PE20080421A1 - Derivados de 5,6-bisaril-2-piridin-carboxamida, su preparacion y su aplicacion en terapeutica como antagonistas de los receptores de urotensina ii - Google Patents
Derivados de 5,6-bisaril-2-piridin-carboxamida, su preparacion y su aplicacion en terapeutica como antagonistas de los receptores de urotensina iiInfo
- Publication number
- PE20080421A1 PE20080421A1 PE2007001066A PE2007001066A PE20080421A1 PE 20080421 A1 PE20080421 A1 PE 20080421A1 PE 2007001066 A PE2007001066 A PE 2007001066A PE 2007001066 A PE2007001066 A PE 2007001066A PE 20080421 A1 PE20080421 A1 PE 20080421A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- pyridin
- cycloalkyl
- halogen
- phenyl
- Prior art date
Links
- 102000012327 Urotensin II receptors Human genes 0.000 title abstract 2
- 108050002984 Urotensin II receptors Proteins 0.000 title abstract 2
- 239000005557 antagonist Substances 0.000 title abstract 2
- 239000003814 drug Substances 0.000 title 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- MAUMSNABMVEOGP-UHFFFAOYSA-N (methyl-$l^{2}-azanyl)methane Chemical class C[N]C MAUMSNABMVEOGP-UHFFFAOYSA-N 0.000 abstract 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical class [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 1
- 206010002329 Aneurysm Diseases 0.000 abstract 1
- 101100516568 Caenorhabditis elegans nhr-7 gene Proteins 0.000 abstract 1
- 206010007559 Cardiac failure congestive Diseases 0.000 abstract 1
- 206010019280 Heart failures Diseases 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical group [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 208000010125 myocardial infarction Diseases 0.000 abstract 1
- 208000031225 myocardial ischemia Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
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- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
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- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE 5,6-BISARIL-2-PIRIDIN-CARBOXAMIDA DE FORMULA (I) DONDE X E Y SON CADA UNO N O CR3, DONDE R3 ES H, HALOGENO, ALCOXI(C1-C5) O ALQUILO(C1-C5); U ES H O NHR7, DONDE R7 ES H O ALQUILO(C1-C5); A ES ARILO(C5-C6), HETEROARILO O HETEROCICLOALQUILO(C3-C8) OPCIONALMENTE SUSTITUIDO; W ES HALOGENO, ALQUILO(C1-C5) O HALOGENOALQUILO(C1-C5); Z ES UN ENLACE, CICLOALQUILENO(C3-C8) O ALQUILENO(C1-C5) OPCIONALMENTE SUSTITUIDO CON HALOGENO, HIDROXI, ALQUILO(C1-C5) O ALCOXI(C1-C5); B ES NR4R5 O UN HETEROCICLO DE FORMULA (i), DONDE R4 Y R5 SON CADA UNO ALQUILO(C1-C5), CICLOALQUILO(C3-C8), FLUOROALQUILO(C1-C5), ENTRE OTROS; m Y n SON CADA UNO DE 0 A 2; R6 Y R7 SON CADA UNO H, ALQUILO(C1-C5) O CICLOALQUILO(C3-C8); R1 Y R2 SON CADA UNO H, ALQUILO(C1-C5), CICLOALQUILO(C3-C8), FENILO, BENCILO, ENTRE OTROS; p ES 0 O 1. SON COMPUESTOS PREFERIDOS: ACIDO 1-({[6-{4-CLORO-3-[3-(DIMETILAMINO)PROPOXI]FENIL}-5-(2,6-DIMETOXIFENIL)PIRIDIN-2-IL]CARBONIL}AMINO)CICLOHEXANOCARBOXILICO, CLORHIDRATO DE ACIDO 9-({[6-{4-CLORO-3-[3-(DIMETILAMINO)PROPOXI]FENIL}-5-(2,6-DIMETOXIFENIL)PIRIDIN-2-IL]CARBONIL}AMINO)BICICLO[3.3.1]NONANO-9-CARBOXILICO, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DE LOS RECEPTORES DE UROTENSINA II SIENDO UTILES EN EL TRATAMIENTO DE INSUFICIENCIA CARDIACA CONGESTIVA, ISQUEMIA CARDIACA, INFARTO DE MIOCARDIO, ANEURISMA
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0607283A FR2904827B1 (fr) | 2006-08-11 | 2006-08-11 | Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antiganistes des recepteurs a l'urotensine ii |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20080421A1 true PE20080421A1 (es) | 2008-06-17 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2007001066A PE20080421A1 (es) | 2006-08-11 | 2007-08-09 | Derivados de 5,6-bisaril-2-piridin-carboxamida, su preparacion y su aplicacion en terapeutica como antagonistas de los receptores de urotensina ii |
Country Status (37)
| Country | Link |
|---|---|
| US (2) | US8110579B2 (es) |
| EP (2) | EP2059508B1 (es) |
| JP (1) | JP5230621B2 (es) |
| KR (1) | KR20090050075A (es) |
| CN (1) | CN101511789B (es) |
| AR (1) | AR062294A1 (es) |
| AT (1) | ATE553082T1 (es) |
| AU (1) | AU2007285659B2 (es) |
| BR (1) | BRPI0716655A2 (es) |
| CA (1) | CA2659928A1 (es) |
| CL (1) | CL2007002329A1 (es) |
| CO (1) | CO6150147A2 (es) |
| CR (1) | CR10603A (es) |
| CY (1) | CY1113129T1 (es) |
| DK (1) | DK2059508T3 (es) |
| EA (1) | EA016352B1 (es) |
| ES (1) | ES2385614T3 (es) |
| FR (1) | FR2904827B1 (es) |
| GT (1) | GT200900026A (es) |
| HR (1) | HRP20120559T1 (es) |
| IL (1) | IL196797A (es) |
| MA (1) | MA30703B1 (es) |
| MX (1) | MX2009001582A (es) |
| MY (1) | MY145644A (es) |
| NO (1) | NO20090779L (es) |
| NZ (1) | NZ574699A (es) |
| PE (1) | PE20080421A1 (es) |
| PL (1) | PL2059508T3 (es) |
| PT (1) | PT2059508E (es) |
| RS (1) | RS52420B (es) |
| SG (1) | SG187993A1 (es) |
| SI (1) | SI2059508T1 (es) |
| TN (1) | TN2009000040A1 (es) |
| TW (1) | TWI388551B (es) |
| UY (1) | UY30534A1 (es) |
| WO (1) | WO2008020124A1 (es) |
| ZA (1) | ZA200900835B (es) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2927330B1 (fr) | 2008-02-07 | 2010-02-19 | Sanofi Aventis | Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antagonistes des recepteurs a l'urotensine ii |
| FR2948119A1 (fr) * | 2009-07-16 | 2011-01-21 | Sanofi Aventis | Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antagonistes des recepteurs a l'urotensine ii |
| FR2948120A1 (fr) | 2009-07-16 | 2011-01-21 | Sanofi Aventis | Derives de 5,6-bisaryl-2-pyrimidine-carboxamide, leur preparation et leur application en therapeutique comme antagonistes des recepteurs a l’urotensine ii |
| 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 |
| SG11201502527UA (en) * | 2012-10-05 | 2015-04-29 | Rigel Pharmaceuticals Inc | Gdf-8 inhibitors |
| WO2014134391A1 (en) | 2013-02-28 | 2014-09-04 | Bristol-Myers Squibb Company | Phenylpyrazole derivatives as potent rock1 and rock2 inhibitors |
| TW201444798A (zh) | 2013-02-28 | 2014-12-01 | 必治妥美雅史谷比公司 | 作爲強效rock1及rock2抑制劑之苯基吡唑衍生物 |
| WO2014144455A1 (en) | 2013-03-15 | 2014-09-18 | Epizyme, Inc. | 1 -phenoxy-3-(alkylamino)-propan-2-ol derivatives as carm1 inhibitors and uses thereof |
| US9346802B2 (en) | 2013-03-15 | 2016-05-24 | Epizyme, Inc. | CARM1 inhibitors and uses thereof |
| EP2970219B1 (en) | 2013-03-15 | 2019-02-27 | Epizyme, Inc. | Carm1 inhibitors and uses thereof |
| NZ736164A (en) * | 2015-03-18 | 2022-07-01 | Vectus Biosystems Ltd | Compositions for the treatment of fibrosis and fibrosis-related conditions |
| CN119775198A (zh) | 2018-05-04 | 2025-04-08 | 治疗方案股份有限公司 | 靶向癌症干细胞的癌症治疗 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6413083A (en) * | 1987-07-07 | 1989-01-17 | Akishiro Nakamura | Streptonigrin derivative and medicinal composition |
| US4916145A (en) * | 1987-07-10 | 1990-04-10 | Hoffmann-La Roche Inc. | Substituted n-[(pyridyl)alkyl]aryl-carboxamide |
| AR033879A1 (es) * | 2001-05-07 | 2004-01-07 | Smithkline Beecham Corp | Compuesto sulfonamida, composicion farmaceutica que lo comprende, su uso para preparar dicha composicion y procedimiento para la obtencion de dicho compuesto |
| SE0104332D0 (sv) * | 2001-12-19 | 2001-12-19 | Astrazeneca Ab | Therapeutic agents |
| WO2004073634A2 (en) * | 2003-02-20 | 2004-09-02 | Encysive Pharmaceuticals Inc. | Phenylenediamine urotensin-ii receptor antagonists and ccr-9 antagonists |
| EP1603884A4 (en) * | 2003-02-28 | 2008-05-28 | Encysive Pharmaceuticals Inc | PYRIDINE, PYRIMIDINE, QUINOLINE, QUINAZOLINE AND NAPHTHALENE UROTENSIN II RECEPTOR ANTAGONISTS |
| FR2856684B1 (fr) * | 2003-06-26 | 2008-04-11 | Sanofi Synthelabo | Derives de diphenylpyridine, leur preparation et leur application en therapeutique |
| WO2005113514A2 (en) * | 2004-05-07 | 2005-12-01 | Janssen Pharmaceutica, N.V. | Substituted pyrimidines as inhibitors of bacterial type iii protein secretion systems |
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2006
- 2006-08-11 FR FR0607283A patent/FR2904827B1/fr not_active Expired - Fee Related
-
2007
- 2007-08-08 TW TW096129256A patent/TWI388551B/zh not_active IP Right Cessation
- 2007-08-09 AU AU2007285659A patent/AU2007285659B2/en not_active Ceased
- 2007-08-09 EP EP07823409A patent/EP2059508B1/fr active Active
- 2007-08-09 ZA ZA200900835A patent/ZA200900835B/xx unknown
- 2007-08-09 NZ NZ574699A patent/NZ574699A/en not_active IP Right Cessation
- 2007-08-09 PE PE2007001066A patent/PE20080421A1/es not_active Application Discontinuation
- 2007-08-09 CA CA002659928A patent/CA2659928A1/fr not_active Abandoned
- 2007-08-09 SI SI200730951T patent/SI2059508T1/sl unknown
- 2007-08-09 JP JP2009523317A patent/JP5230621B2/ja not_active Expired - Fee Related
- 2007-08-09 HR HRP20120559TT patent/HRP20120559T1/hr unknown
- 2007-08-09 CN CN200780033610XA patent/CN101511789B/zh not_active Expired - Fee Related
- 2007-08-09 RS RS20120278A patent/RS52420B/sr unknown
- 2007-08-09 DK DK07823409.3T patent/DK2059508T3/da active
- 2007-08-09 BR BRPI0716655-9A2A patent/BRPI0716655A2/pt not_active IP Right Cessation
- 2007-08-09 EA EA200970192A patent/EA016352B1/ru not_active IP Right Cessation
- 2007-08-09 EP EP11188580.2A patent/EP2439193B1/fr active Active
- 2007-08-09 MY MYPI20090488A patent/MY145644A/en unknown
- 2007-08-09 AR ARP070103513A patent/AR062294A1/es not_active Application Discontinuation
- 2007-08-09 CL CL200702329A patent/CL2007002329A1/es unknown
- 2007-08-09 SG SG2011057080A patent/SG187993A1/en unknown
- 2007-08-09 PT PT07823409T patent/PT2059508E/pt unknown
- 2007-08-09 WO PCT/FR2007/001357 patent/WO2008020124A1/fr not_active Ceased
- 2007-08-09 ES ES07823409T patent/ES2385614T3/es active Active
- 2007-08-09 KR KR1020097004997A patent/KR20090050075A/ko not_active Ceased
- 2007-08-09 AT AT07823409T patent/ATE553082T1/de active
- 2007-08-09 PL PL07823409T patent/PL2059508T3/pl unknown
- 2007-08-09 MX MX2009001582A patent/MX2009001582A/es active IP Right Grant
- 2007-08-10 UY UY30534A patent/UY30534A1/es not_active Application Discontinuation
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2009
- 2009-01-29 IL IL196797A patent/IL196797A/en not_active IP Right Cessation
- 2009-02-04 CO CO09010565A patent/CO6150147A2/es unknown
- 2009-02-04 TN TN2009000040A patent/TN2009000040A1/fr unknown
- 2009-02-05 GT GT200900026A patent/GT200900026A/es unknown
- 2009-02-09 CR CR10603A patent/CR10603A/es not_active Application Discontinuation
- 2009-02-11 US US12/369,200 patent/US8110579B2/en not_active Expired - Fee Related
- 2009-02-18 NO NO20090779A patent/NO20090779L/no not_active Application Discontinuation
- 2009-03-06 MA MA31694A patent/MA30703B1/fr unknown
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2011
- 2011-12-29 US US13/339,810 patent/US8552201B2/en not_active Expired - Fee Related
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2012
- 2012-07-09 CY CY20121100607T patent/CY1113129T1/el unknown
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