MA29759B1 - 1h-imidazopyridines a substituant hydroxy et procedes - Google Patents
1h-imidazopyridines a substituant hydroxy et procedesInfo
- Publication number
- MA29759B1 MA29759B1 MA30694A MA30694A MA29759B1 MA 29759 B1 MA29759 B1 MA 29759B1 MA 30694 A MA30694 A MA 30694A MA 30694 A MA30694 A MA 30694A MA 29759 B1 MA29759 B1 MA 29759B1
- Authority
- MA
- Morocco
- Prior art keywords
- substituted
- methods
- imidazopyridines
- compounds
- hydroxy
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 201000010099 disease Diseases 0.000 abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- UHUHBFMZVCOEOV-UHFFFAOYSA-N 1h-imidazo[4,5-c]pyridin-4-amine Chemical class NC1=NC=CC2=C1N=CN2 UHUHBFMZVCOEOV-UHFFFAOYSA-N 0.000 abstract 1
- GAMYYCRTACQSBR-UHFFFAOYSA-N 4-azabenzimidazole Chemical class C1=CC=C2NC=NC2=N1 GAMYYCRTACQSBR-UHFFFAOYSA-N 0.000 abstract 1
- 102000004127 Cytokines Human genes 0.000 abstract 1
- 108090000695 Cytokines Proteins 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000002955 immunomodulating agent Substances 0.000 abstract 1
- 229940121354 immunomodulator Drugs 0.000 abstract 1
- 230000001939 inductive effect Effects 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 230000001613 neoplastic effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000003612 virological effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
-
- 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
- A61P37/02—Immunomodulators
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
1H-imidazopyridines à substituant hydroxy et procédés Des 1H-imidazo[4,5-c]pyridine-4-amines à substituant hydroxy, avec un substituant hydroxy en position 2, des compositions pharmaceutiques contenant ces composés, des procédés pour la préparation des composés, des intermédiaires, et des méthodes d'utilisation de ces composés comme immunomodulateurs, pour induire la biosynthèse de cytokines chez des animaux et dans le traitement de maladies comprenant des maladies virales et maladies néoplasiques, sont décrits.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71370405P | 2005-09-02 | 2005-09-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA29759B1 true MA29759B1 (fr) | 2008-09-01 |
Family
ID=37561219
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA30694A MA29759B1 (fr) | 2005-09-02 | 2008-02-29 | 1h-imidazopyridines a substituant hydroxy et procedes |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US20100152230A1 (fr) |
| EP (1) | EP1924581A1 (fr) |
| JP (1) | JP4584335B2 (fr) |
| KR (1) | KR20080031496A (fr) |
| CN (1) | CN101253173A (fr) |
| AU (1) | AU2006287157A1 (fr) |
| BR (1) | BRPI0615250A2 (fr) |
| CA (1) | CA2620933A1 (fr) |
| CR (1) | CR9781A (fr) |
| EA (1) | EA200800396A1 (fr) |
| EC (1) | ECSP088225A (fr) |
| IL (1) | IL189262A0 (fr) |
| MA (1) | MA29759B1 (fr) |
| MX (1) | MX2008002414A (fr) |
| NO (1) | NO20081393L (fr) |
| RS (1) | RS20080128A (fr) |
| SV (1) | SV2009002832A (fr) |
| TN (1) | TNSN08099A1 (fr) |
| WO (1) | WO2007028129A1 (fr) |
| ZA (1) | ZA200801645B (fr) |
Families Citing this family (76)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040265351A1 (en) | 2003-04-10 | 2004-12-30 | Miller Richard L. | Methods and compositions for enhancing immune response |
| MXPA06001669A (es) | 2003-08-12 | 2006-04-28 | 3M Innovative Properties Co | Compuestos que contienen imidazo-oxima sustituidos. |
| NZ545412A (en) | 2003-08-27 | 2008-12-24 | Coley Pharm Group Inc | Aryloxy and arylalkyleneoxy substituted imidazoquinolines |
| JP2007504269A (ja) | 2003-09-05 | 2007-03-01 | スリーエム イノベイティブ プロパティズ カンパニー | Cd5+b細胞リンパ腫の治療方法 |
| US7544697B2 (en) | 2003-10-03 | 2009-06-09 | Coley Pharmaceutical Group, Inc. | Pyrazolopyridines and analogs thereof |
| KR101494056B1 (ko) | 2003-10-03 | 2015-02-16 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 피라졸로피리딘 및 그의 유사체 |
| EP1673087B1 (fr) | 2003-10-03 | 2015-05-13 | 3M Innovative Properties Company | Imidazoquinolines a substitution alcoxy |
| CN1906192A (zh) | 2003-11-14 | 2007-01-31 | 3M创新有限公司 | 羟胺取代的咪唑环化合物 |
| WO2005048933A2 (fr) | 2003-11-14 | 2005-06-02 | 3M Innovative Properties Company | Composes d'un anneau d'imidazo substitues par oxime |
| AU2004293078B2 (en) | 2003-11-25 | 2012-01-19 | 3M Innovative Properties Company | Substituted imidazo ring systems and methods |
| JP2007517035A (ja) | 2003-12-29 | 2007-06-28 | スリーエム イノベイティブ プロパティズ カンパニー | アリールアルケニルおよびアリールアルキニル置換されたイミダゾキノリン |
| EP1699788A2 (fr) | 2003-12-30 | 2006-09-13 | 3M Innovative Properties Company | Sulfonamides d'imidazoquinolinyle, d'imidazopyridinyle et d'imidazonaphtyridinyle |
| US8697873B2 (en) | 2004-03-24 | 2014-04-15 | 3M Innovative Properties Company | Amide substituted imidazopyridines, imidazoquinolines, and imidazonaphthyridines |
| US8017779B2 (en) | 2004-06-15 | 2011-09-13 | 3M Innovative Properties Company | Nitrogen containing heterocyclyl substituted imidazoquinolines and imidazonaphthyridines |
| US8541438B2 (en) | 2004-06-18 | 2013-09-24 | 3M Innovative Properties Company | Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines |
| US7915281B2 (en) | 2004-06-18 | 2011-03-29 | 3M Innovative Properties Company | Isoxazole, dihydroisoxazole, and oxadiazole substituted imidazo ring compounds and method |
| WO2006009826A1 (fr) | 2004-06-18 | 2006-01-26 | 3M Innovative Properties Company | Thiazoloquinolines et thiazolonaphtyridines substitues par aryloxy et arylalkyleneoxy |
| JP5209312B2 (ja) | 2004-09-02 | 2013-06-12 | スリーエム イノベイティブ プロパティズ カンパニー | 1−アルコキシ1h−イミダゾ環系および方法 |
| JP5313502B2 (ja) | 2004-12-30 | 2013-10-09 | スリーエム イノベイティブ プロパティズ カンパニー | 置換キラル縮合[1,2]イミダゾ[4,5−c]環状化合物 |
| CA2592904C (fr) | 2004-12-30 | 2015-04-07 | 3M Innovative Properties Company | Composes chiraux a cycle [1,2]imidazo[4,5] fusionne |
| JP2008530022A (ja) | 2005-02-04 | 2008-08-07 | コーリー ファーマシューティカル グループ,インコーポレイテッド | 免疫反応調節物質を含む水性ゲル処方物 |
| CA2602083A1 (fr) | 2005-02-09 | 2006-08-09 | Coley Pharmaceutical Group, Inc. | Composes cycliques du type thiazalo(4,5-c) substitues par un groupe du type oxime et hydroxylamine et methodes connexes |
| US20080318998A1 (en) | 2005-02-09 | 2008-12-25 | Coley Pharmaceutical Group, Inc. | Alkyloxy Substituted Thiazoloquinolines and Thiazolonaphthyridines |
| EP1846405A2 (fr) | 2005-02-11 | 2007-10-24 | 3M Innovative Properties Company | Composes cycliques imidazo 4,5-c substitues par oxime et hydroxylamine et procedes associes |
| CA2597446A1 (fr) | 2005-02-11 | 2006-08-31 | Coley Pharmaceutical Group, Inc. | Imidazoquinolines et imidazonaphthyridines substituees |
| EP1851218A2 (fr) | 2005-02-23 | 2007-11-07 | 3M Innovative Properties Company | Composes d'imidazoquinolines a substitution hydroxyalkyle et procedes |
| AU2006223634A1 (en) | 2005-02-23 | 2006-09-21 | Coley Pharmaceutical Group, Inc. | Hydroxyalkyl substituted imidazoquinolines |
| AU2006216686A1 (en) | 2005-02-23 | 2006-08-31 | Coley Pharmaceutical Group, Inc. | Method of preferentially inducing the biosynthesis of interferon |
| CA2602683A1 (fr) | 2005-04-01 | 2006-10-12 | Coley Pharmaceutical Group, Inc. | Pyrazolopyridine-1,4-diamines et analogues associes |
| CA2602590A1 (fr) | 2005-04-01 | 2006-10-12 | Coley Pharmaceutical Group, Inc. | Composes cycliques 1-pyrazolo[3,4-c] substitues comme modulateurs de la biosynthese de cytokine destines au traitement d'infections virales et de maladies neoplastiques |
| AU2006287270A1 (en) | 2005-09-09 | 2007-03-15 | Coley Pharmaceutical Group, Inc. | Amide and carbamate derivatives of N-{2-[4-amino-2- (ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-1,1-dimethylethyl}methanesulfonamide and methods |
| ZA200803029B (en) | 2005-09-09 | 2009-02-25 | Coley Pharm Group Inc | Amide and carbamate derivatives of alkyl substituted /V-[4-(4-amino-1H-imidazo[4,5-c] quinolin-1-yl)butyl] methane-sulfonamides and methods |
| WO2007056112A2 (fr) | 2005-11-04 | 2007-05-18 | Coley Pharmaceutical Group, Inc. | 1h-imidazoquinolines substituees par hydroxy et alcoxy et procedes correspondants |
| JP2009528989A (ja) | 2006-02-17 | 2009-08-13 | ファイザー・リミテッド | Tlr7変調剤としての3−デアザプリン誘導体 |
| EP1988896A4 (fr) | 2006-02-22 | 2011-07-27 | 3M Innovative Properties Co | Conjugués du modificateur de réponse immune |
| WO2007106854A2 (fr) | 2006-03-15 | 2007-09-20 | Coley Pharmaceutical Group, Inc. | 1h-imidazonaphthyridines hydroxy et alcoxy substituées, et procédés associés |
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| MX2012004706A (es) | 2009-10-22 | 2012-06-08 | Gilead Sciences Inc | Derivados de purina o deazapurina utiles para el tratamiento de (inter alia) infecciones virales. |
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| LT2606047T (lt) | 2010-08-17 | 2017-04-10 | 3M Innovative Properties Company | Imuninio atsako modifikatoriaus junginio lipidizuotos kompozicijos, sudėtys ir būdai |
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| CN103450198B (zh) * | 2012-05-29 | 2015-07-08 | 首都医科大学 | 咪唑并吡啶并咪唑-3-取代乙酸苄酯、其合成、抗肿瘤活性及应用 |
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| PL2922549T3 (pl) | 2012-11-20 | 2017-11-30 | Glaxosmithkline Llc | Nowe związki |
| CA2890201A1 (fr) | 2012-11-20 | 2014-05-30 | Glaxosmithkline Llc | Nouveaux composes |
| WO2014081643A1 (fr) | 2012-11-20 | 2014-05-30 | Glaxosmithkline Llc | Nouveaux composés |
| JP2017526730A (ja) | 2014-09-16 | 2017-09-14 | ギリアード サイエンシーズ, インコーポレイテッド | Toll様受容体モジュレーターの固体形態 |
| EP3728255B1 (fr) | 2017-12-20 | 2022-01-26 | 3M Innovative Properties Company | Composés imidazo [4,5-c]quinoléine à substitution amide ayant un groupe de liaison à chaîne ramifiée destinés à être utilisés en tant que modificateur de la réponse immunitaire |
| WO2019209811A1 (fr) | 2018-04-24 | 2019-10-31 | Bristol-Myers Squibb Company | Agonistes macrocycliques du récepteur 7 de type toll (tlr7) |
| US11554120B2 (en) | 2018-08-03 | 2023-01-17 | Bristol-Myers Squibb Company | 1H-pyrazolo[4,3-d]pyrimidine compounds as toll-like receptor 7 (TLR7) agonists and methods and uses therefor |
| KR20220011685A (ko) | 2019-05-22 | 2022-01-28 | 길리애드 사이언시즈, 인코포레이티드 | Tlr7 조절 화합물과 hiv 백신의 조합 |
| CN115151546A (zh) | 2020-01-27 | 2022-10-04 | 百时美施贵宝公司 | 作为Toll样受体7(TLR7)激动剂的C3-取代的1H-吡唑并[4,3-d]嘧啶化合物 |
| WO2021154661A1 (fr) | 2020-01-27 | 2021-08-05 | Bristol-Myers Squibb Company | Composés 1h-pyrazolo [4,3-d]pyrimidine en tant qu'agonistes du récepteur 7 de type toll (tlr7) |
| KR20220132594A (ko) | 2020-01-27 | 2022-09-30 | 브리스톨-마이어스 스큅 컴퍼니 | 톨-유사 수용체 7 (TLR7) 효능제로서의 1H-피라졸로[4,3-d]피리미딘 화합물 |
| EP4097105A1 (fr) | 2020-01-27 | 2022-12-07 | Bristol-Myers Squibb Company | Composés 1h-pyrazolo[4,3-d]pyrimidine utiles en tant qu'agonistes du récepteur de type toll 7 (tlr7) |
| US20230122249A1 (en) | 2020-01-27 | 2023-04-20 | Bristol-Myers Squibb Company | 1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS |
| KR20220132593A (ko) | 2020-01-27 | 2022-09-30 | 브리스톨-마이어스 스큅 컴퍼니 | 톨-유사 수용체 7 (TLR7) 효능제로서의 1H-피라졸로[4,3-d]피리미딘 화합물 |
| US20230144824A1 (en) | 2020-01-27 | 2023-05-11 | Bristol-Myers Squibb Company | 1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS |
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| FR2860514A1 (fr) * | 2003-10-03 | 2005-04-08 | Sanofi Synthelabo | Derives d'arylalkylcarbamates, leur preparation et leur application en therapeutique |
| WO2005048933A2 (fr) * | 2003-11-14 | 2005-06-02 | 3M Innovative Properties Company | Composes d'un anneau d'imidazo substitues par oxime |
| AU2004293078B2 (en) * | 2003-11-25 | 2012-01-19 | 3M Innovative Properties Company | Substituted imidazo ring systems and methods |
| TW200616604A (en) * | 2004-08-26 | 2006-06-01 | Nicholas Piramal India Ltd | Nitric oxide releasing prodrugs containing bio-cleavable linker |
| JP2009528989A (ja) * | 2006-02-17 | 2009-08-13 | ファイザー・リミテッド | Tlr7変調剤としての3−デアザプリン誘導体 |
-
2006
- 2006-09-01 MX MX2008002414A patent/MX2008002414A/es unknown
- 2006-09-01 EP EP06802901A patent/EP1924581A1/fr not_active Withdrawn
- 2006-09-01 EA EA200800396A patent/EA200800396A1/ru unknown
- 2006-09-01 CN CNA2006800319190A patent/CN101253173A/zh active Pending
- 2006-09-01 US US12/065,490 patent/US20100152230A1/en not_active Abandoned
- 2006-09-01 AU AU2006287157A patent/AU2006287157A1/en not_active Abandoned
- 2006-09-01 WO PCT/US2006/034427 patent/WO2007028129A1/fr not_active Ceased
- 2006-09-01 KR KR1020087005146A patent/KR20080031496A/ko not_active Ceased
- 2006-09-01 RS RSP-2008/0128A patent/RS20080128A/sr unknown
- 2006-09-01 JP JP2008529359A patent/JP4584335B2/ja not_active Expired - Fee Related
- 2006-09-01 CA CA002620933A patent/CA2620933A1/fr not_active Abandoned
- 2006-09-01 BR BRPI0615250-3A patent/BRPI0615250A2/pt not_active IP Right Cessation
-
2008
- 2008-02-04 IL IL189262A patent/IL189262A0/en unknown
- 2008-02-19 ZA ZA200801645A patent/ZA200801645B/xx unknown
- 2008-02-26 EC EC2008008225A patent/ECSP088225A/es unknown
- 2008-02-29 CR CR9781A patent/CR9781A/es not_active Application Discontinuation
- 2008-02-29 SV SV2008002832A patent/SV2009002832A/es not_active Application Discontinuation
- 2008-02-29 TN TNP2008000099A patent/TNSN08099A1/fr unknown
- 2008-02-29 MA MA30694A patent/MA29759B1/fr unknown
- 2008-03-17 NO NO20081393A patent/NO20081393L/no not_active Application Discontinuation
-
2011
- 2011-10-20 US US13/277,619 patent/US20120035209A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0615250A2 (pt) | 2011-05-10 |
| EP1924581A1 (fr) | 2008-05-28 |
| KR20080031496A (ko) | 2008-04-08 |
| US20120035209A1 (en) | 2012-02-09 |
| TNSN08099A1 (fr) | 2009-07-14 |
| ECSP088225A (es) | 2008-03-26 |
| WO2007028129A1 (fr) | 2007-03-08 |
| RS20080128A (sr) | 2009-05-06 |
| US20100152230A1 (en) | 2010-06-17 |
| AU2006287157A1 (en) | 2007-03-08 |
| CA2620933A1 (fr) | 2007-03-08 |
| JP2009507036A (ja) | 2009-02-19 |
| NO20081393L (no) | 2008-05-28 |
| EA200800396A1 (ru) | 2008-08-29 |
| IL189262A0 (en) | 2008-06-05 |
| CR9781A (es) | 2008-03-26 |
| JP4584335B2 (ja) | 2010-11-17 |
| MX2008002414A (es) | 2008-03-27 |
| CN101253173A (zh) | 2008-08-27 |
| SV2009002832A (es) | 2009-02-19 |
| ZA200801645B (en) | 2010-08-25 |
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