PE20030702A1 - PDE9 INHIBITORS FOR THE TREATMENT OF CARDIOVASCULAR DISORDERS - Google Patents
PDE9 INHIBITORS FOR THE TREATMENT OF CARDIOVASCULAR DISORDERSInfo
- Publication number
- PE20030702A1 PE20030702A1 PE2002001070A PE2002001070A PE20030702A1 PE 20030702 A1 PE20030702 A1 PE 20030702A1 PE 2002001070 A PE2002001070 A PE 2002001070A PE 2002001070 A PE2002001070 A PE 2002001070A PE 20030702 A1 PE20030702 A1 PE 20030702A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- ona
- pyrimidin
- dihydro
- treatment
- Prior art date
Links
- 208000024172 Cardiovascular disease Diseases 0.000 title abstract 2
- 229940076380 PDE9 inhibitor Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 101001117256 Drosophila melanogaster High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A Proteins 0.000 abstract 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 2
- OCBFFGCSTGGPSQ-UHFFFAOYSA-N [CH2]CC Chemical group [CH2]CC OCBFFGCSTGGPSQ-UHFFFAOYSA-N 0.000 abstract 1
- KPCZJLGGXRGYIE-UHFFFAOYSA-N [C]1=CC=CN=C1 Chemical class [C]1=CC=CN=C1 KPCZJLGGXRGYIE-UHFFFAOYSA-N 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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Abstract
SE REFIERE A COMPUESTOS DE FORMULA I DONDE R1 ES H, ALQUILO C1-C6 DONDE R1 SE UNE A N1 O N2; R2 ES ALQUILO C1-C6, CICLOALQUILO C3-C7, HETEROCICLO DE 5-6 MIEMBROS CON ALQUILO, OH, ALCOXI; R3 ES ALQUILO C1-C6 CON Ar2, CICLOALQUILO C3-C7, ENTRE OTROS; Ar2 ES EL GRUPO a CONDE R4, R5, R6 SON H, HALO, FENOXI, FENILO, CF3, CF3, ENTRE OTROS. CUANDO R1 ESTA UNIDO A N1, R1 ES ALQUILO C1-C6 Y R2 ES PROPILO ENTONCE R3 NO ES METILO SUSTITUIDO CON Ar1; R1 ESTA UNIDO A N1, R1 ES ALQUILO C1-C6, R2 ES METILO ENTONCES R3 NO ES ALQUILO C1-C4 SUSTITUIDO CON Ar1. SON COMPUESTOS PREFERIDOS 5-(-3-CLOROBENZIL)-3-ISOPROPIL-1,6-DIHIDRO-PIRAZOL[4,3-d]PIRIMIDIN-7-ONA, 3-ISOPROPIL-5-(2-FENOXIBENZIL)-1,6-DIHIDRO-PIRAZOL[4,3-d]PIRIMIDIN-7-ONA. 3-(3-PIRIDINIL)-5-(-2-BENCILOXIBENZIL)-1,6-DIHIDRO-PIRAZOL[4,3-d]PIRIMIDIN-7-ONA. 3-ISOPROPIL-5-(2-TRIFLUOROMETOXIBENCIL)-1,6-DIHIDRO-PIRAZOL[4,3-d]PIRIMIDIN-7-ONA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA Y UN PROCEDIMIENTO PARA LA PREPARACION. LOS COMPUESTOS MENCIONADOS SON INHIBIDORES DE LA FOSFODIESTERASA 9 (PDE9) Y SON UTILES PARA EL TRATAMIENTO DE ENFERMEDADES CARDIOVASCULARESREFERS TO COMPOUNDS OF FORMULA I WHERE R1 IS H, C1-C6 ALKYL WHERE R1 JOINS N1 OR N2; R2 IS C1-C6 ALKYL, C3-C7 CYCLOALKYL, 5-6 MEMBER HETERO CYCLE WITH ALKYL, OH, ALCOXY; R3 IS C1-C6 ALKYL WITH Ar2, C3-C7 CYCLOALKYL, AMONG OTHERS; Ar2 IS THE GROUP to COUNT R4, R5, R6 ARE H, HALO, FENOXI, FENILO, CF3, CF3, AMONG OTHERS. WHEN R1 IS BOUND TO N1, R1 IS ALKYL C1-C6 AND R2 IS PROPYL THEN R3 IS NOT METHYL SUBSTITUTED WITH Ar1; R1 IS JOINTED TO N1, R1 IS C1-C6 ALKYL, R2 IS METHYL THEN R3 IS NOT C1-C4 ALKYL REPLACED WITH Ar1. PREFERRED COMPOUNDS ARE 5 - (- 3-CHLOROBENZIL) -3-ISOPROPIL-1,6-DIHYDRO-PIRAZOL [4,3-d] PYRIMIDIN-7-ONA, 3-ISOPROPYL-5- (2-PHENOXIBENZIL) -1, 6-DIHYDRO-PYRAZOLE [4,3-d] PYRIMIDIN-7-ONA. 3- (3-PYRIDINYL) -5 - (- 2-BENZYLOXIBENZIL) -1,6-DIHYDRO-PYRAZOLE [4,3-d] PYRIMIDIN-7-ONA. 3-ISOPROPYL-5- (2-TRIFLUOROMETOXIBENCIL) -1,6-DIHYDRO-PIRAZOLE [4,3-d] PYRIMIDIN-7-ONA, AMONG OTHERS. IT ALSO REFERS TO A PHARMACEUTICAL COMPOSITION AND A PROCEDURE FOR THE PREPARATION. THE MENTIONED COMPOUNDS ARE INHIBITORS OF PHOSPHODIESTERASE 9 (PDE9) AND ARE USEFUL FOR THE TREATMENT OF CARDIOVASCULAR DISEASES
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0126395A GB0126395D0 (en) | 2001-11-02 | 2001-11-02 | Pyrazolo[4,3]pyrimidine derivatives and their use in treating disease |
| GB0130695A GB0130695D0 (en) | 2001-12-21 | 2001-12-21 | Pyrazola[4,3]pyrimidine |
| GB0216761A GB0216761D0 (en) | 2002-07-18 | 2002-07-18 | PDE9 Inhibitors for treating cardiovascular disorders |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20030702A1 true PE20030702A1 (en) | 2003-08-21 |
Family
ID=27256310
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2002001070A PE20030702A1 (en) | 2001-11-02 | 2002-10-30 | PDE9 INHIBITORS FOR THE TREATMENT OF CARDIOVASCULAR DISORDERS |
Country Status (14)
| Country | Link |
|---|---|
| EP (1) | EP1440073A1 (en) |
| JP (1) | JP2005511575A (en) |
| AR (1) | AR037329A1 (en) |
| BR (1) | BR0214096A (en) |
| CA (1) | CA2466824A1 (en) |
| DO (1) | DOP2002000482A (en) |
| HN (1) | HN2002000317A (en) |
| MX (1) | MXPA04004171A (en) |
| PA (1) | PA8557401A1 (en) |
| PE (1) | PE20030702A1 (en) |
| SV (1) | SV2004001373A (en) |
| TW (1) | TW200300081A (en) |
| UY (1) | UY27522A1 (en) |
| WO (1) | WO2003037899A1 (en) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2459161A1 (en) | 2001-08-31 | 2003-03-13 | The Rockefeller University | Phosphodiesterase activity and regulation of phosphodiesterase 1b-mediated signaling in brain |
| ATE447577T1 (en) | 2001-12-06 | 2009-11-15 | Merck & Co Inc | MITOTIC KINESIN INHIBITORS |
| DE10238724A1 (en) | 2002-08-23 | 2004-03-04 | Bayer Ag | New 6-alkyl-1,5-dihydro-4H-pyrazolo-(3,4-d)-pyrimidin-4-ones useful as selective phosphodiesterase 9A inhibitors for improving attention, concentration, learning and/or memory performance |
| DE10238723A1 (en) | 2002-08-23 | 2004-03-11 | Bayer Ag | Phenyl substituted pyrazolyprimidines |
| DE10238722A1 (en) | 2002-08-23 | 2004-03-11 | Bayer Ag | Improving attention, concentration, cognition, learning and/or memory performance, using selective phosphodiesterase 9A inhibitors, preferably 4H-pyrazolo-(3,4-d)-pyrimidin-4-one derivatives |
| US7141669B2 (en) | 2003-04-23 | 2006-11-28 | Pfizer Inc. | Cannabiniod receptor ligands and uses thereof |
| US8044060B2 (en) | 2003-05-09 | 2011-10-25 | Boehringer Ingelheim International Gmbh | 6-cyclylmethyl- and 6-alkylmethyl pyrazolo[3,4-D]pyrimidines, methods for their preparation and methods for their use to treat impairments of perception, concentration learning and/or memory |
| DE10320785A1 (en) * | 2003-05-09 | 2004-11-25 | Bayer Healthcare Ag | 6-arylmethyl substituted pyrazolopyrimidines |
| DE102004004142A1 (en) * | 2003-05-09 | 2004-11-25 | Bayer Healthcare Ag | 6-Cyclylmethyl- and 6-alkylmethyl-substituted pyrazolopyrimidines |
| JP2006525966A (en) * | 2003-05-09 | 2006-11-16 | バイエル・ヘルスケア・アクチェンゲゼルシャフト | 6-cyclylmethyl- and 6-alkylmethyl substituted pyrazolopyrimidines |
| DE10328479A1 (en) * | 2003-06-25 | 2005-01-13 | Bayer Ag | 6-arylamino-5-cyano-4-pyrimidinones |
| EP2256106B1 (en) | 2003-07-22 | 2015-05-06 | Astex Therapeutics Limited | 3,4-disubstituted 1H-pyrazole compounds and their use as cyclin dependent kinases (CDK) and glycogen synthase kinase-3 (GSK-3) modulators |
| DE102004001873A1 (en) | 2004-01-14 | 2005-09-29 | Bayer Healthcare Ag | Cyanopyrimidinone |
| EP2305352A1 (en) | 2004-04-02 | 2011-04-06 | Merck Sharp & Dohme Corp. | 5-alpha-reductase inhibitors for use in the treatment of men with metabolic and anthropometric disorders |
| US7067659B2 (en) * | 2004-04-23 | 2006-06-27 | Duke University | Reactive oxygen generating enzyme inhibitor with nitric oxide bioactivity and uses thereof |
| AR054425A1 (en) * | 2005-01-21 | 2007-06-27 | Astex Therapeutics Ltd | PIPERIDIN ADDITION SALTS 4-IL-ACID AMID 4- (2,6-DICLORO-BENZOILAMINO) 1H-PIRAZOL-3-CARBOXILICO. |
| US8404718B2 (en) | 2005-01-21 | 2013-03-26 | Astex Therapeutics Limited | Combinations of pyrazole kinase inhibitors |
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| US3939161A (en) * | 1973-10-29 | 1976-02-17 | Abbott Laboratories | 1,3-Dimethyl- 1H-pyrazolo(4,3-D) pyrimidine-7 (6H)-ones |
| US4666908A (en) * | 1985-04-05 | 1987-05-19 | Warner-Lambert Company | 5-Substituted pyrazolo[4,3-d]pyrimidine-7-ones and methods of use |
| GB9722520D0 (en) * | 1997-10-24 | 1997-12-24 | Pfizer Ltd | Compounds |
| DE19838705A1 (en) * | 1998-08-26 | 2000-03-02 | Bayer Ag | New dihydro- (1,2,3) -triazolo- [4,5-d] pyrimidin-7-ones |
| IL139454A0 (en) * | 1999-11-08 | 2001-11-25 | Pfizer | Compounds for the treatment of female sexual dysfunction |
| JP2004534733A (en) * | 2001-02-05 | 2004-11-18 | ドクター・レディーズ・ラボラトリーズ・リミテッド | Aryl-substituted alkyl carboxylic acids as blood cholesterol lowering agents |
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2002
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- 2002-10-09 DO DO2002000482A patent/DOP2002000482A/en unknown
- 2002-10-22 MX MXPA04004171A patent/MXPA04004171A/en unknown
- 2002-10-22 CA CA002466824A patent/CA2466824A1/en not_active Abandoned
- 2002-10-22 JP JP2003540180A patent/JP2005511575A/en active Pending
- 2002-10-22 EP EP02777623A patent/EP1440073A1/en not_active Withdrawn
- 2002-10-22 WO PCT/IB2002/004385 patent/WO2003037899A1/en not_active Ceased
- 2002-10-22 BR BR0214096-9A patent/BR0214096A/en not_active IP Right Cessation
- 2002-10-29 PA PA20028557401A patent/PA8557401A1/en unknown
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- 2002-10-30 UY UY27522A patent/UY27522A1/en not_active Application Discontinuation
- 2002-10-31 AR ARP020104152A patent/AR037329A1/en unknown
- 2002-11-01 SV SV2002001373A patent/SV2004001373A/en not_active Application Discontinuation
- 2002-11-01 TW TW091132424A patent/TW200300081A/en unknown
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| PA8557401A1 (en) | 2003-11-12 |
| AR037329A1 (en) | 2004-11-03 |
| HN2002000317A (en) | 2003-05-21 |
| MXPA04004171A (en) | 2004-09-06 |
| EP1440073A1 (en) | 2004-07-28 |
| CA2466824A1 (en) | 2003-05-08 |
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