MA34373B1 - Composés hétérocycliques agonistes du récepteur ip - Google Patents
Composés hétérocycliques agonistes du récepteur ipInfo
- Publication number
- MA34373B1 MA34373B1 MA35551A MA35551A MA34373B1 MA 34373 B1 MA34373 B1 MA 34373B1 MA 35551 A MA35551 A MA 35551A MA 35551 A MA35551 A MA 35551A MA 34373 B1 MA34373 B1 MA 34373B1
- Authority
- MA
- Morocco
- Prior art keywords
- heterocytic
- agonist
- receiver
- compounds
- relates
- Prior art date
Links
Classifications
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- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
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- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La présente invention concerne des dérivés hétérocycliques qui activent le récepteur IP. L'activation de la voie de signalisation du récepteur IP est utile pour traiter de nombreuses formes de l'hypertension artérielle pulmonaire (HTAP), la fibrose pulmonaire et exercer des effets bénéfiques dans des états fibrotiques de divers organes dans des modèles animaux et des patients. L'invention concerne également des compositions pharmaceutiques comprenant ces dérivés.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36413510P | 2010-07-14 | 2010-07-14 | |
| PCT/EP2011/062028 WO2012007539A1 (fr) | 2010-07-14 | 2011-07-14 | Composés hétérocycliques agonistes du récepteur ip |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA34373B1 true MA34373B1 (fr) | 2013-07-03 |
Family
ID=44628483
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA35551A MA34373B1 (fr) | 2010-07-14 | 2011-07-14 | Composés hétérocycliques agonistes du récepteur ip |
Country Status (35)
| Country | Link |
|---|---|
| US (2) | US8754085B2 (fr) |
| EP (1) | EP2593452B1 (fr) |
| JP (1) | JP5781159B2 (fr) |
| KR (1) | KR101491938B1 (fr) |
| CN (1) | CN103097385B (fr) |
| AU (1) | AU2011278279C1 (fr) |
| BR (1) | BR112013000946B1 (fr) |
| CA (1) | CA2804744C (fr) |
| CL (1) | CL2013000104A1 (fr) |
| CO (1) | CO6660445A2 (fr) |
| CR (1) | CR20130012A (fr) |
| CU (1) | CU24147B1 (fr) |
| CY (1) | CY1118819T1 (fr) |
| DK (1) | DK2593452T3 (fr) |
| EA (1) | EA022046B1 (fr) |
| EC (1) | ECSP13012385A (fr) |
| ES (1) | ES2622519T3 (fr) |
| GT (1) | GT201300018A (fr) |
| HR (1) | HRP20170617T1 (fr) |
| HU (1) | HUE031710T2 (fr) |
| IL (1) | IL224164A (fr) |
| LT (1) | LT2593452T (fr) |
| MA (1) | MA34373B1 (fr) |
| MX (1) | MX2013000537A (fr) |
| MY (1) | MY156795A (fr) |
| NZ (1) | NZ605528A (fr) |
| PE (1) | PE20130404A1 (fr) |
| PH (1) | PH12013500084A1 (fr) |
| PL (1) | PL2593452T3 (fr) |
| PT (1) | PT2593452T (fr) |
| RS (1) | RS55856B1 (fr) |
| SG (1) | SG186989A1 (fr) |
| SI (1) | SI2593452T1 (fr) |
| UA (1) | UA109786C2 (fr) |
| WO (1) | WO2012007539A1 (fr) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RS55856B1 (sr) | 2010-07-14 | 2017-08-31 | Novartis Ag | Heterociklična jedinjenja agonisti ip receptora |
| US8883819B2 (en) | 2011-09-01 | 2014-11-11 | Irm Llc | Bicyclic heterocycle derivatives for the treatment of pulmonary arterial hypertension |
| US20140357641A1 (en) | 2012-01-13 | 2014-12-04 | Novartis Ag | IP receptor agonist heterocyclic compounds |
| CN104053659B (zh) | 2012-01-13 | 2016-11-09 | 诺华股份有限公司 | 用于治疗肺动脉高压(pah)及相关病症的作为ip 受体激动剂的稠合的吡咯类 |
| EP2802585A1 (fr) | 2012-01-13 | 2014-11-19 | Novartis AG | Pipéridines condensées utilisées comme agonistes du récepteur ip pour le traitement de l'htap et de troubles connexes |
| WO2013105063A1 (fr) | 2012-01-13 | 2013-07-18 | Novartis Ag | Pipéridines condensées utilisées comme agonistes du récepteur ip pour le traitement de l'hypertension artérielle pulmonaire (htap) et de troubles associés |
| ES2561353T3 (es) * | 2012-01-13 | 2016-02-25 | Novartis Ag | Sales de un agonista del receptor IP |
| EP2956455B1 (fr) | 2013-02-13 | 2017-05-17 | Novartis AG | Composes heterocycliques a activite agoniste sur le recepteur ip |
| UA119247C2 (uk) | 2013-09-06 | 2019-05-27 | РОЙВЕНТ САЙЕНСИЗ ҐмбГ | Спіроциклічні сполуки як інгібітори триптофангідроксилази |
| US10112926B2 (en) | 2014-04-24 | 2018-10-30 | Novartis Ag | Amino pyridine derivatives as phosphatidylinositol 3-kinase inhibitors |
| PL3134395T3 (pl) | 2014-04-24 | 2018-07-31 | Novartis Ag | Pochodne pirazyny jako inhibitory 3-kinazy fosfatydyloinozytolu |
| EP3134397A1 (fr) | 2014-04-24 | 2017-03-01 | Novartis AG | Dérivés aminés de pyrazine utilisables en tant qu'inhibiteurs de la phosphatidylinositol 3-kinase |
| US9611201B2 (en) | 2015-03-05 | 2017-04-04 | Karos Pharmaceuticals, Inc. | Processes for preparing (R)-1-(5-chloro-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanol and 1-(5-chloro-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanone |
| PH12019500056B1 (en) | 2016-07-12 | 2024-01-31 | Revolution Medicines Inc | 2,5-disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines as allosteric shp2 inhibitors |
| EP4620525A3 (fr) | 2016-12-14 | 2025-12-03 | Respira Therapeutics, Inc. | Procédés et compositions pour le traitement de l'hypertension pulmonaire et d'autres troubles pulmonaires |
| TWI800498B (zh) | 2016-12-21 | 2023-05-01 | 義大利商吉斯藥品公司 | 作為Rho-激酶抑制劑之雙環二氫嘧啶-羧醯胺衍生物 |
| BR112019015075A2 (pt) | 2017-01-23 | 2020-03-10 | Revolution Medicines, Inc. | Compostos bicíclicos como inibidores de shp2 alostéricos |
| SG11201906412SA (en) | 2017-01-23 | 2019-08-27 | Revolution Medicines Inc | Pyridine compounds as allosteric shp2 inhibitors |
| GEP20207202B (en) | 2017-01-30 | 2020-12-25 | Chiesi Farm Spa | Tyrosine amide derivatives as rho-kinase inhibitors |
| BR112020000962A2 (pt) * | 2017-07-18 | 2020-07-14 | Nuvation Bio Inc. | compostos de 1,8-naftiridinona e usos dos mesmos |
| JP2020527588A (ja) | 2017-07-18 | 2020-09-10 | ニューベイション・バイオ・インコーポレイテッドNuvation Bio Inc. | アデノシンアンタゴニストとしてのヘテロ環式化合物 |
| EP3679039B1 (fr) | 2017-09-07 | 2021-06-16 | Chiesi Farmaceutici S.p.A. | Dérivés d'analogues de tyrosine en tant qu'inhibiteurs de rho-kinase |
| SG11202002941WA (en) | 2017-10-12 | 2020-04-29 | Revolution Medicines Inc | Pyridine, pyrazine, and triazine compounds as allosteric shp2 inhibitors |
| CA3084058A1 (fr) | 2017-12-15 | 2019-06-20 | Revolution Medicines, Inc. | Composes polycycliques utilises en tant qu'inhibiteurs allosteriques de shp2 |
| MA51283A (fr) | 2017-12-18 | 2021-05-26 | Chiesi Farm Spa | Dérivés de tyrosine en tant qu'inhibiteurs de kinase rho |
| WO2019121406A1 (fr) | 2017-12-18 | 2019-06-27 | Chiesi Farmaceutici S.P.A. | Dérivés d'azaindole comme inhibiteurs de rho-kinase |
| WO2019121233A1 (fr) | 2017-12-18 | 2019-06-27 | Chiesi Farmaceutici S.P.A. | Dérivés d'oxadiazole utilisés comme inhibiteurs de rho-kinase |
| AR114926A1 (es) | 2018-06-13 | 2020-10-28 | Chiesi Farm Spa | Derivados de azaindol como inhibidores de rho-quinasa |
| TW202019923A (zh) | 2018-07-16 | 2020-06-01 | 義大利商吉斯藥品公司 | 作為Rho-激酶抑制劑之酪胺酸醯胺衍生物 |
| CN113939291A (zh) * | 2019-01-18 | 2022-01-14 | 诺维逊生物股份有限公司 | 1,8-萘啶酮化合物及其用途 |
| BR112021013936A2 (pt) | 2019-01-18 | 2021-09-21 | Nuvation Bio Inc. | Compostos heterocíclicos como antagonistas de adenosina |
| AU2020210013A1 (en) * | 2019-01-18 | 2021-08-26 | Nuvation Bio Inc. | Compounds and uses thereof |
| WO2021252951A1 (fr) | 2020-06-12 | 2021-12-16 | Vanderbilt University | Méthodes de traitement de troubles de motilité gastro-intestinale |
| WO2022128853A1 (fr) | 2020-12-15 | 2022-06-23 | Chiesi Farmaceutici S.P.A. | Dérivés de dihydrofuropyridine utilisés comme inhibiteurs de la rho kinase |
| EP4263548B1 (fr) | 2020-12-15 | 2025-07-02 | Chiesi Farmaceutici S.p.A. | Dérivés de dihydrofuropyridine en tant qu'inhibiteurs de rho-kinase |
| US12534474B2 (en) | 2020-12-15 | 2026-01-27 | Chiesi Farmaceutici S.P.A. | Dihydrofuropyridine derivatives as rho-kinase inhibitors |
| WO2023110700A1 (fr) | 2021-12-13 | 2023-06-22 | Chiesi Farmaceutici S.P.A. | Dérivés de dihydrofuropyridine utilisés comme inhibiteurs de la rho-kinase |
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| DE102008039082A1 (de) | 2008-08-21 | 2010-02-25 | Bayer Schering Pharma Aktiengesellschaft | Azabicyclisch-substituierte 5-Aminopyrazole und ihre Verwendung |
| TWI368513B (en) | 2009-04-30 | 2012-07-21 | Univ Kaohsiung Medical | Synthesis of pulmodil and pulmodil-1, two chlorophenylpiperazine salt derivatives, and rhokinase-dependent inhibition activity on pulmonary artery endothelium dysfunction, medial wall thickness and vascular obstruction thereof |
| WO2011111880A1 (fr) | 2010-03-08 | 2011-09-15 | 주식회사 메디젠텍 | Préparation pharmaceutique pour le traitement ou la prévention de maladies dues à l'export nucléaire de gsk3, comprenant un composé inhibant l'export nucléaire de gsk3 |
| RS55856B1 (sr) | 2010-07-14 | 2017-08-31 | Novartis Ag | Heterociklična jedinjenja agonisti ip receptora |
| EP2802585A1 (fr) | 2012-01-13 | 2014-11-19 | Novartis AG | Pipéridines condensées utilisées comme agonistes du récepteur ip pour le traitement de l'htap et de troubles connexes |
| ES2561353T3 (es) | 2012-01-13 | 2016-02-25 | Novartis Ag | Sales de un agonista del receptor IP |
| US20140357641A1 (en) | 2012-01-13 | 2014-12-04 | Novartis Ag | IP receptor agonist heterocyclic compounds |
| EP2802581A1 (fr) | 2012-01-13 | 2014-11-19 | Novartis AG | 7,8-dihydropyrido[3,4-b]pyrazines utilisées comme agonistes du récepteur ip pour le traitement de l'hypertension artérielle pulmonaire (htap) et des troubles associés |
| CN104053659B (zh) | 2012-01-13 | 2016-11-09 | 诺华股份有限公司 | 用于治疗肺动脉高压(pah)及相关病症的作为ip 受体激动剂的稠合的吡咯类 |
| WO2013105063A1 (fr) | 2012-01-13 | 2013-07-18 | Novartis Ag | Pipéridines condensées utilisées comme agonistes du récepteur ip pour le traitement de l'hypertension artérielle pulmonaire (htap) et de troubles associés |
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