MA32655B1 - Composés modulant sélectivement le récepteur cb2 - Google Patents
Composés modulant sélectivement le récepteur cb2Info
- Publication number
- MA32655B1 MA32655B1 MA33724A MA33724A MA32655B1 MA 32655 B1 MA32655 B1 MA 32655B1 MA 33724 A MA33724 A MA 33724A MA 33724 A MA33724 A MA 33724A MA 32655 B1 MA32655 B1 MA 32655B1
- Authority
- MA
- Morocco
- Prior art keywords
- receptor
- selectively modulating
- compounds selectively
- compounds
- relates
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 208000023275 Autoimmune disease Diseases 0.000 abstract 1
- 208000037765 diseases and disorders Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 201000006417 multiple sclerosis Diseases 0.000 abstract 1
- 230000002035 prolonged effect Effects 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 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
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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
- A61K31/435—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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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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
-
- 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
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- 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
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Transplantation (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La présente invention concerne des composés de formule (i), utiles pour le traitement d'une variété de maladies et de troubles qui sont médiés ou prolongés par l'activité de ccr1 qui comprennent des maladies auto-immunes, telles que la polyarthrite rhumatoïde et la sclérose en plaques. La présente invention concerne également des procédés de fabrication et d'utilisation de ces composés.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10040108P | 2008-09-26 | 2008-09-26 | |
PCT/US2009/057778 WO2010036632A1 (fr) | 2008-09-26 | 2009-09-22 | Composés azaindazole en tant qu’antagonistes des récepteurs ccr1 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA32655B1 true MA32655B1 (fr) | 2011-09-01 |
Family
ID=41349302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA33724A MA32655B1 (fr) | 2008-09-26 | 2011-03-24 | Composés modulant sélectivement le récepteur cb2 |
Country Status (24)
Country | Link |
---|---|
US (4) | US7879873B2 (fr) |
EP (1) | EP2346868B1 (fr) |
JP (1) | JP5507567B2 (fr) |
KR (1) | KR20110060904A (fr) |
CN (1) | CN102227425A (fr) |
AP (1) | AP2739A (fr) |
AR (1) | AR073689A1 (fr) |
AU (1) | AU2009296839A1 (fr) |
BR (1) | BRPI0919844A2 (fr) |
CA (1) | CA2737472A1 (fr) |
CL (1) | CL2011000668A1 (fr) |
CO (1) | CO6351735A2 (fr) |
EA (1) | EA201100524A1 (fr) |
EC (1) | ECSP11010932A (fr) |
IL (1) | IL210857A0 (fr) |
MA (1) | MA32655B1 (fr) |
MX (1) | MX2011002951A (fr) |
NZ (1) | NZ591115A (fr) |
PE (1) | PE20110854A1 (fr) |
TW (1) | TW201018683A (fr) |
UA (1) | UA103634C2 (fr) |
UY (1) | UY32140A (fr) |
WO (1) | WO2010036632A1 (fr) |
ZA (1) | ZA201100625B (fr) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8008327B2 (en) | 2008-04-29 | 2011-08-30 | Boehringer Ingelheim International Gmbh | Indazole compounds as CCR1 receptor antagonists |
CA2722811C (fr) | 2008-05-06 | 2016-07-05 | Boehringer Ingelheim International Gmbh | Composes de pyrazole comme antagonistes de ccr1 |
CN102227425A (zh) | 2008-09-26 | 2011-10-26 | 贝林格尔·英格海姆国际有限公司 | 作为ccr1受体拮抗剂的氮杂吲唑化合物 |
JP5732036B2 (ja) * | 2009-03-19 | 2015-06-10 | メディカル リサーチ カウンシル テクノロジーMedical Research Council Technology | 化合物 |
KR20120087923A (ko) | 2009-10-21 | 2012-08-07 | 베링거 인겔하임 인터내셔날 게엠베하 | Ccr1 수용체 길항제로서의 인다졸 및 피라졸로피리딘 화합물 |
EP2493875B1 (fr) * | 2009-10-27 | 2014-08-06 | Boehringer Ingelheim International GmbH | Composés hétérocycliques utilisés en tant qu'antagonistes des récepteurs ccr1 |
CN102596908A (zh) | 2009-12-08 | 2012-07-18 | 贝林格尔.英格海姆国际有限公司 | 用于制备取代的吲唑和氮杂吲唑化合物的中间体的合成方法 |
JP5793182B2 (ja) * | 2010-04-30 | 2015-10-14 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ccr1受容体アンタゴニストとしてのアザインダゾールアミド化合物 |
EP2388260A1 (fr) * | 2010-05-21 | 2011-11-23 | Archimica GmbH | Procédé de fabrication pour un inhibiteur d'un facteur de coagulation sanguine |
SG188367A1 (en) | 2010-09-03 | 2013-04-30 | Forma Tm Llc | Novel compounds and compositions for the inhibition of nampt |
EP2655371B1 (fr) | 2010-12-23 | 2015-02-25 | Boehringer Ingelheim International GmbH | Composés de pyrazolopipéridine en tant qu'antagonistes de récepteur ccr1 |
JP2014511389A (ja) | 2011-02-28 | 2014-05-15 | エピザイム インコーポレイテッド | 置換6,5−縮合二環式ヘテロアリール化合物 |
CN102775365A (zh) * | 2011-05-10 | 2012-11-14 | 无锡立诺康医药科技有限公司 | 5-氨基取代基-异噁唑类化合物或其酸式盐的合成工艺 |
WO2012163848A1 (fr) | 2011-05-27 | 2012-12-06 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Procédés et compositions pharmaceutiques destinés au traitement de la maladie de crohn |
US9174984B2 (en) | 2011-10-24 | 2015-11-03 | Glaxosmithkline Intellectual Property (No.2) Limited | Chemical compounds |
EP2771484A1 (fr) | 2011-10-28 | 2014-09-03 | Galderma Research & Development | Nouveaux marqueurs d'infiltrat leucocytaire de rosacée et utilisations de ceux-ci |
EP2820017B1 (fr) * | 2012-03-02 | 2016-12-21 | Genentech, Inc. | Dérivés sulfones et sulfoxydes pyridinyliques et pyrimidinyliques |
AR091858A1 (es) * | 2012-07-25 | 2015-03-04 | Sova Pharmaceuticals Inc | INHIBIDORES DE CISTATIONIN-g-LIASA (CSE) |
EP2970306A4 (fr) * | 2013-03-15 | 2016-08-03 | Epizyme Inc | Composés hétéroaryles bicycliques substitués condensés en 6,5 |
US9045477B2 (en) * | 2013-03-15 | 2015-06-02 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
FR3016879A1 (fr) * | 2014-01-29 | 2015-07-31 | Guillaume Laconde | Procede de preparation de benzotriazole n-acyles |
SI3119757T1 (en) | 2014-03-17 | 2018-08-31 | Pfizer Inc. | DIACILGLICEROL-ACILTRANSFERAZE 2 BINDERS FOR THE USE IN THE TREATMENT OF PRECIOUS AND RELATED DISEASES |
BR112016021962A2 (pt) | 2014-04-14 | 2023-01-20 | Boehringer Ingelheim Int | Compostos, composição farmacêutica e seus usos como moduladores de ror gama |
MA44474A (fr) | 2015-10-23 | 2019-01-30 | Vifor Int Ag | Nouveaux inhibiteurs de la ferroportine |
EP3373733A1 (fr) | 2015-11-13 | 2018-09-19 | Basf Se | Oxadiazoles substitués pour lutter contre des champignons phytopathogènes |
WO2017081310A1 (fr) | 2015-11-13 | 2017-05-18 | Basf Se | Oxadiazoles substitués pour lutter contre des champignons phytopathogènes |
WO2017155909A1 (fr) | 2016-03-07 | 2017-09-14 | The Global Alliance For Tb Drug Development, Inc. | Composés antibactériens et utilisations de ceux-ci |
JOP20180036A1 (ar) | 2017-04-18 | 2019-01-30 | Vifor Int Ag | أملاح لمثبطات فروبورتين جديدة |
CN111393376B (zh) * | 2020-05-11 | 2022-05-13 | 安徽赛迪生物科技有限公司 | 一种2-氯嘧啶-4-甲酸的合成方法 |
WO2021262878A1 (fr) * | 2020-06-24 | 2021-12-30 | Oregon Health & Science University | Nouvelle molécule pour la modulation de réponses immunitaires innées régulées par une protéine sting |
Family Cites Families (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5242931A (en) | 1988-06-09 | 1993-09-07 | Kyowa Hakko Kogyo Co., Ltd. | Tricyclic compounds as TXA2 antagonists |
US4999363A (en) | 1988-06-09 | 1991-03-12 | Kyowa Hakko Kogyo Co., Ltd. | Tricyclic compounds |
US5750542A (en) | 1993-09-28 | 1998-05-12 | Pfizer | Benzisoxazole and benzisothizole derivatives as cholinesterase inhibitors |
BR9205811A (pt) | 1991-03-28 | 1994-06-28 | Pfizer | Derivados heterociclicos de aminas ciclicas |
US5612360A (en) | 1992-06-03 | 1997-03-18 | Eli Lilly And Company | Angiotensin II antagonists |
RU2105005C1 (ru) | 1992-07-03 | 1998-02-20 | Кумиай Кемикал Индастри Ко., Лтд. | Конденсированное гетероциклическое производное, способ его получения и гербицидное средство |
WO1995000509A1 (fr) | 1993-06-25 | 1995-01-05 | Kumiai Chemical Industry Co., Ltd. | Derive d'indazolesulfonyluree, son utilisation et intermediaire pour sa production |
CA2207201A1 (fr) | 1994-12-06 | 1996-06-13 | Caroline Henry | Derives de l'azetidine, de la pyrrolidine et de la piperidine utilises comme agonistes des recepteurs 5-ht1 |
GB9519563D0 (en) | 1995-09-26 | 1995-11-29 | Merck Sharp & Dohme | Therapeutic agents |
GB9523583D0 (en) | 1995-11-17 | 1996-01-17 | Merck Sharp & Dohme | Therapeutic agents |
US5760028A (en) | 1995-12-22 | 1998-06-02 | The Dupont Merck Pharmaceutical Company | Integrin receptor antagonists |
WO1997023480A1 (fr) | 1995-12-22 | 1997-07-03 | The Du Pont Merck Pharmaceutical Company | Nouveaux antagonistes de recepteurs d'integrines |
JPH101478A (ja) | 1996-06-11 | 1998-01-06 | Kumiai Chem Ind Co Ltd | インダゾールスルホニル尿素誘導体及び除草剤 |
GB9615449D0 (en) | 1996-07-23 | 1996-09-04 | Merck Sharp & Dohme | Therapeutic agents |
KR20010031783A (ko) | 1997-11-04 | 2001-04-16 | 데이비드 존 우드 | Pde4 억제제 중 인다졸에 의한 카테콜의 생등입체성치환을 기재로 하는 치료상 활성인 화합물 |
US6331640B1 (en) | 1998-10-13 | 2001-12-18 | Hoffmann-La Roche Inc. | Diaminopropionic acid derivatives |
WO2000076970A2 (fr) | 1999-06-14 | 2000-12-21 | Eli Lilly And Company | Composes |
AU5414000A (en) | 1999-06-14 | 2001-01-02 | Eli Lilly And Company | Compounds |
AU5895500A (en) | 1999-06-29 | 2001-01-31 | Cor Therapeutics, Inc. | Novel indazole peptidomimetics as thrombin receptor antagonists |
GB0030306D0 (en) | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
GB0030303D0 (en) | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
GB0030304D0 (en) | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
GB0030305D0 (en) | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
US6897231B2 (en) | 2000-07-31 | 2005-05-24 | Signal Pharmaceuticals, Inc. | Indazole derivatives as JNK inhibitors and compositions and methods related thereto |
US7211594B2 (en) | 2000-07-31 | 2007-05-01 | Signal Pharmaceuticals, Llc | Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith |
US20050009876A1 (en) | 2000-07-31 | 2005-01-13 | Bhagwat Shripad S. | Indazole compounds, compositions thereof and methods of treatment therewith |
US7058826B2 (en) | 2000-09-27 | 2006-06-06 | Amphus, Inc. | System, architecture, and method for logical server and other network devices in a dynamically configurable multi-server network environment |
US20020052373A1 (en) | 2000-10-26 | 2002-05-02 | Zorn Stevin H. | Combination treatment for dementia or cognitive deficits associated with alzheimer's disease and parkinson's disease |
CA2465207C (fr) | 2001-11-01 | 2011-01-04 | Icagen, Inc. | Pyrazole-amides et -sulfonamides |
WO2008011131A2 (fr) | 2006-07-21 | 2008-01-24 | Takeda Pharmaceutical Company Limited | Composés amidés |
WO2003053941A2 (fr) * | 2001-12-20 | 2003-07-03 | Bristol-Myers Squibb Company | Derives de l'acide barbiturique utilises comme inhibiteurs de l'enzyme de conversion du tnf-alpha (tace) et/ou de metalloproteases matricielles |
EP1497278B1 (fr) | 2002-04-11 | 2010-05-26 | Boehringer Ingelheim Pharmaceuticals Inc. | Derives d'amides heterocycliques utilises en tant qu'inhibiteurs de cytokine |
WO2003101968A1 (fr) | 2002-05-31 | 2003-12-11 | Eisai Co., Ltd. | Compose de pyrazole et composition medicinale le contenant |
DE60328690D1 (de) * | 2002-06-12 | 2009-09-17 | Chemocentryx Inc | 1-aryl-4-substituierte piperazin-derivate zur verwendung als ccr1-antagonisten zur behandlung von entzündungen und immunerkrankungen |
TW200500341A (en) | 2002-11-12 | 2005-01-01 | Astrazeneca Ab | Novel compounds |
SE0203825D0 (sv) | 2002-12-20 | 2002-12-20 | Astrazeneca Ab | Novel fused heterocycles and uses thereof |
US7129264B2 (en) | 2003-04-16 | 2006-10-31 | Bristol-Myers Squibb Company | Biarylmethyl indolines and indoles as antithromboembolic agents |
US20040220170A1 (en) | 2003-05-01 | 2004-11-04 | Atkinson Robert N. | Pyrazole-amides and sulfonamides as sodium channel modulators |
JP2007502307A (ja) | 2003-08-15 | 2007-02-08 | アストラゼネカ アクチボラグ | グルタミン酸ラセマーゼ(muri)の阻害剤としての縮合複素環 |
US7960417B2 (en) | 2005-02-24 | 2011-06-14 | Merck Sharp & Dohme Corp. | Benzazole potentiators of metabotropic glutamate receptors |
GB0504828D0 (en) * | 2005-03-09 | 2005-04-13 | Merck Sharp & Dohme | Therapeutic agents |
LT2444079T (lt) | 2005-05-17 | 2017-03-27 | Sarcode Bioscience Inc. | Kompozicijos ir būdai, skirti akių sutrikimų gydymui |
BRPI0612112A8 (pt) * | 2005-06-22 | 2017-12-26 | Chemocentryx Inc | composto, composição farmacêutica, e, método de tratar doenças ou condições mediadas por ccr1. |
WO2007028083A2 (fr) | 2005-09-01 | 2007-03-08 | Eli Lilly And Company | Utilisation de 6-arylalkylamino- 2,3,4,5-tetrahydro-1h-benzo[d]azepines comme agonistes des recepteurs 5-ht2c |
EP1940394A4 (fr) | 2005-10-25 | 2009-07-08 | Smithkline Beecham Corp | Composés chimiques |
TW200829578A (en) * | 2006-11-23 | 2008-07-16 | Astrazeneca Ab | Chemical compounds 537 |
CN101743242A (zh) * | 2007-06-29 | 2010-06-16 | 苏尼西斯制药有限公司 | 用作raf激酶抑制剂的杂环化合物 |
CA2696725A1 (fr) | 2007-08-10 | 2009-03-26 | Crystalgenomics, Inc. | Derives de pyridine et leurs procedes d'utilisation |
GB0716292D0 (en) | 2007-08-21 | 2007-09-26 | Biofocus Dpi Ltd | Imidazopyrazine compounds |
WO2009085256A1 (fr) * | 2007-12-27 | 2009-07-09 | Panacos Pharmaceuticals, Inc. | Composés anti-vih |
US8008327B2 (en) | 2008-04-29 | 2011-08-30 | Boehringer Ingelheim International Gmbh | Indazole compounds as CCR1 receptor antagonists |
CA2722811C (fr) | 2008-05-06 | 2016-07-05 | Boehringer Ingelheim International Gmbh | Composes de pyrazole comme antagonistes de ccr1 |
CN102227425A (zh) | 2008-09-26 | 2011-10-26 | 贝林格尔·英格海姆国际有限公司 | 作为ccr1受体拮抗剂的氮杂吲唑化合物 |
KR20120087923A (ko) | 2009-10-21 | 2012-08-07 | 베링거 인겔하임 인터내셔날 게엠베하 | Ccr1 수용체 길항제로서의 인다졸 및 피라졸로피리딘 화합물 |
EP2493875B1 (fr) | 2009-10-27 | 2014-08-06 | Boehringer Ingelheim International GmbH | Composés hétérocycliques utilisés en tant qu'antagonistes des récepteurs ccr1 |
CN102596908A (zh) | 2009-12-08 | 2012-07-18 | 贝林格尔.英格海姆国际有限公司 | 用于制备取代的吲唑和氮杂吲唑化合物的中间体的合成方法 |
JP5793182B2 (ja) | 2010-04-30 | 2015-10-14 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ccr1受容体アンタゴニストとしてのアザインダゾールアミド化合物 |
EP2655371B1 (fr) | 2010-12-23 | 2015-02-25 | Boehringer Ingelheim International GmbH | Composés de pyrazolopipéridine en tant qu'antagonistes de récepteur ccr1 |
-
2009
- 2009-09-22 CN CN2009801472064A patent/CN102227425A/zh active Pending
- 2009-09-22 NZ NZ591115A patent/NZ591115A/xx not_active IP Right Cessation
- 2009-09-22 MX MX2011002951A patent/MX2011002951A/es active IP Right Grant
- 2009-09-22 PE PE2011000789A patent/PE20110854A1/es not_active Application Discontinuation
- 2009-09-22 JP JP2011529154A patent/JP5507567B2/ja active Active
- 2009-09-22 AU AU2009296839A patent/AU2009296839A1/en not_active Abandoned
- 2009-09-22 UA UAA201105061A patent/UA103634C2/ru unknown
- 2009-09-22 KR KR1020117006720A patent/KR20110060904A/ko not_active Application Discontinuation
- 2009-09-22 US US12/564,129 patent/US7879873B2/en active Active
- 2009-09-22 EA EA201100524A patent/EA201100524A1/ru unknown
- 2009-09-22 CA CA2737472A patent/CA2737472A1/fr not_active Abandoned
- 2009-09-22 WO PCT/US2009/057778 patent/WO2010036632A1/fr active Application Filing
- 2009-09-22 BR BRPI0919844A patent/BRPI0919844A2/pt not_active IP Right Cessation
- 2009-09-22 AP AP2011005685A patent/AP2739A/xx active
- 2009-09-22 EP EP09792818.8A patent/EP2346868B1/fr active Active
- 2009-09-24 UY UY0001032140A patent/UY32140A/es not_active Application Discontinuation
- 2009-09-25 TW TW098132530A patent/TW201018683A/zh unknown
- 2009-09-25 AR ARP090103709A patent/AR073689A1/es unknown
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2010
- 2010-12-16 US US12/969,753 patent/US8063065B2/en active Active
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2011
- 2011-01-25 IL IL210857A patent/IL210857A0/en unknown
- 2011-01-25 ZA ZA2011/00625A patent/ZA201100625B/en unknown
- 2011-03-17 CO CO11033549A patent/CO6351735A2/es active IP Right Grant
- 2011-03-24 MA MA33724A patent/MA32655B1/fr unknown
- 2011-03-25 CL CL2011000668A patent/CL2011000668A1/es unknown
- 2011-03-29 EC EC2011010932A patent/ECSP11010932A/es unknown
- 2011-10-14 US US13/273,509 patent/US8163918B2/en active Active
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2012
- 2012-02-08 US US13/368,397 patent/US8338610B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
AP2739A (en) | 2013-09-30 |
ECSP11010932A (es) | 2011-04-29 |
JP5507567B2 (ja) | 2014-05-28 |
US20110086846A1 (en) | 2011-04-14 |
PE20110854A1 (es) | 2011-12-23 |
US8338610B2 (en) | 2012-12-25 |
IL210857A0 (en) | 2011-04-28 |
BRPI0919844A2 (pt) | 2019-09-24 |
US20120035370A1 (en) | 2012-02-09 |
JP2012503664A (ja) | 2012-02-09 |
EP2346868A1 (fr) | 2011-07-27 |
US7879873B2 (en) | 2011-02-01 |
CN102227425A (zh) | 2011-10-26 |
AR073689A1 (es) | 2010-11-24 |
KR20110060904A (ko) | 2011-06-08 |
UA103634C2 (en) | 2013-11-11 |
WO2010036632A1 (fr) | 2010-04-01 |
CL2011000668A1 (es) | 2011-10-28 |
EP2346868B1 (fr) | 2016-01-27 |
MX2011002951A (es) | 2011-04-26 |
ZA201100625B (en) | 2011-09-28 |
US8163918B2 (en) | 2012-04-24 |
UY32140A (es) | 2010-04-30 |
TW201018683A (en) | 2010-05-16 |
US8063065B2 (en) | 2011-11-22 |
US20100093724A1 (en) | 2010-04-15 |
AU2009296839A1 (en) | 2010-04-01 |
NZ591115A (en) | 2012-10-26 |
CO6351735A2 (es) | 2011-12-20 |
EA201100524A1 (ru) | 2011-10-31 |
CA2737472A1 (fr) | 2010-04-01 |
AP2011005685A0 (en) | 2011-04-30 |
US20120136158A1 (en) | 2012-05-31 |
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