AR035913A1 - Imidazopiridinas sustituidas con fenilo, composiciones que las comprenden y uso de las mismas para la manufactura de medicamentos - Google Patents
Imidazopiridinas sustituidas con fenilo, composiciones que las comprenden y uso de las mismas para la manufactura de medicamentosInfo
- Publication number
- AR035913A1 AR035913A1 ARP010101555A ARP010101555A AR035913A1 AR 035913 A1 AR035913 A1 AR 035913A1 AR P010101555 A ARP010101555 A AR P010101555A AR P010101555 A ARP010101555 A AR P010101555A AR 035913 A1 AR035913 A1 AR 035913A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- phenyl
- alkoxy
- halo
- carbon
- Prior art date
Links
- 239000003814 drug Substances 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- -1 heterocyclic radical Chemical class 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 239000011203 carbon fibre reinforced carbon Substances 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000004857 imidazopyridinyl group Chemical group N1C(=NC2=C1C=CC=N2)* 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 abstract 2
- 150000001408 amides Chemical class 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 150000004677 hydrates Chemical class 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 abstract 1
- 125000006591 (C2-C6) alkynylene group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- 102000000543 Histamine Receptors Human genes 0.000 abstract 1
- 108010002059 Histamine Receptors Proteins 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/12—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Hospice & Palliative Care (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Addiction (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Imidazopiridinas sustituidas con fenilo o sales farmacéuticamente aceptables, amidas, ésteres o hidratos de las mismas que son útiles para el tratamiento y/o prevención de trastornos y condiciones mediados por el receptor H3 de histamina. Tales imidazopiridinas sustituidas con fenilo tienen la fórmula (1) en donde ambas líneas de rayas son un enlace doble carbono-carbono, o ambas están ausentes; R3 es H, alquilo C1-6 fenilo o bencilo, cada uno de R5, R6, R7 y R8 es independientemente H, alquilo C1-6, alcoxi C1-6, halo o amino; uno de Ra, Rb, Rc, Rd, y Re es -WYZ y los otros se seleccionan independientemente entre H, alquilo C1-6, alcoxi C1-6, halo y amino; W es R9, O-R9, NR10, -(CO)(O)R9, -N(R10)SO2-R9, -O(CO)R9, -(CO)R9, -(CO)NR10, o -N(R10)-CO-R9, en donde R9 es alquileno C1-6, alquinileno C2-6, alquenileno C2-6, fenileno o radical bivalente heterocíclico C2-5 y R10 es H, alquilo C1-6, alquinilo C2-6, alquenilo C2-6, fenilo o radical heterocíclico C2-5; Y está ausente, alquilo C1-6, alquinilo C2-6 alquenilo C2-6 o alcoxi C1-6; Z es radical heterocíclico C2-8 con por lo menos un átomo de nitrógeno básico en el anillo, optativamente incluyendo en el anillo hasta 3 heteroátomos adicionales o porciones independientemente seleccionadas entre O, C=O, N, NH, NG, S, SO, y SO2 en donde G es R15, COR15, COOR15, SO2R15, SO2N o CSR15; o Z es NR11R12 donde cada uno de R11 y R12 es independientemente seleccionado entre H, alquilo C1-6, fenilo, bencilo, cicloalquilo C3-8 y radical heterociclico C2-5; y R15 es alquilo C1-6, alquinilo C2-6, alquenilo C2-6, cicloalquilo C3-7, o cicloalquenilo C4-7, siempre que donde Rc es WNR11R12, cada uno de R11 y R12 se selecciona independientemente entre alquilo C1-6, entonces por lo menos uno de los siguientes es verdadero: Rb o Rd es alquilo, alcoxi, amino, o halo; las líneas de rayas representan un doble enlace carbono-carbono o están ausentes; Ra o Re es alquilo, alcoxi, amino o halo; o W es -R9-; -NR10-, (CO)(O)R9-, -O(CO)R9, -(CO)NHR9-, ó -N(R10)(CO)R9-; y además siempre que cada uno de Ra, Rb, Rd y Re es H y W es un alcoxi insustituido, de cadena recta, entonces por lo menos uno de los siguientes es verdadero: Z es cíclico; las líneas de rayas representan un doble enlace carbono-carbono o están ausentes; o R7 o R8 es alquilo, alcoxi, halo, o amino; y cada uno de los grupos hidrocarbilo o heterocíclico antes mencionado es optativamente sustituido con entre 1 y 3 sustituyentes seleccionados entre alquilo C1-3 halo, hidroxi, radical heterocíclico C2-5, fenilo y fenil(alquilo C1-3); y en donde cada uno de los grupos heterocíclicos antes mencionados puede estar adherido al resto de la molécula por un átomo de carbono o un heteroátomo. Se describen también composiciones farmacéuticas que las comprenden y uso de las imidazopiridinas sustituidas con fenilo o sales farmacéuticamente aceptables, amidas, ésteres o hidratos de las mismas para la manufactura de medicamentos.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19407100P | 2000-03-31 | 2000-03-31 | |
US27212101P | 2001-02-28 | 2001-02-28 | |
US09/821,244 US6908929B2 (en) | 2000-03-31 | 2001-03-29 | Phenyl-substituted imidazopyridines |
Publications (1)
Publication Number | Publication Date |
---|---|
AR035913A1 true AR035913A1 (es) | 2004-07-28 |
Family
ID=26889666
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP010101555A AR035913A1 (es) | 2000-03-31 | 2001-03-30 | Imidazopiridinas sustituidas con fenilo, composiciones que las comprenden y uso de las mismas para la manufactura de medicamentos |
Country Status (8)
Country | Link |
---|---|
US (6) | US6908929B2 (es) |
EP (1) | EP1268478B1 (es) |
AR (1) | AR035913A1 (es) |
AT (1) | ATE361297T1 (es) |
AU (1) | AU2001249679A1 (es) |
DE (1) | DE60128211T2 (es) |
ES (1) | ES2286114T3 (es) |
WO (1) | WO2001074815A2 (es) |
Families Citing this family (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE9902987D0 (sv) * | 1999-08-24 | 1999-08-24 | Astra Pharma Prod | Novel compounds |
WO2001074813A2 (en) * | 2000-03-31 | 2001-10-11 | Ortho Mcneil Pharmaceutical, Inc. | METHOD FOR USING 2- OR 3-ARYL SUBSTITUTED IMIDAZO[1,2-a] PYRIDINES AS H3 ANTAGONISTS |
EP1268478B1 (en) | 2000-03-31 | 2007-05-02 | Ortho-McNeil Pharmaceutical, Inc. | Phenyl-substituted imidazopyridines |
US6620839B2 (en) * | 2000-07-13 | 2003-09-16 | Abbott Laboratories | 1,3-disubstituted and 1,3,3-trisubstituted pyrrolidines as histamine-3 receptor ligands and their therapeutic applications |
US6596731B2 (en) | 2001-03-27 | 2003-07-22 | Hoffmann-La Roche Inc. | Substituted imidazo[1,2-A] pyridine derivatives |
US7208497B2 (en) | 2001-07-02 | 2007-04-24 | Novo Nordisk A/S | Substituted piperazines and diazepanes |
WO2003024928A2 (en) | 2001-09-14 | 2003-03-27 | Novo Nordisk A/S | Novel aminoazetidine, -pyrrolidine and -piperidine derivatives |
US6673829B2 (en) | 2001-09-14 | 2004-01-06 | Novo Nordisk A/S | Aminoazetidine,-pyrrolidine and -piperidine derivatives |
DE10247271A1 (de) * | 2002-10-10 | 2004-08-26 | Grünenthal GmbH | Substituierte C-Imidazo[1,2-a]pyridin-3-yle |
US7645756B2 (en) * | 2004-02-18 | 2010-01-12 | Banyu Pharmaceutical Co. Ltd. | Nitrogenous fused heteroaromatic ring derivative |
US7618981B2 (en) * | 2004-05-06 | 2009-11-17 | Cytokinetics, Inc. | Imidazopyridinyl-benzamide anti-cancer agents |
US7795448B2 (en) * | 2004-05-06 | 2010-09-14 | Cytokinetics, Incorporated | Imidazoyl-benzamide anti-cancer agents |
US7504413B2 (en) * | 2004-05-06 | 2009-03-17 | Cytokinetics, Inc. | N-(4-(imidazo[1,2A]pyridin-YL)phenethyl)benzamide inhibitors of the mitotic kinesin CENP-E for treating certain cellular proliferation diseases |
EP1634598A1 (en) * | 2004-09-07 | 2006-03-15 | Laboratorios Del Dr. Esteve, S.A. | Use of piperazine derivatives and analogues for the manufacture of a medicament for the prophylaxis and/or treatment of disorders of food ingestion |
EP1717235A3 (en) * | 2005-04-29 | 2007-02-28 | Bioprojet | Phenoxypropylpiperidines and -pyrrolidines and their use as histamine H3-receptor ligands |
EP1717233A1 (en) | 2005-04-29 | 2006-11-02 | Bioprojet | Histamine H3-receptor ligands and their therapeutic application |
EP1717234A1 (en) * | 2005-04-29 | 2006-11-02 | Bioprojet | Phenoxypropylpiperidines and -pyrrolidines and their use as histamine H3-receptor ligands |
JP5121707B2 (ja) | 2005-07-04 | 2013-01-16 | ハイ ポイント ファーマシューティカルズ,エルエルシー | 新規医薬 |
AR056690A1 (es) * | 2005-10-14 | 2007-10-17 | Athersys Inc | Derivados de indol como inhibidores de indol como inhibidores del receptor 3 de histamina para el tartamiento de trastornos del sueno y cognitivos obesidad y otros trastornos de snc |
JP2009514865A (ja) * | 2005-11-02 | 2009-04-09 | サイトキネティクス・インコーポレーテッド | 有糸分裂キネシン阻害剤 |
RU2008150377A (ru) | 2006-05-19 | 2010-06-27 | Нихон Меди-Физикс Ко., Лтд. (Jp) | Новое соединение, обладающее сродством к амилоиду |
CN102295606A (zh) | 2006-05-29 | 2011-12-28 | 高点制药有限责任公司 | 合成3-(1,3-苯并间二氧杂环戊烯-5-基)-6-(4-环丙基哌嗪-1-基)-哒嗪的方法及其适用的中间体 |
TW200811175A (en) * | 2006-06-21 | 2008-03-01 | Nihon Mediphysics Co Ltd | Novel compound with affinity with amyloid |
EP2042501B1 (en) * | 2006-06-21 | 2017-04-12 | Nihon Medi-Physics Co., Ltd. | Compound having affinity for amyloid |
JP5180838B2 (ja) | 2006-11-30 | 2013-04-10 | 日本メジフィジックス株式会社 | 新規アミロイド親和性化合物 |
CL2008000119A1 (es) | 2007-01-16 | 2008-05-16 | Wyeth Corp | Compuestos derivados de pirazol, antagonistas del receptor nicotinico de acetilcolina; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como demencia senil, alzheimer y esquizofrenia. |
ES2421886T3 (es) | 2007-02-13 | 2013-09-06 | Nihon Mediphysics Co Ltd | Método para producción de un agente de representación de imágenes de diagnóstico por radiación |
EP2014656A3 (en) | 2007-06-11 | 2011-08-24 | High Point Pharmaceuticals, LLC | New heteocyclic h3 antagonists |
ATE503757T1 (de) * | 2007-08-14 | 2011-04-15 | Bayer Schering Pharma Ag | Kondensierte imidazole zur krebsbehandlung |
EP2062893A1 (en) * | 2007-10-18 | 2009-05-27 | Bayer Schering Pharma AG | Fused imidazoles for cancer treatment |
EP2213672A4 (en) * | 2007-10-24 | 2012-05-02 | Nihon Mediphysics Co Ltd | NEW CONNECTION WITH AFFINITY TO AMYLOID |
EP2213671A4 (en) * | 2007-10-26 | 2012-02-22 | Nihon Mediphysics Co Ltd | NOVEL COMPOUND HAVING AFFINITY FOR AMYLOID |
FR2928923B1 (fr) * | 2008-03-21 | 2010-04-23 | Sanofi Aventis | Derives polysubstitues de 2-heteroaryl-6-phenyl-imidazo °1,2-a!pyridines, leur preparation et leur application en therapeutiques |
CN101602687A (zh) * | 2008-06-13 | 2009-12-16 | 上海特化医药科技有限公司 | 6-硝基苯乙酮类化合物、其制备方法及用途 |
US20120172350A1 (en) * | 2009-09-11 | 2012-07-05 | Sunovion Pharmaceuticals Inc. | Histamine h3 inverse agonists and antagonists and methods of use thereof |
PT2694510E (pt) | 2011-04-07 | 2016-02-08 | Bayer Pharma AG | Imidazopiridazinas como inibidores da akt quinase |
WO2013151982A1 (en) | 2012-04-03 | 2013-10-10 | Arena Pharmaceuticals, Inc. | Methods and compounds useful in treating pruritus, and methods for identifying such compounds |
CN103641827B (zh) * | 2013-12-10 | 2015-04-29 | 广西师范大学 | 中氮茚衍生物及其合成方法和应用 |
CN104610255B (zh) * | 2015-01-28 | 2017-01-18 | 常州工程职业技术学院 | 含有异噁唑骨架的[1,2‑a]咪唑并吡啶类衍生物的合成方法 |
ES2928164T3 (es) | 2015-10-19 | 2022-11-15 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
MY199220A (en) | 2015-11-19 | 2023-10-20 | Incyte Corp | Heterocyclic compounds as immunomodulators |
BR112018012756A2 (pt) | 2015-12-22 | 2018-12-04 | Incyte Corp | compostos heterocíclicos como imunomoduladores |
TW201808950A (zh) | 2016-05-06 | 2018-03-16 | 英塞特公司 | 作為免疫調節劑之雜環化合物 |
ES2905980T3 (es) | 2016-05-26 | 2022-04-12 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
SG10202012828TA (en) | 2016-06-20 | 2021-01-28 | Incyte Corp | Heterocyclic compounds as immunomodulators |
MA45669A (fr) | 2016-07-14 | 2019-05-22 | Incyte Corp | Composés hétérocycliques utilisés comme immunomodulateurs |
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JPS5910675B2 (ja) * | 1976-03-22 | 1984-03-10 | ウェルファイド株式会社 | アラルキルアミン誘導体 |
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-
2001
- 2001-03-29 EP EP01922930A patent/EP1268478B1/en not_active Expired - Lifetime
- 2001-03-29 ES ES01922930T patent/ES2286114T3/es not_active Expired - Lifetime
- 2001-03-29 AU AU2001249679A patent/AU2001249679A1/en not_active Abandoned
- 2001-03-29 AT AT01922930T patent/ATE361297T1/de not_active IP Right Cessation
- 2001-03-29 DE DE60128211T patent/DE60128211T2/de not_active Expired - Lifetime
- 2001-03-29 US US09/821,244 patent/US6908929B2/en not_active Expired - Lifetime
- 2001-03-29 WO PCT/US2001/010333 patent/WO2001074815A2/en active IP Right Grant
- 2001-03-30 AR ARP010101555A patent/AR035913A1/es active IP Right Grant
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2004
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- 2004-10-07 US US10/960,363 patent/US7041828B2/en not_active Expired - Lifetime
- 2004-10-07 US US10/960,200 patent/US7041827B2/en not_active Expired - Lifetime
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WO2001074815A2 (en) | 2001-10-11 |
ATE361297T1 (de) | 2007-05-15 |
DE60128211T2 (de) | 2008-01-10 |
DE60128211D1 (de) | 2007-06-14 |
US7087757B2 (en) | 2006-08-08 |
US7041828B2 (en) | 2006-05-09 |
EP1268478B1 (en) | 2007-05-02 |
EP1268478A2 (en) | 2003-01-02 |
US20020006934A1 (en) | 2002-01-17 |
AU2001249679A1 (en) | 2001-10-15 |
WO2001074815A3 (en) | 2002-04-04 |
US20050090523A1 (en) | 2005-04-28 |
ES2286114T3 (es) | 2007-12-01 |
US20050043348A1 (en) | 2005-02-24 |
US20050049277A1 (en) | 2005-03-03 |
US7041827B2 (en) | 2006-05-09 |
US20050085502A1 (en) | 2005-04-21 |
US20050085501A1 (en) | 2005-04-21 |
US6908929B2 (en) | 2005-06-21 |
US7199117B2 (en) | 2007-04-03 |
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