MA34910B1 - Dérivés de 2-methoxy-pyridin-4-yl - Google Patents
Dérivés de 2-methoxy-pyridin-4-ylInfo
- Publication number
- MA34910B1 MA34910B1 MA36184A MA36184A MA34910B1 MA 34910 B1 MA34910 B1 MA 34910B1 MA 36184 A MA36184 A MA 36184A MA 36184 A MA36184 A MA 36184A MA 34910 B1 MA34910 B1 MA 34910B1
- Authority
- MA
- Morocco
- Prior art keywords
- pyridin
- methoxy
- derivatives
- compounds
- immunomodulators
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61P11/02—Nasal agents, e.g. decongestants
-
- 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
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
- A61P17/04—Antipruritics
-
- 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
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (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)
- Diabetes (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Neurology (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Biomedical Technology (AREA)
- Transplantation (AREA)
- Neurosurgery (AREA)
- Hematology (AREA)
- Otolaryngology (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
L'INVENTION CONCERNE DES DÉRIVÉS DE PYRIDINE REPRÉSENTÉS PAR LA FORMULE (I), DANS LAQUELLE A, R1, R2, R3 ET R4 SONT TELS QUE DÉFINIS DANS LA DESCRIPTION, LEUR PRÉPARATION ET LEUR UTILISATION EN TANT DE COMPOSÉS PHARMACEUTIQUEMENT ACTIFS. LES COMPOSÉS AGISSENT EN PARTICULIER EN TANT QU'AGENTS IMMUNOMODULATEURS
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IB2011050241 | 2011-01-19 | ||
PCT/IB2012/050241 WO2012098505A1 (fr) | 2011-01-19 | 2012-01-18 | Dérivés de 2-methoxy-pyridin-4-yl |
Publications (1)
Publication Number | Publication Date |
---|---|
MA34910B1 true MA34910B1 (fr) | 2014-02-01 |
Family
ID=45607310
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA36184A MA34910B1 (fr) | 2011-01-19 | 2012-01-18 | Dérivés de 2-methoxy-pyridin-4-yl |
Country Status (28)
Country | Link |
---|---|
US (1) | US9133179B2 (fr) |
EP (1) | EP2665720B1 (fr) |
JP (1) | JP5859570B2 (fr) |
KR (1) | KR101869120B1 (fr) |
CN (1) | CN103313981B (fr) |
AR (1) | AR084883A1 (fr) |
AU (1) | AU2012208325B2 (fr) |
BR (1) | BR112013017923B1 (fr) |
CA (1) | CA2818470C (fr) |
CL (1) | CL2013002056A1 (fr) |
CY (1) | CY1116657T1 (fr) |
DK (1) | DK2665720T3 (fr) |
ES (1) | ES2544086T3 (fr) |
HK (1) | HK1191645A1 (fr) |
HR (1) | HRP20150919T1 (fr) |
HU (1) | HUE026012T2 (fr) |
IL (1) | IL227509A0 (fr) |
MA (1) | MA34910B1 (fr) |
MX (1) | MX350009B (fr) |
MY (1) | MY163185A (fr) |
PL (1) | PL2665720T3 (fr) |
PT (1) | PT2665720E (fr) |
SG (1) | SG191742A1 (fr) |
SI (1) | SI2665720T1 (fr) |
TW (1) | TWI546300B (fr) |
UA (1) | UA109804C2 (fr) |
WO (1) | WO2012098505A1 (fr) |
ZA (1) | ZA201306193B (fr) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ713080A (en) | 2013-03-15 | 2020-06-26 | Idorsia Pharmaceuticals Ltd | Pyridin-4-yl derivatives |
EP2990055B1 (fr) | 2013-04-26 | 2019-06-05 | Kyoto University | Composition comprenant un agoniste du récepteur 1 de la sphingosine-1-phosphate pour empêcher la formation et/ou l'expansion d'un anévrisme cérébral ou pour réduire un tel anévrisme |
CN105760707B (zh) * | 2014-12-18 | 2018-07-31 | 中国科学院大连化学物理研究所 | 细胞基因翻译过程建模方法 |
HUE047646T2 (hu) * | 2015-05-20 | 2020-05-28 | Idorsia Pharmaceuticals Ltd | Az (S)-3-{4-[5-(2-ciklopentil-6-metoxi-piridin-4-il)-[1,2,4]oxadiazol-3-il]-2-etil-6-metil-fenoxi} -propán-1,2-diol vegyület kristályformája |
CN107382965A (zh) * | 2017-08-14 | 2017-11-24 | 河南科技大学第附属医院 | 具有抗肿瘤活性的新型s1p‑1受体激动剂药物分子的合成方法 |
Family Cites Families (62)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3647809A (en) | 1968-04-26 | 1972-03-07 | Chinoin Gyogyszer Es Vegyeszet | Certain pyridyl-1 2 4-oxadiazole derivatives |
AU7686891A (en) | 1990-04-05 | 1991-10-30 | American National Red Cross, The | A protein family related to immediate-early protein expressed by human endothelial cells during differentiation |
ZA917371B (en) | 1990-09-20 | 1992-06-24 | Merrell Dow Pharma | Calcium uptake inhibitors |
DE4429465A1 (de) | 1994-08-19 | 1996-02-22 | Bayer Ag | Verfahren zur Herstellung von 2-Halogenpyridinaldehyden und neue 2-Halogenpyridinaldehyde |
US6423508B1 (en) | 1998-03-09 | 2002-07-23 | Smithkline Beecham Corporation | Polynucleotide sequences of human EDG-1c |
DE19904389A1 (de) | 1999-02-04 | 2000-08-10 | Bayer Ag | Verwendung von substituierten Isoxazolcarbonsäuren und Derivate und neue Stoffe |
NZ517221A (en) | 1999-08-19 | 2004-01-30 | Nps Pharma Inc | Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
MXPA03007513A (es) | 2001-02-21 | 2004-07-30 | Nps Pharma Inc | Compuestos heteropoliciclicos y su uso como antagonistas del receptor metabotropico de glutamato. |
EP1470137B1 (fr) | 2002-01-18 | 2009-09-02 | Merck & Co., Inc. | Agonistes du recepteur edg |
JP4709488B2 (ja) | 2002-01-18 | 2011-06-22 | メルク・シャープ・エンド・ドーム・コーポレイション | Edg受容体作動薬としてのN−(ベンジル)アミノアルキルカルボン酸化合物、ホスフィン酸化合物、ホスホン酸化合物およびテトラゾール類 |
WO2003105771A2 (fr) | 2002-06-17 | 2003-12-24 | Merck & Co., Inc. | 1-((5-aryl-1,2,4-oxadiazol-3-yl)benzyl)azetidine-3-carboxylates et 1-((5-aryl-1,2,4-oxadiazol-3-yl)benzyl)pyrrolidine-3-carboxylates utilises en tant qu'agonistes du recepteur edg |
DE10237883A1 (de) | 2002-08-19 | 2004-03-04 | Merckle Gmbh Chem.-Pharm. Fabrik | Substituierte Isoxazolderivate und ihre Verwendung in der Pharmazie |
WO2004035538A1 (fr) | 2002-10-15 | 2004-04-29 | Merck & Co., Inc. | Procede de fabrication de l'acide azetidine-3-carboxylique |
US20050004186A1 (en) | 2002-12-20 | 2005-01-06 | Pfizer Inc | MEK inhibiting compounds |
US20060252741A1 (en) | 2003-05-15 | 2006-11-09 | Colandrea Vincent J | 3-(2-amino-1-azacyclyl)-5-aryl-1,2,4-oxadiazoles as s1p receptor agonists |
TW200505416A (en) | 2003-08-12 | 2005-02-16 | Mitsubishi Pharma Corp | Bi-aryl compound having immunosuppressive activity |
CN1859908A (zh) | 2003-10-01 | 2006-11-08 | 默克公司 | 作为s1p受体激动剂的3,5-芳基、杂芳基或环烷基取代的-1,2,4-噁二唑类化合物 |
CA2547198A1 (fr) | 2003-12-17 | 2005-06-30 | Merck & Co., Inc. | Carboxylates propanoiques 3,4-disusbstitues utilises en tant qu'agonistes du recepteur s1p (edg) |
MXPA06013912A (es) | 2004-05-29 | 2007-07-18 | 7Tm Pharma As | Ligandos del receptor de crth2 para usos medicinales. |
WO2006010379A1 (fr) | 2004-07-29 | 2006-02-02 | Actelion Pharmaceuticals Ltd. | Nouveaux derives du thiophene utilises comme agents immunosupresseurs |
WO2006047195A2 (fr) | 2004-10-22 | 2006-05-04 | Merck & Co., Inc. | Carboxylates, sulfonates, phosphonates, phosphinates 2-(aryl)azacyclylmethyle et heterocycles utilises comme agonistes des recepteurs s1p |
JP4318087B2 (ja) | 2004-12-13 | 2009-08-19 | 小野薬品工業株式会社 | アミノカルボン酸誘導体およびその医薬用途 |
PL1863474T3 (pl) | 2005-03-23 | 2009-04-30 | Actelion Pharmaceuticals Ltd | Nowe pochodne tiofenu jako agoniści receptora 1 1-fosforanu sfingozyny |
WO2006100635A2 (fr) | 2005-03-23 | 2006-09-28 | Actelion Pharmaceuticals Ltd | Nouveaux derives de thiophene |
BRPI0609515A8 (pt) | 2005-03-23 | 2017-12-26 | Actelion Pharmaceuticals Ltd | Composto, composição farmacêutica, e, uso de um composto |
WO2006108103A1 (fr) | 2005-04-05 | 2006-10-12 | Pharmacopeia, Inc. | Derives de purine et d'imidazopyridine en vue d'une immunosuppression |
WO2006115188A1 (fr) | 2005-04-22 | 2006-11-02 | Daiichi Sankyo Company, Limited | Compose heterocyclique |
AU2006239418A1 (en) | 2005-04-26 | 2006-11-02 | Neurosearch A/S | Novel oxadiazole derivatives and their medical use |
CA2610310A1 (fr) | 2005-06-08 | 2006-12-14 | Novartis Ag | Oxadiazoles polycycliques ou soxazoles i et leur utilisation comme ligands recepteurs de s1p |
WO2006135694A2 (fr) | 2005-06-10 | 2006-12-21 | Acadia Pharmaceuticals Inc. | Composes modulateurs d'uii et utilisation |
CA2612661A1 (fr) | 2005-06-24 | 2006-12-28 | Actelion Pharmaceuticals Ltd. | Nouveaux derives de thiofene |
WO2007001973A1 (fr) | 2005-06-28 | 2007-01-04 | Astrazeneca Ab | Utilisation |
AR057894A1 (es) | 2005-11-23 | 2007-12-26 | Actelion Pharmaceuticals Ltd | Derivados de tiofeno |
TWI404706B (zh) * | 2006-01-11 | 2013-08-11 | Actelion Pharmaceuticals Ltd | 新穎噻吩衍生物 |
ES2335242T3 (es) | 2006-01-24 | 2010-03-23 | Actelion Pharmaceuticals Ltd. | Derivados novedosos de piridina. |
GB0601744D0 (en) | 2006-01-27 | 2006-03-08 | Novartis Ag | Organic compounds |
RU2008137553A (ru) | 2006-02-21 | 2010-03-27 | Юниверсити Оф Вирджиния Пэтент Фаундейшн (Us) | Фенил-циклоалкильные соединения, содержащие гетероциклические структуры |
CA2651629A1 (fr) | 2006-05-09 | 2007-11-22 | Pfizer Products Inc. | Derives d'acide cycloalkylamine et compositions pharmaceutiques a base de ceux-ci |
TWI408139B (zh) | 2006-09-07 | 2013-09-11 | Actelion Pharmaceuticals Ltd | 新穎噻吩衍生物 |
TWI392671B (zh) | 2006-09-07 | 2013-04-11 | Actelion Pharmaceuticals Ltd | 吡啶-4-基衍生物 |
PL2069335T3 (pl) | 2006-09-08 | 2013-05-31 | Actelion Pharmaceuticals Ltd | Pochodne pirydyn-3-ylu jako środki immunomodulujące |
ES2393412T3 (es) | 2006-09-21 | 2012-12-21 | Actelion Pharmaceuticals Ltd. | Derivados de fenilo y su uso como inmunomoduladores |
EP2081916A1 (fr) | 2006-09-29 | 2009-07-29 | Novartis AG | Dérivés d'oxadiazole ayant des propriétés anti-inflammatoires et immuno-suppressives |
JP2008120794A (ja) | 2006-10-16 | 2008-05-29 | Daiichi Sankyo Co Ltd | ヘテロ環化合物を含有する医薬組成物 |
US20110207704A1 (en) | 2006-12-15 | 2011-08-25 | Abbott Laboratories | Novel Oxadiazole Compounds |
NZ577111A (en) | 2006-12-15 | 2012-05-25 | Abbott Lab | Novel oxadiazole compounds |
WO2008091967A1 (fr) | 2007-01-26 | 2008-07-31 | Smithkline Beecham Corporation | Composés chimiques |
DK2125797T3 (da) | 2007-03-16 | 2014-02-10 | Actelion Pharmaceuticals Ltd | Aminopyridinderivater som s1p1/edg1-receptoragonister |
WO2009024905A1 (fr) | 2007-08-17 | 2009-02-26 | Actelion Pharmaceuticals Ltd | Dérivés pyridiniques utilisés comme modulateurs du récepteur s1p1/edg1 |
CN104478821B (zh) | 2007-10-04 | 2016-09-28 | 默克雪兰诺有限公司 | 噁二唑二芳基化合物 |
EA201070422A1 (ru) | 2007-10-04 | 2010-12-30 | Мерк Сероно С.А. | Производные оксадиазола |
AU2008320374A1 (en) | 2007-11-01 | 2009-05-07 | Actelion Pharmaceuticals Ltd | Novel pyrimidine derivatives |
CA2703987A1 (fr) | 2007-11-08 | 2009-05-14 | Pfizer Inc. | Derives d'acide cyclobutylcarboxylique |
WO2009074950A2 (fr) | 2007-12-10 | 2009-06-18 | Actelion Pharmaceuticals Ltd | Nouveaux dérivés du thiophène |
EP2222668B1 (fr) * | 2007-12-18 | 2011-11-02 | Arena Pharmaceuticals, Inc. | Dérivés d'acide tétrahydrocyclopenta[b]indol-3-ylcarboxylique utiles dans le traitement de troubles auto-immuns et inflammatoires |
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WO2009109907A1 (fr) | 2008-03-06 | 2009-09-11 | Actelion Pharmaceuticals Ltd | Nouveaux dérivés de pyrimidine-pyridine |
EP2262782B1 (fr) * | 2008-03-07 | 2012-07-04 | Actelion Pharmaceuticals Ltd. | Nouveaux dérivés d'aminométhylbenzène |
KR101615779B1 (ko) | 2008-03-07 | 2016-04-26 | 액테리온 파마슈티칼 리미티드 | 면역조절제로서 피리딘-2-일 유도체 |
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TW201107302A (en) | 2009-06-26 | 2011-03-01 | Glaxo Group Ltd | Compounds |
RU2547098C2 (ru) * | 2009-07-16 | 2015-04-10 | Актелион Фармасьютиклз Лтд | Производные пиридин-4-ила |
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2012
- 2012-01-18 WO PCT/IB2012/050241 patent/WO2012098505A1/fr active Application Filing
- 2012-01-18 AR ARP120100163A patent/AR084883A1/es unknown
- 2012-01-18 UA UAA201309611A patent/UA109804C2/ru unknown
- 2012-01-18 MY MYPI2013701260A patent/MY163185A/en unknown
- 2012-01-18 EP EP12704125.9A patent/EP2665720B1/fr active Active
- 2012-01-18 SG SG2013047212A patent/SG191742A1/en unknown
- 2012-01-18 MX MX2013007726A patent/MX350009B/es active IP Right Grant
- 2012-01-18 BR BR112013017923-6A patent/BR112013017923B1/pt active IP Right Grant
- 2012-01-18 HU HUE12704125A patent/HUE026012T2/en unknown
- 2012-01-18 TW TW101101997A patent/TWI546300B/zh active
- 2012-01-18 AU AU2012208325A patent/AU2012208325B2/en not_active Ceased
- 2012-01-18 KR KR1020137020321A patent/KR101869120B1/ko active IP Right Grant
- 2012-01-18 PT PT127041259T patent/PT2665720E/pt unknown
- 2012-01-18 US US13/980,764 patent/US9133179B2/en active Active
- 2012-01-18 MA MA36184A patent/MA34910B1/fr unknown
- 2012-01-18 JP JP2013549917A patent/JP5859570B2/ja not_active Expired - Fee Related
- 2012-01-18 CN CN201280005493.7A patent/CN103313981B/zh active Active
- 2012-01-18 ES ES12704125.9T patent/ES2544086T3/es active Active
- 2012-01-18 PL PL12704125T patent/PL2665720T3/pl unknown
- 2012-01-18 CA CA2818470A patent/CA2818470C/fr active Active
- 2012-01-18 SI SI201230254T patent/SI2665720T1/sl unknown
- 2012-01-18 DK DK12704125.9T patent/DK2665720T3/en active
-
2013
- 2013-07-17 IL IL227509A patent/IL227509A0/en active IP Right Grant
- 2013-07-17 CL CL2013002056A patent/CL2013002056A1/es unknown
- 2013-08-16 ZA ZA2013/06193A patent/ZA201306193B/en unknown
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2014
- 2014-05-23 HK HK14104850.5A patent/HK1191645A1/xx not_active IP Right Cessation
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2015
- 2015-08-28 CY CY20151100762T patent/CY1116657T1/el unknown
- 2015-09-02 HR HRP20150919TT patent/HRP20150919T1/hr unknown
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