AR051802A1 - Heterociclos antagonistas de mchr1 - Google Patents
Heterociclos antagonistas de mchr1Info
- Publication number
- AR051802A1 AR051802A1 ARP050105335A ARP050105335A AR051802A1 AR 051802 A1 AR051802 A1 AR 051802A1 AR P050105335 A ARP050105335 A AR P050105335A AR P050105335 A ARP050105335 A AR P050105335A AR 051802 A1 AR051802 A1 AR 051802A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- alkyl group
- fluorine
- group
- benzofurane
- Prior art date
Links
- 101000581402 Homo sapiens Melanin-concentrating hormone receptor 1 Proteins 0.000 title 1
- 102100027375 Melanin-concentrating hormone receptor 1 Human genes 0.000 title 1
- 239000005557 antagonist Substances 0.000 title 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 13
- 239000011737 fluorine Substances 0.000 abstract 12
- 125000001153 fluoro group Chemical group F* 0.000 abstract 11
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 10
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000002757 morpholinyl group Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000003386 piperidinyl group Chemical group 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 2
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000002393 azetidinyl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 125000004193 piperazinyl group Chemical group 0.000 abstract 2
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 2
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 2
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 2
- 125000003003 spiro group Chemical group 0.000 abstract 2
- 125000004853 tetrahydropyridinyl group Chemical group N1(CCCC=C1)* 0.000 abstract 2
- 125000001113 thiadiazolyl group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- 125000005871 1,3-benzodioxolyl group Chemical group 0.000 abstract 1
- 125000005962 1,4-oxazepanyl group Chemical group 0.000 abstract 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000005330 8 membered heterocyclic group Chemical group 0.000 abstract 1
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 206010012289 Dementia Diseases 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 208000023105 Huntington disease Diseases 0.000 abstract 1
- 208000026139 Memory disease Diseases 0.000 abstract 1
- 208000012902 Nervous system disease Diseases 0.000 abstract 1
- 208000025966 Neurological disease Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 208000002193 Pain Diseases 0.000 abstract 1
- 208000018737 Parkinson disease Diseases 0.000 abstract 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 208000010877 cognitive disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 206010015037 epilepsy Diseases 0.000 abstract 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 125000005956 isoquinolyl group Chemical group 0.000 abstract 1
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 201000006417 multiple sclerosis Diseases 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- -1 phenoxy, 2-pyridyl Chemical group 0.000 abstract 1
- 208000020016 psychiatric disease Diseases 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000002098 pyridazinyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 201000000980 schizophrenia Diseases 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
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- 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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-
- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/00—Drugs for disorders of the nervous system
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
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- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61P9/00—Drugs for disorders of the cardiovascular system
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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
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- 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
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Addiction (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Psychology (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Child & Adolescent Psychology (AREA)
- Cardiology (AREA)
- Reproductive Health (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Los compuestos de formula (1), procesos para preparar tales compuestos, su utilizacion en el tratamiento de la obesidad, trastornos siquiátricos, trastornos cognitivos, trastornos de la memoria, esquizofrenia, epilepsia y afecciones relacionadas, y trastornos neurologicos tales como demencia, esclerosis multiple, mal de Parkinson, corea de Huntington y mal de Alzheimer y trastornos relacionados con el dolor y a composiciones farmacéuticas que los contienen. Reivindicacion 1: Un compuesto de formula (1), A representa N, un grupo alquilo C1-4, un grupo alquenilo C2-4, cicloalquilo C3-8, adamantilo, azetidinilo, pirrolidinilo, piperidinilo, piperazinilo, morfolinilo, 1,3-oxazidinilo, tetrahidro-piridinilo, o espiro[inden-1,4'- piperidinilo]; donde dicho grupo alquilo C1-4 o grupo alquenilo C2-4 está opcionalmente sustituido con uno o más fluor; X representa un enlace o NR3; donde A y X ambos no presentan nitrogeno; donde cuando A es azetidinilo, 1,3-oxazidinilo, pirrolidinilo, piperidinilo, piperazinilo, morfolinilo, tetrahidropiridinilo, o espiro[1,4'-piperidinilo]; el átomo de nitrogeno en A está directamente unido a C(O); R1 y R2 representan independientemente H, alquilo C1-6, un grupo alquenilo C2-6, cicloalquilo C3-10, CONRaRb en el cual Ra y Rb representan independientemente H, un grupo alquilo C1-4 o Ra y Rb, junto con el nitrogeno al cual están unidos, forman un anillo heterocíclico de 4 a 8 miembros; fenilo o naftilo; o un grupo heterocíclico seleccionado entre pirrolilo, imidazolilo, furilo, tienilo, tiazolilo, isotiazolilo, tiadiazolilo, pirazolilo, oxazolilo, isoxazolilo, piridilo, pirazinilo, pirimidinilo, piridazinilo, quinolinilo, isoquinolilo, quinazolilo, indolilo, benzofuranilo, benzo[b]tienilo, benzimidazolilo, benzotiazolilo, 1,4-benzodioxinilo, 1,3-benzodioxolilo, piperidinilo, morfolinilo, 1,4-oxazepanilo, o 4,4-dioxotiomorfolinilo; donde R1 o R2 está opcionalmente sustituido con uno o más de los siguientes: ciano; halo; hidroxi; oxo; un grupo alquilo C1-4 opcionalmente sustituido con uno o más fluor; un grupo alcoxi C1-4 opcionalmente sustituido con uno o más fluor; un grupo NCORaRb o CONRaRb en el cual Ra y Rb representan independientemente un grupo alquilo C1-3; un grupo SO2alquiloC1-4, opcionalmente sustituido con uno o más fluor, un grupo arilo o heteroarilo seleccionado entre tiadiazolilo, pirazolilo, fenilo, fenoxi, 2-piridilo o 3-piridilo donde dicho grupo arilo o heteroarilo puede estar opcionalmente adicionalmente sustituido con uno o más de los siguientes; ciano; halo; hidroxi; un grupo alquilo C1-4 opcionalmente sustituido con uno o más fluor; un grupo alcoxi C1-4 opcionalmente sustituido con uno o más fluor; un grupo NCORaRb o CONRaRb en el que Ra y Rb representan independientemente un grupo alquilo C1-3; un grupo SO2alquiloC1-4, opcionalmente sustituido con uno o más fluor; R1 y/o R2 está unido opcionalmente a A por medio de oxígeno o por medio de un grupo alquilo C1-4, donde uno de los átomos de carbono en dicho grupo alquilo C1-4 opcionalmente se reemplaza con un átomo de oxígeno; Y representa NR3, C(R5R6) o un enlace; donde al menos uno de A, X o Y es N, NR3 o un anillo heterocíclico que contiene nitrogeno; R3, R5 y R6 representan independientemente H o un grupo alquilo C1-4, D representa (CH2)n, donde n es 0 o 1 y E representa (CH2)m, donde m es 0 o 1; R4 representa H o, cuando m y n ambos son 1, R4 representa H o F; Z representa 2,5-tienilo, 2,5-furilo, o pirrolilo, opcionalmente sustituido con uno o más de los siguientes: ciano, halo, un grupo alquilo C1-4 opcionalmente sustituido con uno o más fluor, un grupo alcoxi C1-4 opcionalmente sustituido con uno o más fluor; W representa fenilo, 2-piridilo o 3-piridilo cada uno de los cuales está opcionalmente sustituido con uno o más de los siguientes: ciano, halo, un grupo alquilo C1-4 opcionalmente sustituido con uno o más fluor, un grupo alcoxi C1-4 opcionalmente sustituido con uno o más fluor; un grupo trifluormetilsulfonilo o un grupo 2,2'-difluor-oxolanilo (fusionado con dos átomos de carbono aromáticos adyacentes en W); así como también sus tautomeros, isomeros opticos y sus racematos así como también sus sales farmacéuticamente aceptables; con la condicion de que cuando Y representa NR3 entonces A-X no representa OCH2, CH2CH2 o CH=CH, donde cada átomo de carbono puede estar opcionalmente sustituido con 1 o 2 grupos metilo y/o 1 o 2 fluor.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0403119A SE0403119D0 (sv) | 2004-12-21 | 2004-12-21 | Therapeutic agents |
| SE0501686 | 2005-07-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR051802A1 true AR051802A1 (es) | 2007-02-07 |
Family
ID=36602060
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050105335A AR051802A1 (es) | 2004-12-21 | 2005-12-19 | Heterociclos antagonistas de mchr1 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20080306055A1 (es) |
| EP (1) | EP1831194A4 (es) |
| JP (1) | JP2008524325A (es) |
| AR (1) | AR051802A1 (es) |
| TW (1) | TW200635589A (es) |
| WO (1) | WO2006068594A1 (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005063704A1 (ja) * | 2003-12-25 | 2005-07-14 | Ono Pharmaceutical Co., Ltd. | アゼチジン環化合物およびその医薬 |
| WO2010080864A1 (en) * | 2009-01-12 | 2010-07-15 | Array Biopharma Inc. | Piperidine-containing compounds and use thereof |
| SA110310332B1 (ar) * | 2009-05-01 | 2013-12-10 | Astrazeneca Ab | مركبات ميثانون (3 استبدال -ازيتيدين -1-يل )(5- فينيل -1، 3، 4- أوكساديازول -2-يل ) |
| WO2012004588A2 (en) | 2010-07-06 | 2012-01-12 | Astrazeneca Ab | Therapeutic agents 976 |
| WO2012113103A1 (en) | 2011-02-25 | 2012-08-30 | Helsinn Healthcare S.A. | Asymmetric ureas and medical uses thereof |
| WO2012177893A2 (en) | 2011-06-24 | 2012-12-27 | Amgen Inc. | Trpm8 antagonists and their use in treatments |
| AU2012272898A1 (en) | 2011-06-24 | 2013-04-11 | Amgen Inc. | TRPM8 antagonists and their use in treatments |
| UY34194A (es) | 2011-07-15 | 2013-02-28 | Astrazeneca Ab | ?(3-(4-(espiroheterocíclico)metil)fenoxi)azetidin-1-il)(5-(fenil)-1,3,4-oxadiazol-2-il)metanona en el tratamiento de la obesidad? |
| WO2013078413A1 (en) * | 2011-11-22 | 2013-05-30 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Modulators of lipid storage |
| US8952009B2 (en) | 2012-08-06 | 2015-02-10 | Amgen Inc. | Chroman derivatives as TRPM8 inhibitors |
| JP6223563B2 (ja) | 2013-10-14 | 2017-11-01 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 選択的に置換されたキノリン化合物 |
| RU2671496C2 (ru) | 2013-10-14 | 2018-11-01 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Производные 5-пиперидин-8-цианохинолина |
| TW201627299A (zh) * | 2014-10-29 | 2016-08-01 | 美國禮來大藥廠 | 用於抑制微粒體前列腺素e合成酶1之新穎羧酸化合物 |
| BR112017015291B1 (pt) | 2015-01-16 | 2022-10-11 | Nederlandse Organisatie Voor Toegepast- Natuurwetenschappelijk Onderzoek Tno | Método para preparar um estabilizador de nitrocelulose derivado de ureia aromática |
| BR112018014788B1 (pt) | 2016-03-22 | 2022-03-22 | Helsinn Healthcare Sa | Composto e uso de um composto |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE9902987D0 (sv) * | 1999-08-24 | 1999-08-24 | Astra Pharma Prod | Novel compounds |
| US6727264B1 (en) * | 2001-07-05 | 2004-04-27 | Synaptic Pharmaceutical Corporation | Substituted anilinic piperidines as MCH selective antagonists |
| EP1432693A2 (en) * | 2001-10-01 | 2004-06-30 | Taisho Pharmaceutical Co. Ltd. | Mch receptor antagonists |
| JP2005506338A (ja) * | 2001-10-09 | 2005-03-03 | ニューロクライン バイオサイエンシーズ, インコーポレイテッド | メラノコルチンレセプターのリガンドならびに関連の配合物および方法 |
| JP2005532368A (ja) * | 2002-06-12 | 2005-10-27 | アボット・ラボラトリーズ | メラニン濃縮ホルモン受容体の拮抗薬 |
| WO2004081005A1 (en) * | 2003-03-07 | 2004-09-23 | Neurocrine Biosciences, Inc. | Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto |
| RU2366655C2 (ru) * | 2003-03-14 | 2009-09-10 | Оно Фармасьютикал Ко., Лтд. | Азотсодержащие гетероциклические производные и лекарственные средства, содержащие их в качестве активного ингредиента |
| EP1464335A3 (en) * | 2003-03-31 | 2007-05-09 | Taisho Pharmaceutical Co. Ltd. | Quinoline, tetrahydroquinoline and pyrimidine derivatives as mch antagonist |
-
2005
- 2005-12-19 JP JP2007548144A patent/JP2008524325A/ja active Pending
- 2005-12-19 AR ARP050105335A patent/AR051802A1/es not_active Application Discontinuation
- 2005-12-19 US US11/721,767 patent/US20080306055A1/en not_active Abandoned
- 2005-12-19 WO PCT/SE2005/001966 patent/WO2006068594A1/en not_active Ceased
- 2005-12-19 EP EP05819128A patent/EP1831194A4/en not_active Withdrawn
- 2005-12-21 TW TW094145647A patent/TW200635589A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006068594A1 (en) | 2006-06-29 |
| EP1831194A1 (en) | 2007-09-12 |
| TW200635589A (en) | 2006-10-16 |
| US20080306055A1 (en) | 2008-12-11 |
| JP2008524325A (ja) | 2008-07-10 |
| EP1831194A4 (en) | 2009-12-02 |
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