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
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)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (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 (72)
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 |
WO2005018556A2 (fr) | 2003-08-12 | 2005-03-03 | 3M Innovative Properties Company | Composes contenant une structure imidazo a substitution hydroxylamine |
ES2406730T3 (es) | 2003-08-27 | 2013-06-07 | 3M Innovative Properties Company | Imidazoquinolinas sustituidas con ariloxi y arilalquilenoxi |
AU2004270201A1 (en) | 2003-09-05 | 2005-03-17 | 3M Innovative Properties Company | Treatment for CD5+ B cell lymphoma |
US7544697B2 (en) | 2003-10-03 | 2009-06-09 | Coley Pharmaceutical Group, Inc. | Pyrazolopyridines and analogs thereof |
CA2540598C (fr) | 2003-10-03 | 2013-09-24 | 3M Innovative Properties Company | Pyrazolopyridines et analogues de celles-ci |
CA2540541C (fr) | 2003-10-03 | 2012-03-27 | 3M Innovative Properties Company | Imidazoquinolines a substitution alcoxy |
WO2005048945A2 (fr) | 2003-11-14 | 2005-06-02 | 3M Innovative Properties Company | Composes d'un anneau d'imidazo substitue par hydroxylamine |
EP1685129A4 (fr) | 2003-11-14 | 2008-10-22 | 3M Innovative Properties Co | Composes d'un anneau d'imidazo substitues par oxime |
JP4891088B2 (ja) | 2003-11-25 | 2012-03-07 | スリーエム イノベイティブ プロパティズ カンパニー | 置換されたイミダゾ環系および方法 |
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 |
CA2551399A1 (fr) | 2003-12-30 | 2005-07-21 | 3M Innovative Properties Company | Sulfonamides d'imidazoquinolinyle, d'imidazopyridinyle et d'imidazonaphtyridinyle |
CA2559863A1 (fr) | 2004-03-24 | 2005-10-13 | 3M Innovative Properties Company | Imidazopyridines, imidazoquinolines, et imidazonaphthyridines a substitution amide |
US8017779B2 (en) | 2004-06-15 | 2011-09-13 | 3M Innovative Properties Company | Nitrogen containing heterocyclyl substituted imidazoquinolines and imidazonaphthyridines |
US7915281B2 (en) | 2004-06-18 | 2011-03-29 | 3M Innovative Properties Company | Isoxazole, dihydroisoxazole, and oxadiazole substituted imidazo ring compounds and method |
US8541438B2 (en) | 2004-06-18 | 2013-09-24 | 3M Innovative Properties Company | Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines |
US8026366B2 (en) | 2004-06-18 | 2011-09-27 | 3M Innovative Properties Company | Aryloxy and arylalkyleneoxy substituted thiazoloquinolines and thiazolonaphthyridines |
AU2005326708C1 (en) | 2004-12-30 | 2012-08-30 | 3M Innovative Properties Company | Substituted chiral fused [1,2]imidazo[4,5-c] ring compounds |
AU2005322898B2 (en) | 2004-12-30 | 2011-11-24 | 3M Innovative Properties Company | Chiral fused (1,2)imidazo(4,5-c) ring compounds |
CA2597092A1 (fr) | 2005-02-04 | 2006-08-10 | Coley Pharmaceutical Group, Inc. | Formulations des gel aqueux contenant des modificateurs de reponse immunitaire |
AU2006338521A1 (en) | 2005-02-09 | 2007-10-11 | Coley Pharmaceutical Group, Inc. | Oxime and hydroxylamine substituted thiazolo(4,5-c) ring compounds and methods |
US20080318998A1 (en) | 2005-02-09 | 2008-12-25 | Coley Pharmaceutical Group, Inc. | Alkyloxy Substituted Thiazoloquinolines and Thiazolonaphthyridines |
WO2006086634A2 (fr) | 2005-02-11 | 2006-08-17 | Coley Pharmaceutical Group, Inc. | Composes cycliques imidazo[4,5-c] substitues par oxime et hydroxylamine et procedes associes |
US8658666B2 (en) | 2005-02-11 | 2014-02-25 | 3M Innovative Properties Company | Substituted imidazoquinolines and imidazonaphthyridines |
JP2008538203A (ja) | 2005-02-23 | 2008-10-16 | 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 | インターフェロンの生合成を優先的に誘導する方法 |
EP1851224A2 (fr) | 2005-02-23 | 2007-11-07 | 3M Innovative Properties Company | Imidazoquinolines a substitution hydroxyalkyle |
AU2006216798A1 (en) | 2005-02-23 | 2006-08-31 | Coley Pharmaceutical Group, Inc. | Hydroxyalkyl substituted imidazoquinoline compounds and methods |
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 |
EP1869043A2 (fr) | 2005-04-01 | 2007-12-26 | Coley Pharmaceutical Group, Inc. | Pyrazolopyridine-1,4-diamines et analogues associes |
JP2009507856A (ja) | 2005-09-09 | 2009-02-26 | 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 | N−{2−[4−アミノ−2−(エトキシメチル)−1H−イミダゾ[4,5−c]キノリン−1−イル]−1,1−ジメチルエチル}メタンスルホンアミドのアミドおよびカルバマート誘導体ならびに方法 |
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 |
JP5247458B2 (ja) | 2005-11-04 | 2013-07-24 | スリーエム・イノベイティブ・プロパティーズ・カンパニー | ヒドロキシ及びアルコキシ置換1h−イミダゾキノリン及び方法 |
MX2008010611A (es) | 2006-02-17 | 2008-11-12 | Pfizer Ltd | Derivados de 3-desazapurina como moduladores de receptores similares a toll. |
US8951528B2 (en) | 2006-02-22 | 2015-02-10 | 3M Innovative Properties Company | Immune response modifier conjugates |
WO2007106854A2 (fr) | 2006-03-15 | 2007-09-20 | Coley Pharmaceutical Group, Inc. | 1h-imidazonaphthyridines hydroxy et alcoxy substituées, et procédés associés |
WO2008008432A2 (fr) | 2006-07-12 | 2008-01-17 | Coley Pharmaceutical Group, Inc. | Composés à cycle [1,2] imidazo [4,5-c] fusionné chiral substitué et procédés correspondants |
WO2008030511A2 (fr) | 2006-09-06 | 2008-03-13 | Coley Pharmaceuticial Group, Inc. | 3, 4, 6, 7-tétrahydro-5h-1, 2a, 4a, 8-tétraazacyclopenta[cd]phénalènes substitués |
US20080149123A1 (en) | 2006-12-22 | 2008-06-26 | Mckay William D | Particulate material dispensing hairbrush with combination bristles |
DE602008003764D1 (de) | 2007-02-19 | 2011-01-13 | Glaxosmithkline Llc | Purinderivate als immunmodulatoren |
EP1997805A1 (fr) * | 2007-06-01 | 2008-12-03 | Commissariat à l'Energie Atomique | Compositions à activité antiparasite, applications associées au traitement des maladies infectieuses causées par des apicomplexans |
CA2707030A1 (fr) * | 2007-08-03 | 2009-02-12 | Pfizer Limited | Imidazopyridinones |
LT2320905T (lt) | 2008-08-11 | 2017-09-11 | Glaxosmithkline Llc | Naujieji adenino dariniai |
UA103195C2 (uk) | 2008-08-11 | 2013-09-25 | Глаксосмитклайн Ллк | Похідні пурину для застосування у лікуванні алергій, запальних та інфекційних захворювань |
US8802684B2 (en) | 2008-08-11 | 2014-08-12 | Glaxosmithkline Llc | Adenine derivatives |
US8575181B2 (en) | 2008-08-11 | 2013-11-05 | Glaxosmithkline Llc | Purine derivatives for use in the treatment of allergic, inflammatory and infectious diseases |
EA021377B9 (ru) | 2008-12-09 | 2015-09-30 | Джилид Сайэнс, Инк. | Модуляторы толл-подобных рецепторов |
CA2772071A1 (fr) | 2009-08-28 | 2011-03-03 | Array Biopharma Inc. | Composes inhibiteurs de raf et leurs procedes d'utilisation |
SI2491035T1 (sl) * | 2009-10-22 | 2017-10-30 | Gilead Sciences, Inc. | Derivati purina ali deazapurina uporabni za zdravljenje (med drugimi) virusnih okužb |
US8575340B2 (en) | 2010-02-10 | 2013-11-05 | Glaxosmithkline Llc | Purine derivatives and their pharmaceutical uses |
HUE033901T2 (en) | 2010-08-17 | 2018-01-29 | 3M Innovative Properties Co | Formulations and formulations for lipidized immune response modifying compounds and related processes |
JP6415979B2 (ja) | 2011-06-03 | 2018-10-31 | スリーエム イノベイティブ プロパティズ カンパニー | ヒドラジノ1h−イミダゾキノリン−4−アミン及びこれから調製された複合体 |
CA2838158C (fr) | 2011-06-03 | 2019-07-16 | 3M Innovative Properties Company | Lieurs heterobifonctionnels comportant de segments de polyethylene glycol et conjugues modificateurs de reponse immunitaire obtenus a partir de ceux-ci |
RU2631482C2 (ru) | 2011-07-22 | 2017-09-22 | ГЛАКСОСМИТКЛАЙН ЭлЭлСи | Композиция |
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 |
WO2014031815A1 (fr) | 2012-08-24 | 2014-02-27 | Glaxosmithkline Llc | Composés pyrazolopyrimidine |
KR20150085081A (ko) | 2012-11-20 | 2015-07-22 | 글락소스미스클라인 엘엘씨 | 신규 화합물 |
WO2014081645A1 (fr) | 2012-11-20 | 2014-05-30 | Glaxosmithkline Llc | Nouveaux composés |
EP2922550B1 (fr) | 2012-11-20 | 2017-04-19 | Glaxosmithkline LLC | Nouveaux composés |
UY36298A (es) | 2014-09-16 | 2016-04-29 | Gilead Science Inc | Formas sólidas de un modulador del receptor tipo toll |
JP7197244B2 (ja) | 2017-12-20 | 2022-12-27 | スリーエム イノベイティブ プロパティズ カンパニー | 免疫応答調節剤として使用するための分岐鎖連結基を有するアミド置換イミダゾ[4,5-c]キノリン化合物 |
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 |
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 |
KR20220132591A (ko) | 2020-01-27 | 2022-09-30 | 브리스톨-마이어스 스큅 컴퍼니 | 톨-유사 수용체 7 (TLR7) 효능제로서의 1H-피라졸로[4,3-d]피리미딘 화합물 |
EP4097103A1 (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) |
CN115210236A (zh) | 2020-01-27 | 2022-10-18 | 百时美施贵宝公司 | 作为Toll样受体7(TLR7)激动剂的1H-吡唑并[4,3-d]嘧啶化合物 |
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) |
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 |
JP2023512206A (ja) | 2020-01-27 | 2023-03-24 | ブリストル-マイヤーズ スクイブ カンパニー | トール様受容体7(TLR7)アゴニストとしての1H-ピラゾロ[4,3-d]ピリミジン化合物 |
EP4097107A1 (fr) | 2020-01-27 | 2022-12-07 | Bristol-Myers Squibb Company | Composés 1-pyrazolo[4,3-d]pyrimidine substitués en c3 utiles en tant qu'agonistes du récepteur de type toll 7 (tlr7) |
KR20220132601A (ko) | 2020-01-27 | 2022-09-30 | 브리스톨-마이어스 스큅 컴퍼니 | 톨-유사 수용체 7 (TLR7) 효능제로서의 1H-피라졸로[4,3-d]피리미딘 화합물 |
CN117466808B (zh) * | 2023-12-27 | 2024-03-12 | 烟台新药创制山东省实验室 | 一种6-烷基-2,4-二羟基吡啶类衍生物的制备方法 |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09500128A (ja) * | 1993-07-15 | 1997-01-07 | ミネソタ マイニング アンド マニュファクチャリング カンパニー | イミダゾ〔4,5−c〕ピリジン−4−アミン |
WO1998001448A1 (fr) * | 1996-07-03 | 1998-01-15 | Japan Energy Corporation | Nouveaux derives de purine |
KR100892614B1 (ko) * | 2001-04-17 | 2009-04-09 | 다이닛본 스미토모 세이야꾸 가부시끼가이샤 | 신규 아데닌 유도체 |
EP1389618B1 (fr) * | 2001-04-27 | 2011-06-15 | Eisai R&D Management Co., Ltd. | Pyrazolo 1,5-a pyridines et medicaments les contenant |
AU2003237386A1 (en) * | 2002-06-07 | 2003-12-22 | 3M Innovative Properties Company | Ether substituted imidazopyridines |
TWI325865B (en) * | 2003-02-27 | 2010-06-11 | Palau Pharma Sa | Pyrazolopyridine derivatives |
US7517887B2 (en) * | 2003-04-09 | 2009-04-14 | General Atomics | Reversible inhibitors of S-adenosyl-L-homocysteine hydrolase and uses thereof |
JP2005089334A (ja) * | 2003-09-12 | 2005-04-07 | Sumitomo Pharmaceut Co Ltd | 8−ヒドロキシアデニン化合物 |
CN1997642B (zh) * | 2003-09-22 | 2012-06-13 | 詹森药业有限公司 | 7-氨基亚烷基-杂环喹诺酮类和萘啶酮类 |
FR2860514A1 (fr) * | 2003-10-03 | 2005-04-08 | Sanofi Synthelabo | Derives d'arylalkylcarbamates, leur preparation et leur application en therapeutique |
EP1685129A4 (fr) * | 2003-11-14 | 2008-10-22 | 3M Innovative Properties Co | Composes d'un anneau d'imidazo substitues par oxime |
JP4891088B2 (ja) * | 2003-11-25 | 2012-03-07 | スリーエム イノベイティブ プロパティズ カンパニー | 置換されたイミダゾ環系および方法 |
TW200616604A (en) * | 2004-08-26 | 2006-06-01 | Nicholas Piramal India Ltd | Nitric oxide releasing prodrugs containing bio-cleavable linker |
MX2008010611A (es) * | 2006-02-17 | 2008-11-12 | Pfizer Ltd | Derivados de 3-desazapurina como moduladores de receptores similares a toll. |
-
2006
- 2006-09-01 CN CNA2006800319190A patent/CN101253173A/zh active Pending
- 2006-09-01 JP JP2008529359A patent/JP4584335B2/ja not_active Expired - Fee Related
- 2006-09-01 RS RSP-2008/0128A patent/RS20080128A/sr unknown
- 2006-09-01 MX MX2008002414A patent/MX2008002414A/es unknown
- 2006-09-01 WO PCT/US2006/034427 patent/WO2007028129A1/fr active Application Filing
- 2006-09-01 US US12/065,490 patent/US20100152230A1/en not_active Abandoned
- 2006-09-01 KR KR1020087005146A patent/KR20080031496A/ko not_active Application Discontinuation
- 2006-09-01 AU AU2006287157A patent/AU2006287157A1/en not_active Abandoned
- 2006-09-01 BR BRPI0615250-3A patent/BRPI0615250A2/pt not_active IP Right Cessation
- 2006-09-01 CA CA002620933A patent/CA2620933A1/fr not_active Abandoned
- 2006-09-01 EA EA200800396A patent/EA200800396A1/ru unknown
- 2006-09-01 EP EP06802901A patent/EP1924581A1/fr not_active Withdrawn
-
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 TN TNP2008000099A patent/TNSN08099A1/fr unknown
- 2008-02-29 MA MA30694A patent/MA29759B1/fr unknown
- 2008-02-29 SV SV2008002832A patent/SV2009002832A/es not_active Application Discontinuation
- 2008-02-29 CR CR9781A patent/CR9781A/es not_active Application Discontinuation
- 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 |
---|---|
TNSN08099A1 (fr) | 2009-07-14 |
EP1924581A1 (fr) | 2008-05-28 |
IL189262A0 (en) | 2008-06-05 |
CR9781A (es) | 2008-03-26 |
RS20080128A (en) | 2009-05-06 |
CN101253173A (zh) | 2008-08-27 |
KR20080031496A (ko) | 2008-04-08 |
JP4584335B2 (ja) | 2010-11-17 |
ZA200801645B (en) | 2010-08-25 |
WO2007028129A1 (fr) | 2007-03-08 |
EA200800396A1 (ru) | 2008-08-29 |
SV2009002832A (es) | 2009-02-19 |
ECSP088225A (es) | 2008-03-26 |
AU2006287157A1 (en) | 2007-03-08 |
BRPI0615250A2 (pt) | 2011-05-10 |
JP2009507036A (ja) | 2009-02-19 |
US20100152230A1 (en) | 2010-06-17 |
MX2008002414A (es) | 2008-03-27 |
NO20081393L (no) | 2008-05-28 |
US20120035209A1 (en) | 2012-02-09 |
CA2620933A1 (fr) | 2007-03-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA29759B1 (fr) | 1h-imidazopyridines a substituant hydroxy et procedes | |
WO2008030511A3 (fr) | 3, 4, 6, 7-tétrahydro-5h-1, 2a, 4a, 8-tétraazacyclopenta[cd]phénalènes substitués | |
MY161812A (en) | Substituted imidazo ring systems and methods | |
WO2005079195A3 (fr) | Pyrazolopyridines et analogues de celles-ci | |
MA32070B1 (fr) | Dérivés hétérocycliques réunis par fusion et procédés d'utilisation associés | |
MA47447A (fr) | 2-hétéroaryl-3-oxo-2,3-dihydropyridazine-4-carboxamides pour le traitement du cancer | |
BRPI0414856A (pt) | imidazoquinolinas alcóxi-substituìdas | |
MA40290A1 (fr) | Agents immunorégulateurs | |
MY148480A (en) | Inhibitors of 11-beta-hydroxy steroid dehydrogenase type 1 | |
WO2006091568A3 (fr) | Imidazonaphthyridines a substitution hydroxyalkyle | |
MA27569A1 (fr) | Derives de pyrrolo-pyrazole substitues servant d'inhibiteurs de kinases | |
MA34308B1 (fr) | Triazolopyridines substituées | |
TW200505458A (en) | 1-amino 1h-imidazoquinolines | |
MA27347A1 (fr) | Inhibiteurs de protease du vih, compositions les contenant, leurs utilisations pharmaceutiques et matieres pour leur synthese | |
MA31764B1 (fr) | Composés et compositions en tant que modulateurs de l'activité de gpr119 | |
MA29932B1 (fr) | Inhibiteurs de la proteine d'activation de la 5-lipoxygenase (flap) | |
BRPI0413998A (pt) | imidazoquinolinas arilóxi e arilalquilenóxi substituìdas | |
MA31881B1 (fr) | Dérivés de n-(arylamino)arylsulfonamide comprenant des polymorphes en tant qu'inhibiteurs de mek ainsi que compositions, procédés d'utilisation et procédés de préparation de ceux-ci | |
WO2007106854A3 (fr) | 1h-imidazonaphthyridines hydroxy et alcoxy substituées, et procédés associés | |
MA30352B1 (fr) | Pyridine [3,4-b] pyrazinones | |
WO2007056112A3 (fr) | 1h-imidazoquinolines substituees par hydroxy et alcoxy et procedes correspondants | |
TNSN07476A1 (fr) | Derives de n-(pyridine -2- yl) - sulfonamide | |
MA30821B1 (fr) | Derives de pyrazoline utiles comme antagonistes des recepteurs de mineralocorticoïdes | |
MA30089B1 (fr) | (arylsulfonyl)-pyrasolopiperidines | |
MA31857B1 (fr) | N-phenyl-pyrrolidinylmethylpyrrolidine-amides substitues et utilisation therapeutique de ceux -ci |