PE20090548A1 - Compuestos aza-biciclohexano como inhibidores de trombina - Google Patents
Compuestos aza-biciclohexano como inhibidores de trombinaInfo
- Publication number
- PE20090548A1 PE20090548A1 PE2008001125A PE2008001125A PE20090548A1 PE 20090548 A1 PE20090548 A1 PE 20090548A1 PE 2008001125 A PE2008001125 A PE 2008001125A PE 2008001125 A PE2008001125 A PE 2008001125A PE 20090548 A1 PE20090548 A1 PE 20090548A1
- Authority
- PE
- Peru
- Prior art keywords
- aza
- bicycle
- hexane
- halogen
- alkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
- 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
- C07D403/14—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 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
- C07D405/14—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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hematology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
REFERIDA A UN COMPUESTO DERIVADO DE AZA-BICICLOHEXANO DE FORMULA (I), DONDE EL GRUPO (X) ES UN AZA-BICICLO[3.1.0]HEXANO O AZA-BICICLO[2.1.1]HEXANO; R1 ES UN ANILLO HETEROARILO DE 5 MIEMBROS QUE CONTIENE 2, 3 O 4 HETEROATOMOS SELECCIONADOS ENTRE N, O Y S, DONDE DICHO HETEROARILO ESTA OPCIONALMENTE SUSTITUIDO POR ALQUILO C1-C6, ENTRE OTROS; R2 ES H, HALOGENO, CIANO, ALQUILO C1-C6, ENTRE OTROS; G ES (a), (b) O (c); R3 ES H, ALQUILO C1-C6, ALQUENILO C2-C6, CICLOALQUILO C3-C6, ENTRE OTROS; R4 ES OH O NHR8; R8 ES H O SO2R7; R7 ES ALQUILO C1-C6 OPCIONALMENTE SUSTITUIDO CON OH, HALOGENO, CIANO, ENTRE OTROS; R9 ES HALOGENO, OXO, NH2, ENTRE OTROS; R10 ES HALOGENO, OH, CIANO, ENTRE OTROS; Q ES O, CH2 O S(O)n; W ES C O N; n ES UN ENTERO DE 0 A 2; t ES UN ENTERO DE 0 A 2; u ES 0 O 1. SON COMPUESTOS PREFERIDOS: 5-CLORO-2-TETRAZOL-1-IL-BENCILAMIDA DEL ACIDO (1S,2S,5R)-3-((R)-2-HIDROXI-3,3-DIMETIL-BUTIRIL)-3-AZA-BICICLO[3.1.0]HEXANO-2-CARBOXILICO, 5-CLORO-2-TETRAZOL-1-IL-BENCILAMIDA DEL ACIDO (1S,2S,5R)-3-((R)-2-HIDROXI-2-FENIL-ACETIL)-3-AZA-BICICLO[3.1.0]HEXANO-2-CARBOXILICO, 5-CLORO-2-TETRAZOL-1-IL-BENCILAMIDA DEL ACIDO (1R,2S,5S)-3-((R)-2-HIDROXI-2-FENIL-ACETIL)-3-AZA-BICICLO[3.1.0]HEXANO-2-CARBOXILICO, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES COMPETITIVOS DE SERINA PROTEASAS DE TIPO TRIPSINA TAL COMO LA TROMBINA Y SON UTILES EN EL TRATAMIENTO DE TROMBOSIS Y TRANSTORNOS RELACIONADOS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US94771207P | 2007-07-03 | 2007-07-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20090548A1 true PE20090548A1 (es) | 2009-06-04 |
Family
ID=40002969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2008001125A PE20090548A1 (es) | 2007-07-03 | 2008-07-03 | Compuestos aza-biciclohexano como inhibidores de trombina |
Country Status (5)
Country | Link |
---|---|
US (1) | US20090012087A1 (es) |
PE (1) | PE20090548A1 (es) |
TW (1) | TW200911787A (es) |
UY (1) | UY31203A1 (es) |
WO (1) | WO2009004383A2 (es) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW201002689A (en) | 2008-06-23 | 2010-01-16 | Astrazeneca Ab | Novel compounds |
US8354444B2 (en) | 2008-09-18 | 2013-01-15 | Hoffmann-La Roche Inc. | Substituted pyrrolidine-2-carboxamides |
BRPI1014039A2 (pt) * | 2009-04-08 | 2018-04-03 | Actelion Pharmaceuticals Ltd | 6-(3-aza-biciclo[3.1.0]hex-3-il)-2-fenil-pirimidinas |
DE102011078695A1 (de) | 2011-07-05 | 2013-01-10 | Charité - Universitätsmedizin Berlin | Dialyseverfahren zur Entfernung proteingebundener Toxine aus dem Blut von Patienten unter Einsatz hochfrequenter elektromagnetischer Felder |
WO2014025658A1 (en) * | 2012-08-08 | 2014-02-13 | Merck Sharp & Dohme Corp. | Pyrrolidine thrombin inhibitors |
US20160229839A1 (en) * | 2013-09-27 | 2016-08-11 | Merck Sharp & Dohme Corp. | Factor XIa Inhibitors |
ES2541870B1 (es) | 2013-12-27 | 2016-05-12 | Servicio Andaluz De Salud | Uso de antagonistas no peptídicos de NK1 en una determinada dosis para el tratamiento del cáncer |
CN110256297B (zh) * | 2019-07-05 | 2022-07-26 | 爱斯特(成都)生物制药股份有限公司 | 一种N-Boc-(R)-2-氨基-4,4-二甲基戊酸的制备方法 |
CN110343056B (zh) * | 2019-07-19 | 2022-01-07 | 爱斯特(成都)生物制药股份有限公司 | 一种n-叔丁氧羰基-n-甲基-2-氨基-4,4-二甲基戊酸的制备方法 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2793248B1 (fr) * | 1999-05-03 | 2001-06-29 | Adir | Nouveaux derives de 2,3-methano-aminoacides, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
AU2002230836A1 (en) * | 2000-12-18 | 2002-07-01 | Merck & Co., Inc. | Benzylamine derivatives and their use as thrombin inhibitors |
US6528503B2 (en) * | 2000-12-18 | 2003-03-04 | Merck & Co., Inc. | Thrombin inhibitors |
US7144899B2 (en) * | 2001-02-09 | 2006-12-05 | Merck & Co., Inc. | Thrombin inhibitors |
US7030141B2 (en) * | 2001-11-29 | 2006-04-18 | Christopher Franklin Bigge | Inhibitors of factor Xa and other serine proteases involved in the coagulation cascade |
EP1720844B1 (de) * | 2003-04-03 | 2009-04-29 | MERCK PATENT GmbH | Pyrrolidin-1,2-dicarbonsäure-1-(phenylamid)-2-(4-(3-oxo-morpholin-4-yl)-phenylamid) derivate und verwandte verbindungen als inhibitoren des koagulationsfaktors xa zur behandlung von thromboembolischen erkrankungen |
DE102004045796A1 (de) * | 2004-09-22 | 2006-03-23 | Merck Patent Gmbh | Arzneimittel enthaltend Carbonylverbindungen sowie deren Verwendung |
WO2006055951A2 (en) * | 2004-11-19 | 2006-05-26 | Portola Pharmaceuticals, Inc. | Tetrahydroisoquinolines as factor xa inhibitors |
-
2008
- 2008-07-01 TW TW097124813A patent/TW200911787A/zh unknown
- 2008-07-01 WO PCT/GB2008/050531 patent/WO2009004383A2/en active Application Filing
- 2008-07-02 UY UY31203A patent/UY31203A1/es unknown
- 2008-07-02 US US12/166,407 patent/US20090012087A1/en not_active Abandoned
- 2008-07-03 PE PE2008001125A patent/PE20090548A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
WO2009004383A3 (en) | 2009-04-23 |
US20090012087A1 (en) | 2009-01-08 |
UY31203A1 (es) | 2009-01-30 |
TW200911787A (en) | 2009-03-16 |
WO2009004383A2 (en) | 2009-01-08 |
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Legal Events
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FA | Abandonment or withdrawal |