MA49879A - Composés hétérocycliques utiles en tant qu'inhibiteurs doubles d'atx/ca - Google Patents
Composés hétérocycliques utiles en tant qu'inhibiteurs doubles d'atx/caInfo
- Publication number
- MA49879A MA49879A MA049879A MA49879A MA49879A MA 49879 A MA49879 A MA 49879A MA 049879 A MA049879 A MA 049879A MA 49879 A MA49879 A MA 49879A MA 49879 A MA49879 A MA 49879A
- Authority
- MA
- Morocco
- Prior art keywords
- inhibitors
- heterocyclic compounds
- useful heterocyclic
- atx
- dual
- Prior art date
Links
- 230000009977 dual effect Effects 0.000 title 1
- 150000002391 heterocyclic compounds Chemical class 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- 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
- C07D403/10—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 carbon chain containing aromatic rings
-
- 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
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D401/10—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 carbon chain containing aromatic rings
-
- 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
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07D417/14—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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Ophthalmology & Optometry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicinal Preparation (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP17161249 | 2017-03-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA49879A true MA49879A (fr) | 2020-06-24 |
Family
ID=58347248
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA049879A MA49879A (fr) | 2017-03-16 | 2018-03-13 | Composés hétérocycliques utiles en tant qu'inhibiteurs doubles d'atx/ca |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US11059794B2 (fr) |
| EP (1) | EP3596059B1 (fr) |
| JP (1) | JP7157755B2 (fr) |
| KR (1) | KR20190129924A (fr) |
| CN (1) | CN110392679B (fr) |
| AR (1) | AR111279A1 (fr) |
| AU (1) | AU2018233079B9 (fr) |
| BR (1) | BR112019019017A2 (fr) |
| CA (1) | CA3053329A1 (fr) |
| CL (1) | CL2019002609A1 (fr) |
| CO (1) | CO2019009373A2 (fr) |
| CR (1) | CR20190423A (fr) |
| IL (1) | IL269188B (fr) |
| MA (1) | MA49879A (fr) |
| MX (1) | MX381728B (fr) |
| PE (1) | PE20191757A1 (fr) |
| PH (1) | PH12019502118A1 (fr) |
| RU (1) | RU2019132254A (fr) |
| SG (1) | SG11201908560SA (fr) |
| TW (1) | TW201838982A (fr) |
| WO (1) | WO2018167001A1 (fr) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI633087B (zh) | 2012-06-13 | 2018-08-21 | 赫孚孟拉羅股份公司 | 新穎二氮雜螺環烷及氮雜螺環烷 |
| EP3590940B1 (fr) | 2012-09-25 | 2021-06-09 | F. Hoffmann-La Roche AG | Dérivés du héxahydropyrrolo[3,4-c]pyrrole et composés similaires en tant qu'inhibiteurs de l'autotaxine (atx) et inhibiteurs de la production de l'acid lysophosphatidique (lpa) pour traiter des maladies rénales |
| AR095079A1 (es) | 2013-03-12 | 2015-09-16 | Hoffmann La Roche | Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo |
| NO3074400T3 (fr) | 2013-11-26 | 2018-04-14 | ||
| MA39792B1 (fr) | 2014-03-26 | 2019-12-31 | Hoffmann La Roche | Composés bicycliques en tant qu'inhibiteurs de production d'autotaxine (atx) et d'acide lysophosphatidique (lpa) |
| EP3122751B1 (fr) | 2014-03-26 | 2019-10-30 | F.Hoffmann-La Roche Ag | Composés condensés de [1,4]diazépine en tant qu'inhibiteurs d'autotaxine (atx) et de production d'acide lysophosphatidique (lpa) |
| MA41898A (fr) | 2015-04-10 | 2018-02-13 | Hoffmann La Roche | Dérivés de quinazolinone bicyclique |
| MX387736B (es) | 2015-09-04 | 2025-03-18 | Hoffmann La Roche | Derivados de fenoximetilo. |
| KR20180054634A (ko) | 2015-09-24 | 2018-05-24 | 에프. 호프만-라 로슈 아게 | 이중 오토탁신(atx)/탄산 무수화효소(ca) 억제제로서 신규한 이환형 화합물 |
| CN107635995B (zh) | 2015-09-24 | 2022-08-19 | 豪夫迈·罗氏有限公司 | 作为atx抑制剂的二环化合物 |
| PE20180451A1 (es) | 2015-09-24 | 2018-03-05 | Hoffmann La Roche | Nuevos compuestos biciclicos como inhibidores de atx |
| MX2017015034A (es) | 2015-09-24 | 2018-04-13 | Hoffmann La Roche | Nuevos compuestos biciclicos como inhibidores duales de autotaxina (atx)/anhidrasa carbonica (ca). |
| MA49879A (fr) | 2017-03-16 | 2020-06-24 | Hoffmann La Roche | Composés hétérocycliques utiles en tant qu'inhibiteurs doubles d'atx/ca |
| CN110382484B (zh) | 2017-03-16 | 2022-12-06 | 豪夫迈·罗氏有限公司 | 新的作为atx抑制剂的二环化合物 |
| WO2020119896A1 (fr) * | 2018-12-11 | 2020-06-18 | F. Hoffmann-La Roche Ag | Inhibiteurs hétérocycliques d'atx |
| CN113412113B (zh) * | 2018-12-11 | 2024-07-26 | 豪夫迈·罗氏有限公司 | 氨基嗪酰胺 |
| CN110746450A (zh) * | 2019-09-17 | 2020-02-04 | 济南康和医药科技有限公司 | 一种贝前列素钠关键中间体的合成方法 |
Family Cites Families (141)
| 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 |
| KR910009330B1 (ko) | 1989-10-23 | 1991-11-11 | 재단법인 한국화학연구소 | 항균작용을 갖는 퀴놀린계 화합물과 그의 제조방법 |
| 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 |
| DE4121214A1 (de) | 1991-06-27 | 1993-01-14 | Bayer Ag | 7-azaisoindolinyl-chinolon- und -naphthyridoncarbonsaeure-derivate |
| 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 |
| SK11402000A3 (sk) | 1998-02-04 | 2001-03-12 | Banyu Pharmaceutical Co., Ltd | Cyklické n-acylaminoderiváty |
| 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 |
| AU1400401A (en) | 1999-11-09 | 2001-06-06 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Product inhibiting transduction of G heterotrimeric protein signals combined with another anti-cancer agent for therapeutic use in cancer treatment |
| MXPA03008109A (es) | 2001-03-07 | 2003-12-12 | Pfizer Prod Inc | Moduladores de la actividad de receptores de quimiocinas. |
| JP4459629B2 (ja) | 2002-04-12 | 2010-04-28 | メルク エンド カムパニー インコーポレーテッド | 二環式アミド |
| 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 |
| KR100610731B1 (ko) | 2004-02-24 | 2006-08-09 | 한국과학기술연구원 | Ｔ-형 칼슘 채널 차단제로서 유용한 ３,４-디히드로퀴나졸린유도체 및 그의 제조 방법 |
| CN1950082B (zh) | 2004-03-03 | 2013-02-06 | 凯莫森特里克斯股份有限公司 | 双环和桥连的含氮杂环化物 |
| DK1761542T3 (da) | 2004-06-09 | 2008-04-28 | Hoffmann La Roche | Octahydropyrrolo[3,4-C] pyrrolderivater og anvendelsen deraf som antivirusmidler |
| 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 |
| GB0504019D0 (en) | 2005-02-26 | 2005-04-06 | Astrazeneca Ab | Amide derivatives |
| 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 |
| EP1942108B1 (fr) | 2005-10-28 | 2013-09-04 | Ono Pharmaceutical Co., Ltd. | Compose contenant un groupe basique et son utilisation |
| EP1961744B1 (fr) | 2005-11-18 | 2013-04-17 | Ono Pharmaceutical Co., Ltd. | Composé contenant un groupe basique et son utilisation |
| JP2007176809A (ja) | 2005-12-27 | 2007-07-12 | Hideaki Natsukari | 複素環置換アミド化合物、その製造法および医薬組成物 |
| 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 |
| CN101600698B (zh) | 2006-09-11 | 2012-01-11 | 欧加农股份有限公司;药典有限责任公司 | 喹唑啉酮和异喹啉酮乙酰胺衍生物 |
| CA2663500A1 (fr) | 2006-09-15 | 2008-03-20 | Schering Corporation | Derives d'azetidine spiro-condenses convenant pour le traitement de la douleur, du diabete et des troubles du metabolisme des lipides |
| US8735411B2 (en) | 2006-10-02 | 2014-05-27 | Abbvie Inc. | Macrocyclic benzofused pyrimidine derivatives |
| TWI454262B (zh) | 2006-11-02 | 2014-10-01 | Targacept Inc | 菸鹼乙醯膽鹼受體亞型選擇性之二氮雜雙環烷類醯胺 |
| EP2097388B1 (fr) | 2006-11-15 | 2011-09-07 | High Point Pharmaceuticals, LLC | Nouveaux 2-(2-hydroxyphényl)benzimidazoles utilisés pour traiter l'obésité et le diabète |
| 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 |
| KR20090127178A (ko) | 2007-03-29 | 2009-12-09 | 에프. 호프만-라 로슈 아게 | 비뉴클레오시드 역전사 효소 억제제 |
| 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. |
| JP2010524987A (ja) | 2007-04-27 | 2010-07-22 | サノフィ−アベンティス | ２−ヘテロアリール−ピロロ［３，４−ｃ］ピロール誘導体及びｓｃｄ阻害剤としてのそれらの使用 |
| KR20100039300A (ko) | 2007-08-07 | 2010-04-15 | 애보트 게엠베하 운트 콤파니 카게 | 세로토닌 5-ｈｔ6 수용체의 조절에 반응하는 장애를 치료하는데 적합한 퀴놀린 화합물 |
| DE102007047737A1 (de) | 2007-10-05 | 2009-04-30 | Merck Patent Gmbh | Piperidin- und Piperazinderivate |
| MX2010004281A (es) | 2007-10-19 | 2010-09-10 | Sarcode Corp | Composiciones y metodos para el tratamiento de la retinopatia diabetica. |
| PA8802501A1 (es) | 2007-10-31 | 2009-06-23 | Janssen Pharmaceutica Nv | Diaminas en puente o fusionadas sustituidas con arilo como moduladores de leucotrieno, hidrolasa |
| DE102007054156A1 (de) | 2007-11-12 | 2009-05-14 | Ventech Gmbh | Verfahren zum Feststellen des Druckes und der Profiltiefe bei einem Fahrzeugreifen |
| 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 |
| JPWO2009154132A1 (ja) | 2008-06-19 | 2011-12-01 | Ｍｓｄ株式会社 | スピロジアミン−ジアリールケトオキシム誘導体 |
| WO2010028761A1 (fr) | 2008-09-09 | 2010-03-18 | Sanofi-Aventis | Dérivés de 2-hétéro-aryl-pyrrolo[3, 4-c]pyrrol et leur utilisation en tant qu'inhibiteurs de scd |
| TW201020247A (en) | 2008-11-06 | 2010-06-01 | Gruenenthal Gmbh | Substituierte disulfonamide |
| US8188090B2 (en) | 2008-11-17 | 2012-05-29 | Hoffman-La Roche Inc. | Naphthylacetic acids |
| DE102008059578A1 (de) | 2008-11-28 | 2010-06-10 | Merck Patent Gmbh | Benzo-Naphtyridin Verbindungen |
| EA201100879A1 (ru) | 2008-12-01 | 2012-01-30 | Мерк Патент Гмбх | Производные пиридопиримидина в качестве ингибиторов аутотаксина |
| TW201035102A (en) | 2009-03-04 | 2010-10-01 | Gruenethal Gmbh | Sulfonylated tetrahydroazolopyrazines and their use as medicinal products |
| BRPI1006113A2 (pt) | 2009-03-05 | 2016-02-16 | Daiichi Sankyo Co Ltd | "derivado de piridina". |
| US20120010186A1 (en) | 2009-03-23 | 2012-01-12 | Merck Frosst Canada Ltd. | Heterocyclic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| TW201038572A (en) | 2009-03-25 | 2010-11-01 | Gruenenthal Gmbh | Substituted spiro-amide compounds |
| EP2623101B1 (fr) | 2009-04-02 | 2021-04-21 | Merck Patent GmbH | Dérivés de pipéridine et de pipérazine en tant qu'inhibiteurs de l'autotaxine |
| CA2757415C (fr) | 2009-04-02 | 2018-02-06 | Merck Patent Gmbh | Inhibiteurs de l'autotaxine |
| JP5767205B2 (ja) | 2009-04-02 | 2015-08-19 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | オートタキシン阻害剤としての複素環式化合物 |
| FR2945534B1 (fr) | 2009-05-12 | 2012-11-16 | Sanofi Aventis | DERIVES DE CYCLOPENTAL[c]PYRROLE-2-CARBOXYLATES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE |
| EP2432779A1 (fr) | 2009-05-22 | 2012-03-28 | Exelixis, Inc. | Inhibiteurs de pi3k/mtor à base de benzoxazépines pour lutter contre les maladies prolifératives |
| US20120083476A1 (en) | 2009-06-05 | 2012-04-05 | Janssen Pharmaceutica Nv | Heteroaryl-substituted spirocyclic diamine urea modulators of fatty acid amide hydrolase |
| DE102009033392A1 (de) | 2009-07-16 | 2011-01-20 | Merck Patent Gmbh | Heterocyclische Verbindungen als Autotaxin-Inhibitoren II |
| CN102574822A (zh) | 2009-08-04 | 2012-07-11 | 阿米拉制药公司 | 作为溶血磷脂酸受体拮抗剂的化合物 |
| 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 |
| ES2534516T3 (es) | 2010-01-07 | 2015-04-23 | E.I. Du Pont De Nemours And Company | Compuestos heterocíclicos fungicidas |
| WO2011115813A1 (fr) | 2010-03-18 | 2011-09-22 | Abbott Laboratories | Acétamides de lactame en tant que bloqueurs des canaux calciques |
| PL2547679T3 (pl) | 2010-03-19 | 2016-02-29 | Pfizer | Pochodne 2,3-dihydro-1H-inden-1-ylo-2,7-diazaspiro[3.5]nonanu i ich zastosowanie jako antagonistów lub odwrotnych agonistów receptora greliny |
| WO2011116867A1 (fr) | 2010-03-26 | 2011-09-29 | Merck Patent Gmbh | 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 |
| ES2646834T3 (es) | 2010-08-20 | 2017-12-18 | Amira Pharmaceuticals, Inc. | Inhibidores de autotaxina y usos de los mismos |
| EP2611808B1 (fr) | 2010-09-02 | 2014-11-12 | Merck Patent GmbH | Dérivés de pyrazolopyridinone en tant qu'antagonistes de récepteur de lpa |
| JP5699223B2 (ja) | 2010-12-02 | 2015-04-08 | シャンハイ デュァ ノボ ファルマテック カンパニー リミテッド | 複素環誘導体、その合成法および医療用途 |
| US20140031547A1 (en) | 2010-12-14 | 2014-01-30 | Electrophoretics Limited | CASEIN KINASE 1delta (CK 1delta) INHIBITORS AND THEIR USE IN THE TREATMENT OF NEURODE-GENERATIVE DISEASES SUCH AS TAUOPATHIES |
| US9260416B2 (en) | 2011-05-27 | 2016-02-16 | Amira Pharmaceuticals, Inc. | Heterocyclic autotaxin inhibitors and uses thereof |
| US8664213B2 (en) | 2011-08-29 | 2014-03-04 | Bristol-Myers Squibb Company | Spiro bicyclic diamine derivatives as HIV attachment inhibitors |
| 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 |
| US9815851B2 (en) | 2011-12-02 | 2017-11-14 | Phenex Pharmaceuticals Ag | Pyrrolo carboxamides as modulators of orphan nuclear receptor RAR-related orphan receptor-gamma (RORγ, NR1F3) activity and for the treatment of chronic inflammatory and autoimmune diseases |
| 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 |
| TWI633087B (zh) * | 2012-06-13 | 2018-08-21 | 赫孚孟拉羅股份公司 | 新穎二氮雜螺環烷及氮雜螺環烷 |
| LT3495367T (lt) | 2012-06-13 | 2021-02-25 | Incyte Holdings Corporation | Pakeistieji tricikliniai junginiai, kaip fgfr inhibitoriai |
| CA2871388A1 (fr) | 2012-06-27 | 2014-01-03 | F. Hoffmann-La Roche Ag | Composes 5-azaindazole et methodes d'utilisation |
| TWI631097B (zh) | 2012-07-27 | 2018-08-01 | 百健Ｍａ公司 | 作爲ｓ１ｐ調節劑及／或ａｔｘ調節劑之化合物 |
| WO2014018881A1 (fr) | 2012-07-27 | 2014-01-30 | Biogen Idec Ma Inc. | Agents de modulation d'atx |
| AR092211A1 (es) | 2012-09-24 | 2015-04-08 | Merck Patent Ges Mit Beschränkter Haftung | Derivados de hidropirrolopirrol |
| EP3590940B1 (fr) | 2012-09-25 | 2021-06-09 | F. Hoffmann-La Roche AG | Dérivés du héxahydropyrrolo[3,4-c]pyrrole et composés similaires en tant qu'inhibiteurs de l'autotaxine (atx) et inhibiteurs de la production de l'acid lysophosphatidique (lpa) pour traiter des maladies rénales |
| WO2014048881A1 (fr) | 2012-09-25 | 2014-04-03 | Bayer Pharma Aktiengesellschaft | Combinaison de régorafénib et d'acide acétylsalicylique destinée au traitement du cancer |
| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
| PL2912019T3 (pl) | 2012-10-25 | 2021-11-02 | Tetra Discovery Partners Llc | Heteroarylowe inhibitory pde4 |
| DK2938598T3 (en) | 2012-12-31 | 2017-02-13 | Cadila Healthcare Ltd | Substituted phthalazine-1 (2H) -one derivatives as selective inhibitors of poly (adp-ribose) polymerase-1 |
| JPWO2014133112A1 (ja) | 2013-03-01 | 2017-02-02 | 国立大学法人 東京大学 | オートタキシン阻害活性を有する８−置換イミダゾピリミジノン誘導体 |
| CN105026403B (zh) | 2013-03-12 | 2018-05-18 | 艾伯维公司 | 四环布罗莫结构域抑制剂 |
| AR095079A1 (es) * | 2013-03-12 | 2015-09-16 | Hoffmann La Roche | Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo |
| 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 |
| JP2016512528A (ja) | 2013-03-12 | 2016-04-28 | アクセラ インコーポレイテッド | 眼疾患及び眼障害を治療するための置換された３−フェニルプロピルアミン誘導体 |
| EP2970302A1 (fr) | 2013-03-15 | 2016-01-20 | Biogen MA Inc. | Modulateurs de s1p et/ou de l'atx |
| WO2014179564A1 (fr) | 2013-05-01 | 2014-11-06 | Vitae Pharmaceuticals, Inc. | Inhibiteurs du ror-gamma à base de thiazalopyrrolidine |
| PT3022202T (pt) | 2013-07-18 | 2019-09-03 | Novartis Ag | Inibidores da autotaxina compreendendo um núcleo beteroaromático anel-benzilo-amida-ciclo |
| SI3057959T1 (en) | 2013-10-17 | 2018-07-31 | Vertex Pharmaceuticals Incorporated | DNA-PK INHIBITORS |
| KR102367876B1 (ko) | 2013-11-22 | 2022-02-24 | 사브레 테라퓨틱스 엘엘씨 | 오토탁신 억제제 화합물 |
| AR098475A1 (es) | 2013-11-26 | 2016-06-01 | Bayer Cropscience Ag | Compuestos pesticidas y usos |
| NO3074400T3 (fr) | 2013-11-26 | 2018-04-14 | ||
| EP3122751B1 (fr) | 2014-03-26 | 2019-10-30 | F.Hoffmann-La Roche Ag | Composés condensés de [1,4]diazépine en tant qu'inhibiteurs d'autotaxine (atx) et de production d'acide lysophosphatidique (lpa) |
| BR112016020117B1 (pt) | 2014-03-26 | 2020-03-17 | Basf Se | “compostos, composição e método para o combate dos fungos fitopatogênicos |
| JO3512B1 (ar) | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز |
| MA39792B1 (fr) * | 2014-03-26 | 2019-12-31 | Hoffmann La Roche | Composés bicycliques en tant qu'inhibiteurs de production d'autotaxine (atx) et d'acide lysophosphatidique (lpa) |
| CR20160496A (es) | 2014-04-04 | 2017-01-02 | X-Rx Inc | Inhibidores espirocíclicos sustituidos de la autotaxina |
| JP6632532B2 (ja) | 2014-08-29 | 2020-01-22 | 国立大学法人 東京大学 | オートタキシン阻害活性を有するピリミジノン誘導体 |
| TWI675032B (zh) | 2014-10-14 | 2019-10-21 | 美商維它藥物公司 | ＲＯＲ-γ之二氫吡咯并吡啶抑制劑 |
| WO2016128529A1 (fr) | 2015-02-15 | 2016-08-18 | F. Hoffmann-La Roche Ag | Dérivés de 1-(het)arylsulfonyle- (pyrrolidine ou pipéridine)-2-carboxamide et leur utilisation comme antagonistes de trpa1 |
| MA41898A (fr) | 2015-04-10 | 2018-02-13 | Hoffmann La Roche | Dérivés de quinazolinone bicyclique |
| JP6651546B2 (ja) | 2015-05-11 | 2020-02-19 | カディラ・ヘルスケア・リミテッド | カッパ（κ）オピオイド受容体（ＫＯＲ）アゴニストとしての新規の短鎖ペプチド |
| 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 |
| MX387736B (es) | 2015-09-04 | 2025-03-18 | Hoffmann La Roche | Derivados de fenoximetilo. |
| HK1255699A1 (zh) | 2015-09-24 | 2019-08-23 | Ionis Pharmaceuticals, Inc. | Kras表达的调节剂 |
| MX2017015034A (es) | 2015-09-24 | 2018-04-13 | Hoffmann La Roche | Nuevos compuestos biciclicos como inhibidores duales de autotaxina (atx)/anhidrasa carbonica (ca). |
| PE20180451A1 (es) | 2015-09-24 | 2018-03-05 | Hoffmann La Roche | Nuevos compuestos biciclicos como inhibidores de atx |
| CN107635995B (zh) * | 2015-09-24 | 2022-08-19 | 豪夫迈·罗氏有限公司 | 作为atx抑制剂的二环化合物 |
| KR20180054634A (ko) | 2015-09-24 | 2018-05-24 | 에프. 호프만-라 로슈 아게 | 이중 오토탁신(atx)/탄산 무수화효소(ca) 억제제로서 신규한 이환형 화합물 |
| WO2017087863A1 (fr) | 2015-11-20 | 2017-05-26 | Abide Therapeutics, Inc. | Composés de pyrazole, procédés de production et utilisation |
| WO2017087858A1 (fr) | 2015-11-20 | 2017-05-26 | Abide Therapeutics, Inc. | Composés de pyrazole, procédés de production et utilisation |
| CA3003288A1 (fr) | 2015-11-25 | 2017-06-01 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de bromodomaines bivalents et leurs utilisations |
| CA3006029C (fr) | 2015-12-01 | 2020-08-04 | Nihon Nohyaku Co., Ltd. | Compose 3h-pyrrolopyridine, n-oxyde associe ou sel associe, insecticide agricole et horticole renfermant le compose et methode d'utilisation associee |
| CN110382484B (zh) | 2017-03-16 | 2022-12-06 | 豪夫迈·罗氏有限公司 | 新的作为atx抑制剂的二环化合物 |
| MA49879A (fr) | 2017-03-16 | 2020-06-24 | Hoffmann La Roche | Composés hétérocycliques utiles en tant qu'inhibiteurs doubles d'atx/ca |
| EP3680241A1 (fr) | 2017-03-20 | 2020-07-15 | Forma Therapeutics, Inc. | Compositions de pyrrolopyrrole en tant qu'activateurs de pyruvate kinase (pkr) |
-
2018
- 2018-03-13 MA MA049879A patent/MA49879A/fr unknown
- 2018-03-13 CR CR20190423A patent/CR20190423A/es unknown
- 2018-03-13 SG SG11201908560S patent/SG11201908560SA/en unknown
- 2018-03-13 KR KR1020197030084A patent/KR20190129924A/ko not_active Ceased
- 2018-03-13 WO PCT/EP2018/056140 patent/WO2018167001A1/fr not_active Ceased
- 2018-03-13 CN CN201880017056.4A patent/CN110392679B/zh active Active
- 2018-03-13 BR BR112019019017A patent/BR112019019017A2/pt not_active Application Discontinuation
- 2018-03-13 EP EP18710471.6A patent/EP3596059B1/fr active Active
- 2018-03-13 RU RU2019132254A patent/RU2019132254A/ru not_active Application Discontinuation
- 2018-03-13 AU AU2018233079A patent/AU2018233079B9/en not_active Ceased
- 2018-03-13 JP JP2019550561A patent/JP7157755B2/ja active Active
- 2018-03-13 MX MX2019010772A patent/MX381728B/es unknown
- 2018-03-13 PE PE2019001583A patent/PE20191757A1/es unknown
- 2018-03-13 CA CA3053329A patent/CA3053329A1/fr active Pending
- 2018-03-15 AR ARP180100599A patent/AR111279A1/es unknown
- 2018-03-15 TW TW107108748A patent/TW201838982A/zh unknown
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2019
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- 2019-09-08 IL IL269188A patent/IL269188B/en unknown
- 2019-09-12 CL CL2019002609A patent/CL2019002609A1/es unknown
- 2019-09-12 US US16/569,475 patent/US11059794B2/en active Active
- 2019-09-16 PH PH12019502118A patent/PH12019502118A1/en unknown
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| Publication number | Publication date |
|---|---|
| CR20190423A (es) | 2019-11-01 |
| KR20190129924A (ko) | 2019-11-20 |
| CA3053329A1 (fr) | 2018-09-20 |
| US20200002297A1 (en) | 2020-01-02 |
| AU2018233079A1 (en) | 2019-08-29 |
| CN110392679A (zh) | 2019-10-29 |
| CN110392679B (zh) | 2023-04-07 |
| AU2018233079B9 (en) | 2021-07-22 |
| JP7157755B2 (ja) | 2022-10-20 |
| IL269188B (en) | 2021-12-01 |
| EP3596059C0 (fr) | 2024-04-24 |
| CO2019009373A2 (es) | 2019-09-09 |
| RU2019132254A3 (fr) | 2021-06-04 |
| PE20191757A1 (es) | 2019-12-12 |
| AU2018233079B2 (en) | 2021-06-24 |
| EP3596059A1 (fr) | 2020-01-22 |
| IL269188A (en) | 2019-11-28 |
| EP3596059B1 (fr) | 2024-04-24 |
| PH12019502118A1 (en) | 2020-07-06 |
| US11059794B2 (en) | 2021-07-13 |
| CL2019002609A1 (es) | 2020-02-14 |
| MX381728B (es) | 2025-03-13 |
| SG11201908560SA (en) | 2019-10-30 |
| TW201838982A (zh) | 2018-11-01 |
| BR112019019017A2 (pt) | 2020-04-14 |
| MX2019010772A (es) | 2019-12-16 |
| RU2019132254A (ru) | 2021-04-16 |
| AR111279A1 (es) | 2019-06-26 |
| WO2018167001A1 (fr) | 2018-09-20 |
| JP2020514355A (ja) | 2020-05-21 |
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