MA34765B1 - Antagonistes des récepteurs de l'acide lysophosphatidique et utilisations de ceux-ci - Google Patents
Antagonistes des récepteurs de l'acide lysophosphatidique et utilisations de ceux-ciInfo
- Publication number
- MA34765B1 MA34765B1 MA36060A MA36060A MA34765B1 MA 34765 B1 MA34765 B1 MA 34765B1 MA 36060 A MA36060 A MA 36060A MA 36060 A MA36060 A MA 36060A MA 34765 B1 MA34765 B1 MA 34765B1
- Authority
- MA
- Morocco
- Prior art keywords
- acid receptor
- receptor antagonists
- compounds
- lysophosphatide acid
- relates
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/132—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing rings
- C07C53/134—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing rings monocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
- C07C271/28—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/27—Esters, e.g. nitroglycerine, selenocyanates of carbamic or thiocarbamic acids, meprobamate, carbachol, neostigmine
-
- 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
- A61P11/00—Drugs for disorders of the respiratory system
-
- 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
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/01—Saturated compounds having only one carboxyl group and containing hydroxy or O-metal groups
- C07C59/11—Saturated compounds having only one carboxyl group and containing hydroxy or O-metal groups containing rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C62/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C62/30—Unsaturated compounds
- C07C62/32—Unsaturated compounds containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C69/757—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
- C07D217/14—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
- C07D217/16—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
- C07D217/18—Aralkyl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/28—Two oxygen or sulfur atoms
- C07D231/30—Two oxygen or sulfur atoms attached in positions 3 and 5
- C07D231/32—Oxygen atoms
- C07D231/36—Oxygen atoms with hydrocarbon radicals, substituted by hetero atoms, attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/16—Radicals substituted by singly bound hetero atoms other than halogen by oxygen 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
- C07D401/12—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
- 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
- C07D403/06—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 only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Urology & Nephrology (AREA)
- Biomedical Technology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
La présente invention concerne des composés antagonistes du(des) récepteur(s) de l'acide lysophosphatidique. L'invention concerne également des compositions pharmaceutiques et des médicaments comprenant les composés décrits ici, ainsi que des procédés d'utilisation de tels antagonistes, seuls ou en association avec d'autres composés, dans le but de traiter des états pathologiques ou des maladies dépendantes de l'acide lysophosphatidique ou induites par celui-ci.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42071610P | 2010-12-07 | 2010-12-07 | |
| PCT/US2011/063465 WO2012078593A2 (fr) | 2010-12-07 | 2011-12-06 | Antagonistes des récepteurs de l'acide lysophosphatidique et utilisations de ceux-ci |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA34765B1 true MA34765B1 (fr) | 2013-12-03 |
Family
ID=45418800
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA36060A MA34765B1 (fr) | 2010-12-07 | 2013-06-28 | Antagonistes des récepteurs de l'acide lysophosphatidique et utilisations de ceux-ci |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US9272990B2 (fr) |
| EP (1) | EP2648714B1 (fr) |
| JP (1) | JP2014508111A (fr) |
| KR (1) | KR20130126659A (fr) |
| CN (1) | CN103347510B (fr) |
| AU (1) | AU2011338561A1 (fr) |
| BR (1) | BR112013014019A2 (fr) |
| CA (1) | CA2820817A1 (fr) |
| CL (1) | CL2013001655A1 (fr) |
| CO (1) | CO6771417A2 (fr) |
| EA (1) | EA201390821A1 (fr) |
| IL (1) | IL226491A0 (fr) |
| MA (1) | MA34765B1 (fr) |
| MX (1) | MX2013006040A (fr) |
| PE (1) | PE20140879A1 (fr) |
| PH (1) | PH12013501136A1 (fr) |
| SG (1) | SG190417A1 (fr) |
| WO (1) | WO2012078593A2 (fr) |
| ZA (1) | ZA201304159B (fr) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8975235B2 (en) * | 2011-03-20 | 2015-03-10 | Intermune, Inc. | Lysophosphatidic acid receptor antagonists |
| MX2014014711A (es) * | 2012-06-20 | 2015-03-04 | Hoffmann La Roche | Compuestos de n-ariltriazol como antagonistas del receptor de acido lisofosfatidico (lpar). |
| MA37765A1 (fr) * | 2012-06-20 | 2017-04-28 | Hoffmann La Roche | Composés de pyrazole substitués utilisés comme antagonistes de lpar |
| MA37764A1 (fr) * | 2012-06-20 | 2016-01-29 | Hoffmann La Roche | Composés n-alkyltriazole utilisés comme antagonistes de lpar |
| JP2015524385A (ja) | 2012-07-02 | 2015-08-24 | フィブロスタティン,エス.エル. | Gpbp−1阻害およびその治療的使用 |
| WO2014037303A1 (fr) * | 2012-09-05 | 2014-03-13 | F. Hoffmann-La Roche Ag | Composés de cyanopyrazole substitués antagonistes des lpar |
| BR112015007578B1 (pt) | 2012-10-02 | 2020-05-05 | Bayer Cropscience Ag | Uso não terapêutico de compostos, compostos, composições emétodo não terapêutico para controlar pragas compreendendoos referidos compostos |
| DK2940013T3 (en) | 2012-12-28 | 2018-03-26 | Ube Industries | HALOGEN-SUBSTITUTED HETEROCYCLIC COMPOUND |
| US20140213538A1 (en) * | 2013-01-15 | 2014-07-31 | Intermune, Inc. | Lysophosphatidic acid receptor antagonists |
| EP2961746B1 (fr) | 2013-02-28 | 2018-01-03 | Bristol-Myers Squibb Company | Dérivés de phénylpyrazole en tant que puissants inhibiteurs de rock1 et rock2 |
| AR094929A1 (es) | 2013-02-28 | 2015-09-09 | Bristol Myers Squibb Co | Derivados de fenilpirazol como inhibidores potentes de rock1 y rock2 |
| SG11201507459YA (en) | 2013-03-15 | 2015-10-29 | Epigen Biosciences Inc | Heterocyclic compounds useful in the treatment of disease |
| JP2014231508A (ja) * | 2013-05-02 | 2014-12-11 | 宇部興産株式会社 | ハロゲン置換へテロ環化合物 |
| EA038294B1 (ru) * | 2013-05-24 | 2021-08-05 | Эпиджен Байосайенсиз, Инк. | Гетероциклические соединения, применимые в лечении заболеваний |
| AU2015281021B9 (en) * | 2014-06-27 | 2019-03-28 | Ube Corporation | Salt of halogen-substituted heterocyclic compound |
| WO2016046782A1 (fr) * | 2014-09-26 | 2016-03-31 | Glenmark Pharmaceuticals S.A. | Composés imidazole biaryle en tant qu'inhibiteurs de la s-nitrosoglutathion réductase |
| CA2988306A1 (fr) | 2015-06-05 | 2016-12-08 | Vertex Pharmaceuticals Incorporated | Triazoles pour le traitement de maladies liees a la demyelinisation |
| AR108838A1 (es) | 2016-06-21 | 2018-10-03 | Bristol Myers Squibb Co | Ácidos de carbamoiloximetil triazol ciclohexilo como antagonistas de lpa |
| WO2018106643A1 (fr) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Azoles hétérocycliques pour le traitement de maladies de démyélinisation |
| WO2018106641A1 (fr) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Pyrazoles pour le traitement de maladies démyélinisantes |
| WO2018106646A1 (fr) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Aminotriazoles pour traiter des maladies démyélinisantes |
| WO2019041340A1 (fr) * | 2017-09-04 | 2019-03-07 | Eli Lilly And Company | Composés inhibiteurs du récepteur 1 de l'acide lysophosphatidique (lpar1) |
| EP3728210A1 (fr) | 2017-12-19 | 2020-10-28 | Bristol-Myers Squibb Company | Acides carbamoyle cyclohexyliques à liaison n isoxazole utilisés en tant qu'antagonistes de lpa |
| US11180488B2 (en) | 2017-12-19 | 2021-11-23 | Bristol-Myers Squibb Company | Isoxazole o-linked carbamoyl cyclohexyl acids as LPA antagonists |
| JP7212047B2 (ja) | 2017-12-19 | 2023-01-24 | ブリストル-マイヤーズ スクイブ カンパニー | Lpaアンタゴニストとしてのシクロヘキシル酸ピラゾールアゾール |
| WO2019126087A1 (fr) | 2017-12-19 | 2019-06-27 | Bristol-Myers Squibb Company | Acide cyclohexyle isoxazole azoles en tant qu'antagonistes de lpa |
| KR102698386B1 (ko) | 2017-12-19 | 2024-08-22 | 브리스톨-마이어스 스큅 컴퍼니 | Lpa 길항제로서의 피라졸 n-연결된 카르바모일 시클로헥실 산 |
| KR102725744B1 (ko) * | 2017-12-19 | 2024-11-01 | 브리스톨-마이어스 스큅 컴퍼니 | Lpa 길항제로서의 시클로헥실 산 피라졸 아진 |
| EP3728223B1 (fr) | 2017-12-19 | 2022-12-28 | Bristol-Myers Squibb Company | Azines triazoles d'acide cyclohexyle utilisées en tant qu'antagonistes de lpa |
| US11319309B2 (en) | 2017-12-19 | 2022-05-03 | Bristol-Myers Squibb Company | Cyclohexyl acid isoxazole azines as LPA antagonists |
| AU2018392325A1 (en) | 2017-12-19 | 2020-07-30 | Bristol-Myers Squibb Company | Cyclohexyl acid triazole azoles as LPA antagonists |
| EP3728196B1 (fr) | 2017-12-19 | 2023-04-05 | Bristol-Myers Squibb Company | Acides carbamoyle cyclohexyliques à liaison o pyrazole utilisés en tant qu'antagonistes de lpa |
| ES2941774T3 (es) | 2018-09-18 | 2023-05-25 | Bristol Myers Squibb Co | Acidos oxabiciclo como antagonistas de LPA |
| US12209072B2 (en) | 2018-09-18 | 2025-01-28 | Bristol-Myers Squibb Company | Cyclopentyl acids as LPA antagonists |
| AU2019387370A1 (en) | 2018-11-30 | 2021-06-10 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| CN112574201B (zh) * | 2019-09-29 | 2024-04-19 | 四川科伦博泰生物医药股份有限公司 | 芳基胺类化合物、包含其的药物组合物及其制备方法和用途 |
| CA3158743A1 (fr) | 2019-11-15 | 2021-05-20 | Gilead Sciences, Inc. | Pyridylsulfonamides de carbamate de triazole utilisees en tant qu'antagonistes du recepteur de lpa et leurs utilisations |
| US20230014137A1 (en) * | 2019-11-29 | 2023-01-19 | Ono Pharmaceutical Co., Ltd. | Compound having lysophosphatidic acid receptor agonist activity and pharmaceutical use thereof |
| CA3157600A1 (fr) | 2019-12-12 | 2021-06-17 | Chiesi Farmaceutici S.P.A. | Derives de quinazoline utilises en tant qu'inhibiteurs du recepteur 2 de lpa |
| TWI843503B (zh) | 2020-06-03 | 2024-05-21 | 美商基利科學股份有限公司 | Lpa受體拮抗劑及其用途 |
| US11702407B2 (en) | 2020-06-03 | 2023-07-18 | Gilead Sciences, Inc. | LPA receptor antagonists and uses thereof |
| WO2022006470A1 (fr) | 2020-07-01 | 2022-01-06 | Vanderbilt University | Méthodes de traitement d'une maladie rénale |
| AU2022215844A1 (en) | 2021-02-02 | 2023-09-14 | Liminal Biosciences Limited | Gpr84 antagonists and uses thereof |
| EP4337641A1 (fr) | 2021-05-11 | 2024-03-20 | Gilead Sciences, Inc. | Antagonistes du récepteur lpa et leurs utilisations |
| US12503454B2 (en) | 2021-05-13 | 2025-12-23 | Gilead Sciences, Inc. | LPA receptor antagonists and uses thereof |
| KR20240115978A (ko) | 2021-12-08 | 2024-07-26 | 길리애드 사이언시즈, 인코포레이티드 | Lpa 수용체 길항제 및 이의 용도 |
| TW202342017A (zh) | 2022-02-25 | 2023-11-01 | 美商洛子峰生物有限公司 | 用於治療與lpa受體活性相關的病狀的化合物及組合物 |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4229447A (en) | 1979-06-04 | 1980-10-21 | American Home Products Corporation | Intraoral methods of using benzodiazepines |
| US4476116A (en) | 1982-12-10 | 1984-10-09 | Syntex (U.S.A.) Inc. | Polypeptides/chelating agent nasal compositions having enhanced peptide absorption |
| US5116817A (en) | 1982-12-10 | 1992-05-26 | Syntex (U.S.A.) Inc. | LHRH preparations for intranasal administration |
| US4596795A (en) | 1984-04-25 | 1986-06-24 | The United States Of America As Represented By The Secretary, Dept. Of Health & Human Services | Administration of sex hormones in the form of hydrophilic cyclodextrin derivatives |
| JPS60239743A (ja) * | 1984-05-15 | 1985-11-28 | Canon Inc | 記録媒体 |
| JPS6137885A (ja) * | 1984-07-31 | 1986-02-22 | Canon Inc | El素子 |
| DE3684446D1 (de) | 1985-12-28 | 1992-04-23 | Sumitomo Pharma | Arzneimittel mit verzoegerter stossweiser freisetzung. |
| US4755386A (en) | 1986-01-22 | 1988-07-05 | Schering Corporation | Buccal formulation |
| US5739136A (en) | 1989-10-17 | 1998-04-14 | Ellinwood, Jr.; Everett H. | Intraoral dosing method of administering medicaments |
| US5017381A (en) | 1990-05-02 | 1991-05-21 | Alza Corporation | Multi-unit pulsatile delivery system |
| US5229135A (en) | 1991-11-22 | 1993-07-20 | Prographarm Laboratories | Sustained release diltiazem formulation |
| EP0730019A4 (fr) * | 1994-07-15 | 1996-12-18 | Seiko Epson Corp | Composition de cristaux liquides et element d'affichage a cristaux liquides produit a partir de celle-ci |
| GB9523946D0 (en) | 1995-11-23 | 1996-01-24 | Bayer Ag | Leukotriene antagonistic benzoic acid derivatives |
| US5837284A (en) | 1995-12-04 | 1998-11-17 | Mehta; Atul M. | Delivery of multiple doses of medications |
| US5840329A (en) | 1997-05-15 | 1998-11-24 | Bioadvances Llc | Pulsatile drug delivery system |
| US6391452B1 (en) | 1997-07-18 | 2002-05-21 | Bayer Corporation | Compositions for nasal drug delivery, methods of making same, and methods of removing residual solvent from pharmaceutical preparations |
| DE19907904A1 (de) * | 1999-02-24 | 2000-08-31 | Clariant Gmbh | Verfahren zur Herstellung von [1,1':4',1"]-Terphenylverbindungen |
| JP4396808B2 (ja) | 2001-02-08 | 2010-01-13 | 小野薬品工業株式会社 | Lpa受容体調節剤からなる泌尿器疾患治療剤 |
| DE60226357T2 (de) * | 2001-02-08 | 2009-05-28 | Seimi Chemical Co. Ltd., Chigasaki | Flüssigkristallzusammensetzung enthaltend optisch aktive Verbindungen, und flüssig-kristallines elektrooptisches Element |
| AU2002305450A1 (en) | 2001-05-08 | 2002-11-18 | Yale University | Proteomimetic compounds and methods |
| MXPA05012459A (es) | 2003-05-19 | 2006-02-22 | Irm Llc | Compuestos y composiciones inmunosupresoras. |
| US20050245543A1 (en) | 2004-04-30 | 2005-11-03 | Pfizer Inc | Histamine-3 receptor antagonists |
| AR055041A1 (es) | 2005-03-23 | 2007-08-01 | Merck Frosst Canada Ltd | Tiadiazoles y oxadiazoles como inhibidores de la sintesis de leucotrienos. composiciones farmaceuticas. |
| JP2009504575A (ja) | 2005-08-11 | 2009-02-05 | メルク フロスト カナダ リミテツド | 新規の置換された1,2,3,−トリアゾリルメチル−ベンゾチオフェン又は−インドール並びにロイコトリエン生合成阻害剤としてのそれらの使用 |
| US7405302B2 (en) | 2005-10-11 | 2008-07-29 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (FLAP) inhibitors |
| US20070225285A1 (en) | 2005-11-04 | 2007-09-27 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
| US7977359B2 (en) | 2005-11-04 | 2011-07-12 | Amira Pharmaceuticals, Inc. | 5-lipdxygenase-activating protein (FLAP) inhibitors |
| US20070219206A1 (en) | 2005-11-04 | 2007-09-20 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
| JP5092236B2 (ja) * | 2005-12-20 | 2012-12-05 | 旭硝子株式会社 | 重合性液晶性組成物、高分子液晶、光学素子、及びターフェニル誘導体 |
| WO2007077844A1 (fr) * | 2006-01-06 | 2007-07-12 | Chisso Corporation | Compose terphenyle monofluore ayant un groupe alcenyle, composition de cristaux liquides et ecran a cristaux liquides |
| MX2008009475A (es) | 2006-01-23 | 2008-10-20 | Amira Pharmaceuticals Inc | Inhibidores triciclicos de 5-lipoxigenasa. |
| GB2466121B (en) * | 2008-12-15 | 2010-12-08 | Amira Pharmaceuticals Inc | Antagonists of lysophosphatidic acid receptors |
| JP5399745B2 (ja) * | 2009-03-12 | 2014-01-29 | Jx日鉱日石エネルギー株式会社 | 多孔性金属錯体、多孔性金属錯体の製造方法及びガス貯蔵方法 |
| EP2462128B1 (fr) | 2009-08-04 | 2016-09-21 | Amira Pharmaceuticals, Inc. | Composés en tant qu'antagonistes du récepteur de l'acide lysophosphatidique |
| GB2474120B (en) * | 2009-10-01 | 2011-12-21 | Amira Pharmaceuticals Inc | Compounds as Lysophosphatidic acid receptor antagonists |
| WO2011159550A2 (fr) | 2010-06-14 | 2011-12-22 | Amidra Pharmaceuticals, Inc. | Antagoniste du récepteur de l'acide lysophosphatidique et ses utilisations |
| WO2011159633A1 (fr) | 2010-06-15 | 2011-12-22 | Amira Pharmaceuticals, Inc. | Formulations inhalables d'antagonistes de récepteur d'acide lysophosphatidique |
| EA024967B1 (ru) | 2010-12-07 | 2016-11-30 | Амира Фармасьютикалс, Инк. | Полициклический lpaантагонист и его применение |
-
2011
- 2011-12-06 JP JP2013543256A patent/JP2014508111A/ja active Pending
- 2011-12-06 WO PCT/US2011/063465 patent/WO2012078593A2/fr not_active Ceased
- 2011-12-06 PH PH1/2013/501136A patent/PH12013501136A1/en unknown
- 2011-12-06 EA EA201390821A patent/EA201390821A1/ru unknown
- 2011-12-06 KR KR1020137017645A patent/KR20130126659A/ko not_active Ceased
- 2011-12-06 AU AU2011338561A patent/AU2011338561A1/en not_active Abandoned
- 2011-12-06 SG SG2013040795A patent/SG190417A1/en unknown
- 2011-12-06 EP EP11802233.4A patent/EP2648714B1/fr not_active Not-in-force
- 2011-12-06 PE PE2013001366A patent/PE20140879A1/es not_active Application Discontinuation
- 2011-12-06 CA CA2820817A patent/CA2820817A1/fr not_active Abandoned
- 2011-12-06 MX MX2013006040A patent/MX2013006040A/es not_active Application Discontinuation
- 2011-12-06 US US13/992,053 patent/US9272990B2/en active Active
- 2011-12-06 CN CN201180066991.8A patent/CN103347510B/zh not_active Expired - Fee Related
- 2011-12-06 BR BR112013014019A patent/BR112013014019A2/pt not_active IP Right Cessation
-
2013
- 2013-05-21 IL IL226491A patent/IL226491A0/en unknown
- 2013-06-06 ZA ZA2013/04159A patent/ZA201304159B/en unknown
- 2013-06-07 CL CL2013001655A patent/CL2013001655A1/es unknown
- 2013-06-28 MA MA36060A patent/MA34765B1/fr unknown
- 2013-07-04 CO CO13158409A patent/CO6771417A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2011338561A1 (en) | 2013-07-25 |
| US20130253004A1 (en) | 2013-09-26 |
| SG190417A1 (en) | 2013-07-31 |
| CN103347510A (zh) | 2013-10-09 |
| JP2014508111A (ja) | 2014-04-03 |
| PE20140879A1 (es) | 2014-08-06 |
| EA201390821A1 (ru) | 2013-10-30 |
| CN103347510B (zh) | 2015-11-25 |
| US9272990B2 (en) | 2016-03-01 |
| KR20130126659A (ko) | 2013-11-20 |
| EP2648714A2 (fr) | 2013-10-16 |
| BR112013014019A2 (pt) | 2016-09-13 |
| IL226491A0 (en) | 2013-07-31 |
| CO6771417A2 (es) | 2013-10-15 |
| EP2648714B1 (fr) | 2015-11-18 |
| ZA201304159B (en) | 2014-12-23 |
| PH12013501136A1 (en) | 2013-07-08 |
| MX2013006040A (es) | 2013-08-26 |
| CL2013001655A1 (es) | 2014-04-04 |
| WO2012078593A3 (fr) | 2012-08-02 |
| CA2820817A1 (fr) | 2012-06-14 |
| WO2012078593A2 (fr) | 2012-06-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA34765B1 (fr) | Antagonistes des récepteurs de l'acide lysophosphatidique et utilisations de ceux-ci | |
| MA32226B1 (fr) | Compositions et leurs procedes de preparation et d'utilisation | |
| MA33299B1 (fr) | Nouvelle formulation de naproxène | |
| MA34449B1 (fr) | Formulation de poudre seche comprenant un inhibiteur de phosphodiesterase | |
| MA32131B1 (fr) | Antagonistes aminoalkylbiphényle n, n' disubstitués des récepteurs d2 de la prostaglandine | |
| MA34169B1 (fr) | Dérivés d'acide 1-amino-2-cyclopropyléthylboronique | |
| MA38183A1 (fr) | Composés pyrrolopyrimidines en tant qu'inhibiteurs de kinase | |
| EA201100691A1 (ru) | Антагонисты рецепторов лизофосфатидной кислоты | |
| MA32230B1 (fr) | Formes cristallines et deux formes solvatées de lactates de 4-amino-5-fluoro -3-[5-(4-méthylpipérazin-1-yl)-1h-benzimidazol-2-yl]quinolin-2(1h)-one | |
| MA39033A1 (fr) | Formes solides d'acide {[5-(3-chlorophényl)-3-hydroxypyridine-2-carbonyl] amino}acétique, compositions et leurs utilisations | |
| BR112014026703A2 (pt) | inibidores de dna-pk | |
| MA38391A1 (fr) | Dérivés de pyridinyl et triazolone pyridinyl de fusion | |
| MA33296B1 (fr) | Nouvelle formulation d'indométhacine | |
| MA34650B1 (fr) | Antagonistes du récepteur cgrp de pipéridinone carboxamide azaindane | |
| MA38146B1 (fr) | Nouveaux dérivés du benzimidazole comme antagonistes ep4 | |
| MA37891A1 (fr) | Alcoxypyrazoles comme activateurs de guanylate cyclase soluble | |
| MA33467B1 (fr) | Promédicaments comprenant un conjugué insuline-lieur | |
| MA33295B1 (fr) | Nouvelle formulation de diclofénac | |
| TN2012000192A1 (fr) | N1-pyrazolospirocetones inhibitrices d'acetyl-coa-carboxylase | |
| MA34819B1 (fr) | Dérivés bicyclo[3.2.1]octylamide et leurs utilisations | |
| MA38349A1 (fr) | Œstra-1,3,5(10),16-tétraéno-3-carboxamide pour inhiber la 17-bêta-hydroxystéroïde déshydrogénase (akr1c3) | |
| MA32729B1 (fr) | Derives d'acide 1-amino-2-cyclobutylethylboronique | |
| MA35443B1 (fr) | Composes benzofuranes pour le traitement d'infections par le virus de l'hepatite c | |
| MA35187B1 (fr) | Composés ayant une activité antagoniste d'un récepteur muscarinique et agoniste d'un récepteur béta2 adrénergique | |
| MA34545B1 (fr) | Co-cristaux et sels d'inhibiteurs de ccr3 |