AR034257A1 - Compuesto ureido, composicion farmaceutica que lo comprende y metodo para modular la actividad del receptor de quimiocinas - Google Patents

Compuesto ureido, composicion farmaceutica que lo comprende y metodo para modular la actividad del receptor de quimiocinas

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AR034257A1
AR034257A1 ARP010103133A ARP010103133A AR034257A1 AR 034257 A1 AR034257 A1 AR 034257A1 AR P010103133 A ARP010103133 A AR P010103133A AR P010103133 A ARP010103133 A AR P010103133A AR 034257 A1 AR034257 A1 AR 034257A1
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Argentina
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alkyl
groups
substituted
cycloalkyl
chr
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Du Pont Pharm Co
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Abstract

Un compuesto ureído de la fórmula (1) o estereoisómeros o sales farmacéuticamente aceptables del mismo, en donde: M está ausente o puede ser CH2, CHR5, CHR13, CR13R13 y CR5R13; Q puede ser CH2, CHR5, CHR13, CR13R13 y CR5R13; J y K, independientemente, pueden ser CH2, CHR5, CHR6, CR6R6 y CR5R6; L puede ser CHR5 y CR5R6; a condición de que: cuando M está ausente, J puede ser CH2, CHR5, CHR13 y CR5R13; Z puede ser O, S, NR1a, C(CN)2, CH(NO2) y CHCN; R1a puede ser H, alquilo C1-6, cicloalquilo C3-6, CONR1bR1b, OR1b, CN, NO2 y (CH2)wfenilo; R1b puede ser H, alquilo C1-3, cicloalquilo C3-6 y fenilo; E es un resto de fórmula (2); G puede ser un enlace, C=O y SO2; el anillo B es un anillo heterocíclico saturado de 5, 6 ó 7 miembros, en donde el anillo heterocíclico incluye radicales -NR9-, -O-, -S(O)p-, -NR9dC(O)-, -C(O)NR9d-, -C(O)O-, -OC(O)-, -NR9dC(O)NR9d-, -NR9dC(O)O-, -NR9dS(O)2-, -S(O)2NR9d- ó -OC(O)NR9d-, en donde el anillo heterocíclico opcionalmente está sustituido con 0 a 2 grupos R8; R1 y R2, independientemente, pueden ser H, alquilo C1-8, alquenilo C3-8, alquinilo C3-8 y (CH2)r-cicloalquilo C3-6; R3 puede ser metilo sustituido con 0-1 grupos R10, alquilo C2-8 sustituido con 0-3 grupos R7, alquenilo C3-8 sustituido con 0-3 grupos R7, alquinilo C3-8 sustituido con 0-3 grupos R7, fluoroalquilo C2, haloalquilo C3-8, un residuo (CR3'R3'')r-carboxíclico C3-8 con 0-5 grupos R15 y un sistema (CR3'R3'')r-heterocíclico de 5-10 miembros que contiene de 1-4 heteroátomos que pueden ser N, O y S, sustituido con 0-3 grupos R15; R3' y R3'', en cada ocasión, pueden ser H, alquilo C1-6, (CH2)r-cicloalquilo C3-6 y fenilo; R4 está ausente, se puede considerar junto con el nitrógeno al cual está unido para formar un N-óxido, o puede ser alquilo C1-8, alquenilo C3-8, alquinilo C3-8, (CH2)r-cicloalquilo C3-6, (CH2)qC(O)R4b, (CH2)qC(O)NR4aR4a', (CH2)qC(O)OR4b y un residuo (CH2)r-carbocíclico C3-10 sustituido con 0-3 grupos R4c; R4a y R4a', en cada ocasión, pueden ser H, alquilo C1-6, (CH2)r-cicloalquilo C3-6 y fenilo; R4b, en cada caso, puede ser alquilo C1-6, alquenilo C3-8, (CH2)r-cicloalquilo C3-6, alquinilo C3-8 y fenilo; R4c, en cada ocasión, puede ser alquilo C1-6, alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-6, Cl, F, Br, I, CN, NO2, (CF2)rCF3, (CH2)rO-alquilo C1-5, (CH2)rOH, (CH2)r-S-alquilo C1-5, (CH2)rNR4aR4a' y (CH2)rfenilo; R5 puede ser un residuo (CR5'R5'')t-carboxíclico C3-10 sustituido con 0-5 grupos R16 y un sistema (CR5'R5'')t-heterocíclico de 5-10 miembros que contiene de 1-5 heteroátomos que pueden ser N, O y S, sustituido con 0-3 grupos R16; R5' y R5'', en cada ocasión, pueden ser H, alquilo C1-6, (CH2)r-cicloalquilo C3-6 y fenilo; R6 puede ser alquilo C1-6, alquenilo C2-8, alquinilo C2-8, (CH2)r-cicloalquilo C3-6, (CF2)rCF3, CN, (CH2)rNR6aR6a', (CH2)rOH, (CH2)rOR6b, (CH2)rSH, (CH2)rSR6b, (CH2)rC(O)OH, (CH2)rC(O)R6b, (CH2)rC(O)NR6aR6a', (CH2)rNR6dC(O)R6a, (CH2)rC(O)OR6b, (CH2)rOC(O)R6b, (CH2)rS(O)pR6b, (CH2)rS(O)2NR6aR6a', (CH2)rNR6dS(O)2R6b y (CH2)t-fenilo sustituido con 0-3 grupos R6c; R6a y R6a' pueden ser H, alquilo C1-6, cicloalquilo C3-6 y fenilo sustituido con 0-3 grupos R6c; R6b puede ser alquilo C1-6, cicloalquilo C3-6 y fenilo sustituido con 0-3 grupos R6c; R6c puede ser alquilo C1-6, cicloalquilo C3-6, Cl, F, Br, I, CN, NO2, (CF2)rCF3, (CH2)rO-alquilo C1-5, (CH2)rOH, (CH2)rS-alquilo C1-5 y (CH2)rNR6dR6d; R6d puede ser H, alquilo C1-6 y cicloalquilo C3-6; a condición de que cuando cualquiera entre J ó K sea CR6R6 y R6 es un grupo ciano o está enlazado al carbono al cual se une a través de un heteroátomo, el otro R6 no es un grupo ciano ni está enlazado al carbono al cual se une a través de un heteroátomo; R7 puede ser NO2, CN, NR7aR7a', OH, OR7d, C(O)H, C(O)OH, C(O)R7b, C(O)NR7aR7a', NR7fC(O)OR7d, OC(O)NR7aR7a', NR7fC(O)R7b, NR7fC(O)NR7fR7f, C(O)OR7d, OC(O)R7b, C(=NR7f)NR7aR7a', NHC(=NR7f)NR7fR7f, S(O)pR7b, S(O)2NR7aR7a', NR7fS(O)2R7b y haloalquilo C1-6; R7a y R7a' pueden ser H, alquilo C1-6, alquenilo C3-8, alquinilo C3-8, un residuo (CH2)r-carbocíclico C3-10 sustituido con 0-5 grupos R7e y un sistema (CH2)r-heterocíclico de 5-10 miembros que contiene de 1-4 heteroátomos seleccionados de N, O y S, sustituido con 0-2 grupos R7e; alternativamente, R7a y R7a', junto con el átomo de N al cual están enlazados, juntos forman un sistema heterocíclico de 5-6 miembros que contiene de 1-2 heteroátomos que pueden ser NR7b, O y S, y opcionalmente está fusionado con un anillo bencénico o un heterociclo aromático de 6 miembros; R7b puede ser H, alquilo C1-6, alquenilo C3-8, alquinilo C3-8, un residuo (CH2)r-carbocíclico C3-6 sustituido con 0-3 grupos R7e, y un sistema (CH2)r-heterocíclico de 5-6 miembros que contiene de 1-4 heteroátomos seleccionados de N, O y S, sustituido con 0-2 grupos R7e; R7d puede ser alquenilo C3-8, alquinilo C3-8, metilo, CF3, alquilo C2-6 sustituido con 0-3 grupos R7e, un residuo (CH2)r-carbocíclico C3-10 sustituido con 0-3 grupos R7e y un sistema (CH2)r-heterocíclico de 5-6 miembros que contiene de 1-4 heteroátomos que pueden ser N, O y S, sustituido con 0-3 grupos R7e; R7e, en cada ocasión, puede ser alquilo C1-6, alquenilo C2-8, alquinilo C2-8, (CH2)r-cicloalquilo C3-6, C(O)-alquilo C1-6, C(O)O-alquilo C1-6, Cl, F, Br, I, CN, NO2, (CF2)CF3, (CH2)rO-alquilo C1-5, OH, SH, (CH2)rS-alquilo C1-5, (CH2)rNR7fR7f, (CH2)r-fenilo y un heterociclo sustituido con 0-1 grupos R7g, en donde el heterociclo puede ser imidazol, tiazol, oxazol, pirazol, 1,2,4-triazol, 1,2,3-triazol, isoxazol y tetrazol; R7f puede ser H, alquilo C1-6, cicloalquilo C3-6 y fenilo; R7g puede ser metilo, etilo, acetilo y CF3; R7h puede ser H, alquilo C1-6, cicloalquilo C3-6, (CH2)r-fenilo, C(O)R7f, C(O)OR7i y SO2R7i; R7i puede ser alquilo C1-6 o cicloalquilo C3-6; R8 puede ser alquilo C1-6, alquenilo C2-8, alquinilo C2-8, haloalquilo C1-6, un residuo (CH2)r-carbocíclico C3-10 sustituido con 0-3 grupos R8c y un sistema (CH2)r-heterocíclico de 5-10 miembros que contiene de 1-4 heteroátomos seleccionados de N, O y S, sustituido con 0-2 grupos R8c; R8a puede ser H, alquilo C1-6, alquenilo C2-8, alquinilo C2-8, un residuo (CH2)r-carbocíclico C3-10 sustituido con 0-5 grupos R8e y un sistema (CH2)r-heterocíclico de 5-10 miembros que contiene de 1-4 heteroátomos que pueden ser N, O y S, sustituido con 0-3 grupos R8e; R8b puede ser alquilo C1-6, alquenilo C3-8, alquinilo C3-8, un residuo (CH2)r-carbocíclico C3-6 sustituido con 0-2 grupos R8e y un sistema (CH2)r-heterocíclico de 5-6 miembros que contiene 1-4 heteroátomos seleccionados de N, O y S, sustituido con 0-3 grupos R8e; R8c puede ser alquilo C1-6, alquenilo C2-8, alquinilo C2-8, (CH2)r-cicloalquilo C3-6, Cl, Br, I, F, (CF2)CF3, NO2, CN, (CH2)rNR8fR8f, (CH2)rOH, (CH2)rO-alquilo C1-4, (CH2)rS-alquilo C1-4, (CH2)rC(O)OH, (CH2)rC(O)R8a, (CH2)rC(O)NR8fR8f, (CH2)rNR8fC(O)R8a, (CH2)rC(O)O-alquilo C1-4, (CH2)rOC(O)R8b, (CH2)rS(O)pR8b, (CH2)rS(O)2NR8fR8f, (CH2)rNR8fS(O)2R8b y (CH2)r-fenilo sustituido con 0-3 grupos R8e; R8e puede ser alquilo C1-6, alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-6, Cl, F, BR, I, CN, NO2, (CF2)CF3, (CH2)rO-alquilo C1-5, (CH2)rOH, (CH2)rSH, (CH2)rS-alquilo C1-5, (CH2)rNR8fR8f y (CH2)r-fenilo; R8f puede ser H, alquilo C1-6 y cicloalquilo C3-6; R9 es H, CH3, alquilo C2-6 sustituido con 0-3 grupos R9a, alquenilo C3-8, alquinilo C3-8, haloalquilo C1-6, (CHR')rC(O)-alquilo C1-6 sustituido con 0-3 grupos R9j, (CHR')rC(O)O-alquilo C1-6 sustituido con 0-3 grupos R9b, (CHR')rC(O)NR9dR9d', (CHR')rS(O)2-alquilo C1-6, S(O)2-haloalquilo C1-6, (CHR')rS(O)2NR9dR9d, R9', (CHR')rC(O)R9', (CHR')rC(O)NR9dR9', (CHR')rS(O)2R9' y (CHR')rS(O)2NR9dR9'; R9', en cada ocasión, es (CHR')r-cicloalquilo C3-6 sustituido con 0-3 grupos R9e, (CHR')r-fenilo sustituido con 0-3 grupos R9c, un sistema (CHR')r-heterocíclico de 5-10 miembros que contiene 1 a 4 heteroátomos que se seleccionan de N, O y S, sustituido con 0-3 grupos R9c; R9a, puede ser CN, NO2, O-alquilo C1-5, CF3, OH, OC(O)-alquilo C1-5, S-alquilo C1-5, S(O)p-alquilo C1-5 y NR9dR9d'; R9b, puede ser cicloalquilo C3-6, CN, (CF2)rCF3, (CH2)qO-alquilo C1-5, (CH2)qOH, (CH2)qS-alquilo C1-5, (CH2)rS(O)p-alquilo C1-5 y (CH2)qNR9dR9d'; R9c puede ser alquilo C1-6, cicloalquilo C3-6, Cl, F, Br, I, CN, NO2, (CF2)rCF3, (CH2)rO-alquilo C1-5, (CHR')rC(O)-alquilo C1-5, (CHR')rC(O)O-alquilo C1-5, (CHR')rC(O)NR9dR9d', (CH2)rOH, (CH2)rS-alquilo C1-5, (CH2)rS(O)p-alquilo C1-5 y (CH2)rNR9dR9d'; a condición de que si R9c está unido a un átomo de carbono enlazado con el nitrógeno del anillo B, entonces R9c es (CH2)qOH, (CH2)qO-alquilo C1-5, (CH2)qS-alquilo C1-5, (CH2)qS(O)q-alquilo C1-5 y (CH2)qNR9dR9d'; R9d y R9d' son, en cada ocasión, H, alquilo C1-6, cicloalquilo C3-6 y fenilo; alternativamente, R9d y R9d', junto con el átomo de N al cual están enlazados, juntos forman un sistema heterocíclico de 5-6 miembros que contiene de 1-2 heteroátomos que se seleccionan de NR9h, O, y S, y opcionalmente está fusionado con un anillo bencénico o con un heterociclo aromático de 6 miembros; R9e puede ser alquilo C1-6, cicloalquilo C3-6, Cl, F, Br, I, CN, NO2, (CF2)rCF3, (CH2)rO-alquilo C1-5, (CHR')rC(O)O-alquilo C1-5, (CHR')rC(O)NR9dR9d', (CH2)rOH, (CH2)rS-alquilo C1-5, (CH2)rS(O)p-alquilo C1-5 y (CH2)rNR9dR9d', o, alternativamente, dos grupos R9e en el mismo átomo de C forman un grupo =O; R9h es H, alquilo C1-6, cicloalquilo C3-6, (CH2)r-fenilo, C(O)R9f, C(O)OR9i y SO2R9i; R9i es alquilo C1-6, ó cicloalquilo C3-6; R9j es cicloalquilo C3-6, CN, (CF2)rCF3, (CH2)rO-alquilo C1-5, (CH2)rOH, (CH2)rS-alquilo C1-5, (CH2)rS(O)p-alquilo C1-5 y (CH2)rNR9dR9d'; R10 se selecciona entre C(O)H, C(O)OH, C(O)R10b, C(O)NR10aR10a', C(O)OR10d, C(=NR10f)NR10aR10a', S(O)R10b, S(O)2R10b y S(O)2NR10aR10a'; R10a y R10a', en cada ocasión, son H, alquilo C1-6, alquenilo C3-8, alquinilo C3-8, un residuo (CH2)r-carbocíclico C3-10 sustituido con 0-5 grupos R10e, y un sistema (CH2)r-heterocíclico de 5-10 miembros que contiene de 1-4 heteroátomos que se seleccionan de N, O y S, sustituido
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Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002002525A2 (en) * 2000-06-30 2002-01-10 Bristol-Myers Squibb Pharma Company N-ureidoheterocycloaklyl-piperidines as modulators of chemokine receptor activity
US6434344B1 (en) 2001-02-28 2002-08-13 Toshiba Tec Kabushiki Kaisha Image forming apparatus having a transfer device for transferring a toner image and having a bias voltage controller
TW200303304A (en) * 2002-02-18 2003-09-01 Astrazeneca Ab Chemical compounds
US6835841B2 (en) 2002-09-13 2004-12-28 Bristol-Myers Squibb Company Asymmetric catalytic hydrogenation process for preparation of chiral cyclic β-aminoesters
US7163937B2 (en) 2003-08-21 2007-01-16 Bristol-Myers Squibb Company Cyclic derivatives as modulators of chemokine receptor activity
SE0400208D0 (sv) * 2004-02-02 2004-02-02 Astrazeneca Ab Chemical compounds
US7741479B2 (en) * 2004-12-07 2010-06-22 Locus Pharmaceuticals, Inc. Urea inhibitors of MAP kinases
US7612200B2 (en) * 2004-12-07 2009-11-03 Locus Pharmaceuticals, Inc. Inhibitors of protein kinases
WO2007053499A2 (en) * 2005-11-01 2007-05-10 Millennium Pharmaceuticals, Inc. Compounds useful as antagonists of ccr2
US8067457B2 (en) 2005-11-01 2011-11-29 Millennium Pharmaceuticals, Inc. Compounds useful as antagonists of CCR2
WO2007053495A2 (en) * 2005-11-01 2007-05-10 Millennium Pharmaceuticals, Inc. Compounds useful as antagonists of ccr2
CA2635888A1 (en) * 2006-01-04 2007-07-19 Locus Pharmaceuticals, Inc. Inhibitors of protein kinases
TW200812582A (en) * 2006-04-06 2008-03-16 Astrazeneca Ab Medicaments
US20100056497A1 (en) 2007-01-31 2010-03-04 Dainippon Sumitomo Pharma Co., Ltd Amide derivative
AU2008234834B2 (en) * 2007-04-03 2012-01-19 Novartis Ag New methods
WO2009015166A1 (en) * 2007-07-24 2009-01-29 Bristol-Myers Squibb Company Piperidine derivatives as modulators of chemokine receptor activity
WO2010069979A1 (en) * 2008-12-16 2010-06-24 Nycomed Gmbh Pyran derivatives as ccr3 modulators
EP2398789B1 (en) * 2009-02-20 2014-03-19 Merck Sharp & Dohme Corp. Spiropyrrolidine beta-secretase inhibitors for the treatment of alzheimer's disease
EP2421828A2 (en) 2009-04-24 2012-02-29 Cadila Healthcare Limited Piperidine derivatives as inhibitors of renin
WO2010129351A1 (en) 2009-04-28 2010-11-11 Schepens Eye Research Institute Method to identify and treat age-related macular degeneration
AU2010263641A1 (en) 2009-06-24 2012-01-19 Sumitomo Dainippon Pharma Co., Ltd. N-substituted-cyclic amino derivative
SI2648511T1 (sl) 2010-12-08 2017-11-30 Lycera Corporation Pirazolil gvanidinski inhibitorji F1F0-ATPaze in njihove terapevtske uporabe
US9000014B2 (en) 2010-12-08 2015-04-07 Lycera Corporation Pyridonyl guanidine F1F0-ATPase inhibitors and therapeutic uses thereof
US9169199B2 (en) 2010-12-08 2015-10-27 Lycera Corporation Cycloalkyl guanidine F1F0-ATPase inhibitors and therapeutic uses thereof
HUE030791T2 (en) * 2011-05-13 2017-06-28 Array Biopharma Inc Pyrrolidinylurea, Pyrrolidinylthiocarbamind and Pyrrolidinylguanidine Compounds as Trkaquinase Inhibitors
EP2866796A4 (en) 2012-06-08 2015-11-25 Lycera Corp PYRAZOLYL GUANIDINE F1FO ATPASE HEMMER AND THERAPEUTIC USES THEREOF
US9221814B2 (en) 2012-06-08 2015-12-29 Lycera Corporation Heterocyclic guanidine F1F0-atpase inhibitors and therapeutic uses thereof
WO2013185046A1 (en) 2012-06-08 2013-12-12 Lycera Corporation Saturated acyl guanid1ne for inhibition of f1f0-atpase
DK2922844T3 (en) 2012-11-13 2018-03-05 Array Biopharma Inc N-PYRROLIDINYL, N'-PYRAZOLYL-URINE, THIOURINE, GUANIDINE AND CYANOGUANIDE COMPOUNDS AS TRKA-KINASE INHIBITORS
US9828360B2 (en) 2012-11-13 2017-11-28 Array Biopharma Inc. Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
AU2013344886B2 (en) 2012-11-13 2017-06-29 Array Biopharma Inc. Bicyclic urea, thiourea, guanidine and cyanoguanidine compounds useful for the treatment of pain
WO2014078331A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. N-(arylalkyl)-n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
US9790210B2 (en) 2012-11-13 2017-10-17 Array Biopharma Inc. N-(monocyclic aryl),N'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
WO2014078322A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. Thiazolyl and oxazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
US9809578B2 (en) 2012-11-13 2017-11-07 Array Biopharma Inc. Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trkA kinase inhibitors
US9790178B2 (en) 2012-11-13 2017-10-17 Array Biopharma Inc. Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
WO2014078328A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. N-bicyclic aryl,n'-pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
US9822118B2 (en) 2012-11-13 2017-11-21 Array Biopharma Inc. Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
JP2016539993A (ja) 2013-12-10 2016-12-22 リセラ・コーポレイションLycera Corporation N−置換ピラゾリルグアニジンf1f0−atpアーゼ阻害剤及びその治療用途
CA2931851A1 (en) 2013-12-10 2015-06-18 Lycera Corporation Trifluoromethyl pyrazolyl guanidine f1f0-atpase inhibitors and therapeutic uses thereof
CA2931850A1 (en) 2013-12-10 2015-06-18 Lycera Corporation Alkylpyrazolyl guanidine f1f0-atpase inhibitors and therapeutic uses thereof
WO2015175788A1 (en) 2014-05-15 2015-11-19 Array Biopharma Inc. 1-((3s,4r)-4-(3-fluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)-3-(4-methyl-3-(2-methylpyrimidin-5-yl)-1-phenyl-1h-pyrazol-5-yl)urea as a trka kinase inhibitor
CN108135168B (zh) * 2015-05-21 2021-07-20 凯莫森特里克斯股份有限公司 Ccr2调节剂
JP6812059B2 (ja) * 2015-07-07 2021-01-13 塩野義製薬株式会社 TrkA阻害活性を有する複素環誘導体
AU2018335486B2 (en) 2017-09-25 2024-07-04 Chemocentryx, Inc. Combination therapy using a Chemokine Receptor 2 (CCR2) antagonist and a PD-1/PD-L1 inhibitor
US20190269664A1 (en) 2018-01-08 2019-09-05 Chemocentryx, Inc. Methods of treating solid tumors with ccr2 antagonists
US11154556B2 (en) 2018-01-08 2021-10-26 Chemocentryx, Inc. Methods of treating solid tumors with CCR2 antagonists
CN111630048B (zh) * 2018-03-19 2023-09-29 四川科伦博泰生物医药股份有限公司 脒类和胍类衍生物、其制备方法及其在医药上的应用

Family Cites Families (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3461120A (en) 1965-09-27 1969-08-12 Sterling Drug Inc N-((1-piperidyl)-lower-alkyl)-n-((3-,2-,and 1-indolyl)-lower-alkyl) amines
JP2826826B2 (ja) 1988-04-11 1998-11-18 日本ケミファ株式会社 アルキレンジアミン誘導体
GB8816365D0 (en) 1988-07-08 1988-08-10 Pfizer Ltd Therapeutic agents
IE903957A1 (en) 1989-11-06 1991-05-08 Sanofi Sa Aromatic amine compounds, their method of preparation and¹pharmaceutical compositions in which they are present
IL99320A (en) 1990-09-05 1995-07-31 Sanofi Sa Arylalkylamines, their preparation and pharmaceutical preparations containing them
GB9206757D0 (en) 1992-03-27 1992-05-13 Ferring Bv Novel peptide receptor ligands
WO1994022846A1 (en) 1993-03-30 1994-10-13 Pfizer Inc. Compounds enhancing antitumor activity of other cytotoxic agents
DK60893D0 (da) 1993-05-26 1993-05-26 Novo Nordisk As Piperidinderivater, deres fremstilling og anvendelse
DK60693D0 (da) 1993-05-26 1993-05-26 Novo Nordisk As Kemiske forbindelser, deres fremstilling og anvendelse
US5547966A (en) 1993-10-07 1996-08-20 Bristol-Myers Squibb Company Aryl urea and related compounds
GB9326611D0 (en) 1993-12-31 1994-03-02 Fujisawa Pharmaceutical Co New compound
DE69504300T2 (de) 1994-01-13 1999-04-29 Merck Sharp & Dohme Ltd., Hoddesdon, Hertfordshire Gem-bissubstituierte azazyclische tachykinin-antagonisten
US5661161A (en) 1994-09-29 1997-08-26 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
IL117149A0 (en) 1995-02-23 1996-06-18 Schering Corp Muscarinic antagonists
US5889006A (en) 1995-02-23 1999-03-30 Schering Corporation Muscarinic antagonists
US5668151A (en) 1995-06-07 1997-09-16 Bristol-Myers Squibb Company Dihydropyridine NPY antagonists: piperidine derivatives
CA2237384A1 (en) 1995-11-13 1997-05-22 The Albany Medical College Analgesic compounds and uses thereof
GB9523526D0 (en) 1995-11-17 1996-01-17 Zeneca Ltd Therapeutic compounds
WO1997018813A1 (en) 1995-11-22 1997-05-29 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
ATE219064T1 (de) 1995-12-18 2002-06-15 Fujisawa Pharmaceutical Co Piperazinderivative als tachykinin antagonisten
TW531537B (en) 1995-12-27 2003-05-11 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4-substituted piperidine derivatives
WO1997024325A1 (en) * 1995-12-28 1997-07-10 Takeda Chemical Industries, Ltd. DIPHENYLMETHANE DERIVATIVES AS MIP-1α/RANTES RECEPTOR ANTAGONISTS
CA2243507A1 (en) 1996-01-30 1997-08-07 Christopher J. Dinsmore Inhibitors of farnesyl-protein transferase
US5688955A (en) 1996-03-08 1997-11-18 Adolor Corporation Kappa agonist compounds and pharmaceutical formulations thereof
JP2000504024A (ja) 1996-04-03 2000-04-04 メルク エンド カンパニー インコーポレーテッド ファルネシル―タンパク質トランスフェラーゼ阻害剤
CA2249601A1 (en) 1996-04-03 1997-10-23 Thorsten E. Fisher Inhibitors of farnesyl-protein transferase
EP0891356A1 (en) 1996-04-03 1999-01-20 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
WO1997036876A1 (en) 1996-04-03 1997-10-09 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
AU716381B2 (en) 1996-04-03 2000-02-24 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
CA2249607A1 (en) 1996-04-03 1997-10-09 Neville J. Anthony Inhibitors of farnesyl-protein transferase
AU721952B2 (en) 1996-04-03 2000-07-20 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
JP2001509131A (ja) 1996-04-03 2001-07-10 メルク エンド カンパニー インコーポレーテッド ファルネシルプロテイントランスフェラーゼの阻害剤
EP0904076A1 (en) 1996-04-03 1999-03-31 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
WO1997036890A1 (en) 1996-04-03 1997-10-09 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
AU715606B2 (en) 1996-04-03 2000-02-03 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
GB9612884D0 (en) 1996-06-20 1996-08-21 Smithkline Beecham Plc Novel compounds
US5972966A (en) 1996-12-05 1999-10-26 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
AU5522498A (en) 1996-12-13 1998-07-03 Merck & Co., Inc. Substituted aryl piperazines as modulators of chemokine receptor activity
US5962462A (en) 1996-12-13 1999-10-05 Merck & Co., Inc. Spiro-substituted azacycles as modulators of chemokine receptor activity
WO1998025604A1 (en) 1996-12-13 1998-06-18 Merck & Co., Inc. Spiro-substituted azacycles as modulators of chemokine receptor activity
JP2001508798A (ja) 1997-01-21 2001-07-03 メルク エンド カンパニー インコーポレーテッド ケモカインレセプター活性のモジュレーターとしての3,3−二置換ピペリジン類
AU7371998A (en) 1997-05-07 1998-11-27 University Of Pittsburgh Inhibitors of protein isoprenyl transferases
US6001836A (en) 1997-05-28 1999-12-14 Bristol-Myers Squibb Company Dihydropyridine NPY antagonists: cyanoguanidine derivatives
US5889016A (en) 1997-06-26 1999-03-30 Bristol-Myers Squibb Company Dihydropyrimidone derivatives as NPY antagonists
EP1003514A4 (en) 1997-07-25 2000-10-11 Merck & Co Inc CYCLIC AMINE MODULATORS OF CHEMOKIN RECEPTORS
IL125658A0 (en) * 1997-08-18 1999-04-11 Hoffmann La Roche Ccr-3 receptor antagonists
EP1009405A4 (en) 1997-08-28 2001-05-09 Merck & Co Inc MODULATORS OF PYRROLIDINE AND PIPERIDINE OF CHEMOKINE RECEPTOR ACTIVITY
AU3716499A (en) 1998-04-21 1999-11-08 Aventis Pharma Limited Substituted diamines and their use as cell adhesion inhibitors
SE9802209D0 (sv) 1998-06-22 1998-06-22 Astra Pharma Inc Novel compounds
AU2057200A (en) 1998-12-18 2000-07-03 Du Pont Pharmaceuticals Company N-ureidoalkyl-piperidines as modulators of chemokine receptor activity
CA2347912A1 (en) 1998-12-18 2000-06-22 Soo S. Ko Heterocyclic piperidines as modulators of chemokine receptor activity
AU3126600A (en) 1998-12-18 2000-07-03 Du Pont Pharmaceuticals Company N-ureidoalkyl-piperidines as modulators of chemokine receptor activity
US6331541B1 (en) 1998-12-18 2001-12-18 Soo S. Ko N-ureidoalkyl-piperidines as modulators of chemokine receptor activity
AU2056700A (en) 1998-12-18 2000-07-03 Du Pont Pharmaceuticals Company 2-substituted-4-nitrogen heterocycles as modulators of chemokine receptor activity
US6444686B1 (en) 1998-12-18 2002-09-03 Brsitol-Myers Squibb Pharma Company N-ureidoalkyl-piperidines as modulators of chemokine receptor activity
WO2000035449A1 (en) 1998-12-18 2000-06-22 Du Pont Pharmaceuticals Company N-ureidoalkyl-piperidines as modulators of chemokine receptor activity
CA2348923A1 (en) 1998-12-18 2000-06-22 Dean A. Wacker N-ureidoalkyl-piperidines as modulators of chemokine receptor activity
AU760174B2 (en) * 1999-02-09 2003-05-08 Bristol-Myers Squibb Company Lactam inhibitors of FXa and method
WO2002002525A2 (en) * 2000-06-30 2002-01-10 Bristol-Myers Squibb Pharma Company N-ureidoheterocycloaklyl-piperidines as modulators of chemokine receptor activity
WO2003045917A2 (en) * 2001-11-30 2003-06-05 F. Hoffmann-Laroche Ag Ccr-3 receptor antagonists vii

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WO2002002525A3 (en) 2002-08-29
US20040058961A1 (en) 2004-03-25
US20030032654A1 (en) 2003-02-13
MXPA02012712A (es) 2003-04-25
IL153123A0 (en) 2003-06-24
AU2001273129A1 (en) 2002-01-14
JP2004517805A (ja) 2004-06-17
US6949546B2 (en) 2005-09-27
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US6627629B2 (en) 2003-09-30
HK1054032A1 (zh) 2003-11-14
CA2413245A1 (en) 2002-01-10

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