AR076928A1 - Derivados de 3h-pirido[4, 3-d]pirimidin-4-ona, un metodo para su preparacion, composiciones farmaceuticas que los comprenden y su uso en la manufactura de un medicamento para el tratamiento o prevencion de enfermedades relacionadas con el estres. - Google Patents
Derivados de 3h-pirido[4, 3-d]pirimidin-4-ona, un metodo para su preparacion, composiciones farmaceuticas que los comprenden y su uso en la manufactura de un medicamento para el tratamiento o prevencion de enfermedades relacionadas con el estres.Info
- Publication number
- AR076928A1 AR076928A1 ARP100101834A ARP100101834A AR076928A1 AR 076928 A1 AR076928 A1 AR 076928A1 AR P100101834 A ARP100101834 A AR P100101834A AR P100101834 A ARP100101834 A AR P100101834A AR 076928 A1 AR076928 A1 AR 076928A1
- Authority
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- Argentina
- Prior art keywords
- group
- lower alkyl
- halogen
- cycloalkyl
- substituted
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 229940126601 medicinal product Drugs 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 230000002265 prevention Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 31
- -1 phenyloxy group Chemical group 0.000 abstract 12
- 125000003545 alkoxy group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 125000002757 morpholinyl group Chemical group 0.000 abstract 3
- 125000004043 oxo group Chemical group O=* 0.000 abstract 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 3
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 3
- 125000003386 piperidinyl group Chemical group 0.000 abstract 3
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 3
- 125000001544 thienyl group Chemical group 0.000 abstract 3
- 125000001425 triazolyl group Chemical group 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000004598 dihydrobenzofuryl group Chemical group O1C(CC2=C1C=CC=C2)* 0.000 abstract 2
- 125000002541 furyl group Chemical group 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000005059 halophenyl group Chemical group 0.000 abstract 2
- 125000002883 imidazolyl group Chemical group 0.000 abstract 2
- 125000002971 oxazolyl group Chemical group 0.000 abstract 2
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 2
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 2
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 2
- 125000000335 thiazolyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 abstract 1
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 1
- 125000004946 alkenylalkyl group Chemical group 0.000 abstract 1
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000006383 alkylpyridyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000002047 benzodioxolyl group Chemical group O1OC(C2=C1C=CC=C2)* 0.000 abstract 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000005169 cycloalkylcarbonylamino group Chemical group 0.000 abstract 1
- 125000005434 dihydrobenzoxazinyl group Chemical group O1N(CCC2=C1C=CC=C2)* 0.000 abstract 1
- 125000005435 dihydrobenzoxazolyl group Chemical group O1C(NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004639 dihydroindenyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000004925 dihydropyridyl group Chemical group N1(CC=CC=C1)* 0.000 abstract 1
- 125000005053 dihydropyrimidinyl group Chemical group N1(CN=CC=C1)* 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000005945 imidazopyridyl group Chemical group 0.000 abstract 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 abstract 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 abstract 1
- 125000005956 isoquinolyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000002098 pyridazinyl group Chemical group 0.000 abstract 1
- 125000005554 pyridyloxy group Chemical group 0.000 abstract 1
- 125000005493 quinolyl group Chemical group 0.000 abstract 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000005886 tetrahydrobenzothienyl group Chemical group 0.000 abstract 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 abstract 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 abstract 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 abstract 1
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 1
- 125000001113 thiadiazolyl group Chemical group 0.000 abstract 1
- 125000001984 thiazolidinyl group Chemical group 0.000 abstract 1
- 125000004588 thienopyridyl group Chemical group S1C(=CC2=C1C=CC=N2)* 0.000 abstract 1
- 125000005505 thiomorpholino group Chemical group 0.000 abstract 1
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 abstract 1
Classifications
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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Abstract
Estos compuestos son utilizados en el tratamiento del estrés y además se proveen un método para su produccion. Reivindicacion 1: Un compuesto heterocíclico caracterizado por la formula general [1] donde, R1 y R2 cada uno en forma independiente representan hidrogeno; un grupo fenilalquilo inferior que puede tener uno o más sustituyente(s) seleccionado/s del grupo que consiste de un grupo alquilo inferior, un grupo alcoxi inferior, halogeno, un grupo alquilo inferior sustituido con halogeno, un grupo alcoxi inferior sustituido con halogeno, un grupo cicloalquilo C3-8 y un grupo ciano, en un anillo benceno y/o en un grupo alquilo inferior; un grupo cicloalquil alquilo C3-8 inferior; un grupo cicloalquilo C3-8 que puede tener uno o más grupo(s) halofenilo; o R1 y R2 pueden formar un anillo pirrolidino junto con el nitrogeno adyacente a R1 y R2 y el anillo pirrolidino puede tener uno o más sustituyente(s) seleccionado/s del grupo que consiste de un grupo halofenilo y un grupo fenilo que presenta un grupo alquilo inferior sustituido con halogeno; R3 representa un grupo alquinilo inferior; un grupo amino que puede tener uno o más grupo(s) alquilo inferior; un grupo alcoxi inferior; un grupo piperazinilo que puede tener uno o más grupo(s) alquilo inferior; un grupo feniloxi; un grupo morfolinilo o un grupo pirrolidinilo; R4 representa cualquiera de los grupos representados por los siguientes (1) a (91): (1) un grupo fenilo; (2) un grupo naftilo; (3) un grupo dihidroindenilo; (4) un grupo fenilalquilo inferior; (5) un grupo piridilo; (6) un grupo piridazinilo; (7) un grupo triazolilo; (8) un grupo pirimidinilo; (9) un grupo imidazolilo; (10) un grupo dihidropiridilo; (11) un grupo quinolilo; (12) un grupo isoquinolilo; (13) un grupo tetrahidroquinolilo; (14) un grupo dihidroquinolilo; (15) un grupo imidazopiridilo; (16) un grupo pirazolopiridilo; (17) un grupo indolinilo; (18) un grupo naftiridinilo; (19) un grupo benzoimidazolilo; (20) un grupo indolizinilo; (21) un grupo tienilo; (22) un grupo benzotienilo; (23) un grupo benzodioxolilo; (24) un grupo benzofurilo; (25) un grupo tienopiridilo; (26) un grupo tienopirrolilo; (27) un grupo dihidrobenzotiazinilo; (28) un grupo isoxazolilo; (29) un grupo tetrahidrobenzoxazepinilo; (30) un grupo indolilo; (31) un grupo benzotiazolilo; (32) un grupo dihidrotienodioxinilo; (33) un grupo pirrolidinilo; (34) un grupo dihidrobenzoxazinilo; (35) un grupo tetrahidroquinazolinilo; (36) un grupo tetrahidroquinoxalinilo; (37) un grupo dihidrobenzodioxinilo; (38) un grupo cromanilo; (39) un grupo dihidropiridooxazinilo; (40) un grupo tetrahidronaftilo; (41) un grupo dihidrobenzofurilo; (42) un grupo dihidrobenzoxazolilo; (43) un grupo tetrahidrobenzotienilo; (44) un grupo tetrahidrociclopentapirazolilo; (45) un grupo benzotriazolilo; (46) un grupo dihidrobenzoimidazolilo; (47) un grupo dihidrobenzotiazolilo; (48) un grupo isoindolinilo; (49) un grupo tetrahidrobenzodiazepinilo; (50) un grupo dihidrobenzodioxepinilo; (51) un grupo quinoxalinilo; (52) un grupo indazolilo; (53) un grupo cinolinilo; (54) un grupo dihidroftalazinilo; (55) un grupo dihidronaftiridinilo; (56) un grupo hexahidroquinolinilo; (57) un grupo furopirrolilo; (58) un grupo tienopirazinilo; (59) un grupo imidazotiazolilo; (60) un grupo xantenilo; (61) un grupo piperidinilo; (62) un grupo pirrolilo; (63) un grupo pirazolilo; (64) un grupo tiazolilo; (65) un grupo furilo; (66) un grupo pirazinilo; (67) un grupo dihidropirazolilo; (68) un grupo tiazolidinilo; (69) un grupo tetrahidrofuranilo; (70) un grupo tetrahidropiranilo; (71) un grupo tiadiazolilo; (72) un grupo dihidropiridazinilo; (73) un grupo tienil alquilo inferior; (74) un grupo cicloalquilo C3-8; (75) un grupo alquilo inferior; (76) un grupo benzodioxoliloxi; (77) un grupo feniltio alquilo inferior; (78) un grupo fenil-cicloalquilo C3-8; (79) un grupo fenoxi alquilo inferior; (80) un grupo fenilo alquenilo inferior; (81) un grupo ciclo alquilo C3-8 alquenilo inferior; (82) un grupo piridil alquilo inferior; (83) un grupo benzofurilo alquenilo inferior; (84) un grupo dihidrobenzofurilo alquenilo inferior; (85) un grupo dihidrobenzodioxinilo alquenilo inferior; (86) un grupo dihidrobenzodioxiniloxi alquilo inferior; (87) un grupo oxazolilo; (88) un grupo dihidroindeniloxi alquilo inferior; (89) un grupo dihidropirimidinilo; (90) un grupo piridiloxi alquilo inferior; (91) un grupo alcoxi inferior alquilo inferior; donde en el grupo alquilo inferior, el anillo cicloalquilo, el anillo aromático o en el anillo heterocíclico, pueden existir uno o más sustituyente(s) seleccionados de los siguientes (1-1) a (1-46): (1-1) un átomo de halogeno; (1-2) un grupo alquilo inferior; (1-3) un grupo alcanoilo inferior; (1-4) un grupo alquilo inferior sustituido con halogeno; (1-5) un grupo alcoxi inferior sustituido con halogeno; (1-6) un grupo ciano; (1-7) un grupo alcoxi inferior; (1-8) un grupo inferior alquiltio; (1-9) un grupo imidazolilo que puede tener uno o más grupo(s) alquilo inferior; (1-10) un grupo oxazolilo; (1-11) un grupo oxadiazolilo que puede tener uno o más grupo(s) alquilo inferior; (1-12) un grupo triazolilo; (1-13) un grupo benzoilo; (1-14) un grupo piridilo; (1-15) un grupo oxo; (1-16) un grupo fenilo que puede tener uno o más sustituyente(s) seleccionado/s del grupo que consiste de un grupo alquilo inferior, un grupo alcoxi inferior sustituido con halogeno, un grupo alquilo inferior sustituido con halogeno y un átomo de halogeno; (1-17) un grupo tienilo; (1-18) un grupo furilo; (1-19) un grupo tiazolilo; (1-20) un grupo triazolil alquilo inferior; (1-21) un grupo ciclo alquiloxi C3-8; (1-22) un grupo fenilalquilo inferior; (1-23) un grupo fenoxi; (1-24) un grupo cicloalquilo C3-8; (1-25) un grupo pirazolilo; (1-26) un grupo pirrolilo; (1-27) un grupo alquenilo inferior; (1-28) un grupo pirrolidinilo que puede tener uno o más grupos oxo; (1-29) un grupo dihidropirazolilo que puede tener uno o más sustituyente(s) seleccionado/s del grupo que consiste de un grupo oxo y un grupo alquilo inferior; (1-30) un grupo hidroxi; (1-31) un grupo tetrazolilo; (1-32) un grupo morfolinilo; (1-33) un grupo pirimidinilo; (1-34) un grupo homo-piperazinilo que puede tener uno o más grupo(s) alquilo inferior; (1-35) un grupo alcanoilamino inferior; (1-36) un grupo cicloalquilcarbonilamino C3-8; (1-37) un grupo fenoxi alquilo inferior; (1-38) un grupo tiomorfolino; (1-39) un grupo piperidinilo; (1-40) un grupo alcoxi inferior alquilo inferior; (1-41) un grupo amino que puede tener uno o más sustituyente(s) seleccionado/s del grupo que consiste de un grupo alquilo inferior, un grupo alcanoilo inferior y un grupo cicloalquilo C3-8; (1-42) un grupo morfolinil alquilo inferior; (1-43) un grupo piperidinil alquilo inferior; (1-44) un grupo alquilsulfonilo inferior; (1-45) un grupo adamantil alquilo inferior; (1-46) un grupo carbamoilo que puede tener uno o más grupo(s) alquilo inferior; o una sal de los mismos.
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| JP2009129002 | 2009-05-28 |
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| ES (1) | ES2430663T3 (es) |
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| EP2576536B1 (en) * | 2010-06-01 | 2016-09-14 | The University of Queensland | Haematopoietic-prostaglandin d2 synthase inhibitors |
| EP2642998B1 (en) | 2010-11-24 | 2020-09-16 | The Trustees of Columbia University in the City of New York | A non-retinoid rbp4 antagonist for treatment of age-related macular degeneration and stargardt disease |
| WO2013166037A1 (en) | 2012-05-01 | 2013-11-07 | The Trustees Of Columbia University In The City Of New York | Non-retinoid antagonists for treatment of eye disorders |
| WO2014151936A1 (en) | 2013-03-14 | 2014-09-25 | The Trustees Of Columbia University In The City Of New York | Octahydropyrrolopyrroles, their preparation and use |
| WO2014151959A1 (en) | 2013-03-14 | 2014-09-25 | The Trustees Of Columbia University In The City Of New York | N-alkyl-2-phenoxyethanamines, their preparation and use |
| EP2968303B1 (en) | 2013-03-14 | 2018-07-04 | The Trustees of Columbia University in the City of New York | Octahydrocyclopentapyrroles, their preparation and use |
| EP2968304B1 (en) | 2013-03-14 | 2018-10-10 | The Trustees of Columbia University in the City of New York | 4-phenylpiperidines, their preparation and use |
| SG11201608943VA (en) | 2014-04-30 | 2016-11-29 | Univ Columbia | Substituted 4-phenylpiperidines, their preparaiton and use |
| ES2838573T3 (es) * | 2014-08-21 | 2021-07-02 | Bristol Myers Squibb Co | Derivados de benzamida ligados como inhibidores potentes de ROCK |
| JP7471818B2 (ja) | 2016-08-18 | 2024-04-22 | ヴィダック ファーマ リミテッド | ピペラジン誘導体、医薬組成物、及びその使用方法 |
| EP3765459A1 (en) | 2018-03-13 | 2021-01-20 | Shire Human Genetic Therapies, Inc. | Substituted imidazopyridines as inhibitors of plasma kallikrein and uses thereof |
| HRP20240793T1 (hr) | 2018-04-18 | 2024-09-13 | Constellation Pharmaceuticals, Inc. | Modulatori enzima koji modificiraju metil, njihovi pripravci i upotreba |
| CN112262143A (zh) | 2018-05-21 | 2021-01-22 | 星座制药公司 | 甲基修饰酶的调节剂、其组合物和用途 |
| PH12022550188A1 (en) | 2019-07-24 | 2022-11-21 | Constellation Pharmaceuticals Inc | Crystalline forms of 7-chloro-2-(4-(3-methoxyazetidin-1-yl)cyclohexyl)-2,4-dimethyl-n-((6-methyl-4-(methylthio)-2-oxo-1,2-dihydropyridin-3-yl)methyl)benzo[d][1,3]dioxole-5-carboxamide |
| JP7695232B2 (ja) | 2019-09-18 | 2025-06-18 | 武田薬品工業株式会社 | ヘテロアリール血漿カリクレインインヒビター |
| US11787796B2 (en) | 2019-09-18 | 2023-10-17 | Takeda Pharmaceutical Company Limited | Plasma Kallikrein inhibitors and uses thereof |
| CN113912622B (zh) * | 2020-07-10 | 2023-12-01 | 上海纽思克生物科技有限公司 | 三环嘧啶酮类化合物、其制备方法、其组合物和用途 |
| AU2024264196A1 (en) * | 2023-04-28 | 2025-11-27 | Pharmaengine, Inc. | Mta-cooperative prmt5 inhibitor |
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| US6383764B1 (en) | 2000-04-28 | 2002-05-07 | The Regents Of The University Of California | Methods of identifying compounds for controlling absence seizures in a mammal relating to prolactin-releasing peptide(PrRP) |
| WO2004014909A1 (en) * | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Fused tetrahydropyridine derivatives as matrix metalloproteinase inhibitors |
| US20040216177A1 (en) | 2003-04-25 | 2004-10-28 | Otsuka Pharmaceutical Co., Ltd. | Congenic rats containing a mutant GPR10 gene |
| WO2005025293A2 (en) * | 2003-09-10 | 2005-03-24 | Icagen, Inc. | Fused ring heterocycles as potassium channel modulators |
| DE102004020908A1 (de) | 2004-04-28 | 2005-11-17 | Grünenthal GmbH | Substituierte 5,6,7,8,-Tetrahydro-pyrido[4,3-d]pyrimidin-2-yl- und 5,6,7,8,-Tetrahydro-chinazolin-2-yl-Verbindungen |
| GB0506147D0 (en) * | 2005-03-24 | 2005-05-04 | Merck Sharp & Dohme | Therapeutic agents |
| JPWO2008038768A1 (ja) * | 2006-09-28 | 2010-01-28 | 大日本住友製薬株式会社 | 二環性ピリミジン構造を有する化合物及びそれを含有する医薬組成物 |
| JP2010524941A (ja) * | 2007-04-20 | 2010-07-22 | シェーリング コーポレイション | ピリミジノン誘導体およびそれらの使用方法 |
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| EP2435046A1 (en) | 2012-04-04 |
| US20120065189A1 (en) | 2012-03-15 |
| EP2435046B1 (en) | 2013-09-04 |
| TW201109327A (en) | 2011-03-16 |
| ES2430663T3 (es) | 2013-11-21 |
| JP5624560B2 (ja) | 2014-11-12 |
| JP2012528076A (ja) | 2012-11-12 |
| US9206173B2 (en) | 2015-12-08 |
| WO2010137738A1 (en) | 2010-12-02 |
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