AR053728A1 - Pirimidinas condensadas como agonistas del receptor de acido nicotinico para el tratamiento de dislipidemia y composiciones farmaceuticas que las contienen en combinacion con otros agentes terapeuticos - Google Patents
Pirimidinas condensadas como agonistas del receptor de acido nicotinico para el tratamiento de dislipidemia y composiciones farmaceuticas que las contienen en combinacion con otros agentes terapeuticosInfo
- Publication number
- AR053728A1 AR053728A1 ARP060101969A ARP060101969A AR053728A1 AR 053728 A1 AR053728 A1 AR 053728A1 AR P060101969 A ARP060101969 A AR P060101969A AR P060101969 A ARP060101969 A AR P060101969A AR 053728 A1 AR053728 A1 AR 053728A1
- Authority
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- Prior art keywords
- alkyl
- aryl
- alkylene
- substituted
- groups
- Prior art date
Links
- 208000032928 Dyslipidaemia Diseases 0.000 title abstract 2
- 208000017170 Lipid metabolism disease Diseases 0.000 title abstract 2
- 239000003814 drug Substances 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 229940124597 therapeutic agent Drugs 0.000 title abstract 2
- 102100030643 Hydroxycarboxylic acid receptor 2 Human genes 0.000 title 1
- 101710125793 Hydroxycarboxylic acid receptor 2 Proteins 0.000 title 1
- 239000000556 agonist Substances 0.000 title 1
- 125000003118 aryl group Chemical group 0.000 abstract 29
- 125000000217 alkyl group Chemical group 0.000 abstract 23
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 13
- 125000001072 heteroaryl group Chemical group 0.000 abstract 13
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 150000002367 halogens Chemical class 0.000 abstract 8
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 125000005275 alkylenearyl group Chemical group 0.000 abstract 5
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- -1 -alkylene-aryl Chemical group 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- 208000001145 Metabolic Syndrome Diseases 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
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- 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
-
- 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
- A61K31/495—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
-
- 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
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—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
- 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
- C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Gastroenterology & Hepatology (AREA)
- Neurology (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Biomedical Technology (AREA)
- Emergency Medicine (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
Abstract
util en el tratamiento de enfermedades, trastornos o afecciones tales como síndrome metabolico y dislipidemia. Se proveen además composiciones farmacéuticas que contienen otros agentes terapéuticos. Reivindicacion 1: Un compuesto de la formula (1), o una sal, un solvato, éster o tautomero de dicho compuesto, aceptables para uso farmacéutico, donde: Q se selecciona del grupo que consiste en las formulas (2) a (6); L se selecciona del grupo que consiste en las formulas (7) a (10); R1 se selecciona del grupo que consiste en H, alquilo, alquenilo, alquinilo, haloalquilo, alquilo sustituido con uno o más grupos hidroxilo, cicloalquilo, -C(O)-alquilo, -alquileno-C(O)-O-alquilo, -O-R10, -alquilen-O-alquilo; arilo, -alquilen-arilo, heteroarilo, -alquileno-heteroarilo, halogeno, -(CH2)n-N(R7)2, -alquileno-cicloalquilo y -alquileno-cicloalquenilo; donde dicho cicloalquilo o la porcion cicloalquilo de dicho -alquileno-cicloalquilo de R1 están no sustituidos o sustituidos con uno o más grupos X; dicho arilo o la porcion arilo de dicho -alquileno-arilo de R1 están no sustituidos o sustituidos con uno o más grupos Y; y dicho heteroarilo o la porcion heteroarilo de dicho -alquileno-heteroarilo de R1 están no sustituidos o sustituidos con uno o más grupos Y; R2 se selecciona del grupo que consiste en H, halogeno, alquilo, haloalquilo, alquilo sustituido con uno o más -OH, -C(O)-alquilo, -C(O)-O-alquilo, -C(O)-OH, -O-R10, -alquileno-O- alquilo, arilo no sustituido, arilo sustituido con uno o más grupos Y, heteroarilo no sustituido, heteroarilo sustituido con uno o más grupos Y, y halogeno; o R1 y R2 junto con los átomos de carbono de anillo a los cuales se los expone unidos forman un anillo cicloalquileno de 5 o 6 miembros, o un anillo heterocíclico de 5 o 6 miembros que tiene 1 o 2 heteroátomos; R3 se selecciona del grupo que consiste en H, alquilo, alquilo sustituido con uno o más grupos hidroxilo; -alquilen-O-alquilo, cicloalquilo, -alquileno- cicloalquilo, -alquilen-C(O)-O- alquilo, -alquileno-O-C(O)-alquilo, alquenilo, arilo y heteroarilo; donde dicho cicloalquilo o la porcion cicloalquilo de dicho -alquileno- cicloalquilo de R3 están no sustituidos o sustituidos con uno o más grupos X; dicho arilo de R3 está no sustituido o sustituido con uno o más grupos Y; y dicho heteroarilo de R3 está no sustituido o sustituido con uno o más grupos Y; R4 se selecciona del grupo que consiste en H, halogeno, alquilo, -O-R10, -C(O)-O-alquilo, - S(O)m-R9, -N(R7)2, -N(R7)-NH-C(O)-alquilo, -N(R7)-NH-C(O)-O-alquilo, -O-N=C(R12) 2, -N(R7)-N=C(R12)2, -C(O)-alquilo, heterociclilo no sustituido, heterociclilo sustituido con uno o más grupos X; -O-N(R7)-C(O)O-alquilo, -C(O)-N(R7)2, -CN, -N3 y -O- C(O)-alquilo; R5 se selecciona del grupo que consiste en H, alquilo, -alquileno-C(O)-R8, -alquileno-C(O)- N(R11)2, -alquileno-C(=N-O-alquil)-arilo, cicloalquilo, -alquileno-cicloalquilo, -alquileno-C(O)-O-alquilo, -alquileno-O-C(O)-alquilo, - alquileno-C(O)-heterociclilo y alquenilo; donde dicho cicloalquilo o la porcion cicloalquilo de dicho -alquileno-cicloalquilo de R5 están no sustituidos o sustituidos con uno o más grupos X; y la porcion arilo de dicho -alquileno-C(=N-O-alquil)- arilo de R5 está no sustituida o sustituida con uno o más grupos Y; R6 se selecciona del grupo que consiste en H, alquilo, alquenilo, alquilo sustituido con uno o más grupos hidroxilo, -alquileno-O-alquilo, -O-R10, halogeno, arilo, heteroarilo y - N(R7)2; donde dicho arilo de R6 está no sustituido o sustituido con uno o más grupos Y; y dicho heteroarilo de R6 está no sustituido o sustituido con uno o más grupos Z; cada R7 se selecciona de manera independiente del grupo que consiste en H, alquilo, cicloalquilo, arilo, -C(O)-alquilo, y -C(O)-arilo; donde dicho cicloalquilo de R7 está no sustituido o sustituido con uno o más grupos X; y la porcion arilo de dicho -C(O)-arilo o dicho arilo de R7 están no sustituidos o sustituidos con uno o más grupos Y; o dos grupos R7, junto con el átomo de N al cual están enlazados forman un heterociclilo; R8 se selecciona del grupo que consiste en arilo, -OH y heterociclilo; donde dicho heterociclilo de R8 está no sustituido o sustituido con uno o más grupos X; y dicho arilo de R8 está no sustituido o sustituido con uno o más grupos Y; R9 se selecciona del grupo que consiste en alquilo, -alquileno-cicloalquilo, alquenilo, -N(R11)2 y alquileno-arilo; donde la porcion cicloalquilo de dicho - alquileno-cicloalquilo de R9 está no sustituida o sustituida con uno o más grupos X; y la porcion arilo de dicho -alquileno-arilo de R9 está no sustituida o sustituida con uno o más grupos Y; y con la condicion de que cuando R9 es -N(R11)2, m es 1 o 2; R10 se selecciona del grupo que consiste en H, alquilo, -alquileno-arilo, -alquenileno-arilo, -alquileno-heteroarilo, alquenilo, -C(O)-alquilo, alquinilo y -alquileno- cicloalquilo; donde la porcion cicloalquilo de dicho -alquileno-cicloalquilo de R10 está no sustituida o sustituida con uno o más grupos X; la porcion arilo de dicho -alquileno-arilo o -alquenileno-arilo de R10 está no sustituida o sustituida con uno o más grupos Y; y la porcion heteroarilo de dicho -alquileno-heteroarilo de R10 está no sustituida o sustituida con uno o más grupos Z; cada R11 se selecciona de manera independiente del grupo que consiste en H, alquilo y arilo; donde dicho arilo de R11 está no sustituido o sustituido con uno o más grupos Y; o dos grupos R11, junto con el átomo de N al cual están unidos, forman un heterociclilo; cada R12 se selecciona de manera independiente del grupo que consiste en alquilo, arilo y heteroarilo; donde dicho arilo de R12 está no sustituido o sustituido con uno o más grupos Y; y dichos heteroarilo de R12 está no sustituido o sustituido con uno o más grupos Z; Ra y Rb se seleccionan de manera independiente del grupo que consiste en H, alquilo, arilo y heteroarilo; donde dicho arilo de Ra y Rb está no sustituido o sustituido con uno o más grupos Y; y dicho heteroarilo de Ra y Rb está no sustituido o sustituido con uno o más grupos Z; Rc se selecciona del grupo que consiste en H, alquilo, alquileno-arilo y -C(O)-alquilo; donde la porcion arilo de dicho alquileno-arilo de Rc está no sustituida o sustituida con uno o más grupos Y; Rd se selecciona del grupo que consiste en H, alquilo y alquileno-arilo; donde la porcion arilo de dicho alquileno-arilo de Rd está no sustituida o sustituida con uno o más grupos Y; cada X se selecciona de manera independiente del grupo que consiste en halogeno, alquilo, haloalquilo, -O-alquilo, -O-haloalquilo y -OH; cada Y se selecciona de manera independiente del grupo que consiste en halogeno, alquilo, haloalquilo, -O-alquilo, -O-haloalquilo, -CN, -NO2, -OH, -S(O2)-alquilo, -S(O2)-arilo, -S(O2)- NH2, -S(O2)-NH-alquilo, -S(O2)-NH-arilo, -S(O2)-N(alquilo)2, -S(O2)-N(arilo)2, -S(O2)-N(alquilo)(arilo) y arilo; cada Z se selecciona de manera independientemente del grupo que consiste en alquilo, haloalquilo, halogeno, -O-alquilo, -O-haloalquilo, -CN, -OH, arilo y N- oxido; n es 0, 1, 2, o 3; m es 0, 1 o 2; y con la condicion de que cuando L es la formula (7), y R2, R3 y R5 son H, entonces R1 no es - CH3.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68184805P | 2005-05-17 | 2005-05-17 | |
| US71556505P | 2005-09-09 | 2005-09-09 | |
| US73103905P | 2005-10-28 | 2005-10-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR053728A1 true AR053728A1 (es) | 2007-05-16 |
Family
ID=37431860
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060101969A AR053728A1 (es) | 2005-05-17 | 2006-05-16 | Pirimidinas condensadas como agonistas del receptor de acido nicotinico para el tratamiento de dislipidemia y composiciones farmaceuticas que las contienen en combinacion con otros agentes terapeuticos |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US7723342B2 (es) |
| EP (1) | EP1885726B1 (es) |
| JP (1) | JP4975739B2 (es) |
| KR (1) | KR20080016567A (es) |
| AR (1) | AR053728A1 (es) |
| AU (1) | AU2006247695B2 (es) |
| BR (1) | BRPI0610133A2 (es) |
| CA (1) | CA2608405A1 (es) |
| IL (1) | IL187302A0 (es) |
| MX (1) | MX2007014517A (es) |
| NO (1) | NO20076450L (es) |
| PE (1) | PE20061442A1 (es) |
| TW (1) | TW200716648A (es) |
| WO (1) | WO2006124490A2 (es) |
Families Citing this family (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7737155B2 (en) * | 2005-05-17 | 2010-06-15 | Schering Corporation | Nitrogen-containing heterocyclic compounds and methods of use thereof |
| US7750015B2 (en) * | 2005-05-17 | 2010-07-06 | Schering Corporation | Nitrogen-containing heterocyclic compounds and methods of use thereof |
| PL1901731T3 (pl) | 2005-06-28 | 2011-08-31 | Merck Sharp & Dohme | Agoniści receptora niacyny, kompozycje zawierające te związki i sposoby leczenia |
| CN101400682A (zh) * | 2006-01-20 | 2009-04-01 | 先灵公司 | 治疗异常脂血症的杂环烟酸受体激动剂 |
| GB0614471D0 (en) | 2006-07-20 | 2006-08-30 | Syngenta Ltd | Herbicidal Compounds |
| JP2010500300A (ja) | 2006-08-08 | 2010-01-07 | サノフィ−アベンティス | アリールアミノアリール−アルキル−置換イミダゾリジン−2,4−ジオン、それらの製造法、それらの化合物を含有する薬剤、およびそれらの使用 |
| EP2139895A1 (en) * | 2007-03-23 | 2010-01-06 | F. Hoffmann-Roche AG | Aza-pyridopyrimidinone derivatives |
| JPWO2008120655A1 (ja) | 2007-03-30 | 2010-07-15 | 株式会社医薬分子設計研究所 | I型11βヒドロキシステロイド脱水素酵素阻害活性を有するオキサゾリジノン誘導体 |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| MX2010004450A (es) | 2007-10-22 | 2010-05-05 | Schering Corp | Derivados heterociclo biciclicos y su uso como moduladores de la actividad de gpr119. |
| DE102007063671A1 (de) | 2007-11-13 | 2009-06-25 | Sanofi-Aventis Deutschland Gmbh | Neue kristalline Diphenylazetidinonhydrate, diese Verbindungen enthaltende Arzneimittel und deren Verwendung |
| DE102007061764A1 (de) * | 2007-12-20 | 2009-06-25 | Bayer Healthcare Ag | Anellierte Cyanopyridine und ihre Verwendung |
| CA2724426A1 (en) | 2008-05-19 | 2009-11-26 | Schering Corporation | Bicyclic heterocycle derivatives and use thereof as gpr119 modulators |
| US8206943B1 (en) | 2008-06-30 | 2012-06-26 | Schering Corporation | Assay for PCSK9 inhibitors |
| WO2010003624A2 (en) | 2008-07-09 | 2010-01-14 | Sanofi-Aventis | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
| JP2011528365A (ja) | 2008-07-16 | 2011-11-17 | シェーリング コーポレイション | Gpr119モジュレーターとしての二環式ヘテロ環誘導体およびそれらの使用方法 |
| WO2010009210A2 (en) * | 2008-07-17 | 2010-01-21 | Schering Corporation | Acetylsalicyclic acid derivatives useful to treat metabolic syndromes |
| WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
| US20110243940A1 (en) * | 2008-12-16 | 2011-10-06 | Schering Corporation | Bicyclic pyranone derivatives and methods of use thereof |
| WO2010075068A1 (en) | 2008-12-16 | 2010-07-01 | Schering Corporation | Pyridopyrimidine derivatives and methods of use thereof |
| JP2012513470A (ja) | 2008-12-23 | 2012-06-14 | シェーリング コーポレイション | 二環式複素環誘導体及びその使用方法 |
| WO2010075273A1 (en) | 2008-12-23 | 2010-07-01 | Schering Corporation | Bicyclic heterocycle derivatives and methods of use thereof |
| US8580807B2 (en) | 2009-04-03 | 2013-11-12 | Merck Sharp & Dohme Corp. | Bicyclic piperidine and piperazine derivatives as GPCR modulators for the treatment of obesity, diabetes and other metabolic disorders |
| AR076024A1 (es) | 2009-04-03 | 2011-05-11 | Schering Corp | Derivados de heterociclos biciclicos puenteados y metodos de uso de los mismos |
| KR20120060207A (ko) | 2009-08-26 | 2012-06-11 | 사노피 | 신규한 결정성 헤테로방향족 플루오로글리코시드 수화물, 이들 화합물을 포함하는 약제 및 이들의 용도 |
| WO2011053688A1 (en) | 2009-10-29 | 2011-05-05 | Schering Corporation | Bridged bicyclic piperidine derivatives and methods of use thereof |
| US20120232073A1 (en) | 2009-11-23 | 2012-09-13 | Santhosh Francis Neelamkavil | Fused bicyclic pyrimidine derivatives and methods of use thereof |
| US8912206B2 (en) | 2009-11-23 | 2014-12-16 | Merck Sharp & Dohme Corp. | Pyrimidine ether derivatives and methods of use thereof |
| US9301929B2 (en) | 2009-11-24 | 2016-04-05 | Merck Sharp & Dohme Corp. | Substituted biaryl derivatives and methods of use thereof |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| WO2011157827A1 (de) | 2010-06-18 | 2011-12-22 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| US20130197043A1 (en) | 2010-08-31 | 2013-08-01 | Snu R&Db Foundation | Use of the fetal reprogramming of a ppar agonist |
| US8828994B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2766349B1 (de) | 2011-03-08 | 2016-06-01 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| WO2012120055A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US8828995B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| WO2012120056A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2013072882A1 (en) | 2011-11-18 | 2013-05-23 | Actelion Pharmaceuticals Ltd | 2 -amino- 1, 8 -naphthyridine-3 -carboxamide derivatives as antimicrobial agents |
| WO2013151982A1 (en) | 2012-04-03 | 2013-10-10 | Arena Pharmaceuticals, Inc. | Methods and compounds useful in treating pruritus, and methods for identifying such compounds |
| US9255154B2 (en) | 2012-05-08 | 2016-02-09 | Alderbio Holdings, Llc | Anti-PCSK9 antibodies and use thereof |
| EP2931716B1 (en) | 2012-12-13 | 2016-11-02 | Novartis Ag | Pyridone derivatives and uses thereof in the treatment of tuberculosis |
| MX2015011898A (es) | 2013-03-13 | 2016-05-05 | Genentech Inc | Compuestos de pirazolo y usos de los mismos. |
| UA118034C2 (uk) * | 2013-11-14 | 2018-11-12 | Елі Ліллі Енд Компані | Заміщений піперидилетилпіримідин як інгібітор грелін-o-ацилтрансферази |
| WO2017003723A1 (en) | 2015-07-01 | 2017-01-05 | Crinetics Pharmaceuticals, Inc. | Somatostatin modulators and uses thereof |
| WO2017205432A1 (en) * | 2016-05-23 | 2017-11-30 | Dai Lu | Functionalized pyrano[2,3-d]pyrimidin-7-one derivatives and methods for their preparation and use |
| EP3658560A4 (en) | 2017-07-25 | 2021-01-06 | Crinetics Pharmaceuticals, Inc. | SOMATOSTAT IN MODULATORS AND USES THEREOF |
| CA3129569A1 (en) | 2019-03-14 | 2020-09-17 | Thomas Weimbs | Methods and compositions for supporting renal health |
| US20230048576A1 (en) * | 2019-03-19 | 2023-02-16 | City Of Hope | Compounds for the treatment of neuropathic pain |
| KR20240089791A (ko) * | 2021-10-20 | 2024-06-20 | 인실리코 메디신 아이피 리미티드 | 메티오닌 아데노실트랜스퍼라제 2a (mat2a) 억제제 및 그의 용도 |
Family Cites Families (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2826580A (en) | 1958-03-11 | Derivatives of y | ||
| US2628560A (en) * | 1946-02-26 | 1953-02-17 | Keyes Fibre Co | Molded pulp wad |
| US3139432A (en) * | 1963-06-24 | 1964-06-30 | Mead Johnson & Co | Pyrido [2, 3-d] pyrimidine-2, 4, 5, 7-tetraones |
| US4215216A (en) * | 1979-04-18 | 1980-07-29 | American Home Products Corporation | 7,8-Dihydro-2,5,8-trisubstituted-7-oxo-pyrido[2,3-d]pyrimidine-6-carboxylic acid derivatives |
| GB8410485D0 (en) * | 1984-04-24 | 1984-05-31 | Waddington John Plc | Label cutting |
| DD263891A3 (de) | 1986-12-23 | 1989-01-18 | Dresden Arzneimittel | Verbessertes verfahren zur herstellung von 2,4,6,8-tetrahydroxy-yrimido[5,4-d] pyrimidin und seinen salzen |
| DD265760A3 (de) | 1987-05-25 | 1989-03-15 | Dresden Arzneimittel | Verfahren zur herstellung von 2,4,6,8-tetrachlorpyrimido-[5,4-d]pyrimidin |
| US5547954A (en) * | 1994-05-26 | 1996-08-20 | Fmc Corporation | 2,4-Diamino-5,6-disubstituted-and 5,6,7-trisubstituted-5-deazapteridines as insecticides |
| US5620981A (en) * | 1995-05-03 | 1997-04-15 | Warner-Lambert Company | Pyrido [2,3-D]pyrimidines for inhibiting protein tyrosine kinase mediated cellular proliferation |
| DE19624154A1 (de) * | 1996-06-18 | 1998-01-08 | Hoechst Ag | Ringannelierte Dihydropyrane, Verfahren zur Herstellung sowie deren Verwendung |
| AU4694999A (en) * | 1998-08-06 | 2000-02-28 | Warner-Lambert Company | Use of thiazolidinedione derivatives for the treatment or prevention of cataracts |
| US20040137563A9 (en) * | 1998-10-13 | 2004-07-15 | Ruoping Chen | Endogenous and non-endogenous versions of human G protein-coupled receptors |
| US6468990B1 (en) | 1999-05-17 | 2002-10-22 | Queen's University At Kingston | Method of inhibiting binding of nerve growth factor to p75 NTR receptor |
| JP2004504303A (ja) * | 2000-07-05 | 2004-02-12 | シナプティック・ファーマスーティカル・コーポレーション | 選択的メラニン凝集ホルモン−1(mch1)受容体アンタゴニストおよびその使用 |
| MXPA03002478A (es) * | 2000-09-22 | 2004-05-05 | Akzo Nobel Nv | Compuestos heteroaromaticos biciclicos. |
| CN1847229B (zh) * | 2000-10-23 | 2011-05-04 | 史密丝克莱恩比彻姆公司 | 2,4,8-三取代-8H-吡啶并[2,3-d]嘧啶-7-酮化合物 |
| AU2002242910A1 (en) | 2001-04-11 | 2002-10-28 | Glaxo Group Limited | Medicaments which are modulators of hm74 and/or hm74a activity |
| US6825180B2 (en) * | 2001-05-18 | 2004-11-30 | Cell Therapeutics, Inc. | Pyridopyrimidine compounds and their uses |
| US6902902B2 (en) * | 2001-11-27 | 2005-06-07 | Arena Pharmaceuticals, Inc. | Human G protein-coupled receptors and modulators thereof for the treatment of metabolic-related disorders |
| WO2003049739A1 (en) * | 2001-12-07 | 2003-06-19 | Vertex Pharmaceuticals, Inc. | Pyrimidine-based compounds useful as gsk-3 inhibitors |
| JP2004083587A (ja) * | 2002-08-06 | 2004-03-18 | Tanabe Seiyaku Co Ltd | 医薬組成物 |
| WO2004037159A2 (en) | 2002-10-23 | 2004-05-06 | Obetherapy Biotechnology | Compounds, compositions and methods for modulating fat metabolism |
| AU2003293006A1 (en) * | 2002-11-22 | 2004-06-18 | Japan Tobacco Inc. | Fused bicyclic nitrogen-containing heterocycles |
| US20040122033A1 (en) * | 2002-12-10 | 2004-06-24 | Nargund Ravi P. | Combination therapy for the treatment of obesity |
| WO2004083388A2 (en) | 2003-03-14 | 2004-09-30 | Bristol-Myers Squibb Company | Polynucleotide encoding a novel human g-protein coupled receptor variant of hm74, hgprbmy74 |
| AR041089A1 (es) * | 2003-05-15 | 2005-05-04 | Merck & Co Inc | Procedimiento y composiciones farmaceutiicas para tratar aterosclerosis, dislipidemias y afecciones relacionadas |
| EP1635813A4 (en) | 2003-06-06 | 2009-07-01 | Merck & Co Inc | COMBINATION THERAPY FOR THE TREATMENT OF DYSLIPIDEMIA |
| EP1635773A2 (en) | 2003-06-06 | 2006-03-22 | Merck & Co., Inc. (a New Jersey corp.) | Combination therapy for the treatment of hypertension |
| US20070099884A1 (en) | 2003-06-06 | 2007-05-03 | Erondu Ngozi E | Combination therapy for the treatment of diabetes |
| WO2005010000A2 (de) * | 2003-07-18 | 2005-02-03 | Basf Aktiengesellschaft | Arylkondensierte 3-arylpyridinverbindungen und ihre verwendung zur bekämpfung von schadpilzen |
| BRPI0507604A (pt) | 2004-02-14 | 2007-07-03 | Smithkline Beecham Corp | medicamentos com atividade de receptor hm74a |
| WO2005105097A2 (en) | 2004-04-28 | 2005-11-10 | Gpc Biotech Ag | Pyridopyrimidines for treating inflammatory and other diseases |
| US20050251869A1 (en) * | 2004-05-04 | 2005-11-10 | Tian-Quan Cai | Animal model for raising HDL-cholesterol with niacin |
| FR2873118B1 (fr) * | 2004-07-15 | 2007-11-23 | Sanofi Synthelabo | Derives de pyrido-pyrimidine, leur application en therapeutique |
| WO2006045565A1 (en) | 2004-10-22 | 2006-05-04 | Smithkline Beecham Corporation | Xanthine derivatives with hm74a receptor activity |
| WO2006045564A1 (en) | 2004-10-22 | 2006-05-04 | Smithkline Beecham Corporation | Xanthine derivatives with hm74a receptor activity |
| CN101146798A (zh) | 2005-01-21 | 2008-03-19 | 詹森药业有限公司 | 用作雌激素受体调节剂的新的杂环苯并[c]色烯衍生物 |
| JP2008538277A (ja) | 2005-02-18 | 2008-10-23 | アリーナ ファーマシューティカルズ, インコーポレイテッド | 脂質関連障害の治療用の組成物および方法 |
| US9271963B2 (en) | 2005-03-03 | 2016-03-01 | Universitat Des Saarlandes | Selective inhibitors of human corticosteroid synthases |
| US7750015B2 (en) * | 2005-05-17 | 2010-07-06 | Schering Corporation | Nitrogen-containing heterocyclic compounds and methods of use thereof |
| US7737155B2 (en) * | 2005-05-17 | 2010-06-15 | Schering Corporation | Nitrogen-containing heterocyclic compounds and methods of use thereof |
| US20090117559A1 (en) | 2005-08-10 | 2009-05-07 | Liaw Chen W | Methods for Determining Probability of an Adverse or Favorable Reaction to a Niacin Receptor Agonist |
| US8691498B2 (en) | 2005-09-02 | 2014-04-08 | Arena Pharmaceuticals, Inc. | Methods of screening for a compound that reduces atherogenesis |
| CN101400682A (zh) * | 2006-01-20 | 2009-04-01 | 先灵公司 | 治疗异常脂血症的杂环烟酸受体激动剂 |
| CA2683915A1 (en) | 2007-04-13 | 2008-10-23 | Schering Corporation | Pyrimidinedione derivatives and methods of use thereof |
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- 2006-05-11 KR KR1020077026812A patent/KR20080016567A/ko not_active Withdrawn
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| US20060264489A1 (en) | 2006-11-23 |
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| CA2608405A1 (en) | 2006-11-23 |
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| US7723342B2 (en) | 2010-05-25 |
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| BRPI0610133A2 (pt) | 2010-06-01 |
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| AU2006247695A1 (en) | 2006-11-23 |
| KR20080016567A (ko) | 2008-02-21 |
| EP1885726B1 (en) | 2016-12-14 |
| MX2007014517A (es) | 2008-02-11 |
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