CL2008002142A1 - Compuestos derivados de 2-amino-6-({[2-(4-clorofenil)-1,3-tiazol-4-il]metil}tio)-4-[4-(2-hidroxietoxi) fenil] piridin-3,5-dicarbonitrilo; procedimiento de preparacion; composicion farmaceutica y uso en enfermedades cardiovasculares. - Google Patents
Compuestos derivados de 2-amino-6-({[2-(4-clorofenil)-1,3-tiazol-4-il]metil}tio)-4-[4-(2-hidroxietoxi) fenil] piridin-3,5-dicarbonitrilo; procedimiento de preparacion; composicion farmaceutica y uso en enfermedades cardiovasculares.Info
- Publication number
- CL2008002142A1 CL2008002142A1 CL2008002142A CL2008002142A CL2008002142A1 CL 2008002142 A1 CL2008002142 A1 CL 2008002142A1 CL 2008002142 A CL2008002142 A CL 2008002142A CL 2008002142 A CL2008002142 A CL 2008002142A CL 2008002142 A1 CL2008002142 A1 CL 2008002142A1
- Authority
- CL
- Chile
- Prior art keywords
- pharmaceutical composition
- dicarbonitrile
- hydroxyethoxy
- thiazol
- pyridin
- Prior art date
Links
- 208000024172 Cardiovascular disease Diseases 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- CITWCLNVRIKQAF-UHFFFAOYSA-N 2-amino-6-[[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methylsulfanyl]-4-[4-(2-hydroxyethoxy)phenyl]pyridine-3,5-dicarbonitrile Chemical compound N#CC=1C(C=2C=CC(OCCO)=CC=2)=C(C#N)C(N)=NC=1SCC(N=1)=CSC=1C1=CC=C(Cl)C=C1 CITWCLNVRIKQAF-UHFFFAOYSA-N 0.000 title 1
Classifications
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- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
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- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
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- C07K5/06086—Dipeptides with the first amino acid being basic
-
- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
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- Emergency Medicine (AREA)
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Abstract
COMPUESTO DE FORMULA (I) CARACTERIZADO PORQUE LA FORMULA (I) ES: EN DONDE RA ES LO INDICADO EN LA REIVINDICACIÓN 1. PROCEDIMIENTO DE PREPARACIÓN; COMPOSICIÓN FARMACÉUTICA Y USO EN ENFERMEDADES CARDIOVASCULARES.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007036076A DE102007036076A1 (de) | 2007-08-01 | 2007-08-01 | Dipeptoid-Produgs und ihre Verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2008002142A1 true CL2008002142A1 (es) | 2009-02-06 |
Family
ID=40010616
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2008002142A CL2008002142A1 (es) | 2007-08-01 | 2008-07-21 | Compuestos derivados de 2-amino-6-({[2-(4-clorofenil)-1,3-tiazol-4-il]metil}tio)-4-[4-(2-hidroxietoxi) fenil] piridin-3,5-dicarbonitrilo; procedimiento de preparacion; composicion farmaceutica y uso en enfermedades cardiovasculares. |
Country Status (26)
| Country | Link |
|---|---|
| US (3) | US8703696B2 (es) |
| EP (1) | EP2185552B1 (es) |
| JP (1) | JP5486492B2 (es) |
| KR (1) | KR101550077B1 (es) |
| CN (1) | CN101821263B (es) |
| AR (1) | AR067779A1 (es) |
| AU (1) | AU2008280983B2 (es) |
| BR (1) | BRPI0814963A2 (es) |
| CA (1) | CA2695036C (es) |
| CL (1) | CL2008002142A1 (es) |
| CY (1) | CY1115114T1 (es) |
| DE (1) | DE102007036076A1 (es) |
| DK (1) | DK2185552T3 (es) |
| ES (1) | ES2459441T3 (es) |
| HR (1) | HRP20140470T1 (es) |
| IL (1) | IL202892A (es) |
| JO (1) | JO2941B1 (es) |
| PE (1) | PE20090891A1 (es) |
| PL (1) | PL2185552T3 (es) |
| PT (1) | PT2185552E (es) |
| RU (2) | RU2486183C9 (es) |
| SI (1) | SI2185552T1 (es) |
| TW (1) | TWI436766B (es) |
| UY (1) | UY31244A1 (es) |
| WO (1) | WO2009015811A1 (es) |
| ZA (1) | ZA201000707B (es) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004042607A1 (de) | 2004-09-03 | 2006-03-09 | Bayer Healthcare Ag | Substituierte Phenylaminothiazole und ihre Verwendung |
| DE102006042143A1 (de) | 2006-09-08 | 2008-03-27 | Bayer Healthcare Aktiengesellschaft | Neue substituierte Bipyridin-Derivate und ihre Verwendung |
| DE102006056739A1 (de) | 2006-12-01 | 2008-06-05 | Bayer Healthcare Ag | Substituierte 4-Amino-3,5-dicyano-2-thiopyridine und ihre Verwendung |
| DE102006056740A1 (de) | 2006-12-01 | 2008-06-05 | Bayer Healthcare Ag | Cyclisch substituierte 3,5-Dicyano-2-thiopyridine und ihre Verwendung |
| DE102007035367A1 (de) | 2007-07-27 | 2009-01-29 | Bayer Healthcare Ag | Substituierte Aryloxazole und ihre Verwendung |
| DE102007036076A1 (de) * | 2007-08-01 | 2009-02-05 | Bayer Healthcare Aktiengesellschaft | Dipeptoid-Produgs und ihre Verwendung |
| DE102007061763A1 (de) * | 2007-12-20 | 2009-06-25 | Bayer Healthcare Ag | Substituierte azabicyclische Verbindungen und ihre Verwendung |
| DE102007061764A1 (de) * | 2007-12-20 | 2009-06-25 | Bayer Healthcare Ag | Anellierte Cyanopyridine und ihre Verwendung |
| DE102008013587A1 (de) * | 2008-03-11 | 2009-09-17 | Bayer Schering Pharma Aktiengesellschaft | Heteroaryl-substituierte Dicyanopyridine und ihre Verwendung |
| CA2726020C (en) * | 2008-05-29 | 2016-08-16 | Bayer Schering Pharma Aktiengesellschaft | 2-alkoxy-substituted dicyanopyridines and use thereof |
| DE102008062567A1 (de) * | 2008-12-16 | 2010-06-17 | Bayer Schering Pharma Aktiengesellschaft | Dipeptoid-Prodrugs und ihre Verwendung |
| DE102009006602A1 (de) * | 2009-01-29 | 2010-08-05 | Bayer Schering Pharma Aktiengesellschaft | Alkylamino-substituierte Dicyanopyridine und deren Aminosäureester-Prodrugs |
| DE102010030688A1 (de) | 2010-06-30 | 2012-01-05 | Bayer Schering Pharma Aktiengesellschaft | Substituierte Dicyanopyridine und ihre Verwendung |
| US20120058983A1 (en) * | 2010-09-02 | 2012-03-08 | Bayer Pharma Aktiengesellschaft | Adenosine A1 agonists for the treatment of glaucoma and ocular hypertension |
| AU2011336304B2 (en) | 2010-12-03 | 2017-03-30 | Nalpropion Pharmaceuticals Llc | Increasing drug bioavailability in naltrexone therapy |
| MA39101A1 (fr) * | 2013-12-12 | 2017-08-31 | Bayer Pharma AG | Agonistes a1 de l'adénosine utilisés comme médicaments contre les maladies des reins |
| JP6855243B2 (ja) | 2014-01-24 | 2021-04-07 | エイアイ・セラピューティクス・インコーポレーテッド | 癌治療のためのアピリモド(apilimod)組成物 |
| ES2741399T3 (es) * | 2014-11-07 | 2020-02-10 | Ai Therapeutics Inc | Apilimod para el uso en el tratamiento de cáncer renal |
| WO2017137528A1 (en) | 2016-02-12 | 2017-08-17 | Charité - Universitätsmedizin Berlin | Adenosine a1 receptor agonist for use in treatment of status epilepticus |
| WO2018153899A1 (de) * | 2017-02-22 | 2018-08-30 | Bayer Pharma Aktiengesellschaft | Selektive partielle adenosin a1 rezeptor-agonisten in kombination mit stimulatoren und/oder aktivatoren der löslichen guanylatcyclase (sgc) |
| WO2018153898A1 (de) * | 2017-02-22 | 2018-08-30 | Bayer Pharma Aktiengesellschaft | Selektive partielle adenosin a1 rezeptor-agonisten in kombination mit mineralocorticoid-rezeptor-antagonisten |
| WO2018153895A1 (de) * | 2017-02-22 | 2018-08-30 | Bayer Pharma Aktiengesellschaft | Selektive partielle adenosin a1 rezeptor-agonisten in kombination mit einem inhibitor der neutralen endopeptidase und/oder einem angiotensin ii rezeptor-antagonisten |
| WO2018153897A1 (de) * | 2017-02-22 | 2018-08-30 | Bayer Pharma Aktiengesellschaft | Selektive partielle adenosin a1 rezeptor-agonisten in kombination mit hcn-kanal-hemmern |
| WO2018153900A1 (de) | 2017-02-22 | 2018-08-30 | Bayer Aktiengesellschaft | Selektive partielle adenosin a1 rezeptor-agonisten in kombination mit sglt-2-hemmern |
| CN117122743A (zh) * | 2023-08-10 | 2023-11-28 | 南京圣德医疗科技有限公司 | 一种人工心脏生物瓣膜的制备方法 |
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-
2007
- 2007-08-01 DE DE102007036076A patent/DE102007036076A1/de not_active Withdrawn
-
2008
- 2008-07-21 CL CL2008002142A patent/CL2008002142A1/es unknown
- 2008-07-22 PE PE2008001244A patent/PE20090891A1/es not_active Application Discontinuation
- 2008-07-22 UY UY31244A patent/UY31244A1/es not_active Application Discontinuation
- 2008-07-23 PT PT87849865T patent/PT2185552E/pt unknown
- 2008-07-23 SI SI200831218T patent/SI2185552T1/sl unknown
- 2008-07-23 PL PL08784986T patent/PL2185552T3/pl unknown
- 2008-07-23 DK DK08784986.5T patent/DK2185552T3/da active
- 2008-07-23 KR KR1020107002102A patent/KR101550077B1/ko not_active Expired - Fee Related
- 2008-07-23 WO PCT/EP2008/006027 patent/WO2009015811A1/de not_active Ceased
- 2008-07-23 RU RU2010106877/04A patent/RU2486183C9/ru not_active IP Right Cessation
- 2008-07-23 US US12/671,694 patent/US8703696B2/en not_active Expired - Fee Related
- 2008-07-23 CA CA2695036A patent/CA2695036C/en not_active Expired - Fee Related
- 2008-07-23 JP JP2010518541A patent/JP5486492B2/ja not_active Expired - Fee Related
- 2008-07-23 BR BRPI0814963-1A2A patent/BRPI0814963A2/pt not_active IP Right Cessation
- 2008-07-23 AU AU2008280983A patent/AU2008280983B2/en not_active Ceased
- 2008-07-23 EP EP08784986.5A patent/EP2185552B1/de not_active Not-in-force
- 2008-07-23 ES ES08784986.5T patent/ES2459441T3/es active Active
- 2008-07-23 CN CN200880101445.1A patent/CN101821263B/zh not_active Expired - Fee Related
- 2008-07-23 HR HRP20140470AT patent/HRP20140470T1/hr unknown
- 2008-07-29 JO JO2008339A patent/JO2941B1/en active
- 2008-07-31 TW TW097128917A patent/TWI436766B/zh not_active IP Right Cessation
- 2008-08-01 AR ARP080103358A patent/AR067779A1/es unknown
-
2009
- 2009-12-22 IL IL202892A patent/IL202892A/en not_active IP Right Cessation
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2010
- 2010-01-29 ZA ZA2010/00707A patent/ZA201000707B/en unknown
-
2013
- 2013-03-13 RU RU2013111077A patent/RU2629558C2/ru not_active IP Right Cessation
-
2014
- 2014-03-19 US US14/219,872 patent/US8957017B2/en not_active Expired - Fee Related
- 2014-05-29 CY CY20141100384T patent/CY1115114T1/el unknown
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2015
- 2015-01-16 US US14/598,902 patent/US20150133364A1/en not_active Abandoned
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