(alquilo inferior)-N-acilamino-alquilo (inferior); carboxi-alquilo (inferior): alcoxi-carbonilo inferior-alquilo (inferior); carbamoil-alquilo(inferior) sustituido de manera opcional con uno o dos alquilo inferi or; o -(CH2)j-NR12R13 (enel cual R12 y R13, cada uno de ellos en forma independiente, es hidrogeno o alquilo inferior, o R12 y R13 pueden estar enlazadas para formar una cadena de
ARP990104285A 1998-08-26 1999-08-26 Compuestos derivados de aminoalcoholes de aplicacion como agonistas de receptores adrenergicos y sus sales, proceso para prepararlos composicionesfarmaceuticas formuladas con dichos compuestos, uso de los mismos en la preparacion de dichas composiciones y metodo para el tratamiento profilactico y/ot AR020276A1 (es)

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AUPQ407699A0 (en) * 1999-11-16 1999-12-09 Fujisawa Pharmaceutical Co., Ltd. Aminoalcohol derivatives
AUPQ575300A0 (en) * 2000-02-21 2000-03-16 Fujisawa Pharmaceutical Co., Ltd. New compound
AUPR034000A0 (en) 2000-09-25 2000-10-19 Fujisawa Pharmaceutical Co., Ltd. Aminoalcohol derivatives
AUPR120400A0 (en) * 2000-11-02 2000-11-23 Fujisawa Pharmaceutical Co., Ltd. New compound
JP4044740B2 (ja) * 2001-05-31 2008-02-06 信越化学工業株式会社 レジスト材料及びパターン形成方法
WO2003024483A1 (fr) * 2001-09-11 2003-03-27 Fujisawa Pharmaceutical Co., Ltd. Potentialisateur d'effets inhibiteurs sur la frequence des mictions et l'incontinence urinaire
CN101039902B (zh) * 2004-09-21 2010-11-10 安斯泰来制药有限公司 氨基醇衍生物
DE102004050952A1 (de) * 2004-10-18 2006-04-20 Boehringer Ingelheim Pharma Gmbh & Co. Kg Pharmazeutische Zusammensetzung zur Behandlung von Beschwerden, die mit krankhaften Veränderungen oder Irritationen der Prostata verbunden sind
EP2096105A1 (en) * 2008-02-28 2009-09-02 Laboratorios Almirall, S.A. Derivatives of 4-(2-amino-1-hydroxyethyl)phenol as agonists of the b2 adrenergic receptor

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US5451677A (en) * 1993-02-09 1995-09-19 Merck & Co., Inc. Substituted phenyl sulfonamides as selective β 3 agonists for the treatment of diabetes and obesity
US5726165A (en) * 1994-07-29 1998-03-10 Smithkline Beecham P.L.C. Derivatives of 4-(2-aminoethyl)phenoxymethyl-phosphonic and -phosphinic acid and pharmaceutical and veterinary uses therefor
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US5541204A (en) * 1994-12-02 1996-07-30 Bristol-Myers Squibb Company Aryloxypropanolamine β 3 adrenergic agonists
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