MA33675B1 - Composé indazole et pyrazolopyridine en tant qu'antagonistes du récepteur ccr1 - Google Patents
Composé indazole et pyrazolopyridine en tant qu'antagonistes du récepteur ccr1Info
- Publication number
- MA33675B1 MA33675B1 MA34779A MA34779A MA33675B1 MA 33675 B1 MA33675 B1 MA 33675B1 MA 34779 A MA34779 A MA 34779A MA 34779 A MA34779 A MA 34779A MA 33675 B1 MA33675 B1 MA 33675B1
- Authority
- MA
- Morocco
- Prior art keywords
- receptor antagonists
- pyrazolobidine
- indazole
- compound
- ccr1 receptor
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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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
- 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
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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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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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
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- 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
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- 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P17/06—Antipsoriatics
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- 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
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- 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
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- 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
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- 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]
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- 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
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- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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
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- 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
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- 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
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'INVENTION PORTE SUR DES ANTAGONISTES DU RÉCEPTEUR CCR1 REPRÉSENTÉ PAR LA FORMULE (I) (FORMULE (I)) DANS LAQUELLE X REPRÉSENTE L'AZOTE OU C-R2; AR1 REPRÉSENTE UN CARBOCYCLE, UN HÉTÉROARYLE OU UN HÉTÉROCYCLYLE CHACUN ÉVENTUELLEMENT SUBSTITUÉ PAR UN À TROIS RA ; AR2 REPRÉSENTE UN CARBOCYCLE, UN HÉTÉROARYLE OU UN HÉTÉROCYCLYLE CHACUN ÉVENTUELLEMENT SUBSTITUÉ PAR UN À TROIS RB; G CYCLIQUE REPRÉSENTE UN CARBOCYCLE OU UN HÉTÉROCYCLYLE CHACUN ÉVENTUELLEMENT SUBSTITUÉ PAR UN À DEUX R8; R1 REPRÉSENTE HYDROGÈNE, ALKYLE EN C1-6 OU (ALCOXY EN C1-6)(ALKYLE EN C1-6). L'INVENTION PORTE ÉGALEMENT SUR DES COMPOSITIONS, SUR DES PROCÉDÉS DE FABRICATION ET D'UTILISATION DE COMPOSÉS REPRÉSENTÉS PAR LA FORMULE (I).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25359009P | 2009-10-21 | 2009-10-21 | |
PCT/US2010/053142 WO2011049917A1 (fr) | 2009-10-21 | 2010-10-19 | Composés d'indazole et de pyrazolopyridine comme antagonistes du récepteur ccr1 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA33675B1 true MA33675B1 (fr) | 2012-10-01 |
Family
ID=43126891
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA34779A MA33675B1 (fr) | 2009-10-21 | 2012-04-16 | Composé indazole et pyrazolopyridine en tant qu'antagonistes du récepteur ccr1 |
Country Status (29)
Country | Link |
---|---|
US (1) | US9056858B2 (fr) |
EP (1) | EP2491028B1 (fr) |
JP (1) | JP5542946B2 (fr) |
KR (1) | KR20120087923A (fr) |
CN (1) | CN102666526A (fr) |
AP (1) | AP2012006204A0 (fr) |
AU (1) | AU2010308277A1 (fr) |
BR (1) | BR112012009331A2 (fr) |
CA (1) | CA2778060A1 (fr) |
CL (1) | CL2012000967A1 (fr) |
CO (1) | CO6531488A2 (fr) |
DK (1) | DK2491028T3 (fr) |
EA (1) | EA021015B1 (fr) |
EC (1) | ECSP12011904A (fr) |
ES (1) | ES2444780T3 (fr) |
GE (1) | GEP20146103B (fr) |
HR (1) | HRP20140213T1 (fr) |
IL (1) | IL218823A0 (fr) |
IN (1) | IN2012DN03449A (fr) |
MA (1) | MA33675B1 (fr) |
MX (1) | MX2012004644A (fr) |
NZ (1) | NZ599132A (fr) |
PE (1) | PE20121433A1 (fr) |
PL (1) | PL2491028T3 (fr) |
PT (1) | PT2491028E (fr) |
RS (1) | RS53130B (fr) |
SI (1) | SI2491028T1 (fr) |
TN (1) | TN2012000180A1 (fr) |
WO (1) | WO2011049917A1 (fr) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2722923C (fr) | 2008-04-29 | 2016-08-02 | Boehringer Ingelheim International Gmbh | Composes indazole comme antagonistes des recepteurs ccr1 |
CA2722811C (fr) | 2008-05-06 | 2016-07-05 | Boehringer Ingelheim International Gmbh | Composes de pyrazole comme antagonistes de ccr1 |
PE20110854A1 (es) | 2008-09-26 | 2011-12-23 | Boehringer Ingelheim Int | DERIVADOS DE 1-FENIL-1H-PIRAZOLO[3,4-c]PIRIDINA-4-CARBONILAMINA COMO ANTAGONISTAS DE LOS RECEPTORES CCR1 |
EA021015B1 (ru) | 2009-10-21 | 2015-03-31 | Бёрингер Ингельхайм Интернациональ Гмбх | Индазолы и пиразолопиридины в качестве антагонистов рецептора ccr1 |
US8927550B2 (en) | 2009-10-27 | 2015-01-06 | Boehringer Ingelheim International Gmbh | Heterocyclic compounds as CCR1 receptor antagonists |
WO2011137109A1 (fr) | 2010-04-30 | 2011-11-03 | Boehringer Ingelheim International Gmbh | Composés azaindazole amides en tant qu'antagonistes des récepteurs ccr1 |
WO2012087782A1 (fr) | 2010-12-23 | 2012-06-28 | Boehringer Ingelheim International Gmbh | Composés de pyrazolopipéridine en tant qu'antagonistes de récepteur ccr1 |
CA2852160A1 (fr) | 2011-10-28 | 2013-05-02 | Galderma Research & Development | Nouveaux marqueurs d'infiltrat leucocytaire de rosacee et utilisations de ceux-ci |
JP6282759B2 (ja) | 2014-04-14 | 2018-02-21 | 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 | Rorガンマのモジュレーターとしての化合物 |
CN112707831A (zh) * | 2021-02-05 | 2021-04-27 | 阿里生物新材料(常州)有限公司 | 一种3-(1-氨基环丙基)苯甲酸甲酯的合成方法 |
Family Cites Families (60)
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 |
CA1338625C (fr) | 1988-06-09 | 1996-10-01 | Kyowa Hakko Kogyo Co., Ltd. | Composes tricycliques |
BR9205811A (pt) | 1991-03-28 | 1994-06-28 | Pfizer | Derivados heterociclicos de aminas ciclicas |
US5750542A (en) | 1993-09-28 | 1998-05-12 | Pfizer | Benzisoxazole and benzisothizole derivatives as cholinesterase inhibitors |
US5612360A (en) | 1992-06-03 | 1997-03-18 | Eli Lilly And Company | Angiotensin II antagonists |
AU662997B2 (en) | 1992-07-03 | 1995-09-21 | Ihara Chemical Industry Co. Ltd. | Condensed heterocyclic derivative and weedkiller |
ES2122290T3 (es) | 1993-06-25 | 1998-12-16 | Kumiai Chemical Industry Co | Derivado de indazolsulfonilurea, su utilizacion e intermediario para su produccion. |
JPH10509721A (ja) | 1994-12-06 | 1998-09-22 | メルク シヤープ エンド ドーム リミテツド | 5ht1レセプターアゴニストとしてのアゼチジン、ピロリジン及びピペリジン誘導体 |
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 |
AU1345697A (en) | 1995-12-22 | 1997-07-17 | Du Pont Merck Pharmaceutical Company, The | Novel integrin receptor antagonists |
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 |
NZ503995A (en) | 1997-11-04 | 2003-02-28 | Pfizer Prod Inc | Indazole compounds, and pharmaceutical compositions and uses thereof, based on indazole bioisostere replacement of catechol in PDE4 inhibitors |
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 |
WO2000076971A2 (fr) | 1999-06-14 | 2000-12-21 | Eli Lilly And Company | Composes |
AU5895500A (en) | 1999-06-29 | 2001-01-31 | Cor Therapeutics, Inc. | Novel indazole peptidomimetics as thrombin receptor antagonists |
KR20020095186A (ko) | 2000-03-02 | 2002-12-20 | 엔디씨 인프라레드 엔지니어링 리미티드 | 전자기 검출 장치 |
GB0030305D0 (en) | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
GB0030306D0 (en) | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
GB0030304D0 (en) | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
GB0030303D0 (en) | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
US20050009876A1 (en) | 2000-07-31 | 2005-01-13 | Bhagwat Shripad S. | Indazole compounds, compositions thereof and methods of treatment therewith |
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 |
US6897231B2 (en) | 2000-07-31 | 2005-05-24 | Signal Pharmaceuticals, Inc. | Indazole derivatives as JNK inhibitors and compositions and methods related thereto |
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 |
ATE455104T1 (de) | 2001-11-01 | 2010-01-15 | Icagen Inc | Pyrazolamide zur anwendung in der behandlung von schmerz |
WO2008011131A2 (fr) | 2006-07-21 | 2008-01-24 | Takeda Pharmaceutical Company Limited | Composés amidés |
CA2478232C (fr) | 2002-04-11 | 2011-06-14 | Boehringer Ingelheim Pharmaceuticals, Inc. | Derives d'amides heterocycliques utilises en tant qu'inhibiteurs de cytokine |
IL164209A0 (en) | 2002-05-31 | 2005-12-18 | Eisai Co Ltd | Pyrazole derivatives and pharmaceutical compositions containing the same |
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 |
WO2004014905A1 (fr) | 2002-08-08 | 2004-02-19 | Boehringer Ingelheim Pharmaceuticals, Inc. | Composes benzimidazole substitues |
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 |
WO2005016929A1 (fr) | 2003-08-15 | 2005-02-24 | Astrazeneca Ab | Heterocycles fusionnes utilises en tant qu'inhibiteurs de la glutamate racemase (muri) |
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 |
CA2960117C (fr) | 2005-05-17 | 2018-01-30 | Sarcode Bioscience Inc. | Antagonistes de lfa-1 destines au traitement de troubles de l'oeil |
US20070155738A1 (en) | 2005-05-20 | 2007-07-05 | Alantos Pharmaceuticals, Inc. | Heterobicyclic metalloprotease inhibitors |
WO2007002667A2 (fr) | 2005-06-22 | 2007-01-04 | Chemocentryx, Inc. | Composés d'azaindazole et procédés d'utilisation |
ES2397400T3 (es) | 2005-09-01 | 2013-03-06 | Eli Lilly & Company | 6-arilalquilamino-2,3,4,5-tetrahidro-1H-benzo[D]azepinas como agonistas del receptor 5-HT2C |
WO2007102883A2 (fr) * | 2005-10-25 | 2007-09-13 | Smithkline Beecham Corporation | Composés chimiques |
KR20090111847A (ko) | 2007-01-19 | 2009-10-27 | 아디아 바이오사이언스즈 인크. | Mek 억제제 |
RU2470023C2 (ru) | 2007-06-26 | 2012-12-20 | Астразенека Аб | 1-цианоциклопропильные производные в качестве ингибиторов катепсина к |
US20110028507A1 (en) | 2007-08-10 | 2011-02-03 | Crystalgenomics, Inc. | Pyridine derivatives and methods of use thereof |
GB0716292D0 (en) | 2007-08-21 | 2007-09-26 | Biofocus Dpi Ltd | Imidazopyrazine compounds |
AU2008329909B2 (en) | 2007-11-29 | 2013-10-03 | Boehringer Ingelheim International Gmbh | Derivatives of 6,7-dihydro-5H-imidazo[1,2-alpha]imidazole-3- carboxylic acid amides |
CA2722923C (fr) | 2008-04-29 | 2016-08-02 | Boehringer Ingelheim International Gmbh | Composes indazole comme antagonistes des recepteurs ccr1 |
CA2722811C (fr) | 2008-05-06 | 2016-07-05 | Boehringer Ingelheim International Gmbh | Composes de pyrazole comme antagonistes de ccr1 |
PE20110854A1 (es) | 2008-09-26 | 2011-12-23 | Boehringer Ingelheim Int | DERIVADOS DE 1-FENIL-1H-PIRAZOLO[3,4-c]PIRIDINA-4-CARBONILAMINA COMO ANTAGONISTAS DE LOS RECEPTORES CCR1 |
EA021015B1 (ru) | 2009-10-21 | 2015-03-31 | Бёрингер Ингельхайм Интернациональ Гмбх | Индазолы и пиразолопиридины в качестве антагонистов рецептора ccr1 |
US8927550B2 (en) | 2009-10-27 | 2015-01-06 | Boehringer Ingelheim International Gmbh | Heterocyclic compounds as CCR1 receptor antagonists |
EP2509952A1 (fr) | 2009-12-08 | 2012-10-17 | Boehringer Ingelheim International GmbH | Procédé de synthèse d'intermédiaires utiles pour la fabrication de for composés à substitution indazole et aza-indazole |
WO2011137109A1 (fr) | 2010-04-30 | 2011-11-03 | Boehringer Ingelheim International Gmbh | Composés azaindazole amides en tant qu'antagonistes des récepteurs ccr1 |
WO2012087782A1 (fr) | 2010-12-23 | 2012-06-28 | Boehringer Ingelheim International Gmbh | Composés de pyrazolopipéridine en tant qu'antagonistes de récepteur ccr1 |
-
2010
- 2010-10-19 EA EA201200602A patent/EA021015B1/ru not_active IP Right Cessation
- 2010-10-19 GE GEAP201012715A patent/GEP20146103B/en unknown
- 2010-10-19 JP JP2012535292A patent/JP5542946B2/ja active Active
- 2010-10-19 MX MX2012004644A patent/MX2012004644A/es active IP Right Grant
- 2010-10-19 NZ NZ599132A patent/NZ599132A/en not_active IP Right Cessation
- 2010-10-19 BR BR112012009331A patent/BR112012009331A2/pt not_active IP Right Cessation
- 2010-10-19 RS RS20140024A patent/RS53130B/en unknown
- 2010-10-19 KR KR1020127010143A patent/KR20120087923A/ko not_active Application Discontinuation
- 2010-10-19 IN IN3449DEN2012 patent/IN2012DN03449A/en unknown
- 2010-10-19 DK DK10768356.7T patent/DK2491028T3/da active
- 2010-10-19 PT PT107683567T patent/PT2491028E/pt unknown
- 2010-10-19 SI SI201030538T patent/SI2491028T1/sl unknown
- 2010-10-19 CN CN2010800578454A patent/CN102666526A/zh active Pending
- 2010-10-19 WO PCT/US2010/053142 patent/WO2011049917A1/fr active Application Filing
- 2010-10-19 AU AU2010308277A patent/AU2010308277A1/en not_active Abandoned
- 2010-10-19 EP EP10768356.7A patent/EP2491028B1/fr active Active
- 2010-10-19 US US13/499,939 patent/US9056858B2/en active Active
- 2010-10-19 PL PL10768356T patent/PL2491028T3/pl unknown
- 2010-10-19 AP AP2012006204A patent/AP2012006204A0/xx unknown
- 2010-10-19 PE PE2012000493A patent/PE20121433A1/es not_active Application Discontinuation
- 2010-10-19 CA CA2778060A patent/CA2778060A1/fr not_active Abandoned
- 2010-10-19 ES ES10768356.7T patent/ES2444780T3/es active Active
-
2012
- 2012-03-25 IL IL218823A patent/IL218823A0/en unknown
- 2012-04-16 MA MA34779A patent/MA33675B1/fr unknown
- 2012-04-16 CL CL2012000967A patent/CL2012000967A1/es unknown
- 2012-04-19 TN TNP2012000180A patent/TN2012000180A1/en unknown
- 2012-04-26 CO CO12068976A patent/CO6531488A2/es active IP Right Grant
- 2012-05-16 EC ECSP12011904 patent/ECSP12011904A/es unknown
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Also Published As
Publication number | Publication date |
---|---|
EP2491028B1 (fr) | 2013-12-11 |
CA2778060A1 (fr) | 2011-04-28 |
BR112012009331A2 (pt) | 2019-09-24 |
EA021015B1 (ru) | 2015-03-31 |
CO6531488A2 (es) | 2012-09-28 |
TN2012000180A1 (en) | 2013-12-12 |
CL2012000967A1 (es) | 2012-09-14 |
AP2012006204A0 (en) | 2012-04-30 |
AU2010308277A1 (en) | 2012-04-26 |
HRP20140213T1 (hr) | 2014-04-11 |
PL2491028T3 (pl) | 2014-05-30 |
US9056858B2 (en) | 2015-06-16 |
IN2012DN03449A (fr) | 2015-10-23 |
KR20120087923A (ko) | 2012-08-07 |
GEP20146103B (en) | 2014-05-27 |
ES2444780T3 (es) | 2014-02-26 |
DK2491028T3 (da) | 2014-01-13 |
MX2012004644A (es) | 2012-05-08 |
JP2013508376A (ja) | 2013-03-07 |
JP5542946B2 (ja) | 2014-07-09 |
CN102666526A (zh) | 2012-09-12 |
ECSP12011904A (es) | 2012-10-30 |
PT2491028E (pt) | 2014-02-04 |
SI2491028T1 (sl) | 2014-03-31 |
PE20121433A1 (es) | 2012-11-10 |
EA201200602A1 (ru) | 2012-12-28 |
WO2011049917A1 (fr) | 2011-04-28 |
NZ599132A (en) | 2014-05-30 |
US20120270870A1 (en) | 2012-10-25 |
RS53130B (en) | 2014-06-30 |
EP2491028A1 (fr) | 2012-08-29 |
IL218823A0 (en) | 2012-06-28 |
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