AR069078A1 - Derivados de piridina y pirazina - Google Patents
Derivados de piridina y pirazinaInfo
- Publication number
- AR069078A1 AR069078A1 ARP080104644A ARP080104644A AR069078A1 AR 069078 A1 AR069078 A1 AR 069078A1 AR P080104644 A ARP080104644 A AR P080104644A AR P080104644 A ARP080104644 A AR P080104644A AR 069078 A1 AR069078 A1 AR 069078A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- amino
- con
- hydroxy
- Prior art date
Links
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 53
- 125000000217 alkyl group Chemical group 0.000 abstract 26
- 229910052757 nitrogen Inorganic materials 0.000 abstract 19
- 125000003545 alkoxy group Chemical group 0.000 abstract 11
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 abstract 10
- 125000001424 substituent group Chemical group 0.000 abstract 10
- -1 cyano, amino Chemical group 0.000 abstract 8
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 229910052760 oxygen Inorganic materials 0.000 abstract 7
- 229910052717 sulfur Inorganic materials 0.000 abstract 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 6
- 125000001589 carboacyl group Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 5
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 4
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 3
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 3
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 3
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 2
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 2
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000004423 acyloxy group Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000005153 alkyl sulfamoyl group Chemical group 0.000 abstract 2
- 125000005281 alkyl ureido group Chemical group 0.000 abstract 2
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000002431 aminoalkoxy group Chemical group 0.000 abstract 1
- VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 208000035269 cancer or benign tumor Diseases 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 230000037431 insertion Effects 0.000 abstract 1
- 238000003780 insertion Methods 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Composiciones farmacéuticas que los contienen y su uso en la elaboracion de un medicamento en el tratamiento de trastornos de proliferacion celular. Reivindicacion 1: Un compuesto caracterizado porque responde a la formula (1) donde W es CH o N; J es O o S; cada uno de G1, G2, G3 y G4 se selecciona entre CH y N con la condicion de que no más de dos de G1, G2, G3 y G4 representan N; el Anillo A se selecciona entre (i) fenilo sustituido con R1 y sustituido opcionalmente con hasta tres grupos R2; o (ii) un anillo heteroarilo monocíclico de 5 o 6 miembros con hasta tres heteroátomos del anillo que se seleccionan entre oxígeno, nitrogeno y azufre, donde dicho anillo está sustituido con R1 y opcionalmente está sustituido con hasta tres grupos R2; o (iii) un sistema de anillos bicíclico de 8, 9 o 10 miembros, donde dicho sistema de anillos bicíclico opcionalmente tiene hasta tres heteroátomos del anillo que se seleccionan entre oxígeno, nitrogeno y azufre y está sustituido opcionalmente por R1 y opcionalmente está sustituido con hasta tres grupos R2; R1 es un grupo con la formula: R4-X1- donde X1 es un enlace directo o se selecciona entre O, S, SO, SO2, N(R5), CO, CH(OR5), CON(R5), N(R5)CO, N(R5)CON(R5), SO2N(R5), N(R5)SO2, C(R5)2O, OC(R5)2, C(R5)2S, SC(R5)2, C(R5)2, C(R5)2N(R5) y N(R5)C(R5)2, donde cada R5 se selecciona independientemente entre hidrogeno, (C1-8)alquilo C1-8, hidroxi-alquilo C1-6, alcoxi C1-6-alquilo C1-6, ciano-alquilo C1-6, halogeno-alquilo C1-6, di-[alquil C1-6]amino-alquilo C1-6, alquilamino C1-6-alquilo C1-6 o amino-alquilo C1-6, y cuando X1 es un enlace directo o se selecciona entre CH(OR5), C(R5)2O, C(R5)2S, C(R5)2 o C(R5)2N(R5), donde R5 tiene cualquiera de los significados que se definieron anteriormente;, R4 es hidroxi-alquilo C1-6, alcoxi C1-6-alquilo C1-6, R5-S, R5-S(O), R5-SO2, R5-SO2-O, R5-S-alquilo C1-6, R5-S(O)-alquilo C1-6, R5-SO2-alquilo C1-6, N,N-di(R5)sulfamoilo, N,N-di-(R5)sulfamoil-alquilo C1-6, R5-SO2N(R5), R5-SO2N(R5)-alquilo C1-6, R5-CON(R5), R5O-CON(R5), R5-CON(R5)-alquilo C1-6, R5O-CON(R5)-alquilo C1-6, (R5)2N-SO2N(R5), (R5)2N-SO2N(R5)-alquilo C1-6, (R5)2N-CON(R5), (R5)2N-CON(R5)-alquilo C1-6, R5-CO, R5-CO-alquilo C1-6, R5O-CO-alquilo C1-6, (R5)2NCO, (R5)2NCO-alquilo C1-6, (R5)2N-COO, (R5)2NCOO-alquilo C1-6, ciano, amino, (R6)-amino, di-(R6)-amino, amino-alquilo C1-6, (R6)-amino-alquilo C1-6 o di(R6)-amino-alquilo C1-6, donde cada R6 que está presente es alquilo C1-6 sustituido opcionalmente con 1, 2 o 3 sustituyentes que se seleccionan independientemente entre halogeno, ciano, hidroxi y alcoxi C1-6; y cuando X1 se selecciona entre O, S, SO, SO2, N(R5), CO, CON(R5), N(R5)CO, N(R5)CON(R5), SO2N(R5), N(R5)SO2, OC(R5)2, SC(R5)2 y N(R5)C(R5)2, donde R5 tiene cualquiera de los significados que se definieron anteriormente, R4 es hidroxi-alquilo C1-6, alcoxi C1-6-alquilo C1-6, R5-S-alquilo C1-6, R5-S(O)-alquilo C1-6, R5-SO2-alquilo C1-6, N,N-di-(R5)sulfamoil-alquilo C1-6, R5-SO2N(R5)-alquilo C1-6, R5-CON(R5)-alquilo C1-6, R5O-CON(R5)-alquilo C1-6, (R5)2N-SO2N(R5)-alquilo C1-6, (R5)2N-CON(R5)-alquilo C1-6, R5-CO, R5-CO-alquilo C1-6, R5O-CO, R5O-CO-alquilo C1-6, (R5)2NCO, (R5)2NCO-alquilo C1-6, (R5)2NCOO-alquilo C1-6, amino-alquilo C1-6, (R6)-amino-alquilo C1-6 o di-(R6)-amino-alquilo C1-6, donde cada R6 que está presente es alquilo C1-6 sustituido opcionalmente con 1, 2 o 3 sustituyentes que se seleccionan independientemente entre halogeno, ciano, hidroxi y alcoxi C1-6; o R1 es un grupo con la formula: Q1-X2- donde X2 es un enlace directo o se selecciona entre O, S, SO, SO2, N(R7), N[C(O)R7], N[C(O)N(R7)2], N[C(O)OR7], N[SO2-N(R7)2], CO, CH(OR7), CON(R7), N(R7)CO, N(R7)CON(R7), SO2N(R7), N(R7)SO2, O-SO2, SO2O, C(R7)2O, OC(R7)2, C(R7)2S, SC(R7)2, C(R7)2, C(R7)2N(R7) y N(R7)C(R7)2, donde cada R7 se selecciona independientemente entre hidrogeno, alquilo C1-8, hidroxi-alquilo C1-6, alcoxi C1-6-alquilo C1-6, ciano-alquilo C1-6, halogenoalquilo C1-6, di-(R8)amino-alquilo C1-6, (R8)-amino-alquilo C1-6 o amino-alquilo C1-6, donde R8 es alquilo C1-6 sustituido opcionalmente con 1, 2 o 3 sustituyentes que se seleccionan independientemente entre halogeno, ciano, hidroxi y alcoxi C1-6; y Q1 es arilo, aril-alquilo C1-6, cicloalquilo C3-8, cicloalquil C3-8-alquilo C1-6, heterociclilo, heterociclil-alquilo C1-6, heteroarilo o heteroaril-alquilo C1-6, donde cualquier grupo arilo o cicloalquilo C3-8 en un sustituyente R1 lleva 1, 2 o 3 sustituyentes y cualquier grupo heterociclilo o heteroarilo en un sustituyente R1 opcionalmente tiene 1, 2 o 3 sustituyentes, donde dichos sustituyentes se seleccionan independientemente entre halogeno, trifluorometilo, ciano, nitro, hidroxi, amino, carboxi, carbamoilo, ureido, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, alcoxi C1-6, halogeno-alcoxi C1-6, hidroxi-alquilo C1-6, alcoxi C1-6-alquilo C1-6, alquilsulfonil C1-6-alquilo C1-6, ciano-alquilo C1-6, halogeno-alquilo C1-6, amino-alquilo C1-6, alquilamino C1-6-alquilo C1-6, di-[alquil C1-6]amino-alquilo C1-6, alqueniloxi C2-6, alquiniloxi C2-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, alquilamino C1-6, di-[alquil C1-6]amino, alcoxicarbonilo C1-6, alcanoilo C2-6, hidroxi-alcanoilo C2-6, alcoxi C1-6-alcanoilo C2-6, alcanoiloxi C2-6, N-alquilcarbamoilo C1-6, N,N-di-[alquil C1-6]carbamoilo, carbamoil-alquilo C1-6, N-alquil-carbamoil C1-6-alquilo C1-6, N,N-di-[alquil C1-6]carbamoil-alquilo C1-6, alcanoilamino C1-6, N-alquil C1-6-alcanoilamino C1-6, N-alquilureido C1-6, N'-alquilureido C1-6, N',N'-di-[alquil C1-6]ureido, N,N'-di-[alquil C1-6]ureido, N,N',N'-tri-[alquil C1-6]ureido, N-alquilsulfamoilo C1-6, N,N-di-[alquil C1-6]sulfamoilo, alcansulfonilamino C1-6, N-alquil C1-6-alcansulfonilamino C1-6, alcoxi C1-6-alcoxicarbonilo C1-6, alquilamino C1-6-alcanoilo C2-6, di-[alquil C1-6]amino-alcanoilo C2-6, alcanoilamino C1-6-alcanoilo C2-6, alcoxi C1-6-alcoxi C1-6-alcanoilo C2-6, heterociclilo, heterociclilalquilo C1-6, heteroarilo o heteroaril-alquilo C1-6 y algun grupo heterociclilo dentro de un sustituyente R1 opcionalmente tiene 1 o 2 sustituyentes oxo; donde, cualquier CH, CH2, o CH3 en cualquiera de los grupos alquilo que esté presente en la definicion de R4 que se conecta a X1 o que esté presente en la definicion de Q1 que se conecta a X2, opcionalmente tiene un grupo hidroxi o ciano y opcionalmente tiene hasta tres grupos halogenos, y se puede reemplazar opcionalmente por un átomo que se selecciona entre O, S o N o un grupo SO2 y los átomos de carbono adyacentes en una cadena alquilo opcionalmente pueden estar separados por la insercion en la cadena de un grupo CsC; cada uno de los grupos R2 puede ser igual o diferente y se selecciona entre halogeno, ciano, hidroxi, amino, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, halogeno-alcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, alquilamino C1-6, di-[alquil C1-6]amino, alcoxicarbonilo C1-6, alcanoilo C2-6, alcanoiloxi C2-6, carbamoilo, N-alquilcarbamoilo C1-6, N,N-di-{alquil C1-6}carbamoilo, alcanoilamino C1-6, N-alquil C1-6-alcanoilamino C1-6, alcoxi C1-6-alquilo C1-6, hidroxi-alquilo C1-6, amino-alquilo C1-6, alquilamino C1-6-alquilo C1-6, di-{alquil C1-6]amino-alquilo C1-6, alcoxi C1-6-alcoxi C1-6, hidroxi-alcoxi C1-6, amino-alcoxi C1-6, alquilamino C1-6-alcoxi C1-6 y di-[alquil C1-6]amino-alcoxi C1-6; n es 0, 1, 2 o 3 y, cuando n es 2 o 3, cada uno de los grupos R3 puede ser igual o diferente, y cada uno de los grupos R3 presente se selecciona entre hidrogeno, halogeno, amino, ciano, sulfamoilo, OR9, N-alquil-sulfamoilo C1-6, N,N-di-[alquil C1-6]sulfamoilo, trifluorometilo, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, alcoxi C1-6, alcoxicarbonilo C1-6, halogeno-alcoxi C1-6, carbamoilo, N-alquilcarbamoilo C1-6, N,N-di-[alquil C1-6]carbamoilo, alcanoilamino C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, hidroxi-alquilo C1-6, alcoxi C1-6-alquilo C1-6, alcanoilo C2-6, alcansulfonilamino C1-6, amino-alquilo C1-6, alquilamino C1-6-alquilo C1-6, di-[alquil C1-6]amino-alquilo C1-6, alcoxi C1-6-alcoxi C1-6, hidroxi-alcoxi C1-6, amino-alcoxi C1-6, alquilamino C1-6-alcoxi C1-6 y di-{alquil C1-6]amino-alcoxi C1-6, donde R9 es fluoro-alquilo C1-6, arilo, aril-alquilo C1-6, heterociclilo, heterociclil-alquilo C1-6, heteroarilo o heteroaril-alquilo C1-6, donde cualquier grupo arilo, heterociclilo o heteroarilo dentro de la definicion de R9 opcionalmente tiene 1, 2 o 3 sustituyentes que se seleccionan independientemente entre halogeno, fluoroalquilo C1-6, oxo, ciano, hidroxi, amino, carboxi, carbamoilo, alquilo C1-8, alquenilo C2-8, alquinilo C2-8 o alcoxi C1-6; o una sal del mismo aceptable para uso farmacéutico.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07301491 | 2007-10-25 | ||
| EP07305005 | 2007-12-21 | ||
| EP08305180 | 2008-05-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR069078A1 true AR069078A1 (es) | 2009-12-30 |
Family
ID=40580139
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080104644A AR069078A1 (es) | 2007-10-25 | 2008-10-24 | Derivados de piridina y pirazina |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US8017611B2 (es) |
| EP (1) | EP2215085B1 (es) |
| JP (1) | JP2011500778A (es) |
| KR (1) | KR20100089090A (es) |
| CN (1) | CN101910158A (es) |
| AR (1) | AR069078A1 (es) |
| AT (1) | ATE523508T1 (es) |
| AU (1) | AU2008315746A1 (es) |
| CA (1) | CA2703653A1 (es) |
| CL (1) | CL2008003188A1 (es) |
| CO (1) | CO6270364A2 (es) |
| EC (1) | ECSP10010197A (es) |
| IL (1) | IL205108A0 (es) |
| MX (1) | MX2010004491A (es) |
| PE (1) | PE20091116A1 (es) |
| TW (1) | TW200920367A (es) |
| UY (1) | UY31430A1 (es) |
| WO (1) | WO2009053737A2 (es) |
Families Citing this family (142)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007026341A1 (de) | 2007-06-06 | 2008-12-11 | Merck Patent Gmbh | Benzoxazolonderivate |
| DE102007032507A1 (de) | 2007-07-12 | 2009-04-02 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102007061963A1 (de) | 2007-12-21 | 2009-06-25 | Merck Patent Gmbh | Pyridazinonderivate |
| EP2265270A1 (en) | 2008-02-04 | 2010-12-29 | OSI Pharmaceuticals, Inc. | 2-aminopyridine kinase inhibitors |
| AR070317A1 (es) | 2008-02-06 | 2010-03-31 | Osi Pharm Inc | Furo (3,2-c) piridina y tieno (3,2-c) piridinas |
| JP2011511078A (ja) * | 2008-02-06 | 2011-04-07 | レアド トヘラペウトイクス,インコーポレーテッド | ポリ(adpリボース)ポリメラーゼ(parp)のベンズオキサゾールカルボキサミド阻害剤 |
| DE102008019907A1 (de) | 2008-04-21 | 2009-10-22 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102008028905A1 (de) | 2008-06-18 | 2009-12-24 | Merck Patent Gmbh | 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate |
| CN102264721B (zh) | 2008-11-10 | 2015-12-09 | 沃泰克斯药物股份有限公司 | 用作atr激酶抑制剂的化合物 |
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| ATE492544T1 (de) | 2004-08-26 | 2011-01-15 | Pfizer | Pyrazol-substituierte aminoheteroarylverbindungen als proteinkinasehemmer |
| JP4954086B2 (ja) | 2004-12-08 | 2012-06-13 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー | 1h−ピロロ[2,3−b]ピリジン |
| DE602007004092D1 (de) | 2006-03-22 | 2010-02-11 | Vertex Pharma | C-met-proteinkinasehemmer zur behandlung proliferativer erkrankungen |
| ES2340093T3 (es) | 2006-06-22 | 2010-05-28 | Biovitrum Ab (Publ) | Derivados pirazina y piridina como inhibidores de cinasa mnk. |
| EP1900727A1 (en) | 2006-08-30 | 2008-03-19 | Cellzome Ag | Aminopyridine derivatives as kinase inhibitors |
| GB0619342D0 (en) | 2006-09-30 | 2006-11-08 | Vernalis R&D Ltd | New chemical compounds |
| GB0625659D0 (en) | 2006-12-21 | 2007-01-31 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
| KR100979439B1 (ko) | 2008-04-10 | 2010-09-02 | 한국화학연구원 | 신규 피라졸 및 벤즈옥사졸 치환된 피리딘 유도체 또는이의 약학적으로 허용가능한 염, 이의 제조방법 및 이를유효성분으로 함유하는 이상세포 성장 질환의 예방 및치료용 약학적 조성물 |
-
2008
- 2008-10-22 WO PCT/GB2008/050974 patent/WO2009053737A2/en not_active Ceased
- 2008-10-22 AU AU2008315746A patent/AU2008315746A1/en not_active Abandoned
- 2008-10-22 KR KR1020107011254A patent/KR20100089090A/ko not_active Withdrawn
- 2008-10-22 MX MX2010004491A patent/MX2010004491A/es not_active Application Discontinuation
- 2008-10-22 JP JP2010530561A patent/JP2011500778A/ja active Pending
- 2008-10-22 CA CA2703653A patent/CA2703653A1/en not_active Abandoned
- 2008-10-22 CN CN200880122861XA patent/CN101910158A/zh active Pending
- 2008-10-22 AT AT08841876T patent/ATE523508T1/de not_active IP Right Cessation
- 2008-10-22 EP EP08841876A patent/EP2215085B1/en active Active
- 2008-10-23 US US12/256,739 patent/US8017611B2/en not_active Expired - Fee Related
- 2008-10-24 UY UY31430A patent/UY31430A1/es unknown
- 2008-10-24 TW TW097141072A patent/TW200920367A/zh unknown
- 2008-10-24 AR ARP080104644A patent/AR069078A1/es unknown
- 2008-10-24 PE PE2008001832A patent/PE20091116A1/es not_active Application Discontinuation
- 2008-10-24 CL CL2008003188A patent/CL2008003188A1/es unknown
-
2010
- 2010-04-15 IL IL205108A patent/IL205108A0/en unknown
- 2010-04-29 CO CO10050944A patent/CO6270364A2/es not_active Application Discontinuation
- 2010-05-21 EC EC2010010197A patent/ECSP10010197A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CL2008003188A1 (es) | 2009-11-27 |
| JP2011500778A (ja) | 2011-01-06 |
| IL205108A0 (en) | 2010-11-30 |
| EP2215085A2 (en) | 2010-08-11 |
| ATE523508T1 (de) | 2011-09-15 |
| CA2703653A1 (en) | 2009-04-30 |
| CN101910158A (zh) | 2010-12-08 |
| WO2009053737A3 (en) | 2009-07-30 |
| WO2009053737A2 (en) | 2009-04-30 |
| KR20100089090A (ko) | 2010-08-11 |
| PE20091116A1 (es) | 2009-08-29 |
| AU2008315746A1 (en) | 2009-04-30 |
| CO6270364A2 (es) | 2011-04-20 |
| TW200920367A (en) | 2009-05-16 |
| US20090118305A1 (en) | 2009-05-07 |
| MX2010004491A (es) | 2010-06-21 |
| UY31430A1 (es) | 2009-05-29 |
| EP2215085B1 (en) | 2011-09-07 |
| ECSP10010197A (es) | 2010-06-29 |
| US8017611B2 (en) | 2011-09-13 |
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