AR074902A1 - Derivados de 1,2,4-oxadiazoles agonistas de receptores s1p1 - Google Patents
Derivados de 1,2,4-oxadiazoles agonistas de receptores s1p1Info
- Publication number
- AR074902A1 AR074902A1 ARP090105087A ARP090105087A AR074902A1 AR 074902 A1 AR074902 A1 AR 074902A1 AR P090105087 A ARP090105087 A AR P090105087A AR P090105087 A ARP090105087 A AR P090105087A AR 074902 A1 AR074902 A1 AR 074902A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- groups
- alkyl
- hydrogen atom
- optionally substituted
- Prior art date
Links
- 102100025750 Sphingosine 1-phosphate receptor 1 Human genes 0.000 title 1
- 101710155454 Sphingosine 1-phosphate receptor 1 Proteins 0.000 title 1
- 239000000556 agonist Substances 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 9
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 5
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 5
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 abstract 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000002431 aminoalkoxy group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical group OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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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
- A61K31/4245—Oxadiazoles
-
- 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
- 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
- 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
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P25/04—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
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Transplantation (AREA)
- Virology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Reivindicación 1: Un compuesto de fórmula general (1), o una sal farmacéuticamente aceptable o N-óxido del mismo: Fórmula (1). Donde: (i) A se selecciona del grupo que consiste en -N-, -O- y -S-; B y C se seleccionan independientemente del grupo que consiste en -N- y -O-, con la condición de que dos de A, B y C sean átomos de nitrógeno; o (ii) dos de A, B y C son -N- y uno de A, B, y C es -NH-; G1 se selecciona del grupo que consiste en -CH2-, -NH- y -O-; G2 se selecciona del grupo que consiste en -NR4- y -O-; R1 representa: - un grupo heteroarilo que contiene N, bicílico, de 8 a 10 miembros, opcionalmente sustituido con un grupo carboxialquiIo C1-4 o un grupo aminoalquilo C1-4, - un grupo piridilo opcionalmente sustituido con uno o más sustituyentes seleccionados de grupos hidroxi, grupos alquilo C1-4, grupos carboxialquilo C1-4, grupos haloalquilo C1-4, grupos alcoxi C1-4, grupos amino, grupos aminoalquilo C1-4 y grupos aminoalcoxi C1-4, - un grupo piridona sustituido con uno o más grupos alquilo C1-4; grupos haloalquilo C1-4 o grupos aminoalquilo C1-4, o un grupo de fórmula (2) donde: - Ra representa un átomo de hidrógeno, un átomo de halógeno, un grupo alquilo C1-4 , un grupo cicloalquilo C3-4 o un grupo -CF3; - Rb representa un átomo de hidrógeno, un átomo de halógeno, un grupo alquilo C1-4, un grupo -CF3 o un grupo alcoxi C1-4; - Rd representa un átomo de hidrógeno, un grupo alquilo C1-4 o un grupo alcoxi C1-4; - Rc representa: -Un átomo de hidrógeno, un grupo hidroxialquilo C1-4, un grupo aminoalquilo C1-4 que está opcionalmente sustituido con uno o más sustituyentes seleccionados de átomos de halógeno, grupos hidroxi y grupos -CF3; -un anillo heterocíclico que contiene N, saturado, de 4 a 6 miembros, opcionalmente sustituido con un grupo carboxialquilo C1-2; - -(CH2)(0-4)-C(O)OR', -(CH2)(0-4)-C(O)NR'R”, -(CH2)(0-4)-NHC(O)R”, -S(O)2NR'R”, -O-(CH2)(2-4)NR'R”, -O-(CH2)(1-4)C(O)OR'', -O-(CH2)(1-4)-C(O)NR'R”, -(CH2)(0-4)NR'R”, -(CH2)(0-4)-CONHS(O)2R', -(CH2)(0-4)-NHS(O)2R' o -(CH2)(0-3)-NH-(CH2)((1-3)(NH)(0-1)S(O)2R' donde, * R' representa un átomo de hidrógeno o un grupo alquilo C1-4, * R” representa un átomo de hidrógeno, un grupo alquilo C1-4, un grupo cicloalquilo C3-4, un grupo carboxialquilo C1-4 un grupo haloaquilo C1-4, un grupo hidroxialquilo C1-4 o un anillo heterocíclico que contiene N, saturado, de 6 miembros, o * R' y R” junio con el átomo de nitrógeno al que están unidos forman un grupo heterocíclico de 4 a 6 miembros que contiene, como heteroátomos, un átomo de N y, opcionalmente, un átomo adicional seleccionado de N y O, y que está opcionalmente sustituido con un grupo carboxi o carboxialquilo C1-4, o Rc junto con Rd forman un grupo cicloalquilo C5-6 opcionalmente sustituido con un grupo -NHRf, donde Rf se selecciona del grupo que consiste en un átomo de hidrógeno y un grupo carboximetilo; R2 y R3 se seleccionan independientemente del grupo que consiste en átomos de hidrógeno, átomos de halógeno y grupos alquilo C1-4 ; y R4 se selecciona del grupo que consiste en un átomo de hidrógeno, un grupo fenilo, un grupo cicloalquil C3-4-alquilo C1-4, un grupo aminoalquilo C1-4, un grupo haloalquilo C1-4 y un grupo alquilo C1-4 lineal o ramificado que está opcionalmente sustituido con un grupo fenilo o piridilo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08382090A EP2202232A1 (en) | 2008-12-26 | 2008-12-26 | 1,2,4-oxadiazole derivatives and their therapeutic use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR074902A1 true AR074902A1 (es) | 2011-02-23 |
Family
ID=40671021
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090105087A AR074902A1 (es) | 2008-12-26 | 2009-12-23 | Derivados de 1,2,4-oxadiazoles agonistas de receptores s1p1 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US20110311485A1 (es) |
| EP (2) | EP2202232A1 (es) |
| JP (1) | JP2012513958A (es) |
| KR (1) | KR20110104075A (es) |
| CN (1) | CN102264731A (es) |
| AR (1) | AR074902A1 (es) |
| AU (1) | AU2009331959A1 (es) |
| BR (1) | BRPI0918194A2 (es) |
| CA (1) | CA2748397A1 (es) |
| CO (1) | CO6341631A2 (es) |
| EA (1) | EA201100975A1 (es) |
| EC (1) | ECSP11011083A (es) |
| IL (1) | IL213168A0 (es) |
| MX (1) | MX2011006505A (es) |
| SG (1) | SG172152A1 (es) |
| TW (1) | TW201024287A (es) |
| UY (1) | UY32296A (es) |
| WO (1) | WO2010072352A1 (es) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8399451B2 (en) | 2009-08-07 | 2013-03-19 | Bristol-Myers Squibb Company | Heterocyclic compounds |
| EP2366702A1 (en) * | 2010-03-18 | 2011-09-21 | Almirall, S.A. | New oxadiazole derivatives |
| US8247436B2 (en) | 2010-03-19 | 2012-08-21 | Novartis Ag | Pyridine and pyrazine derivative for the treatment of CF |
| JP2013530139A (ja) | 2010-05-08 | 2013-07-25 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | ヒドロキシアルキルベンジルピラゾール類およびその使用 |
| EA201291167A1 (ru) | 2010-05-08 | 2013-05-30 | Байер Интеллектуэль Проперти Гмбх | Замещенные гетероциклилбензилпиразолы и их применение |
| EP2595969B1 (en) * | 2010-07-20 | 2015-04-22 | Bristol-Myers Squibb Company | Substituted 3-phenyl-1,2,4-oxadiazole compounds |
| WO2012061459A1 (en) * | 2010-11-03 | 2012-05-10 | Bristol-Myers Squibb Company | Heterocyclic compounds as s1p1 agonists for the treatment of autoimmune and vascular diseases |
| EP2455080A1 (en) * | 2010-11-23 | 2012-05-23 | Almirall, S.A. | S1P1 receptor agonists for use in the treatment of multiple sclerosis |
| EP2455081A1 (en) * | 2010-11-23 | 2012-05-23 | Almirall, S.A. | S1P1 receptor agonists for use in the treatment of crohn's disease |
| KR101299512B1 (ko) * | 2011-04-19 | 2013-08-22 | 전북대학교산학협력단 | 스핑고신 1-포스페이트를 유효성분으로 함유하는 관절염 질환 치료 조성물 |
| WO2013025984A2 (en) * | 2011-08-18 | 2013-02-21 | Temple University | Cannabinoid receptor treatments |
| US9242976B2 (en) * | 2012-01-13 | 2016-01-26 | Bristol-Myers Squibb Company | Thiazolyl- or thiadiazolyl-substituted pyridyl compounds useful as kinase inhibitors |
| AU2013286860B2 (en) | 2012-07-02 | 2017-10-26 | Monsanto Technology Llc | Processes for the preparation of 3,5-disubstituted-1,2,4-oxadiazoles |
| PT2958913T (pt) | 2013-02-20 | 2018-12-03 | Lg Chemical Ltd | Agonistas de recetores de esfingosina-1-fosfato, métodos para a sua preparação e composições farmacêuticas que os contêm como agente ativo |
| UY35338A (es) | 2013-02-21 | 2014-08-29 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | Compuestos bicíclicos moduladores de la actividad de s1p1 y composiciones farmacéuticas que los contienen |
| TW201534586A (zh) | 2013-06-11 | 2015-09-16 | Orion Corp | 新穎cyp17抑制劑/抗雄激素劑 |
| TWI689487B (zh) | 2014-08-20 | 2020-04-01 | 美商必治妥美雅史谷比公司 | 經取代雙環化合物 |
| MA41139B1 (fr) | 2014-12-11 | 2026-02-27 | Laboratoires Juvise Pharmaceuticals | Combinaison pharmaceutique comprenant du ponesimod et son utilisation dans le traitement de la sclérose en plaque |
| EA036075B1 (ru) | 2014-12-11 | 2020-09-23 | Актелион Фармасьютиклз Лтд | Схема дозирования для селективного агониста рецептора s1p1 |
| WO2018162607A1 (en) * | 2017-03-07 | 2018-09-13 | F. Hoffmann-La Roche Ag | Oxadiazole transient receptor potential channel inhibitors |
| WO2018187479A1 (en) | 2017-04-04 | 2018-10-11 | Case Western Reserve University | Method of modulating ribonucleotide reductase |
| CN108546266B (zh) * | 2018-07-25 | 2020-09-22 | 上海毕得医药科技有限公司 | 一种1,4,6,7-四氢吡喃[4,3-c]吡唑-3-羧酸的合成方法 |
| BR112021026837A2 (pt) * | 2019-08-06 | 2022-02-22 | Domain Therapeutics | Compostos de 5-heteroaril-piridin-2-amina como anta-gonistas do receptor de neuropeptídeo ff |
| CN115087655A (zh) | 2019-12-20 | 2022-09-20 | 辉瑞公司 | 苯并咪唑衍生物 |
| AU2022376961A1 (en) | 2021-10-29 | 2024-05-16 | Arcus Biosciences, Inc. | Inhibitors of hif-2alpha and methods of use thereof |
| JP2025525162A (ja) * | 2022-08-01 | 2025-08-01 | ヴァロ ヘルス インコーポレイテッド | 6-置換-1-(2h)-イソキノリノン及び中間体化合物の製造方法 |
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| MX2008009579A (es) | 2006-01-27 | 2008-09-25 | Univ Virginia | Metodo para el tratamiento de dolor neuropatico. |
| TWI389683B (zh) | 2006-02-06 | 2013-03-21 | Kyorin Seiyaku Kk | A therapeutic agent for an inflammatory bowel disease or an inflammatory bowel disease treatment using a 2-amino-1,3-propanediol derivative as an active ingredient |
| TWI382984B (zh) * | 2006-04-03 | 2013-01-21 | Astellas Pharma Inc | 雜環化合物 |
| EP2046315B1 (en) | 2006-06-02 | 2013-04-10 | The Ohio State University Research Foundation | Therapeutic agents for the treatment of mantle cell lymphoma |
| GB0612721D0 (en) | 2006-06-27 | 2006-08-09 | Novartis Ag | Organic compounds |
| AU2007284337B2 (en) | 2006-08-17 | 2012-07-19 | University Of Chicago | Treatment of inflammatory diseases |
| JO2701B1 (en) * | 2006-12-21 | 2013-03-03 | جلاكسو جروب ليميتد | Vehicles |
-
2008
- 2008-12-26 EP EP08382090A patent/EP2202232A1/en not_active Withdrawn
-
2009
- 2009-12-04 UY UY0001032296A patent/UY32296A/es not_active Application Discontinuation
- 2009-12-14 TW TW098142730A patent/TW201024287A/zh unknown
- 2009-12-15 SG SG2011043510A patent/SG172152A1/en unknown
- 2009-12-15 KR KR1020117017302A patent/KR20110104075A/ko not_active Withdrawn
- 2009-12-15 AU AU2009331959A patent/AU2009331959A1/en not_active Abandoned
- 2009-12-15 MX MX2011006505A patent/MX2011006505A/es not_active Application Discontinuation
- 2009-12-15 CN CN2009801528657A patent/CN102264731A/zh active Pending
- 2009-12-15 EP EP09771316A patent/EP2370431A1/en not_active Withdrawn
- 2009-12-15 BR BRPI0918194A patent/BRPI0918194A2/pt not_active Application Discontinuation
- 2009-12-15 US US13/142,104 patent/US20110311485A1/en not_active Abandoned
- 2009-12-15 WO PCT/EP2009/008968 patent/WO2010072352A1/en not_active Ceased
- 2009-12-15 JP JP2011542702A patent/JP2012513958A/ja active Pending
- 2009-12-15 EA EA201100975A patent/EA201100975A1/ru unknown
- 2009-12-15 CA CA2748397A patent/CA2748397A1/en not_active Abandoned
- 2009-12-23 AR ARP090105087A patent/AR074902A1/es unknown
-
2011
- 2011-05-25 EC EC2011011083A patent/ECSP11011083A/es unknown
- 2011-05-26 IL IL213168A patent/IL213168A0/en unknown
- 2011-06-17 CO CO11075839A patent/CO6341631A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO2010072352A1 (en) | 2010-07-01 |
| KR20110104075A (ko) | 2011-09-21 |
| SG172152A1 (en) | 2011-07-28 |
| TW201024287A (en) | 2010-07-01 |
| CA2748397A1 (en) | 2010-07-01 |
| AU2009331959A1 (en) | 2011-06-30 |
| US20110311485A1 (en) | 2011-12-22 |
| EA201100975A1 (ru) | 2012-02-28 |
| EP2202232A1 (en) | 2010-06-30 |
| CN102264731A (zh) | 2011-11-30 |
| JP2012513958A (ja) | 2012-06-21 |
| BRPI0918194A2 (pt) | 2015-12-01 |
| ECSP11011083A (es) | 2011-06-30 |
| IL213168A0 (en) | 2011-07-31 |
| UY32296A (es) | 2010-05-31 |
| MX2011006505A (es) | 2011-07-12 |
| EP2370431A1 (en) | 2011-10-05 |
| CO6341631A2 (es) | 2011-11-21 |
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