PA8653501A1 - NEW COMPOUNDS - Google Patents
NEW COMPOUNDSInfo
- Publication number
- PA8653501A1 PA8653501A1 PA20058653501A PA8653501A PA8653501A1 PA 8653501 A1 PA8653501 A1 PA 8653501A1 PA 20058653501 A PA20058653501 A PA 20058653501A PA 8653501 A PA8653501 A PA 8653501A PA 8653501 A1 PA8653501 A1 PA 8653501A1
- Authority
- PA
- Panama
- Prior art keywords
- rent
- alcoxi
- het
- members
- heterocicle
- Prior art date
Links
Classifications
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- 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
- A61P15/10—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D207/14—Nitrogen atoms not forming part of a nitro radical
Abstract
UN COMPUESTO DE FORMULA (l) Y SUS DERIVADOS FARMACEUTICA Y/O VETERINARIAMENTE ACEPTABLES, EN LA QUE R1, R2, R3 Y R20 SON CADA UNO INDEPENDIENTEMENTE H, CI, BR, F CF3, OCF3, ME O ET; R4 ES HET O CICLOALQUILO DE C3-7 OPCIONALMENTE SUBSTITUIDO CON ALQUILO DE C1-4, ALCOXI DE C1-4, ALCOXIALQUILO QUE CONTIENE DE 2 A 4 ATOMOS DE CARBONO, O S-(ALQUILO DE C1-4); A ES O O 1; Y HET ES UN HETEROCICLO NO AROMATICO DE 4, 5 O 6 MIEMBROS QUE CONTIENEN POR LO MENOS UN HETEROATOMO DE N, O ó S, OPCIONALMENTE CONDENSADO CON UN GRUPO CARBOCICLICO DE 5 O 6 MIEMBROS O UN SEGUNDO HETEROCICLO DE 4, 5 O 6 MIEMBROS QUE CONTIENE POR LO MENOS UN HETEROATOMO DE N O o S, EN EL QUE EL GRUPO HET ESTA OPCIONALMENTE SUBSTITUIDO POR LO MENOS CON UN SUBSTITUYENTE SELECCIONADO INDEPENDIENTEMENTE DE ALQUILO DE C1-8, ALCOXI DE C1-8, OH, HALO, CF3, OCF3, SCF3, HIDROXI-ALQUILO DE C1-6, ALCOXI DE C1-4-AQUILO DE C1-6 Y ALQUIL DE C1-4-S-ALQUILO DE C1-4; CON TAL DE QUE POR LO MENOS UNO DE R1,R2,Y R3 SEA DISTINTO DE H. LOS COMPUESTOS DE LA INVENCION EXHIBEN ACTIVIDAD COMO INHIBIDORES DE LA RECAPTACION TANTO DE SEROTONINA COMO DE NORADRENALINA Y POR LO TANTO TIENEN UTILIDAD EN VARIAS AREAS TERAPEUTICAS, POR EJEMPLO, INCONTINENCIA URINARIA.A COMPOSITE OF FORMULA (l) AND ITS PHARMACEUTICAL AND / OR VETERINARLY ACCEPTABLE DERIVATIVES, IN WHICH R1, R2, R3 AND R20 ARE EACH INDEPENDENTLY H, CI, BR, F CF3, OCF3, ME OR ET; R4 IS HET OR C3-7 CYCLALKYL OPTIONALLY SUBSTITUTED WITH C1-4 RENT, C1-4 ALCOXI, ALCOXIALQUIL CONTAINING FROM 2 TO 4 CARBON ATOMS, OR S- (C1-4 RENT); A ES O O 1; AND HET IS A NON-AROMATIC HETEROCICLE OF 4, 5 OR 6 MEMBERS CONTAINING AT LEAST ONE HETEROATOMY OF N, OR OR S, OPTIONALLY CONDENSED WITH A CARBOYCLIC GROUP OF 5 OR 6 MEMBERS OR A SECOND HETEROCICLE OF 4, 5 OR 6 MEMBERS THAT CONTAINS AT LEAST ONE HETEROATOMO OF NO or S, IN WHICH THE GROUP HET IS OPTIONALLY SUBSTITUTED AT LEAST WITH A SUBSTITUENTLY SELECTED FROM RENT OF C1-8, ALCOXI OF C1-8, OH, HALO, CF3, OCF3, SCF3, HYDROXI-RENT OF C1-6, ALCOXI OF C1-4-AQUILO OF C1-6 AND RENT OF C1-4-S-RENT OF C1-4; SO THAT AT LEAST ONE OF R1, R2, AND R3 IS DIFFERENT FROM H. THE COMPOUNDS OF THE INVENTION EXHIBIT ACTIVITY AS INHIBITORS OF THE RECAPTATION OF BOTH SEROTONIN AND NORADRENALINE AND THEREFORE THEY ARE USED IN VARIOUS THERAPEUTIC AREAS EXAMPLE, URINARY INCONTINENCE.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0425766.3A GB0425766D0 (en) | 2004-11-23 | 2004-11-23 | Novel compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
PA8653501A1 true PA8653501A1 (en) | 2006-06-02 |
Family
ID=33548739
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PA20058653501A PA8653501A1 (en) | 2004-11-23 | 2005-11-23 | NEW COMPOUNDS |
Country Status (26)
Country | Link |
---|---|
EP (1) | EP1817281A1 (en) |
JP (1) | JP4233596B2 (en) |
KR (1) | KR100886294B1 (en) |
CN (1) | CN101065355A (en) |
AP (1) | AP2007004003A0 (en) |
AR (1) | AR052243A1 (en) |
AU (1) | AU2005308534A1 (en) |
BR (1) | BRPI0518486A2 (en) |
CA (1) | CA2589258A1 (en) |
CR (1) | CR9171A (en) |
EA (1) | EA011217B1 (en) |
GB (1) | GB0425766D0 (en) |
GT (1) | GT200500337A (en) |
IL (1) | IL183191A0 (en) |
MA (1) | MA29038B1 (en) |
MX (1) | MX2007006138A (en) |
NL (2) | NL1030485C2 (en) |
NO (1) | NO20072486L (en) |
PA (1) | PA8653501A1 (en) |
PE (1) | PE20061056A1 (en) |
SV (1) | SV2006002311A (en) |
TN (1) | TNSN07201A1 (en) |
TW (1) | TWI300776B (en) |
UY (1) | UY29224A1 (en) |
WO (1) | WO2006056884A1 (en) |
ZA (1) | ZA200703910B (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH628885A5 (en) * | 1978-01-01 | 1982-03-31 | Anphar Sa | Piperidine derivative |
GB0314054D0 (en) * | 2003-06-17 | 2003-07-23 | Pfizer Ltd | Amide derivatives as selective serotonin re-uptake inhibitors |
CA2530159C (en) * | 2003-06-17 | 2010-02-02 | Pfizer Inc. | N-pyrrolidin-3-yl-amide derivatives as serotonin and noradrenaline re-uptake inhibitors |
-
2004
- 2004-11-23 GB GBGB0425766.3A patent/GB0425766D0/en not_active Ceased
-
2005
- 2005-11-18 MX MX2007006138A patent/MX2007006138A/en active IP Right Grant
- 2005-11-18 EP EP05808510A patent/EP1817281A1/en not_active Withdrawn
- 2005-11-18 JP JP2007542360A patent/JP4233596B2/en not_active Expired - Fee Related
- 2005-11-18 CA CA002589258A patent/CA2589258A1/en not_active Abandoned
- 2005-11-18 KR KR1020077014351A patent/KR100886294B1/en not_active IP Right Cessation
- 2005-11-18 AU AU2005308534A patent/AU2005308534A1/en not_active Abandoned
- 2005-11-18 EA EA200700920A patent/EA011217B1/en not_active IP Right Cessation
- 2005-11-18 WO PCT/IB2005/003643 patent/WO2006056884A1/en active Application Filing
- 2005-11-18 CN CNA2005800401025A patent/CN101065355A/en active Pending
- 2005-11-18 BR BRPI0518486-0A patent/BRPI0518486A2/en not_active IP Right Cessation
- 2005-11-18 AP AP2007004003A patent/AP2007004003A0/en unknown
- 2005-11-21 AR ARP050104866A patent/AR052243A1/en not_active Application Discontinuation
- 2005-11-21 PE PE2005001362A patent/PE20061056A1/en not_active Application Discontinuation
- 2005-11-22 TW TW094140922A patent/TWI300776B/en active
- 2005-11-22 UY UY29224A patent/UY29224A1/en not_active Application Discontinuation
- 2005-11-22 NL NL1030485A patent/NL1030485C2/en not_active IP Right Cessation
- 2005-11-22 GT GT200500337A patent/GT200500337A/en unknown
- 2005-11-23 PA PA20058653501A patent/PA8653501A1/en unknown
- 2005-11-23 SV SV2005002311A patent/SV2006002311A/en unknown
-
2006
- 2006-10-27 NL NL1032760A patent/NL1032760C2/en not_active IP Right Cessation
-
2007
- 2007-05-14 IL IL183191A patent/IL183191A0/en unknown
- 2007-05-15 NO NO20072486A patent/NO20072486L/en not_active Application Discontinuation
- 2007-05-15 ZA ZA200703910A patent/ZA200703910B/en unknown
- 2007-05-22 TN TNP2007000201A patent/TNSN07201A1/en unknown
- 2007-05-23 MA MA29935A patent/MA29038B1/en unknown
- 2007-06-07 CR CR9171A patent/CR9171A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EA200700920A1 (en) | 2007-12-28 |
PE20061056A1 (en) | 2006-11-08 |
JP2008520646A (en) | 2008-06-19 |
EA011217B1 (en) | 2009-02-27 |
GB0425766D0 (en) | 2004-12-22 |
KR100886294B1 (en) | 2009-03-04 |
WO2006056884A1 (en) | 2006-06-01 |
CN101065355A (en) | 2007-10-31 |
ZA200703910B (en) | 2008-09-25 |
CA2589258A1 (en) | 2006-06-01 |
UY29224A1 (en) | 2006-06-30 |
AR052243A1 (en) | 2007-03-07 |
NL1030485A1 (en) | 2006-05-24 |
NL1030485C2 (en) | 2006-11-07 |
NL1032760C2 (en) | 2007-04-17 |
EP1817281A1 (en) | 2007-08-15 |
AU2005308534A1 (en) | 2006-06-01 |
KR20070086599A (en) | 2007-08-27 |
MA29038B1 (en) | 2007-11-01 |
TWI300776B (en) | 2008-09-11 |
NL1032760A1 (en) | 2006-12-13 |
TW200626543A (en) | 2006-08-01 |
AP2007004003A0 (en) | 2007-06-30 |
NO20072486L (en) | 2007-06-20 |
GT200500337A (en) | 2006-06-13 |
JP4233596B2 (en) | 2009-03-04 |
BRPI0518486A2 (en) | 2008-11-18 |
CR9171A (en) | 2007-07-04 |
IL183191A0 (en) | 2007-08-19 |
MX2007006138A (en) | 2007-07-19 |
TNSN07201A1 (en) | 2008-11-21 |
SV2006002311A (en) | 2006-09-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PA8605301A1 (en) | NEW COMPOUNDS | |
NI200700270A (en) | BENZODIOXAN AND BENZODIOXOLAN DERIVATIVES AND USES OF THE SAME | |
ECSP066898A (en) | SELECTED CGRP ANTAGONISTS, PROCEDURE FOR PREPARATION AS WELL AS ITS USE AS A MEDICINAL PRODUCT | |
GT200400092A (en) | PREPARATION AND USE OF RENTAL DERIVATIVES FOR THE TREATMENT OF OBESITY | |
ECSP088638A (en) | BENCENSULFONIL-CHROMANE, THIOCHROMANE, TETRAHYDRONAFTALENE AND RELATED GAMMA SECRETASE INHIBITORS | |
UY28215A1 (en) | USEFUL KINAZOLINES AS IONIC CHANNEL MODULATORS | |
CR8482A (en) | NEW DERIVATIVES OF QUINOLINA | |
UY28026A1 (en) | 4-PIPERAZINILBENCENOSULFONILINDOLES AND USES OF THE SAME. | |
PA8575401A1 (en) | DERIVATIVES OF BENZOCONDENSED HETEROARILAMIDE OF USEFUL TIENOPIRIDINS AS THERAPEUTIC AGENTS, PHARMACEUTICAL COMPOSITIONS THAT INCLUDE THE SAME AND METHODS FOR USE | |
AR074358A1 (en) | PIRAZINE DERIVATIVES AS INHIBITORS OF PHOSPHODIESTERASE 10 | |
DE602006006850D1 (en) | AZABICYCLO (3,1,0) -HEXAN DERIVATIVES SUITABLE AS MODULATORS OF DOPAMINE D3 RECEPTORS | |
CR10327A (en) | "PIRIDIN (3-4-b) PIRAZINONAS" | |
UY28848A1 (en) | SELECTED CGRP ANTAGONISTS, PROCEDURES FOR THEIR PREPARATION, AND THEIR EMPLOYMENT AS MEDICATIONS | |
ECSP099394A (en) | DERIVATIVES OF QUINUCLIDINOL AS ANTOGONISTS OF MUSCARINIC RECEPTORS | |
ECSP099216A (en) | NEW DERIVATIVES OF DIOSMETINE, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
ECSP088194A (en) | SELECTED CGRP ANTAGONISTS, PROCEDURES FOR THEIR PREPARATION, AS WELL AS ITS USE AS MEDICATIONS | |
GT200600161A (en) | NEW THERAPEUTIC COMBINATIONS FOR THE TREATMENT OR PREVENTION OF PSYCHOTIC DISORDERS | |
TW200800962A (en) | Selected CGRP antagonists, processes for preparing them and their use as pharmaceutical compositions | |
UY27685A1 (en) | INDOLIL-UREA DERIVED FROM USEFUL TIENOPIRIDINS AS ANTIANGIOGEN AGENTS, AND PROCEDURES FOR USE | |
CR9499A (en) | NEW DERIVATIVES OF PHENYLPIRIDINYLPIPERAZINE, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
CR10255A (en) | "NEW THERAPEUTIC COMPOSITIONS FOR THE TREATMENT OR PREVENTION OF PSYCHOTIC DISORDERS" | |
AR035434A1 (en) | FLUORALCOXIFENILSULFONILUREAS REPLACED, PROCEDURE FOR PREPARATION, PROCEDURE TO COMBAT THE INDESEABLE GROWTH OF PLANTS OR MICROORGANISMS, USE OF THESE COMPOUNDS TO COMBAT THE INDESEABLE GROWTH OF THE PLANTS OR THE MICRO ORGANISTS AND HER | |
PA8563601A1 (en) | ACIDS-3- (IMIDAZOLIL) -2- ALCOXIPROPANOICS | |
ECSP10010578A (en) | PHARMACEUTICAL COMPOSITION 271 | |
PA8653501A1 (en) | NEW COMPOUNDS |