AR019256A1 - Utilizacion de derivados tetraciclo[6-6-2-0(2.27).0(9.14)] hexadeca-2(7), 3, 5, 9(14), 10,12-hexaeno, para la preparacion de preparados farmaceuticos conaccion inhibitoria de la fosfolipasa, los referidos derivados y preparado farmaceutico que contiene por lo menos a uno de dichos derivados - Google Patents

Utilizacion de derivados tetraciclo[6-6-2-0(2.27).0(9.14)] hexadeca-2(7), 3, 5, 9(14), 10,12-hexaeno, para la preparacion de preparados farmaceuticos conaccion inhibitoria de la fosfolipasa, los referidos derivados y preparado farmaceutico que contiene por lo menos a uno de dichos derivados

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AR019256A1
AR019256A1 ARP980104764A ARP980104764A AR019256A1 AR 019256 A1 AR019256 A1 AR 019256A1 AR P980104764 A ARP980104764 A AR P980104764A AR P980104764 A ARP980104764 A AR P980104764A AR 019256 A1 AR019256 A1 AR 019256A1
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derivatives
formula
pharmaceutical preparations
hydrogen
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Roche Olivier
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    • C07C259/16Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines having carbon atoms of hydroxamidine groups bound to carbon atoms of rings other than six-membered aromatic rings
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Abstract

Utilizacion de derivados tetraciclo[6.6.2.0(2.7).0(9.14)]-hexadeca-2(7), 3, 5, 9, (14), 10, 12-hexaeno de formula (1): caracterizado porque: R1 y R2 soniguales o diferentes y significan hidrogeno o un átomo de halogeno, X simboliza hidrogeno e Ysimb oliza un grupo NR3R4 o un grupo -N+CH3R3R4, o X e Y juntasforman un grupo-CH2-NR5, y Z representa un grupo >C=NH un grupo >CH2, R3 simboliza hidrogeno o un grupo alquilo inferior y R4 simboliza hidroxilo, carbamoilo,amidino, héteroarilo,N-aralquilhé teroarilo o un grupo alquilo inferior, o R3 y R4 juntas con el átomo de nitrogeno al cual se encuentran unidas forman unanillo heterocíclico que opcionalmente puede estar roto por un heteroátomo adicional y que opcionalmente puede estarsustituido un a o varia veces, R5representa hidrogeno, un grupo amidino o un héterociclo que opcionalmente se encuentra roto por uno o varios heteroátomos, para la produccion de preparadosfarmacéuticos con accion inhibitoria de la fosfolipasa, comoasí también los compuestos de formula (I), las sales, los ésteres, las formas opticamente activasy los racematos de los mismos fisiologicamente tolerados y también los derivados que se pueden metabolizar en vivo para formar compuestos de formulageneral(1), y los p reparados farmacéuticos que contienen a dichos compuestos de formula (1).
ARP980104764A 1997-09-24 1998-09-23 Utilizacion de derivados tetraciclo[6-6-2-0(2.27).0(9.14)] hexadeca-2(7), 3, 5, 9(14), 10,12-hexaeno, para la preparacion de preparados farmaceuticos conaccion inhibitoria de la fosfolipasa, los referidos derivados y preparado farmaceutico que contiene por lo menos a uno de dichos derivados AR019256A1 (es)

Applications Claiming Priority (1)

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DE19742014A DE19742014A1 (de) 1997-09-24 1997-09-24 Neue Tetracyclen, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel

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AR019256A1 true AR019256A1 (es) 2002-02-13

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AU (1) AU9746698A (es)
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AUPS282602A0 (en) 2002-06-07 2002-06-27 Garvan Institute Of Medical Research Method of inhibiting cell proliferation
WO2004009017A2 (en) * 2002-07-18 2004-01-29 Bristol-Myers Squibb Company Modulators of the glucocorticoid receptor and method
US7326728B2 (en) 2004-01-16 2008-02-05 Bristol-Myers Squibb Company Modulators of glucocorticoid receptor, AP-1, and/or NF-κβ activity and use thereof
US7273881B2 (en) 2004-01-16 2007-09-25 Bristol-Myers Squibb Company Modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US7569689B2 (en) * 2004-01-16 2009-08-04 Bristol-Myers Squibb Company Modulators of the glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US7253283B2 (en) * 2004-01-16 2007-08-07 Bristol-Myers Squibb Company Tricyclic modulators of the glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US7625921B2 (en) 2004-01-16 2009-12-01 Bristol-Myers Squibb Company Modulators of the glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US7605264B2 (en) * 2004-01-16 2009-10-20 Bristol-Myers Squibb Company Heterocyclic modulators of the glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US7411071B2 (en) 2005-01-13 2008-08-12 Bristol-Myers Squibb Company Modulators of the glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US7361654B2 (en) 2005-01-13 2008-04-22 Bristol-Myers Squibb Co. Substituted heteroaryl amide modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US7642273B2 (en) 2005-01-13 2010-01-05 Bristol-Myers Squibb Company Modulators of the glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US7317024B2 (en) 2005-01-13 2008-01-08 Bristol-Myers Squibb Co. Heterocyclic modulators of the glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US9498460B1 (en) 2016-04-06 2016-11-22 King Saud University Halogenated tetracyclic compounds

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CH429711A (de) * 1963-10-21 1967-02-15 Geigy Ag J R Verfahren zur Herstellung von neuen Aethanoanthracenderivaten
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FR1459843A (fr) * 1965-07-27 1966-06-17 Soc Ind Fab Antibiotiques Sifa Nouveaux sels d'ammonium quaternaire dérivés de l'éthano-9, 10 dihydro-9, 10 anthracène et procédé de préparation
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WO1995033715A1 (en) * 1994-06-02 1995-12-14 Smithkline Beecham Corporation Anti-inflammatory compounds

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CA2304879A1 (en) 1999-04-01
CN1278789A (zh) 2001-01-03
JP2002505999A (ja) 2002-02-26
TR200001222T2 (tr) 2000-09-21
DE19742014A1 (de) 1999-03-25
EP1034162A1 (de) 2000-09-13
AU9746698A (en) 1999-04-12
WO1999015493A8 (de) 1999-05-06
BR9813217A (pt) 2000-08-29
KR20010024258A (ko) 2001-03-26
ZA988711B (en) 2000-03-23
WO1999015493A1 (de) 1999-04-01

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