PE20010736A1 - PIRAZOL-[4,3-d]-PIRIMIDIN-7-ONA COMO INHIBIDORES DE LA 3`,5'-GUANOSINMONOFOSFATO CICLICO FOSFODIESTERASA - Google Patents
PIRAZOL-[4,3-d]-PIRIMIDIN-7-ONA COMO INHIBIDORES DE LA 3`,5'-GUANOSINMONOFOSFATO CICLICO FOSFODIESTERASAInfo
- Publication number
- PE20010736A1 PE20010736A1 PE2000001084A PE0010842000A PE20010736A1 PE 20010736 A1 PE20010736 A1 PE 20010736A1 PE 2000001084 A PE2000001084 A PE 2000001084A PE 0010842000 A PE0010842000 A PE 0010842000A PE 20010736 A1 PE20010736 A1 PE 20010736A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- het
- pyrimidin
- ocor7
- cor8
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 101710111837 Cyclic phosphodiesterase Proteins 0.000 title 1
- -1 CYANE Chemical class 0.000 abstract 5
- 101100134927 Gallus gallus COR8 gene Proteins 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 201000001881 impotence Diseases 0.000 abstract 2
- ZOOGRGPOEVQQDX-UUOKFMHZSA-N 3',5'-cyclic GMP Chemical compound C([C@H]1O2)OP(O)(=O)O[C@H]1[C@@H](O)[C@@H]2N1C(N=C(NC2=O)N)=C2N=C1 ZOOGRGPOEVQQDX-UUOKFMHZSA-N 0.000 abstract 1
- BKAWJIRCKVUVED-UHFFFAOYSA-N 5-(2-hydroxyethyl)-4-methylthiazole Chemical group CC=1N=CSC=1CCO BKAWJIRCKVUVED-UHFFFAOYSA-N 0.000 abstract 1
- 101100189582 Dictyostelium discoideum pdeD gene Proteins 0.000 abstract 1
- 208000010228 Erectile Dysfunction Diseases 0.000 abstract 1
- 206010057671 Female sexual dysfunction Diseases 0.000 abstract 1
- 101150098694 PDE5A gene Proteins 0.000 abstract 1
- 102000004861 Phosphoric Diester Hydrolases Human genes 0.000 abstract 1
- 108090001050 Phosphoric Diester Hydrolases Proteins 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 102100029175 cGMP-specific 3',5'-cyclic phosphodiesterase Human genes 0.000 abstract 1
- 230000004064 dysfunction Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/12—Drugs for genital or sexual disorders; Contraceptives for climacteric disorders
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Reproductive Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Endocrinology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Gynecology & Obstetrics (AREA)
- Pregnancy & Childbirth (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
SE REFIERE A PIRAZOL[3,4-d]PIRIMIDIN-7-ONA DE FORMULA I, DONDE X ES O, NR5; R1 ES H, ALQUILO, HET, ALQUIL-HET, ARILO, ALQUILARILO, OR6, OCOR7, COR8, COOR9, CONR10R11, NR12R13, SO2NR14R15; R2 ES H, HALOGENO, CIANO, NITRO, OR6, OCOR7, COR8, COOR9, ENTRE OTROS; R3 ES H, ALQUILO, ALQUILHET, ALQUILARILO, OR6, ENTRE OTROS; R4 ES H, HALOGENO, CIANO, NITRO, OR6, ENTRE OTROS; Y ES C, SO; A ES ALQUILENO, Z ES OR6, HALOGENO, HET, ARILO; R10 Y R11 SON H, ALQUILO, OR6, OCOR7, COR8, ENTRE OTROS; R12 Y R13 SON H, ALQUILO O UNO DE R12 O R13 ES CO-ALQUILO, CO-HET, O JUNTOS SON ALQUILENO C3-C7, R14 Y R15 SON H, ALQUILO O JUNTO CON N FORMAN UN ANILLO HETEROCICLICO; R5, R6, R7, R8, R9 SON H, ALQUILO; HET ES UN HETEROCICLO DE 4-12 MIEMBROS, CON LA CONDICION QUE R4 NO ES NH2, CUANDO R1 ES ALQUILO C1-C3 OPCIONALMENTE SUSTITUIDO CON FENILO, HET, PIPERIDINILO, MORFOLINILO. UN COMPUESTO PREFERIDO ES 5-(2-BUTOXI-5-YODO-3-PIRIDINIL)-3-ETIL-2-(2-METOXIETIL)-2,6-DIHIDRO-7H-PIRAZOL[4,3-d]PIRIMIDIN-7-ONA, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION. EL COMPUESTO I ES UN INHIBIDOR DE 3`,5'- GUANOSINMONOFOSFATO CICLICO FOSFODIESTERASA cGMP PDE5 Y PUEDE SER UTIL PARA EL TRATAMIENTO DE LA DISFUNCIN ERECTIL MASCULINA, IMPOTENCIA, DISFUNCION SEXUAL FEMENINA, DISFUNCION DEL CLITORIS
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9924041.8A GB9924041D0 (en) | 1999-10-11 | 1999-10-11 | Pharmaceutically active compounds |
| GB0018660A GB0018660D0 (en) | 2000-07-28 | 2000-07-28 | Pharmaceutically active compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20010736A1 true PE20010736A1 (es) | 2001-07-19 |
Family
ID=26244758
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2000001084A PE20010736A1 (es) | 1999-10-11 | 2000-10-10 | PIRAZOL-[4,3-d]-PIRIMIDIN-7-ONA COMO INHIBIDORES DE LA 3`,5'-GUANOSINMONOFOSFATO CICLICO FOSFODIESTERASA |
Country Status (34)
| Country | Link |
|---|---|
| US (1) | US6756373B1 (es) |
| EP (1) | EP1222190A1 (es) |
| JP (1) | JP2003511452A (es) |
| KR (1) | KR20020038941A (es) |
| CN (1) | CN1378547A (es) |
| AP (1) | AP2002002455A0 (es) |
| AR (1) | AR022665A1 (es) |
| AU (1) | AU7547900A (es) |
| BG (1) | BG106568A (es) |
| BR (1) | BR0014695A (es) |
| CA (1) | CA2387353A1 (es) |
| CO (1) | CO5261539A1 (es) |
| CZ (1) | CZ20021151A3 (es) |
| DZ (1) | DZ3218A1 (es) |
| EA (1) | EA200200240A1 (es) |
| EE (1) | EE200200192A (es) |
| GT (1) | GT200000168A (es) |
| HK (1) | HK1049834A1 (es) |
| HU (1) | HUP0203438A3 (es) |
| IL (1) | IL149025A0 (es) |
| IS (1) | IS6288A (es) |
| MA (1) | MA26824A1 (es) |
| NO (1) | NO20021695L (es) |
| NZ (1) | NZ517324A (es) |
| OA (1) | OA12058A (es) |
| PA (1) | PA8504401A1 (es) |
| PE (1) | PE20010736A1 (es) |
| PL (1) | PL357522A1 (es) |
| SK (1) | SK4562002A3 (es) |
| SV (1) | SV2002000192A (es) |
| TN (1) | TNSN00198A1 (es) |
| TR (1) | TR200200954T2 (es) |
| UY (1) | UY26383A1 (es) |
| WO (1) | WO2001027112A1 (es) |
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| GB0105893D0 (en) * | 2001-03-09 | 2001-04-25 | Pfizer Ltd | Pharmaceutically active compounds |
| GB0106661D0 (en) * | 2001-03-16 | 2001-05-09 | Pfizer Ltd | Pharmaceutically active compounds |
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| US11590209B2 (en) | 2020-01-21 | 2023-02-28 | Palatin Technologies, Inc. | Use of bremelanotide in patients with controlled hypertension |
| CN113493459B (zh) * | 2020-04-07 | 2022-12-13 | 广州白云山医药集团股份有限公司白云山制药总厂 | Pde5抑制剂化合物及其制备方法和应用 |
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- 2000-10-04 JP JP2001530330A patent/JP2003511452A/ja not_active Withdrawn
- 2000-10-04 KR KR1020027004589A patent/KR20020038941A/ko not_active Ceased
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