MA37940A2 - Nouveaux dérivés bicycliques - Google Patents
Nouveaux dérivés bicycliquesInfo
- Publication number
- MA37940A2 MA37940A2 MA37940A MA37940A MA37940A2 MA 37940 A2 MA37940 A2 MA 37940A2 MA 37940 A MA37940 A MA 37940A MA 37940 A MA37940 A MA 37940A MA 37940 A2 MA37940 A2 MA 37940A2
- Authority
- MA
- Morocco
- Prior art keywords
- bicyclic derivatives
- new bicyclic
- new
- derivatives
- relates
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Abstract
L'invention concerne de nouveaux composés ayant la formule générale (i) où r
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP12185941 | 2012-09-25 | ||
PCT/EP2013/069679 WO2014048865A1 (fr) | 2012-09-25 | 2013-09-23 | Nouveaux dérivés bicycliques |
Publications (2)
Publication Number | Publication Date |
---|---|
MA37940A2 true MA37940A2 (fr) | 2016-06-30 |
MA37940B1 MA37940B1 (fr) | 2018-09-28 |
Family
ID=47073290
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA37940A MA37940B1 (fr) | 2012-09-25 | 2013-09-23 | Derives d'octahydro-cyclopenta(c)pyrrole substitues inhibiteurs de l'autotaxine, utiles pour traiter les affections renales, hepatiques et inflammatoires, les affections du systeme nerveux, les maladies fibreuses. |
Country Status (33)
Country | Link |
---|---|
US (4) | US20150353559A1 (fr) |
EP (2) | EP2900669B1 (fr) |
JP (1) | JP6285444B2 (fr) |
KR (1) | KR102179599B1 (fr) |
CN (1) | CN104684915B (fr) |
AR (1) | AR092645A1 (fr) |
AU (1) | AU2013322838B2 (fr) |
BR (1) | BR112015004111A2 (fr) |
CA (1) | CA2878442A1 (fr) |
CL (1) | CL2015000706A1 (fr) |
CR (1) | CR20150120A (fr) |
DK (1) | DK2900669T3 (fr) |
EA (1) | EA036630B1 (fr) |
ES (1) | ES2753163T3 (fr) |
HK (1) | HK1206722A1 (fr) |
HR (1) | HRP20191937T1 (fr) |
HU (1) | HUE045797T2 (fr) |
IL (1) | IL237126A (fr) |
IN (1) | IN2015DN00960A (fr) |
LT (1) | LT2900669T (fr) |
MA (1) | MA37940B1 (fr) |
MX (1) | MX368615B (fr) |
PE (1) | PE20150758A1 (fr) |
PH (1) | PH12015500263B1 (fr) |
PL (1) | PL2900669T3 (fr) |
PT (1) | PT2900669T (fr) |
RS (1) | RS59512B1 (fr) |
SG (1) | SG11201500572YA (fr) |
SI (1) | SI2900669T1 (fr) |
TW (1) | TWI609018B (fr) |
UA (1) | UA116547C2 (fr) |
WO (1) | WO2014048865A1 (fr) |
ZA (1) | ZA201500345B (fr) |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG11201407534PA (en) | 2012-06-13 | 2014-12-30 | Hoffmann La Roche | New diazaspirocycloalkane and azaspirocycloalkane |
IN2015DN00960A (fr) | 2012-09-25 | 2015-06-12 | Hoffmann La Roche | |
CN104968656B (zh) | 2012-12-19 | 2017-08-11 | 诺华股份有限公司 | 自分泌运动因子抑制剂 |
US9409895B2 (en) | 2012-12-19 | 2016-08-09 | Novartis Ag | Autotaxin inhibitors |
AR095079A1 (es) | 2013-03-12 | 2015-09-16 | Hoffmann La Roche | Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo |
JP6647592B2 (ja) * | 2013-07-03 | 2020-02-14 | ルンドベック ラ ホーヤ リサーチ センター,インク. | ピロロピロールカルバメート、および関連する有機化合物、医薬組成物、ならびにその医学的使用 |
WO2015048507A1 (fr) | 2013-09-26 | 2015-04-02 | Mnemosyne Pharmaceuticals, Inc. | Modulateurs de nrb2, à base d'octahydro-cyclopenta[c] pyrrole, à modulation négative sélective |
CN105793253B (zh) | 2013-11-22 | 2019-08-23 | 法玛克亚公司 | 自分泌运动因子抑制剂化合物 |
MY187449A (en) | 2013-11-26 | 2021-09-22 | Hoffmann La Roche | New octahydro-cyclobuta [1,2-c;3,4-c']dipyrrol-2-yl |
HUE046820T2 (hu) * | 2014-03-26 | 2020-03-30 | Hoffmann La Roche | Biciklusos vegyületek autotaxin (ATX) és lizofoszfatidsav (LPA) termelésgátlókként |
JP6554481B2 (ja) | 2014-03-26 | 2019-07-31 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | オートタキシン(atx)及びリゾホスファチジン酸(lpa)産生の阻害剤としての縮合[1,4]ジアゼピン化合物 |
US9051320B1 (en) | 2014-08-18 | 2015-06-09 | Pharmakea, Inc. | Methods for the treatment of metabolic disorders by a selective small molecule autotaxin inhibitor |
JO3579B1 (ar) * | 2014-09-26 | 2020-07-05 | Luc Therapeutics Inc | مُعدِلات تفاغرية سالبة لمستقبل nr2b من المركب n-ألكيل أريل-5-أوكسي أريل-ثامن هيدرو-خماسي الحلقة [c] بيرول |
GB201501870D0 (en) | 2015-02-04 | 2015-03-18 | Cancer Rec Tech Ltd | Autotaxin inhibitors |
GB201502020D0 (en) | 2015-02-06 | 2015-03-25 | Cancer Rec Tech Ltd | Autotaxin inhibitory compounds |
MA41898A (fr) | 2015-04-10 | 2018-02-13 | Hoffmann La Roche | Dérivés de quinazolinone bicyclique |
AU2016268250B2 (en) | 2015-05-27 | 2020-08-27 | Sabre Therapeutics Llc | Autotaxin inhibitors and uses thereof |
WO2016197009A1 (fr) | 2015-06-05 | 2016-12-08 | Vertex Pharmaceuticals Incorporated | Triazoles pour le traitement de maladies liées à la démyélinisation |
CR20180058A (es) | 2015-09-04 | 2018-02-26 | Hoffmann La Roche | Nuevos derivados de fenoximetilo |
MX2018001890A (es) * | 2015-09-24 | 2018-06-20 | Hoffmann La Roche | Compuestos biciclicos como inhibidores de autotaxina (atx). |
KR20180054830A (ko) * | 2015-09-24 | 2018-05-24 | 에프. 호프만-라 로슈 아게 | 오토탁신(atx) 억제제로서의 이환형 화합물 |
MX2017015034A (es) * | 2015-09-24 | 2018-04-13 | Hoffmann La Roche | Nuevos compuestos biciclicos como inhibidores duales de autotaxina (atx)/anhidrasa carbonica (ca). |
CN107922415B (zh) | 2015-09-24 | 2022-04-15 | 豪夫迈·罗氏有限公司 | 新的作为双重atx/ca抑制剂的二环化合物 |
CN106986789B (zh) * | 2016-01-20 | 2019-07-16 | 中国人民解放军军事医学科学院生物医学分析中心 | 对苯二酚类化合物及其制备方法与在抗肿瘤或免疫调节中的应用 |
US10030020B2 (en) | 2016-05-12 | 2018-07-24 | Abide Therapeutics, Inc. | Spirocycle compounds and methods of making and using same |
JOP20190107A1 (ar) | 2016-11-16 | 2019-05-09 | Lundbeck La Jolla Research Center Inc | مثبطات أحادي أسيل جليسرول ليباز (magl) |
WO2018106646A1 (fr) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Aminotriazoles pour traiter des maladies démyélinisantes |
WO2018106641A1 (fr) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Pyrazoles pour le traitement de maladies démyélinisantes |
WO2018106643A1 (fr) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Azoles hétérocycliques pour le traitement de maladies de démyélinisation |
WO2018114677A2 (fr) | 2016-12-19 | 2018-06-28 | Bayer Pharma Aktiengesellschaft | [(phénylsulfonyl)octahydro-épiminoisoindol-yl](1h-1,2,3-triazol-5-yl)méthanones |
CR20190423A (es) | 2017-03-16 | 2019-11-01 | Hoffmann La Roche | Nuevos compuestos biciclícos como inhibidores dobles de atx/ca |
WO2018167113A1 (fr) * | 2017-03-16 | 2018-09-20 | F. Hoffmann-La Roche Ag | Nouveaux composés bicycliques utilisés en tant qu'inhibiteurs d'atx |
EA201992215A1 (ru) | 2017-03-20 | 2020-02-06 | Форма Терапьютикс, Инк. | Пирролопирроловые композиции в качестве активаторов пируваткиназы (pkr) |
MX2020002254A (es) | 2017-08-29 | 2020-07-20 | Lundbeck La Jolla Research Center Inc | Compuestos espirociclicos y sus metodos de preparacion y uso. |
MX2020002251A (es) | 2017-08-29 | 2020-07-20 | Lundbeck La Jolla Research Center Inc | Compuestos espirociclicos y sus metodos de preparacion y uso. |
CA3079478A1 (fr) | 2017-10-19 | 2019-04-25 | Js Innopharm (Shanghai) Ltd. | Composes heterocycliques, compositions comprenant le compose heterocyclique, et leurs procedes d'utilisation |
TWI780281B (zh) * | 2017-12-14 | 2022-10-11 | 丹麥商Nmd藥品公司 | 用於治療神經肌肉病症的化合物 |
EP3852791A4 (fr) | 2018-09-19 | 2022-06-15 | Forma Therapeutics, Inc. | Activation de la pyruvate kinase r |
US20220031671A1 (en) | 2018-09-19 | 2022-02-03 | Forma Therapeutics, Inc. | Treating sickle cell disease with a pyruvate kinase r activating compound |
CN111620866A (zh) * | 2019-02-27 | 2020-09-04 | 南京药石科技股份有限公司 | 一种顺式-7,7-二氟-六氢-1H 吡咯并[3,4-c]吡啶衍生物及其制备方法 |
CN113549063B (zh) * | 2020-04-23 | 2024-04-05 | 南京药石科技股份有限公司 | 一种光学异构的八氢-2H-吡咯并[3,4-c]吡啶-2-羧酸叔丁酯的制备方法 |
TW202211918A (zh) * | 2020-06-30 | 2022-04-01 | 印度商卡地拉保健有限公司 | 新穎奧特他新(autotaxin)抑制劑 |
TW202229255A (zh) | 2020-11-13 | 2022-08-01 | 丹麥商H 朗德貝克公司 | Magl抑制劑 |
CN113214111A (zh) * | 2021-04-30 | 2021-08-06 | 上海立科化学科技有限公司 | 3-(2-氰基苯基)丙酸及4-氰基-1-茚满酮的制备方法 |
Family Cites Families (125)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1252898B (de) | 1965-06-12 | 1967-10-26 | Bayer Ag | Verfahren zur Herstellung von Copolymerisaten des Trioxans |
US5240928A (en) | 1989-07-03 | 1993-08-31 | Merck & Co., Inc. | Substituted quinazolinones as angiotensin II antagonists |
DE3930262A1 (de) | 1989-09-11 | 1991-03-21 | Thomae Gmbh Dr K | Kondensierte diazepinone, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
CA2037630C (fr) | 1990-03-07 | 2001-07-03 | Akira Morimoto | Composes heterocycliques renfermant de l'azote, methode de production et applications correspondantes |
US5470975A (en) | 1990-10-16 | 1995-11-28 | E.R. Squibb & Sons, Inc. | Dihydropyrimidine derivatives |
US5290780A (en) | 1991-01-30 | 1994-03-01 | American Cyanamid Co. | Angiotensin II receptor blocking 2,3,6 substituted quinazolinones |
US5238942A (en) | 1991-05-10 | 1993-08-24 | Merck & Co., Inc. | Substituted quinazolinones bearing acidic functional groups as angiotensin ii antagonists |
US5202322A (en) | 1991-09-25 | 1993-04-13 | Merck & Co., Inc. | Quinazolinone and pyridopyrimidine a-II antagonists |
US5532243A (en) | 1992-02-14 | 1996-07-02 | The Dupont Merck Pharmaceutical Company | Antipsychotic nitrogen-containing bicyclic compounds |
US5358951A (en) | 1993-04-23 | 1994-10-25 | American Cyanamid Company | Angiotensin II receptor blocking 2, 3, 6 substituted quinazolinones |
DE4407047A1 (de) * | 1994-03-03 | 1995-09-07 | Merck Patent Gmbh | Acetamide |
US20010016657A1 (en) * | 1997-03-18 | 2001-08-23 | Smithkline Beecham P.L.C. | Substituted isoquinoline derivatives and their use as anticonvulsants |
KR20010040693A (ko) | 1998-02-04 | 2001-05-15 | 나가사까 겐지로 | N-아실 환상 아민유도체 |
JP2001039950A (ja) | 1999-07-30 | 2001-02-13 | Banyu Pharmaceut Co Ltd | N−アシル環状アミン誘導体 |
DE60005545D1 (de) | 1999-10-27 | 2003-10-30 | Millennium Pharm Inc | Pyridyl enthaltende spirocyclische verbindungen als inhibitoren der fibrinogen-abhängigen blutplättchen aggregation |
RU2298417C2 (ru) | 1999-11-09 | 2007-05-10 | Сосьете Де Консей Де Решерш Э Д`Аппликасьон Сьентифик (С.К.Р.А.С.) | Продукт, включающий ингибитор трансдукции сигналов гетеротримерных протеинов g в комбинации с другим цитостатическим средством, для терапевтического применения при лечении рака |
CA2440803A1 (fr) | 2001-03-07 | 2002-09-12 | Pfizer Products Inc. | Modulateurs de l'activite du recepteur de la chimiokine |
US7667053B2 (en) | 2002-04-12 | 2010-02-23 | Merck & Co., Inc. | Bicyclic amides |
GB0303852D0 (en) | 2003-02-19 | 2003-03-26 | Pfizer Ltd | Triazole compounds useful in therapy |
WO2005023762A1 (fr) | 2003-09-04 | 2005-03-17 | Abbott Laboratories | Derives de pyrrolidine-2-carbonitrile et leur utilisation comme inhibiteurs de la dipeptidyle peptidase-iv (dpp-iv) |
SE0302811D0 (sv) | 2003-10-23 | 2003-10-23 | Astrazeneca Ab | Novel compounds |
GB0324790D0 (en) | 2003-10-24 | 2003-11-26 | Astrazeneca Ab | Amide derivatives |
US7226951B2 (en) | 2003-12-17 | 2007-06-05 | Allergan, Inc. | Compounds having selective cytochrome P450RAI-1 or selective cytochrome P450RAI-2 inhibitory activity and methods of obtaining the same |
US7435831B2 (en) * | 2004-03-03 | 2008-10-14 | Chemocentryx, Inc. | Bicyclic and bridged nitrogen heterocycles |
EP1720545B1 (fr) | 2004-03-03 | 2014-10-29 | ChemoCentryx, Inc. | Heterocycles d'azote bicycliques et ponts |
EP1761542B1 (fr) | 2004-06-09 | 2008-01-02 | F.Hoffmann-La Roche Ag | Dérivés octahydropyrrolo[3,4-c]pyrrole et leur utilisation comme agents antiviraux |
RU2401833C2 (ru) | 2004-08-10 | 2010-10-20 | Янссен Фармацевтика Н.В. | Производные 1, 2, 4-триазин-6-она, ингибирующие вич |
US7410949B2 (en) | 2005-01-18 | 2008-08-12 | Hoffmann-La Roche Inc. | Neuropeptide-2 receptor (Y-2R) agonists and uses thereof |
MX2007013469A (es) | 2005-04-28 | 2008-01-22 | Wyeth Corp | Forma ii polimorfa de tanaproget. |
US7737279B2 (en) * | 2005-05-10 | 2010-06-15 | Bristol-Myers Squibb Company | 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same |
TW200800999A (en) | 2005-09-06 | 2008-01-01 | Astrazeneca Ab | Novel compounds |
WO2007049771A1 (fr) | 2005-10-28 | 2007-05-03 | Ono Pharmaceutical Co., Ltd. | Compose contenant un groupe basique et son utilisation |
ES2601525T3 (es) * | 2005-11-14 | 2017-02-15 | Purdue Research Foundation | Indenoisoquinolinas N-sustituidas y síntesis de las mismas |
ES2407115T3 (es) | 2005-11-18 | 2013-06-11 | Ono Pharmaceutical Co., Ltd. | Compuesto que contiene un grupo básico y uso del mismo |
WO2007103719A2 (fr) | 2006-03-03 | 2007-09-13 | Incyte Corporation | MODULATEURS DE LA 11-β-HYDROXYSTÉROÏDE DÉSHYDROGÉNASE DE TYPE 1, LEURS COMPOSITIONS PHARMACEUTIQUES ET LEURS PROCÉDÉS D'UTILISATION |
JP2008031064A (ja) | 2006-07-27 | 2008-02-14 | Astellas Pharma Inc | ジアシルピペラジン誘導体 |
AU2007296634B2 (en) | 2006-09-11 | 2012-09-20 | Merck Sharp & Dohme B.V. | Quinazolinone and isoquinolinone acetamide derivatives |
US7638526B2 (en) | 2006-09-15 | 2009-12-29 | Schering Corporation | Azetidine derivatives useful in treating pain, diabetes and disorders of lipid metabolism |
US8735411B2 (en) | 2006-10-02 | 2014-05-27 | Abbvie Inc. | Macrocyclic benzofused pyrimidine derivatives |
US7915299B2 (en) | 2006-11-15 | 2011-03-29 | High Point Pharmaceuticals, Llc | 2-(2-hydroxyphenyl)benzimidazoles useful for treating obesity and diabetes |
TW200831085A (en) | 2006-12-13 | 2008-08-01 | Merck & Co Inc | Non-nucleoside reverse transcriptase inhibitors |
EP1975165A1 (fr) | 2007-03-27 | 2008-10-01 | Boehringer Ingelheim Pharma GmbH & Co. KG | Pyrrolidinamide substituée, sa fabrication et son utilisation en tant que médicament |
AU2008233929A1 (en) | 2007-03-29 | 2008-10-09 | F. Hoffmann-La Roche Ag | Non-nucleoside reverse transcriptase inhibitors |
CL2008001002A1 (es) | 2007-04-11 | 2008-10-17 | Actelion Pharmaceuticals Ltd | Compuestos derivados de oxazolidinona; composicion farmaceutica que comprende a dichos compuestos; y su uso para preparar un medicamento para tratar una infeccion bacteriana. |
EP2152711B1 (fr) | 2007-04-27 | 2010-11-24 | Sanofi-Aventis | Dérivés de 2 -hétéroaryl- pyrrolo [3, 4-c]pyrrole et utilisation comme inhibiteurs de scd |
DE102007047737A1 (de) | 2007-10-05 | 2009-04-30 | Merck Patent Gmbh | Piperidin- und Piperazinderivate |
US20090155176A1 (en) | 2007-10-19 | 2009-06-18 | Sarcode Corporation | Compositions and methods for treatment of diabetic retinopathy |
PE20091017A1 (es) | 2007-10-31 | 2009-07-16 | Janssen Pharmaceutica Nv | Diaminas en puente o fusionadas sustituidas con arilo como moduladores de leucotrieno a4 hidrolasa |
JP2009161449A (ja) | 2007-12-28 | 2009-07-23 | Lion Corp | Ppar活性促進剤並びに美容用飲食品、皮膚外用剤及び医薬 |
EP2301936A1 (fr) | 2008-06-19 | 2011-03-30 | Banyu Pharmaceutical Co., Ltd. | Dérivé de spirodiamine-diarylcétoxime |
EP2328898B1 (fr) | 2008-09-09 | 2014-12-24 | Sanofi | Dérivés 2-hétéroaryl-pyrrolo[3,4-c]pyrrole et leur utilisation comme inhibiteurs de scd |
TW201020247A (en) | 2008-11-06 | 2010-06-01 | Gruenenthal Gmbh | Substituierte disulfonamide |
JP5373104B2 (ja) | 2008-11-17 | 2013-12-18 | エフ.ホフマン−ラ ロシュ アーゲー | Crth2アンタゴニスト又は部分アゴニストとして使用されるナフチル酢酸 |
DE102008059578A1 (de) | 2008-11-28 | 2010-06-10 | Merck Patent Gmbh | Benzo-Naphtyridin Verbindungen |
CN102216299B (zh) | 2008-12-01 | 2015-02-11 | 默克专利有限公司 | 作为自体毒素抑制剂的2,5-二氨基取代的吡啶并[4,3-d]嘧啶化合物 |
TW201035102A (en) | 2009-03-04 | 2010-10-01 | Gruenethal Gmbh | Sulfonylated tetrahydroazolopyrazines and their use as medicinal products |
TW201038572A (en) | 2009-03-25 | 2010-11-01 | Gruenenthal Gmbh | Substituted spiro-amide compounds |
EA201101396A1 (ru) * | 2009-04-02 | 2012-09-28 | Мерк Патент Гмбх | Ингибиторы аутотаксина |
CN102369186B (zh) | 2009-04-02 | 2014-07-09 | 默克专利有限公司 | 作为自分泌运动因子抑制剂的哌啶和哌嗪衍生物 |
ES2527788T3 (es) | 2009-04-02 | 2015-01-30 | Merck Patent Gmbh | Compuestos heterocíclicos como inhibidores de autotaxina |
FR2945534B1 (fr) | 2009-05-12 | 2012-11-16 | Sanofi Aventis | DERIVES DE CYCLOPENTAL[c]PYRROLE-2-CARBOXYLATES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE |
CA2763099A1 (fr) | 2009-05-22 | 2010-11-25 | Exelixis, Inc. | Inhibiteurs de pi3k/mtor a base de benzoxazepines pour lutter contre les maladies proliferatives |
WO2010141817A1 (fr) | 2009-06-05 | 2010-12-09 | Janssen Pharmaceutica Nv | Modulateurs d'amide d'acide gras hydrolase de type diamine urée spirocyclique substituée par un groupe hétéroaryle |
DE102009033392A1 (de) * | 2009-07-16 | 2011-01-20 | Merck Patent Gmbh | Heterocyclische Verbindungen als Autotaxin-Inhibitoren II |
WO2011017350A2 (fr) | 2009-08-04 | 2011-02-10 | Amira Pharmaceuticals, Inc. | Composés en tant qu'antagonistes du récepteur de l'acide lysophosphatidique |
UA107360C2 (en) | 2009-08-05 | 2014-12-25 | Biogen Idec Inc | Bicyclic aryl sphingosine 1-phosphate analogs |
AR079022A1 (es) | 2009-11-02 | 2011-12-21 | Sanofi Aventis | Derivados de acido carboxilico ciclico sustituidos con acilamino, su uso como productos farmaceuticos, composicion farmaceutica y metodo de preparacion |
MX2012007935A (es) * | 2010-01-07 | 2012-08-15 | Du Pont | Compuestos heterociclicos fungicidas. |
WO2011115813A1 (fr) | 2010-03-18 | 2011-09-22 | Abbott Laboratories | Acétamides de lactame en tant que bloqueurs des canaux calciques |
HUE025774T2 (en) | 2010-03-19 | 2016-05-30 | Pfizer | 2,3-Dihydro-1H-inden-1-yl-2,7-diazaspiro [3.6] nonane derivatives and their use as antagonists or inverse agonists of the ghrelin receptor |
CA2794211A1 (fr) | 2010-03-26 | 2011-09-29 | Wolfgang Staehle | Benzonaphthyridinamines en tant qu'inhibiteurs d'autotaxine |
GB201008005D0 (en) | 2010-05-13 | 2010-06-30 | Sentinel Oncology Ltd | Pharmaceutical compounds |
EP2575794A2 (fr) | 2010-06-04 | 2013-04-10 | B.S.R.C. "Alexander Fleming" | Modulation de la voie autotaxine et utilisations correspondantes |
AR082590A1 (es) | 2010-08-12 | 2012-12-19 | Hoffmann La Roche | Inhibidores de la tirosina-quinasa de bruton |
EP2606031B1 (fr) * | 2010-08-20 | 2017-09-27 | Amira Pharmaceuticals, Inc. | Inhibiteurs de l'autotaxine et leurs utilisations |
CA2809892C (fr) * | 2010-09-02 | 2019-05-28 | Merck Patent Gmbh | Derives de pyrazolopyridinone en tant qu'antagonistes de recepteur de lpa |
CN103298460B (zh) | 2010-12-14 | 2016-06-01 | 电泳有限公司 | 酪蛋白激酶1δ(CK1δ)抑制剂 |
US9260416B2 (en) | 2011-05-27 | 2016-02-16 | Amira Pharmaceuticals, Inc. | Heterocyclic autotaxin inhibitors and uses thereof |
ES2609579T3 (es) | 2011-08-29 | 2017-04-21 | VIIV Healthcare UK (No.5) Limited | Derivados espiro de diamina bicíclica como inhibidores de la unión del VIH |
WO2013054185A1 (fr) | 2011-10-13 | 2013-04-18 | Pfizer, Inc. | Dérivés de pyrimidine et de pyridine utiles en thérapie |
JPWO2013065712A1 (ja) | 2011-10-31 | 2015-04-02 | 東レ株式会社 | ジアザスピロウレア誘導体及びその医薬用途 |
US8809552B2 (en) | 2011-11-01 | 2014-08-19 | Hoffmann-La Roche Inc. | Azetidine compounds, compositions and methods of use |
WO2013079223A1 (fr) | 2011-12-02 | 2013-06-06 | Phenex Pharmaceuticals Ag | Pyrrolocarboxamides en tant que modulateurs de l'activité d'un récepteur orphelin gamma (rorϒ, nr1f3) apparenté au récepteur nucléaire orphelin rar et destinés au traitement de maladies inflammatoires chroniques et auto-immunes |
TWI638802B (zh) | 2012-05-24 | 2018-10-21 | 芬蘭商奧利安公司 | 兒茶酚o-甲基轉移酶活性抑制化合物 |
SG11201407534PA (en) | 2012-06-13 | 2014-12-30 | Hoffmann La Roche | New diazaspirocycloalkane and azaspirocycloalkane |
PT3176170T (pt) | 2012-06-13 | 2019-02-05 | Incyte Holdings Corp | Compostos tricíclicos substituídos como inibidores de fgfr |
EA028364B1 (ru) | 2012-07-27 | 2017-11-30 | Биоген Айдек Ма Инк. | Аутотаксин-модулирующие соединения |
US9550798B2 (en) | 2012-07-27 | 2017-01-24 | Biogen Ma Inc. | Compounds that are S1P modulating agents and/or ATX modulating agents |
IN2015DN00960A (fr) | 2012-09-25 | 2015-06-12 | Hoffmann La Roche | |
MX357035B (es) | 2012-09-25 | 2018-06-25 | Bayer Pharma AG | Combinacion de regorafenib y acido acetilsalicilico para el tratamiento del cancer. |
AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
DK2912019T3 (da) | 2012-10-25 | 2021-05-25 | Tetra Discovery Partners Llc | Heteroarylhæmmere af pde4 |
US20160002247A1 (en) | 2013-03-01 | 2016-01-07 | The University Of Tokyo | 8-substituted imidazopyrimidinone derivative having autotaxin inhibitory activity |
UY35395A (es) | 2013-03-12 | 2014-10-31 | Abbvie Inc | Inhibidores de bromodominios tetracíclicos |
TWI593692B (zh) | 2013-03-12 | 2017-08-01 | 美國禮來大藥廠 | 四氫吡咯并噻嗪化合物 |
CN105209428A (zh) | 2013-03-12 | 2015-12-30 | 奥克塞拉有限公司 | 用于治疗眼科疾病和病症的取代的3-苯基丙胺衍生物 |
AR095079A1 (es) | 2013-03-12 | 2015-09-16 | Hoffmann La Roche | Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo |
TW201446768A (zh) | 2013-03-15 | 2014-12-16 | Biogen Idec Inc | S1p及/或atx調節劑 |
AU2014291711B2 (en) | 2013-07-18 | 2017-02-02 | Novartis Ag | Autotaxin inhibitors comprising a heteroaromatic ring-benzyl-amide-cycle core |
PT3057959T (pt) | 2013-10-17 | 2018-06-04 | Vertex Pharma | Inibidores de adn-pk |
CN105793253B (zh) | 2013-11-22 | 2019-08-23 | 法玛克亚公司 | 自分泌运动因子抑制剂化合物 |
AR098475A1 (es) | 2013-11-26 | 2016-06-01 | Bayer Cropscience Ag | Compuestos pesticidas y usos |
MY187449A (en) | 2013-11-26 | 2021-09-22 | Hoffmann La Roche | New octahydro-cyclobuta [1,2-c;3,4-c']dipyrrol-2-yl |
JO3512B1 (ar) | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز |
PL3122732T3 (pl) | 2014-03-26 | 2018-08-31 | Basf Se | Podstawione związki [1,2,4]triazolowe i imidazolowe jako fungicydy |
JP6554481B2 (ja) | 2014-03-26 | 2019-07-31 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | オートタキシン(atx)及びリゾホスファチジン酸(lpa)産生の阻害剤としての縮合[1,4]ジアゼピン化合物 |
HUE046820T2 (hu) | 2014-03-26 | 2020-03-30 | Hoffmann La Roche | Biciklusos vegyületek autotaxin (ATX) és lizofoszfatidsav (LPA) termelésgátlókként |
MX2016013049A (es) | 2014-04-04 | 2017-04-27 | X-Rx Inc | Inhibidores de autotaxina espirociclicos sustituidos. |
WO2016061160A1 (fr) | 2014-10-14 | 2016-04-21 | Vitae Pharmaceuticals, Inc. | Inhibiteurs de ror-gamma à base de dihydropyrrolopyridine |
AU2016217851A1 (en) | 2015-02-15 | 2017-08-03 | F. Hoffmann-La Roche Ag | 1-(het)arylsulfonyl-(pyrrolidine or piperidine)-2-carboxamide derivatives and their use as TRPA1 antagonists |
MA41898A (fr) | 2015-04-10 | 2018-02-13 | Hoffmann La Roche | Dérivés de quinazolinone bicyclique |
CN104927727B (zh) | 2015-07-06 | 2017-01-11 | 香山红叶建设有限公司 | 一种玻璃幕墙用结构密封胶及其制备方法 |
PL415078A1 (pl) | 2015-09-04 | 2017-03-13 | Oncoarendi Therapeutics Spółka Z Ograniczoną Odpowiedzialnością | Podstawione aminotriazole przydatne jako inhibitory kwaśnej chitynazy ssaków |
CR20180058A (es) | 2015-09-04 | 2018-02-26 | Hoffmann La Roche | Nuevos derivados de fenoximetilo |
MX2017015034A (es) | 2015-09-24 | 2018-04-13 | Hoffmann La Roche | Nuevos compuestos biciclicos como inhibidores duales de autotaxina (atx)/anhidrasa carbonica (ca). |
CN107922415B (zh) | 2015-09-24 | 2022-04-15 | 豪夫迈·罗氏有限公司 | 新的作为双重atx/ca抑制剂的二环化合物 |
KR20180054830A (ko) | 2015-09-24 | 2018-05-24 | 에프. 호프만-라 로슈 아게 | 오토탁신(atx) 억제제로서의 이환형 화합물 |
MX2018001890A (es) | 2015-09-24 | 2018-06-20 | Hoffmann La Roche | Compuestos biciclicos como inhibidores de autotaxina (atx). |
EP3353328A4 (fr) | 2015-09-24 | 2019-06-12 | Ionis Pharmaceuticals, Inc. | Modulateurs de l'expression de kras |
WO2017091673A2 (fr) | 2015-11-25 | 2017-06-01 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de bromodomaines bivalents et leurs utilisations |
CN108290858B (zh) | 2015-12-01 | 2021-07-06 | 日本农药株式会社 | 3h-吡咯并吡啶化合物或其n-氧化物、或它们的盐类及含有该化合物的农业园艺用杀虫剂及其使用方法 |
WO2017139978A1 (fr) | 2016-02-19 | 2017-08-24 | 吴伟东 | Procédé et système d'actualisation d'application de téléphone mobile |
CR20190423A (es) | 2017-03-16 | 2019-11-01 | Hoffmann La Roche | Nuevos compuestos biciclícos como inhibidores dobles de atx/ca |
WO2018167113A1 (fr) | 2017-03-16 | 2018-09-20 | F. Hoffmann-La Roche Ag | Nouveaux composés bicycliques utilisés en tant qu'inhibiteurs d'atx |
EA201992215A1 (ru) | 2017-03-20 | 2020-02-06 | Форма Терапьютикс, Инк. | Пирролопирроловые композиции в качестве активаторов пируваткиназы (pkr) |
-
2013
- 2013-09-23 IN IN960DEN2015 patent/IN2015DN00960A/en unknown
- 2013-09-23 EA EA201590534A patent/EA036630B1/ru not_active IP Right Cessation
- 2013-09-23 DK DK13766056T patent/DK2900669T3/da active
- 2013-09-23 CA CA2878442A patent/CA2878442A1/fr active Pending
- 2013-09-23 PL PL13766056T patent/PL2900669T3/pl unknown
- 2013-09-23 CN CN201380049392.4A patent/CN104684915B/zh active Active
- 2013-09-23 MX MX2015002090A patent/MX368615B/es active IP Right Grant
- 2013-09-23 BR BR112015004111A patent/BR112015004111A2/pt active Search and Examination
- 2013-09-23 MA MA37940A patent/MA37940B1/fr unknown
- 2013-09-23 ES ES13766056T patent/ES2753163T3/es active Active
- 2013-09-23 UA UAA201503793A patent/UA116547C2/uk unknown
- 2013-09-23 HU HUE13766056A patent/HUE045797T2/hu unknown
- 2013-09-23 RS RS20191402A patent/RS59512B1/sr unknown
- 2013-09-23 AU AU2013322838A patent/AU2013322838B2/en not_active Ceased
- 2013-09-23 EP EP13766056.9A patent/EP2900669B1/fr active Active
- 2013-09-23 JP JP2015533548A patent/JP6285444B2/ja active Active
- 2013-09-23 EP EP19187624.2A patent/EP3590940B1/fr active Active
- 2013-09-23 PT PT137660569T patent/PT2900669T/pt unknown
- 2013-09-23 KR KR1020157007381A patent/KR102179599B1/ko active IP Right Grant
- 2013-09-23 WO PCT/EP2013/069679 patent/WO2014048865A1/fr active Application Filing
- 2013-09-23 SG SG11201500572YA patent/SG11201500572YA/en unknown
- 2013-09-23 AR ARP130103396A patent/AR092645A1/es not_active Application Discontinuation
- 2013-09-23 SI SI201331606T patent/SI2900669T1/sl unknown
- 2013-09-23 PE PE2015000230A patent/PE20150758A1/es active IP Right Grant
- 2013-09-23 LT LT13766056T patent/LT2900669T/lt unknown
- 2013-09-24 TW TW102134348A patent/TWI609018B/zh not_active IP Right Cessation
-
2015
- 2015-01-16 ZA ZA2015/00345A patent/ZA201500345B/en unknown
- 2015-02-05 IL IL237126A patent/IL237126A/en active IP Right Grant
- 2015-02-06 PH PH12015500263A patent/PH12015500263B1/en unknown
- 2015-03-06 CR CR20150120A patent/CR20150120A/es unknown
- 2015-03-20 CL CL2015000706A patent/CL2015000706A1/es unknown
- 2015-05-21 US US14/719,063 patent/US20150353559A1/en not_active Abandoned
- 2015-07-27 HK HK15107163.9A patent/HK1206722A1/xx unknown
-
2016
- 2016-10-12 US US15/291,933 patent/US20170050960A1/en not_active Abandoned
-
2017
- 2017-05-01 US US15/583,679 patent/US10669268B2/en active Active
-
2019
- 2019-10-23 HR HRP20191937TT patent/HRP20191937T1/hr unknown
-
2020
- 2020-03-13 US US16/818,409 patent/US20200339570A1/en not_active Abandoned
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA37940A2 (fr) | Nouveaux dérivés bicycliques | |
MA35664B1 (fr) | Nouveaux dérivés bicycliques de la dihydroisoquinoline-1-one | |
MA34389B1 (fr) | Nouvelles aminopyrazoloquinazolines | |
MA35049B1 (fr) | Triazolopyridines | |
CO6852084A2 (es) | Nuevos compuestos sustituidos con halógeno | |
AU2014270524A8 (en) | 2-phenylimidazo [1,2-a]pyrimidines as imaging agents | |
MA35089B1 (fr) | Inhibiteurs de la production de leucotrienes de type benzodioxane | |
IN2014MN02496A (fr) | ||
MA37756A1 (fr) | Nouveaux composés diazaspirocycloalcane et azaspirocycloalcane | |
AU2012334173A8 (en) | [1, 2, 3] triazolo [4, 5 -d] pyrimidine derivatives as agonists of the cannabinoid receptor 2 | |
CO6831982A2 (es) | Pirazolo[4,3-d]pirimidinas útiles como inhibidores de cinasas | |
CR20140132A (es) | Derivados de pirrolopirimidina y purina | |
CR20140042A (es) | Indazoles | |
CR20130470A (es) | INHIBIDORES DE QUINASA RELACIONADOS CON PIRROLO [2,3-d]PIRIMIDINA TROMPOMIOSINA | |
MA35086B1 (fr) | Compose de triazolopyridine | |
UY34445A (es) | Nuevos compuestos inhibidores de la fosfodiesterasa del tipo 10a | |
MA35357B1 (fr) | Composes de type anilines | |
CR20140510A (es) | Nucleósidos de espirooxetano de uracilo | |
CR20130369A (es) | Novedosos derivados heterocíclicos | |
CR20120295A (es) | Triazolopiridinas | |
EA202190619A1 (ru) | Противовирусные соединения | |
CR20120297A (es) | Espironucleósidos uracílicos oxetánicos | |
EA201491002A1 (ru) | Производные [1,2,3]триазоло[4,5-d]пиримидина в качестве агонистов каннабиноидного рецептора 2 | |
IN2014MN01521A (fr) | ||
MA38645B1 (fr) | Nouveaux inhibiteurs de cyp17/antiandrogènes |