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AR038955A1 - PIRIMIDINONE AND PIRIDONA SUBSTITUTED COMPOUNDS AND METHODS FOR USE - Google Patents

PIRIMIDINONE AND PIRIDONA SUBSTITUTED COMPOUNDS AND METHODS FOR USE

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Publication number
AR038955A1
AR038955A1 ARP970105716A ARP970105716A AR038955A1 AR 038955 A1 AR038955 A1 AR 038955A1 AR P970105716 A ARP970105716 A AR P970105716A AR P970105716 A ARP970105716 A AR P970105716A AR 038955 A1 AR038955 A1 AR 038955A1
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Argentina
Prior art keywords
radicals
alkyl
optionally substituted
alkylthio
cyano
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ARP970105716A
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Spanish (es)
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Michael J Malone
Nathan B Mantlo
Jeffery A Zablocki
Ulrike D Spohr
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Amgen Inc
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Publication of AR038955A1 publication Critical patent/AR038955A1/en

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Abstract

Los compuestos de pirimidinona y piridona sustituidos seleccionados son efectivos para la profilaxis y tratamiento de enfermedades, tales como enfermedades mediadas por TNF-alfa, IL-1beta, IL-6 y/o IL-8, y otras afecciones, tales como dolor y diabetes. Nuevos compuestos, análogos, prodrogas y sales farmacéuticamente aceptables de las mismas, composiciones farmacéuticas y métodos para la profilaxis y el tratamiento de enfermedades y otras afecciones y condiciones que involucran inflamación, dolor, diabetes y lo similar. Procesos para preparar estos compuestos así como productos intermedios útiles en estos procesos. Reivindicación 1: Un compuesto de la fórmula (1) o una sal farmacéuticamente aceptable del mismo, donde X es O, S ó NR5; el grupo molecular (2) es elegido del grupo de fórmulas (3) siempre que el número total combinado de radicales arilo, heteroarilo, cicloalquilo y heterociclilo en -VC(R)W- sea 0-3; U es NR21 ó CHR21; n es un entero de 1-3; R1 y R2 son independientemente -Y ó -Z-Y, y R3 y R4 son cada uno independientemente -Z-Y; siempre que R4 no sea un radical arilo sustituido, (aril sustituido)metilo ó (aril sustituido)etilo, y el número total de radicales arilo, heteroarilo, cicloalquilo y heterociclilo en cada -Y y -Z-Y sea 0-3; donde cada Z es independientemente: (1) un radical alquilo, alquenilo ó alquinilo sustituido optativamente por (a) 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, ciano ó halo, y (b) 1-2 radicales de heterociclilo, arilo o heteroarilo sustituidos optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, halo, alquilo ó haloalquilo; (2) un radical heterociclilo sustituido optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, alquilo ó haloalquilo; o (3) un radical arilo ó heteroarilo sustituido optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, ciano, halo, alquilo ó haloalquilo; cada Y es independientemente: (1) un radical hidrógeno; (2) un radical halo, ciano ó nitro; (3) un radical -C(O)-R20, -C(O)-OR21, -C(O)-NR5R21 ó -C(NR5)-NR5R21; (4) un radical -OR21, -O-C(O)-R21, -O-C(O)-NR5R21 u -O-C(O)-NR22-S(O)2-R20; (5) un radical -SR21, -S(O)-R20, -S(O)2-R20, -S(O)2-NR5R21, -S(O)2NR22-C(O)-R21, -S(O)2-NR22-C(O)-OR20 ó -S(O)2-NR22-C(O)NR5R21; ó (6) un radical -NR5R21, -NR22-C(O)-R21, -NR22-C(O)-OR20, -NR22-C(O)NR5R21, -NR22-C(NR5)-NR5R21, -NR22-S(O)2-R20 ó -NR22S(O)2-NR5R21; donde cada R5 es independientemente (1) radicales hidrógeno; (2) radicales alquilo, alquenilo ó alquinilo sustituidos optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, hidroxi, alcoxi, alquiltio, ciano ó halo; ó (3) radicales arilo, heteroarilo, aralquilo, heteroaralquilo, heterociclilo, heterociclilalquilo, cicloalquilo ó cicloalquilalquilo sustituidos optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, hidroxi, alcoxi, alquiltio, ciano, alquilo ó haloalquilo; donde cada R20 es independientemente (1) un radical alquilo, alquenilo ó alquinilo optativamente sustituidos por 1-3 radicales de -CO2R23 amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, N-(alcoxicarbonil)-N-(alquil)amino, aminocarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, ciano, halo ó aralcoxi, aralquiltio, aralquilsulfonilo, cicloalquilo, heterociclilo, arilo ó heteroarilo optativamente sustituidos por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, alcanoilo, alcoxicarbonilo, hidroxi, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, ciano, halo, alquilo ó haloalquilo; (2) un radical heterociclilo sustituido optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, alcoxicarbonilo, hidroxi, alcoxi, alquiltio, ciano, alquilo ó haloalquilo; o (3) radicales arilo ó heteroarilo sustituidos optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, alcoxicarbonilo, hidroxi, alcoxi, alquiltio, ciano, halo, azido, alquilo ó haloalquilo; cada R22 es independientemente un radical hidrógeno ó R20; cada R22 es independientemente (1) un radical hidrógeno; (2) un radical alquilo sustituido optativamente por un radical de heterociclilo, arilo ó heteroarilo sustituido optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, ciano, halo, alquilo ó haloalquilo; ó (3) radicales heterociclilo, arilo ó heteroarilo sustituidos optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, ciano, halo, alquilo ó haloalquilo; y cada R23 es independientemente hidrógeno ó alquilo, ó arilo, heteroarilo, aralquilo ó heteroaralquilo sustituido optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, ciano, halo, alquilo ó haloalquilo; y R11 y R12 son independientemente un radical arilo ó heteroarilo sustituido optativamente por 1-3 radicales de (1) R30; (2) radicales halo ó ciano; (3) radicales -C(O)-R30, -C(O)-OR29, -C(O)-NR31R32 ó -C(NR31)NR31R32; (4) radicales -OR29, -O-C(O)-R29, -O-C(O)-NR31R32 ó -O-C(O)-NR33S(O)2-R30; (5) radicales -SR29, -S(O)-R30, -S(O)2-R30, -S(O)2-NR31R32, -S(O)2-NR33-C(O)-R30, -S(O)2-NR33-C(O)-OR30 ó -S(O)2-NR33-C(O)-NR31R32; ó (6) -NR31R32, -NR33-C(O)-R29, -NR33-C(O)-OR30, -NR33-C(O)-NR31R32, -NR33-C(NR31)-NR31R32, -NR33-S(O)2-R30 ó -NR33S(O)2-NR31R32; siempre que (1) R11 no sea un radical 4-piridilo, 4-pirimidinilo, 4-quinolilo ó 6-isoquinolinilo sustituido optativamente por 1-2 sustituyentes; y (2) el número total de radicales arilo, heteroarilo, cicloalquilo y heterociclilo sustituidos en cada uno de R11 y R12 sea 0-1; donde cada R30 es independientemente (1) un radical alquilo, alquenilo ó alquinilo optativamente sustituido por 1-3 radicales de -NR31R31, -CO2R23, hidroxi, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, ciano, halo ó aralcoxi, aralquiltio, aralquilsulfonilo, heterociclilo, arilo ó heteroarilo optativamente sustituidos por 1-3 radicales de los radicales amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, ciano, halo, alquilo ó haloalquilo; (2) un radical heterociclilo sustituido optativamente por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, ciano, halo, alquilo ó haloalquilo; o (3) radicales arilo ó heteroarilo optativamente sustituidos por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, ciano, alquilo ó haloalquilo; cada R29 es independientemente un radical hidrógeno ó R30; cada R31 y R32 es independientemente (1) radicales hidrógeno; (2) un radical alquilo sustituido optativamente por un radical cicloalquilo, arilo, heterociclilo ó heteroarilo sustituido optativamente por 1-3 radicales de los radicales amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, ciano, alquilo ó haloalquilo; ó (3) un radical arilo, heteroarilo, heterociclilo ó cicloalquilo sustituido optativamente por 1-3 radicales de los radicales amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, ciano, alquilo ó haloalquilo; y donde cada R33 es independientemente (1) un radical hidrógeno; ó (2) un radical alquilo sustituido optativamente por un radical de los radicales heterociclilo, arilo ó heteroarilo optativamente sustituido por 1-3 radicales de amino, alquilamino, dialquilamino, alcanoilamino, alcoxicarbonilamino, alquilsulfonilamino, hidroxi, alcoxi, alquiltio, ciano, alquilo ó haloalquilo.Selected substituted pyrimidinone and pyridone compounds are effective for the prophylaxis and treatment of diseases, such as diseases mediated by TNF-alpha, IL-1 beta, IL-6 and / or IL-8, and other conditions, such as pain and diabetes. . New compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for the prophylaxis and treatment of diseases and other conditions and conditions involving inflammation, pain, diabetes and the like. Processes to prepare these compounds as well as intermediate products useful in these processes. Claim 1: A compound of the formula (1) or a pharmaceutically acceptable salt thereof, wherein X is O, S or NR5; the molecular group (2) is chosen from the group of formulas (3) provided that the combined total number of aryl, heteroaryl, cycloalkyl and heterocyclyl radicals in -VC (R) W- is 0-3; U is NR21 or CHR21; n is an integer of 1-3; R1 and R2 are independently -Y or -Z-Y, and R3 and R4 are each independently -Z-Y; provided that R4 is not a substituted aryl radical, (substituted aryl) methyl or (substituted aryl) ethyl, and the total number of aryl, heteroaryl, cycloalkyl and heterocyclyl radicals in each -Y and -Z-Y is 0-3; where each Z is independently: (1) an alkyl, alkenyl or alkynyl radical optionally substituted by (a) 1-3 amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, cyano or halo radicals, and (b) 1-2 heterocyclyl, aryl or heteroaryl radicals optionally substituted by 1-3 amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, halo, alkyl or haloalkyl radicals; (2) a heterocyclyl radical optionally substituted by 1-3 radicals of amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, alkyl or haloalkyl; or (3) an aryl or heteroaryl radical optionally substituted by 1-3 amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, cyano, halo, alkyl or haloalkyl radicals; each Y is independently: (1) a hydrogen radical; (2) a halo, cyano or nitro radical; (3) a radical -C (O) -R20, -C (O) -OR21, -C (O) -NR5R21 or -C (NR5) -NR5R21; (4) a radical -OR21, -O-C (O) -R21, -O-C (O) -NR5R21 or -O-C (O) -NR22-S (O) 2-R20; (5) a radical -SR21, -S (O) -R20, -S (O) 2-R20, -S (O) 2-NR5R21, -S (O) 2NR22-C (O) -R21, -S (O) 2-NR22-C (O) -OR20 or -S (O) 2-NR22-C (O) NR5R21; or (6) a radical -NR5R21, -NR22-C (O) -R21, -NR22-C (O) -OR20, -NR22-C (O) NR5R21, -NR22-C (NR5) -NR5R21, -NR22 -S (O) 2-R20 or -NR22S (O) 2-NR5R21; where each R5 is independently (1) hydrogen radicals; (2) alkyl, alkenyl or alkynyl radicals optionally substituted by 1-3 amino, alkylamino, dialkylamino, hydroxy, alkoxy, alkylthio, cyano or halo radicals; or (3) aryl, heteroaryl, aralkyl, heteroaralkyl, heterocyclyl, heterocyclylalkyl, cycloalkyl or cycloalkylalkyl radicals optionally substituted by 1-3 amino, alkylamino, dialkylamino, hydroxy, alkoxy, alkylthio, cyano, alkyl or haloalkyl radicals; where each R20 is independently (1) an alkyl, alkenyl or alkynyl radical optionally substituted by 1-3 radicals of -CO2R23 amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, N- (alkoxycarbonyl) -N- (alkyl) amino, aminocarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, cyano, halo or aralkoxy, aralkylthio, aralkylsulfonyl, cycloalkyl, heterocyclyl, aryl or heteroaryl optionally substituted by 1-3 radicals of amino, alkylamino, dialkylamino, alkanoylamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino, alkylaminolamino , alkoxycarbonyl, hydroxy, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, cyano, halo, alkyl or haloalkyl; (2) a heterocyclyl radical optionally substituted by 1-3 radicals of amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, alkoxycarbonyl, hydroxy, alkoxy, alkylthio, cyano, alkyl or haloalkyl; or (3) aryl or heteroaryl radicals optionally substituted by 1-3 amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, alkoxycarbonyl, hydroxy, alkoxy, alkylthio, cyano, halo, azido, alkyl or haloalkyl radicals; each R22 is independently a hydrogen radical or R20; each R22 is independently (1) a hydrogen radical; (2) an alkyl radical optionally substituted by a heterocyclyl, aryl or heteroaryl radical optionally substituted by 1-3 radicals of amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, cyano, halo , alkyl or haloalkyl; or (3) heterocyclyl, aryl or heteroaryl radicals optionally substituted by 1-3 amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, cyano, halo, alkyl or haloalkyl radicals; and each R23 is independently hydrogen or alkyl, or aryl, heteroaryl, aralkyl or heteroaralkyl optionally substituted by 1-3 radicals of amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, cyano, halo , alkyl or haloalkyl; and R11 and R12 are independently an aryl or heteroaryl radical optionally substituted by 1-3 radicals of (1) R30; (2) halo or cyano radicals; (3) radicals -C (O) -R30, -C (O) -OR29, -C (O) -NR31R32 or -C (NR31) NR31R32; (4) radicals -OR29, -O-C (O) -R29, -O-C (O) -NR31R32 or -O-C (O) -NR33S (O) 2-R30; (5) radicals -SR29, -S (O) -R30, -S (O) 2-R30, -S (O) 2-NR31R32, -S (O) 2-NR33-C (O) -R30, - S (O) 2-NR33-C (O) -OR30 or -S (O) 2-NR33-C (O) -NR31R32; or (6) -NR31R32, -NR33-C (O) -R29, -NR33-C (O) -OR30, -NR33-C (O) -NR31R32, -NR33-C (NR31) -NR31R32, -NR33- S (O) 2-R30 or -NR33S (O) 2-NR31R32; provided that (1) R11 is not a 4-pyridyl, 4-pyrimidinyl, 4-quinolyl or 6-isoquinolinyl radical optionally substituted by 1-2 substituents; and (2) the total number of aryl, heteroaryl, cycloalkyl and heterocyclyl radicals substituted in each of R11 and R12 is 0-1; where each R30 is independently (1) an alkyl, alkenyl or alkynyl radical optionally substituted by 1-3 radicals of -NR31R31, -CO2R23, hydroxy, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, cyano, halo or aralkoxy, aralkylthio, aralkylsulfonyl, heterocyclyl , aryl or heteroaryl optionally substituted by 1-3 radicals of the amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, cyano, halo, alkyl or haloalkyl radicals; (2) a heterocyclyl radical optionally substituted by 1-3 radicals of amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, cyano, halo, alkyl or haloalkyl; or (3) aryl or heteroaryl radicals optionally substituted by 1-3 amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, cyano, alkyl or haloalkyl radicals; each R29 is independently a hydrogen radical or R30; each R31 and R32 is independently (1) hydrogen radicals; (2) an alkyl radical optionally substituted by a cycloalkyl, aryl, heterocyclyl or heteroaryl radical optionally substituted by 1-3 radicals of the amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, cyano, alkyl or haloalkyl; or (3) an aryl, heteroaryl, heterocyclyl or cycloalkyl radical optionally substituted by 1-3 radicals of the amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, cyano, alkyl or haloalkyl radicals; and where each R33 is independently (1) a hydrogen radical; or (2) an alkyl radical optionally substituted by a radical of the heterocyclyl, aryl or heteroaryl radicals optionally substituted by 1-3 radicals of amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, hydroxy, alkoxy, alkylthio, cyano, alkyl or haloalkyl

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Families Citing this family (87)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6613942B1 (en) 1997-07-01 2003-09-02 Novo Nordisk A/S Glucagon antagonists/inverse agonists
EP1087963B1 (en) * 1998-06-19 2004-08-25 Chiron Corporation Inhibitors of glycogen synthase kinase 3
AR023052A1 (en) 1998-09-25 2002-09-04 Mitsuharu Yoshimura Milton DERIVATIVES OF PIRIMIDONA
ES2212657T3 (en) 1998-11-04 2004-07-16 Smithkline Beecham Corporation REPLACED PIRAZINAS PIRIDIN-4-IL OR PIRIMIDIN-4-IL.
US6350744B1 (en) * 1998-11-20 2002-02-26 Merck & Co., Inc. Compounds having cytokine inhibitory activity
WO2000040243A1 (en) 1999-01-08 2000-07-13 Smithkline Beecham Corporation Novel compounds
US6503949B1 (en) 1999-05-17 2003-01-07 Noro Nordisk A/S Glucagon antagonists/inverse agonists
US7122666B2 (en) 1999-07-21 2006-10-17 Sankyo Company, Limited Heteroaryl-substituted pyrrole derivatives, their preparation and their therapeutic uses
GB9927844D0 (en) * 1999-11-26 2000-01-26 Glaxo Group Ltd Chemical compounds
US6906067B2 (en) 1999-12-28 2005-06-14 Bristol-Myers Squibb Company N-heterocyclic inhibitors of TNF-α expression
WO2001047897A1 (en) * 1999-12-28 2001-07-05 Pharmacopeia, Inc. Cytokine, especially tnf-alpha, inhibitors
GB0003224D0 (en) 2000-02-11 2000-04-05 Glaxo Group Ltd Chemical compounds
EP1136484A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-(Arylalkylamino)pyrimidone derivatives
EP1136486A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-[Indanylamino]pyrimidone and 2-[tetrahydronaphthalenylamino]pyrimidone derivatives
WO2001070728A1 (en) * 2000-03-23 2001-09-27 Sanofi-Synthelabo 2-[nitrogen-heterocyclic]pyrimidone derivatives
AU2001248365A1 (en) * 2000-03-23 2001-10-03 Mitsubishi Pharma Corporation 2-(arylalkylamino)pyrimidone derivatives and 2-(heteroarylalkylamino)pyrimidone derivatives
EP1136491A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-[(Heteroaryl)alkylamino]pyrimidone derivatives
EP1136489A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-[Piperidin-1-yl]pyrimidone derivatives
EP1136483A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-[Piperazinyl]pyrimidone derivatives
EP1136099A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-(Indolylalkylamino)pyrimidone derivatives as GSK3beta inhibitors
EP1136485A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo Aminophenyl pyrimidone derivatives
EP1136482A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-Amino-3-(alkyl)-pyrimidone derivatives as GSK3beta inhibitors
EP1136493A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-(Thienopyridinyl)pyrimidone, 2-(furopyridinyl)pyrimidone 2-(isoquinolinyl)pyrimidone, 2-(pyridoindolyl)pyrimidone and 2-(benzofuropyridinyl)pyrimidone derivatives
EP1510222A3 (en) 2000-04-26 2007-05-23 Eisai R&D Management Co., Ltd. Medicinal compositions promoting bowel movement
CA2781858C (en) * 2000-05-12 2015-03-31 Genzyme Corporation Modulators of tnf-.alpha. signaling
US6562807B2 (en) 2000-06-23 2003-05-13 Novo Nordisk A/S Glucagon antagonists/inverse agonists
GB0021494D0 (en) * 2000-09-01 2000-10-18 Glaxo Group Ltd Chemical comkpounds
JP2004514656A (en) * 2000-09-06 2004-05-20 カイロン コーポレイション Inhibitors of glycogen synthase kinase 3
US6670362B2 (en) 2000-09-20 2003-12-30 Pfizer Inc. Pyridazine endothelin antagonists
US6821960B2 (en) 2000-11-17 2004-11-23 Noyo Nordisk Pharmaceuticals, Inc. Glucagon antagonists/inverse agonists
EP1345890A1 (en) 2000-11-17 2003-09-24 Novo Nordisk A/S Glucagon antagonists/inverse agonists
US6706744B2 (en) 2000-11-17 2004-03-16 Novo Nordisk A/S Glucagon antagonists/inverse agonists
GB0112810D0 (en) * 2001-05-25 2001-07-18 Glaxo Group Ltd Pyrimidine derivatives
GB0112802D0 (en) 2001-05-25 2001-07-18 Glaxo Group Ltd Pyrimidine derivatives
GB0119477D0 (en) 2001-08-09 2001-10-03 Glaxo Group Ltd Pyrimidine derivatives
JP4368682B2 (en) 2001-09-21 2009-11-18 田辺三菱製薬株式会社 3-Substituted-4-pyrimidone derivatives
CN1810802B (en) * 2001-09-21 2011-04-27 三菱制药株式会社 3-substituted-4-pyrimidone derivatives
HUP0401900A3 (en) 2001-09-21 2005-08-29 Sanofi Aventis 3-substituted-4-pyrimidone derivatives, pharmaceutical compositions containing them and their intermediates
TWI330183B (en) 2001-10-22 2010-09-11 Eisai R&D Man Co Ltd
TWI301834B (en) * 2001-10-22 2008-10-11 Eisai R&D Man Co Ltd Pyrimidone compound and pharmaceutical composition including the same
US6921762B2 (en) 2001-11-16 2005-07-26 Amgen Inc. Substituted indolizine-like compounds and methods of use
US6762318B2 (en) 2001-12-03 2004-07-13 Novo Nordisk A/S Glucagon antagonists
US6881746B2 (en) 2001-12-03 2005-04-19 Novo Nordick A/S Glucagon antagonists/inverse agonists
AR038368A1 (en) 2002-02-01 2005-01-12 Novartis Ag N-PYRIMIDIN-2-IL-AMINAS SUBSTITUTED COMPOUNDS AS IGE INHIBITORS, A PHARMACEUTICAL COMPOSITION AND THE USE OF SUCH COMPOUNDS FOR THE PREPARATION OF A MEDICINAL PRODUCT
EP1476428B1 (en) 2002-02-22 2010-11-17 Pharmacia & Upjohn Company LLC Pyridyl sulfone derivatives as 5-ht6 receptor ligands
DE60302221T2 (en) * 2002-02-28 2006-08-03 Sanofi-Aventis HETEROARYL SUBSTITUTED 2-PYRIDINYL AND 2-PYRIMIDINYL-6,7,8,9-TETRAHYDROPYRIMIDO [1,2-A] PYRIMIDIN-4-ONDERIVATE
US20030232813A1 (en) * 2002-04-10 2003-12-18 Orchid Chemicals & Pharmaceuticals Limited Novel amino substituted pyrimidinone derivatives
US7026326B2 (en) 2002-05-21 2006-04-11 Amgen Inc. Substituted heterocyclic compounds and methods of use
CA2492033A1 (en) 2002-07-09 2004-01-15 Boehringer Ingelheim Pharma Gmbh & Co. Kg Pharmaceutical compositions of anticholinergics and p38 kinase inhibitors in the treatment of respiratory diseases
ATE325115T1 (en) 2002-08-19 2006-06-15 Glaxo Group Ltd PYRIMIDINE DERIVATIVES AS SELECTIVE COX-2 INHIBITORS
GB0221443D0 (en) 2002-09-16 2002-10-23 Glaxo Group Ltd Pyridine derivates
NZ541074A (en) 2002-12-16 2008-04-30 Mitsubishi Pharma Corp 3-Substituted-4-pyrimidone derivatives
PL378402A1 (en) * 2003-02-06 2006-04-03 Basf Aktiengesellschaft Pyrimidines, methods for the production thereof, and use thereof
TWI357408B (en) 2003-03-26 2012-02-01 Mitsubishi Tanabe Pharma Corp 3-substituted-4-pyrimidone derivatives
JP2007534624A (en) * 2003-07-16 2007-11-29 ニューロジェン・コーポレーション Biaryl piperazinyl-pyridine analogues
WO2005039485A2 (en) * 2003-08-13 2005-05-06 Chiron Corporation Gsk-3 inhibitors and uses thereof
AU2004267096B2 (en) * 2003-08-20 2008-10-02 Amgen Inc. Substituted pyrimdinone derivatives and methods of use
GB0323137D0 (en) 2003-10-03 2003-11-05 Chang Lisa C W 2,4,6- Trisubstituted pyrimidines and their different uses
US7897607B2 (en) 2004-04-07 2011-03-01 Takeda Pharmaceutical Company Limited Cyclic compounds
US20060035893A1 (en) 2004-08-07 2006-02-16 Boehringer Ingelheim International Gmbh Pharmaceutical compositions for treatment of respiratory and gastrointestinal disorders
MY145822A (en) 2004-08-13 2012-04-30 Neurogen Corp Substituted biaryl piperazinyl-pyridine analogues
PE20060777A1 (en) 2004-12-24 2006-10-06 Boehringer Ingelheim Int INDOLINONE DERIVATIVES FOR THE TREATMENT OR PREVENTION OF FIBROTIC DISEASES
US8193206B2 (en) 2005-06-14 2012-06-05 Taigen Biotechnology Co., Ltd. Pyrimidine compounds
EA015890B1 (en) * 2005-06-14 2011-12-30 Тайджен Байотекнолоджи Ко. Лтд. Pyrimidine compounds
ES2270715B1 (en) 2005-07-29 2008-04-01 Laboratorios Almirall S.A. NEW DERIVATIVES OF PIRAZINA.
WO2007022964A2 (en) 2005-08-24 2007-03-01 Abbott Gmbh & Co. Kg Hetaryl-substituted guanidine compounds and use thereof as binding partners for 5-ht5-receptors
ES2274712B1 (en) 2005-10-06 2008-03-01 Laboratorios Almirall S.A. NEW IMIDAZOPIRIDINE DERIVATIVES.
EP2079728B1 (en) 2006-10-10 2013-09-25 Amgen Inc. N-aryl pyrazole compounds for use against diabetes
EP1992344A1 (en) 2007-05-18 2008-11-19 Institut Curie P38 alpha as a therapeutic target in pathologies linked to FGFR3 mutation
EA201000104A1 (en) * 2007-07-26 2010-08-30 Новартис Аг DERIVATIVES OF PYRIMIDINE APPLICABLE FOR THE TREATMENT OF INFLAMMATORY OR ALLERGIC PATHOLOGICAL CONDITIONS
DK2268635T3 (en) * 2008-04-21 2015-09-14 Taigen Biotechnology Co Ltd Heterocyclic Compounds
US9023834B2 (en) 2008-11-13 2015-05-05 Taigen Biotechnology Co., Ltd. Lyophilization formulation
EP2629776B1 (en) 2010-10-18 2017-08-16 Cerenis Therapeutics Holding SA Compounds, compositions and methods useful for cholesterol mobilisation
GB201106829D0 (en) 2011-04-21 2011-06-01 Proximagen Ltd Heterocyclic compounds
NZ611529A (en) 2010-12-23 2015-06-26 Pfizer Glucagon receptor modulators
ME02502B (en) 2011-02-08 2017-02-20 Pfizer Glucagon receptor modulator
JP5647379B2 (en) 2011-07-22 2014-12-24 ファイザー・インク Quinolinyl glucagon receptor modulator
AU2012335220B2 (en) 2011-11-11 2017-06-01 Pfizer Inc. 2-thiopyrimidinones
EP3083584B1 (en) 2013-12-19 2018-02-21 Sunshine Lake Pharma Co., Ltd. Nitrogenous heterocyclic derivatives and their application in the treatment of tissue fibrosis
TWI651310B (en) * 2014-02-20 2019-02-21 日商日本煙草產業股份有限公司 Triterpenoids and their medical use
MA42035A (en) 2015-05-05 2018-03-14 Pfizer 2-THIOPYRIMIDINONES
AU2016346557B2 (en) * 2015-10-29 2020-10-29 Aska Pharmaceutical Co., Ltd. Pyrimidine derivative
SG11201802927VA (en) * 2015-11-04 2018-05-30 Merck Patent Gmbh Methods for treating cancer using pyrimidine and pyridine compounds with btk inhibitory activity
SI3377484T1 (en) * 2015-11-17 2024-02-29 Merck Patent Gmbh Methods for treating multiple sclerosis using pyrimidine and pyridine compounds with btk inhibitory activity
TW201811766A (en) 2016-08-29 2018-04-01 瑞士商諾華公司 N-(pyridin-2-yl)pyridine-sulfonamide derivatives and their use in the treatment of disease
BR112022009202A2 (en) * 2019-11-12 2022-09-06 Genzyme Corp 6-limb heteroarylaminosulfonamides for the treatment of diseases and conditions mediated by deficient CFTR activity
US11993580B1 (en) 2022-12-02 2024-05-28 Neumora Therapeutics, Inc. Methods of treating neurological disorders

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1271116B (en) * 1965-05-04 1968-06-27 Bayer Ag Process for the preparation of 4-hydroxypyrimidines
BE759176A (en) * 1969-11-20 1971-05-19 Sandoz Sa PYRIMIDINE DERIVATIVES, THEIR PREPARATION AND MEDICINAL PRODUCTS CONTAINING THESE DERIVES
US4438117A (en) * 1980-09-03 1984-03-20 E. I. Du Pont De Nemours And Company 2-Substituted thio-4,5-diarylpyrimidines
DE3319843A1 (en) * 1983-06-01 1984-12-06 Ali-Akbar Dipl.-Chem. Dr. 4300 Mülheim Pourzal Process for the preparation of pyrimidines from nitrile and alkynes
US4500533A (en) * 1983-06-22 1985-02-19 Eli Lilly And Company 2,4,5-Triaryl pyrimidines and a method of treating pain, fever, thrombosis, inflammation and arthritis
US5077142A (en) * 1989-04-20 1991-12-31 Ricoh Company, Ltd. Electroluminescent devices
US5620999A (en) * 1994-07-28 1997-04-15 Weier; Richard M. Benzenesulfonamide subtituted imidazolyl compounds for the treatment of inflammation
JP3382951B2 (en) * 1995-10-06 2003-03-04 メルク エンド カムパニー インコーポレーテッド Substituted imidazoles having anticancer activity and cytocan inhibitory activity
WO1997016442A1 (en) * 1995-10-31 1997-05-09 Merck & Co., Inc. Substituted pyridyl pyrroles, compositions containing such compounds and methods of use
EP0888335A4 (en) * 1996-03-13 2002-01-02 Smithkline Beecham Corp Novel pyrimidine compounds useful in treating cytokine mediated diseases

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