AR020138A1 - COMPUESTOS DERIVADOS DE N-{3-[1-(1H-IMIDAZOL-4-IL)-ALQUIL C1-4]-fenil}-ALCAN-SULFONAMIDA, COMPOSICION FARMACEUTICA QUE LOS CONTIENE Y METODO PARA ACTIVARADRENO RECEPTORES a1 EN UN MAMIFERO. - Google Patents
COMPUESTOS DERIVADOS DE N-{3-[1-(1H-IMIDAZOL-4-IL)-ALQUIL C1-4]-fenil}-ALCAN-SULFONAMIDA, COMPOSICION FARMACEUTICA QUE LOS CONTIENE Y METODO PARA ACTIVARADRENO RECEPTORES a1 EN UN MAMIFERO.Info
- Publication number
- AR020138A1 AR020138A1 ARP990103957A ARP990103957A AR020138A1 AR 020138 A1 AR020138 A1 AR 020138A1 AR P990103957 A ARP990103957 A AR P990103957A AR P990103957 A ARP990103957 A AR P990103957A AR 020138 A1 AR020138 A1 AR 020138A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- alkoxy
- arylalkyl
- cycloalkyl
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- 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
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/84—Sulfur atoms
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Compuesto que tiene la formula 1: amida éster o prodroga aceptable para uso farmacéutico, donde R1 se selecciona del grupo formado por -S(O)2R9 y -C(O)R10;R9 se selecciona del grupo que consiste de alquenilo C2-10, alquilo C1-10, alquinilo C2-10, arilo, arilalquenilo C2-5, arilalquilo C2-5, cicloalquilo C3-8,cicloalquil C3-7 alquilo C1-4, haloalquilo C1-5, heterociclo mono y bi-ciclo, y -NZ1Z2 donde Z1 y Z2 se seleccionan independientemente del grupo formado porhidrogeno, alquilo C1-10, alquil C1-4 carbonilo, arilo, arilalquilo C2-5, y formilo; R10 se selecciona del grupo formado por alquenilo C2-10, alcoxi C1-6,alquilo C1-10, alquinilo C2-10, arilo, arilalquilo C2-5, cicloalquilo C3-8, cicloalquil C3-7 alquilo C1-5, halo C1-5, y -NZ1Z2 definido precedentemente; R2 seselecciona del grupo formado por hidrogeno, alquenilo C2-10, alcoxi C1-6, alquilo C1-10, halo, halo C1-5 alquilo C1-5, e hidroxi; R3 se selecciona del grupoformado por alqueniloxi C2-5, alquilo C1-10, alcoxi C1-6, alcoxi C1-4 alquilo C1-4, alquinil C1-4 oxi, arilalquilo C2-5, cicloalquil C3-7 alquilo C1-4, haloC1-5 alquilo C1-5, e hidroxi; con la condicion de que cuando R3 es seleccionado del grupo que consiste de alqueniloxi, alquilo, alcoxi, alcoxi-alquilo-alquinil-oxi, aril-alquilo, ciclaoalquil-alquilo, halo-alquilo e hidroxi, con los alcances indicados precedentemente, entonces R4 es seleccionado del grupo queconsiste de hidrogeno, alquilo C1-10, alcoxi C1-6, halo C1-5, e hidroxi; o R3 y R4 junto con los átomos de carbono a los cuales se encuentran unidos forman unanillo carbocíclico de 5, 6 o 7 miembros; o R3 y R4 junto con los átomos de carbono a los cuales se encuentran unidos forman un anillo de 5 o 6 miembros quecontiene 1 heteroátomo seleccionadodel grupo formado por O, NR11, y S(O)n; R11 se selecciona del grupo formado por hidrogneo, alquenilo C2-10, alcoxi C1-4,carbonilo, alquilo C1-10, alquil C1-4, carbonilo, alquinilo C2-10, arilalquilo C2-5, formilo, -C(O)NZ1Z2, y -SO2NZ1Z2; n es 0-2: R5 se selecciona del grupoformado por imidazol-4-ilo, imidazol-5-ilo, pirazol, oxazol, isoxazol, tiazol, isotiazol, oxidiazol, triazol, tiadiazol, piridina, pirimidina, pirazina y
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13079998A | 1998-08-07 | 1998-08-07 | |
US09/364,901 US6503935B1 (en) | 1998-08-07 | 1999-07-29 | Imidazoles and related compounds as α1A agonists |
Publications (1)
Publication Number | Publication Date |
---|---|
AR020138A1 true AR020138A1 (es) | 2002-04-10 |
Family
ID=22446384
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP990103957A AR020138A1 (es) | 1998-08-07 | 1999-08-06 | COMPUESTOS DERIVADOS DE N-{3-[1-(1H-IMIDAZOL-4-IL)-ALQUIL C1-4]-fenil}-ALCAN-SULFONAMIDA, COMPOSICION FARMACEUTICA QUE LOS CONTIENE Y METODO PARA ACTIVARADRENO RECEPTORES a1 EN UN MAMIFERO. |
Country Status (8)
Country | Link |
---|---|
US (1) | US6503935B1 (es) |
EP (1) | EP1102754A1 (es) |
JP (1) | JP2002522423A (es) |
AR (1) | AR020138A1 (es) |
AU (1) | AU5338699A (es) |
CA (1) | CA2338594A1 (es) |
TW (1) | TW517050B (es) |
WO (1) | WO2000007997A1 (es) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6503935B1 (en) | 1998-08-07 | 2003-01-07 | Abbott Laboratories | Imidazoles and related compounds as α1A agonists |
US20030073850A1 (en) * | 1998-08-07 | 2003-04-17 | Altenbach Robert J. | 4-Imidazole derivatives of benzyl and restricted benzyl sulfonamides, sulfamides, ureas, carbamates, and amides and their use |
FI20000073A0 (fi) * | 2000-01-14 | 2000-01-14 | Orion Yhtymae Oy | Uusia imidatsolijohdannaisia |
US6388090B2 (en) | 2000-01-14 | 2002-05-14 | Orion Corporation | Imidazole derivatives |
US20020183357A1 (en) * | 2000-02-17 | 2002-12-05 | Brioni Jorge D. | Use of alpha- 1- alpha adrenoceptor agonists with alpha-1-Beta antagonism for the treatment of stress urinary incontinence |
US6323231B1 (en) | 2000-02-17 | 2001-11-27 | Abbott Laboratories | Use of α1A adrenoceptor agonists with α1B and α1D antagonism for the treatment of stress urinary incontinence |
US7071220B2 (en) * | 2000-09-18 | 2006-07-04 | Toa Eiyo Ltd. | N-substituted benzothiophenesulfonamide derivatives |
AU2003216312A1 (en) * | 2002-02-19 | 2003-09-09 | Northwestern University | NON-COVALENT INHIBITORS OF AmpC ss-LACTAMASE |
AR040241A1 (es) | 2002-06-10 | 2005-03-23 | Merck & Co Inc | Inhibidores de la 11-beta-hidroxiesteroide deshidrogrenasa 1 para el tratamiento de la diabetes obesidad y dislipidemia |
AU2005207925B2 (en) | 2004-01-26 | 2008-09-04 | Merck Sharp & Dohme Corp. | Novel crystalline forms of an inhibitor of 11-beta-hydroxysteroid dehydrogenase Type 1 |
BRPI0611370A2 (pt) * | 2005-05-23 | 2010-08-31 | Sagami Chem Res | derivados de pirazol-1-carboxilato, processos para a producão destes e processos para a producão de derivados de pirazol |
Family Cites Families (31)
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AU518569B2 (en) | 1979-08-07 | 1981-10-08 | Farmos-Yhtyma Oy | 4-benzyl- and 4-benzoyl imidazole derivatives |
EP0025136B1 (de) | 1979-08-27 | 1983-07-06 | Bayer Ag | Lichtsammelsystem und Verwendung von Cumarinderivaten als Energiewandler in solchen Systemen |
GB2071655B (en) | 1980-03-04 | 1983-06-22 | Erba Farmitalia | N-amidazolyl derivatives of1-chroman and process for their preparation |
US4320148A (en) | 1980-11-24 | 1982-03-16 | Smithkline Corporation | 2-Aminotetralin compounds, pharmaceutical compositions and method of producing central alpha1 agonist activity |
PT77219B (fr) | 1982-08-24 | 1986-02-04 | May & Baker Ltd | Procede de preparation des derives de la benzamide |
US4634705A (en) | 1984-06-06 | 1987-01-06 | Abbott Laboratories | Adrenergic amidines |
US4813998A (en) | 1986-02-27 | 1989-03-21 | Janssen Pharmaceutica N.V. | Herbicidal 1H-imidazole-5-carboxylic acid derivatives |
IT1216256B (it) | 1986-08-13 | 1990-02-22 | Menarini Sas | (benzofuran-2-il) imidazoli, con attivita' farmacologica,loro sali e procedimenti di fabbricazione relativi. |
US5043447A (en) | 1987-04-24 | 1991-08-27 | Syntex Pharmaceuticals, Ltd. | Substituted imidazolyl-alkyl-piperazine and -diazepine derivatives |
IL91542A0 (en) | 1988-10-06 | 1990-04-29 | Erba Carlo Spa | N-imidazolyl-and n-imidazolyl-methyl derivatives of substituted bicyclic compounds,their preparation and pharmaceutical compositions containing them |
US5073566A (en) | 1989-11-30 | 1991-12-17 | Eli Lilly And Company | Angiotensin ii antagonist 1,3-imidazoles and use thereas |
JP3393891B2 (ja) | 1992-08-18 | 2003-04-07 | 塩野義製薬株式会社 | イミダゾール類の製造方法 |
US5296609A (en) | 1993-04-09 | 1994-03-22 | Syntex Pharmaceuticals, Ltd. | Process for the preparation of 1,2,4-substituted imidazoles and related aminoalkylimidazole derivatives |
SE9302333D0 (sv) | 1993-07-06 | 1993-07-06 | Ab Astra | New compounds |
ATE234290T1 (de) | 1993-11-15 | 2003-03-15 | Schering Corp | Phenylalkyl-imidazole als h3-rezeptor- antagonisten |
US5616601A (en) | 1994-07-28 | 1997-04-01 | Gd Searle & Co | 1,2-aryl and heteroaryl substituted imidazolyl compounds for the treatment of inflammation |
GB9425211D0 (en) | 1994-12-14 | 1995-02-15 | Ucb Sa | Substituted 1H-imidazoles |
DE19514579A1 (de) | 1995-04-20 | 1996-10-24 | Boehringer Ingelheim Kg | Verwendung von alpha¶1¶¶L¶-Agonisten zur Behandlung der Harninkontinenz |
WO1996038143A1 (en) | 1995-06-02 | 1996-12-05 | Synaptic Pharmaceutical Corporation | The use of alpha-1c-selective adrenoceptor agonists for the treatment of urinary incontinence |
US5610174A (en) | 1995-06-02 | 1997-03-11 | Synaptic Pharmaceutical Corporation | Use of α1A -selective adrenoceptor agonists for the treatment of urinary incontinence |
US5756528A (en) | 1995-06-06 | 1998-05-26 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
HUP9901190A3 (en) | 1996-02-09 | 2002-05-28 | Black James Foundation | Sulfonamide derivatives of imidazole, process for producing them and pharmaceutical compositions containing them |
WO1997036876A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
AU2381397A (en) | 1996-04-19 | 1997-11-12 | Novo Nordisk A/S | Modulators of molecules with phosphotyrosine recognition units |
GB9702194D0 (en) | 1997-02-04 | 1997-03-26 | Lilly Co Eli | Sulphonide derivatives |
US5866579A (en) | 1997-04-11 | 1999-02-02 | Synaptic Pharmaceutical Corporation | Imidazole and imidazoline derivatives and uses thereof |
SG72827A1 (en) | 1997-06-23 | 2000-05-23 | Hoffmann La Roche | Phenyl-and aminophenyl-alkylsulfonamide and urea derivatives |
US6407132B1 (en) | 1997-07-25 | 2002-06-18 | James Black Foundation Limited | Substituted imidazole derivatives and their use as histamine H3 receptor ligands |
FR2768055A1 (fr) | 1997-09-11 | 1999-03-12 | Synthelabo | Utilisation de derives de sulfonanilide pour obtenir un medicament destine au traitement de l'ejaculation retrograde ou de l'aspermie |
FR2768054A1 (fr) | 1997-09-11 | 1999-03-12 | Synthelabo | Utilisation de derives de benzene sulfonamide pour obtenir un medicament destine au traitement de l'ejaculation retrograde ou de l'aspermie |
US6503935B1 (en) | 1998-08-07 | 2003-01-07 | Abbott Laboratories | Imidazoles and related compounds as α1A agonists |
-
1999
- 1999-07-29 US US09/364,901 patent/US6503935B1/en not_active Expired - Fee Related
- 1999-08-06 CA CA002338594A patent/CA2338594A1/en not_active Abandoned
- 1999-08-06 EP EP99939019A patent/EP1102754A1/en not_active Withdrawn
- 1999-08-06 WO PCT/US1999/017739 patent/WO2000007997A1/en not_active Application Discontinuation
- 1999-08-06 AU AU53386/99A patent/AU5338699A/en not_active Abandoned
- 1999-08-06 JP JP2000563631A patent/JP2002522423A/ja not_active Withdrawn
- 1999-08-06 AR ARP990103957A patent/AR020138A1/es not_active Application Discontinuation
- 1999-09-14 TW TW088113524A patent/TW517050B/zh not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JP2002522423A (ja) | 2002-07-23 |
EP1102754A1 (en) | 2001-05-30 |
AU5338699A (en) | 2000-02-28 |
US6503935B1 (en) | 2003-01-07 |
CA2338594A1 (en) | 2000-02-17 |
WO2000007997A1 (en) | 2000-02-17 |
TW517050B (en) | 2003-01-11 |
WO2000007997A8 (en) | 2000-05-04 |
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FA | Abandonment or withdrawal |