PE20020407A1 - Derivados de quinazolina como antagonistas del receptor adrenergico alfa-1 - Google Patents

Derivados de quinazolina como antagonistas del receptor adrenergico alfa-1

Info

Publication number
PE20020407A1
PE20020407A1 PE2001000870A PE2001000870A PE20020407A1 PE 20020407 A1 PE20020407 A1 PE 20020407A1 PE 2001000870 A PE2001000870 A PE 2001000870A PE 2001000870 A PE2001000870 A PE 2001000870A PE 20020407 A1 PE20020407 A1 PE 20020407A1
Authority
PE
Peru
Prior art keywords
alkyl
metil
amino
antagonists
alpha
Prior art date
Application number
PE2001000870A
Other languages
English (en)
Inventor
Cyrus Kephra Becker
Chris Richard Melville
Juerg Roland Pfister
Xiaoming Zhang
Original Assignee
Hoffmann La Roche
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20020407A1 publication Critical patent/PE20020407A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/10Drugs for genital or sexual disorders; Contraceptives for impotence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/14Heterocyclic 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 three or more hetero rings

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Anesthesiology (AREA)
  • Psychiatry (AREA)
  • Gynecology & Obstetrics (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

SE REFIERE A COMPUESTOS DE FORMULA I DONDE R1 ES H, ALQUILO C1-C6; R2 ES ALQUILO C1-C6, HETEROCICLILO CON ARILO, ALCOXI, HALOGENO; R' Y R'' SON ALQUILO C1-C6; A ES H, COR3, SO2R3, COOR3, ENTRE OTROS; R3 ES ALQUILO C1-C6, ARILO, ARILALQUILO, HETEROALQUILO, HETEROARILALQUILIO, CICLOALQUILO; R4 Y R5 SON H; R4 Y R5 JUNTO A C FORMAN UN ANILLO DE 5 A 7 MIEMBROS; R6 ES H, ALQUILO, CIANO; n ES 0-2; SON COMPUESTOS PREFERIDOS 1-(4-{[(4-AMINO-6,7-DIMETOXI-QUINAZOLIN-2-IL)-METIL-AMINO]-METIL}-4-FENIL-PIPERIDIN-1-IL)-1-(TETRAHIDRO-FURAN-2-IL)-METANONA, 1-(4-{[(4-AMINO-6,7-DIMETOXI-QUINAZOLIN-2-IL)-METIL-AMINO]-METIL}-4-FENIL-PIPERIDIN-1-IL)-1-PIRROLIDIN-2-IL-METANONA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA Y UN PROCEDIMIENTO PARA LA PREPARACION. LOS COMPUESTOS MENCIONADOS SON ANTAGONISTAS DEL RECEPTOR ADRENERGICO ALFA-1 Y SON UTILES PARA EL TRATAMIENTO DE LA DISFUNCION SEXUAL, TRASTORNOS DEL TRACTO URINARIO
PE2001000870A 2000-08-31 2001-08-29 Derivados de quinazolina como antagonistas del receptor adrenergico alfa-1 PE20020407A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US22950300P 2000-08-31 2000-08-31

Publications (1)

Publication Number Publication Date
PE20020407A1 true PE20020407A1 (es) 2002-05-21

Family

ID=22861517

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2001000870A PE20020407A1 (es) 2000-08-31 2001-08-29 Derivados de quinazolina como antagonistas del receptor adrenergico alfa-1

Country Status (19)

Country Link
US (1) US6559153B2 (es)
EP (1) EP1315714B1 (es)
JP (1) JP3971299B2 (es)
KR (1) KR100602929B1 (es)
CN (1) CN1308324C (es)
AR (1) AR032475A1 (es)
AT (1) ATE309240T1 (es)
AU (2) AU9378801A (es)
BR (1) BR0113585A (es)
CA (1) CA2420177C (es)
DE (1) DE60114852T2 (es)
ES (1) ES2251512T3 (es)
GT (1) GT200100181A (es)
MX (1) MXPA03001777A (es)
PA (1) PA8527901A1 (es)
PE (1) PE20020407A1 (es)
UY (1) UY26919A1 (es)
WO (1) WO2002018348A2 (es)
ZA (1) ZA200301082B (es)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003014122A1 (en) * 2001-08-10 2003-02-20 Polychip Pharmaceuticals Pty Ltd Derivatives of morphine-like opioid compounds
AU2003219199A1 (en) * 2002-04-03 2003-10-13 Orion Corporation Use of an alfa2-adrenoreceptor antagonist for cns-related diseases
TW200403058A (en) * 2002-04-19 2004-03-01 Bristol Myers Squibb Co Heterocyclo inhibitors of potassium channel function
ITMI20030151A1 (it) * 2003-01-30 2004-07-31 Recordati Ind Chimica E Farma Ceutica S P A Uso di antagonisti selettivi del recettore mglu5 per il trattamento di disfunzioni neuromuscolari del tratto urinario inferiore.
EP1646615B1 (en) * 2003-06-06 2009-08-26 Vertex Pharmaceuticals Incorporated Pyrimidine derivatives as modulators of atp-binding cassette transporters
DK1648878T3 (da) * 2003-07-24 2009-08-10 Euro Celtique Sa Piperidinforbindelser og farmaceutiske sammensætninger, som indeholder dem
WO2006021345A2 (en) * 2004-08-27 2006-03-02 Bayer Healthcare Ag Diagnostics and therapeutics for diseases associated with adrenergic alpha-1b receptor (adra1b)
MY179032A (en) 2004-10-25 2020-10-26 Cancer Research Tech Ltd Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors
US7413607B2 (en) * 2005-03-31 2008-08-19 3M Innovative Properties Company Templated semiconductor particles and methods of making
US7344583B2 (en) * 2005-03-31 2008-03-18 3M Innovative Properties Company Methods of making metal particles within cored dendrimers
ATE449082T1 (de) * 2005-05-04 2009-12-15 Hoffmann La Roche (3,4-dihydro-chinazolin-2-yl)-(2-aryloxy-ethyl) amine mit aktivität am 5-ht-rezeptor
EP2043655A2 (en) 2006-04-25 2009-04-08 Astex Therapeutics Limited Purine and deazapurine derivatives as pharmaceutical compounds
JP5144666B2 (ja) * 2006-09-19 2013-02-13 スリーエム イノベイティブ プロパティズ カンパニー 鋳型化された金属酸化物粒子及び製造方法
PL2201012T3 (pl) 2007-10-11 2014-11-28 Astrazeneca Ab Pochodne pirolo[2,3-d]pirymidyny jako inhibitory kinazy białkowej b
TW200944526A (en) 2008-04-22 2009-11-01 Vitae Pharmaceuticals Inc Carbamate and urea inhibitors of 11β-hydroxysteroid dehydrogenase 1
ES2761311T3 (es) 2011-04-01 2020-05-19 Astrazeneca Ab Tratamiento terapéutico
MY175800A (en) 2011-11-30 2020-07-09 Astrazeneca Ab Combination treatment of cancer
AU2013204533B2 (en) 2012-04-17 2017-02-02 Astrazeneca Ab Crystalline forms
BR112019018774A2 (pt) 2017-03-12 2020-04-07 Wang Xiaodong composto tendo uma estrutura de acordo com a fórmula i, sal farmaceuticamente aceitável, composição farmacêutica, método para prevenir ou tratar uma doença ou afeção e método para imunomodulação, inibição ou prevenção de rejeição de enxertos de órgãos ou pele ou tratamento de tumores ou câncer
WO2019088095A1 (ja) * 2017-11-02 2019-05-09 国立大学法人九州大学 鎮痛剤及びその使用

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0853479A4 (en) 1995-09-29 2001-04-11 Merck & Co Inc ALPHA 1b ADRENERGIC RECEPTOR ANTAGONISTS
GB9526546D0 (en) * 1995-12-23 1996-02-28 Pfizer Ltd Compounds useful in therapy
GB9700504D0 (en) 1997-01-11 1997-02-26 Pfizer Ltd Pharmaceutical compounds
US6355641B1 (en) 1999-03-17 2002-03-12 Syntex (U.S.A.) Llc Oxazolone derivatives and uses thereof

Also Published As

Publication number Publication date
AR032475A1 (es) 2003-11-12
WO2002018348A3 (en) 2002-07-11
CA2420177C (en) 2008-07-08
US6559153B2 (en) 2003-05-06
KR100602929B1 (ko) 2006-07-20
JP3971299B2 (ja) 2007-09-05
BR0113585A (pt) 2003-07-29
EP1315714B1 (en) 2005-11-09
UY26919A1 (es) 2002-02-28
WO2002018348A2 (en) 2002-03-07
EP1315714A2 (en) 2003-06-04
ES2251512T3 (es) 2006-05-01
PA8527901A1 (es) 2002-07-30
AU9378801A (en) 2002-03-13
GT200100181A (es) 2002-05-23
MXPA03001777A (es) 2003-06-04
DE60114852T2 (de) 2006-07-27
CA2420177A1 (en) 2002-03-07
AU2001293788B2 (en) 2007-10-11
KR20030022421A (ko) 2003-03-15
JP2004507527A (ja) 2004-03-11
ZA200301082B (en) 2004-05-07
DE60114852D1 (de) 2005-12-15
CN1545510A (zh) 2004-11-10
CN1308324C (zh) 2007-04-04
US20020045614A1 (en) 2002-04-18
ATE309240T1 (de) 2005-11-15

Similar Documents

Publication Publication Date Title
PE20020407A1 (es) Derivados de quinazolina como antagonistas del receptor adrenergico alfa-1
RU2294932C2 (ru) Новые производные индола со сродством к рецептору 5-ht6
DE60309498T2 (de) 4-piperazinylbenzolsulfonyl-indole mit 5-ht6 rezeptor-affinität
PE20060625A1 (es) Derivados de benzazepina como antagonistas y/o agonistas del receptor h3 de histamina
PE20020735A1 (es) Derivados de quinazolona como antagonistas de receptores adrenergicos alfa-1a/b
PE20050525A1 (es) Derivados de pirazol sustituido y compuestos relacionados como antagonistas del receptor de bradiquinina b1
ES2238583T3 (es) Derivados de benzo(d)azepina como antagonistas del receptor 5-ht6.
PE20050465A1 (es) Compuestos derivados de quinuclidina como antagonistas del receptor muscarinico m3
US9522150B2 (en) Alpha adrenergic receptor modulators
PE20011371A1 (es) Derivados de 3-(3-isopropil-5-metil-4h-1,2,4-triazol-4-il)-exo-8-azabiciclo[3.2.1]octano como antagonistas de los receptores de quimiocina ccr5
PE20010574A1 (es) Derivados de indol como ligandos del receptor 5-ht2
PE20001467A1 (es) Derivados de 4-fenilpiridina como antagonistas del receptor de neuroquinina
PE20020298A1 (es) Derivados de 1,3,8-triaza-espiro[4,5]decan-4-ona como antagonistas de receptores de neuroquinina nk-1
PE20010575A1 (es) Derivados de indol y su uso como ligandos del receptor 5ht2
PE20021072A1 (es) DERIVADOS DE DIHIDRO-BENZO(b) (1,4)-DIAZEPIN-2-ONA COMO ANTAGONISTAS I DE mGLUR2
PE20091335A1 (es) Derivados de ftalazinona
PE20010854A1 (es) USO DE DERIVADOS DE PIRIMIDINA 4 SUSTITUIDOS COMO ANTAGONISTAS DE LOS RECEPTORES DE GLUTAMATO mGluR1
NO333165B1 (no) Forbindelse og sammensetning, og anvendelse av samme
CA2272640C (en) Guanidinyl heterocycle compounds useful as alpha-2 adrenoceptor agonists
JP3869723B2 (ja) バソプレッシン・アゴニストとしての縮合アゼピン
PE20011258A1 (es) Derivados de benzocicloalquilenilamina como antagonistas de receptores muscarinicos
RU2135503C1 (ru) N-замещенные производные 3-азабицикло (3.2.0)гептана или их соли с физиологически совместимыми кислотами
JP2004532240A5 (es)
AU2009314221B2 (en) 1-(Arylsulfonyl)-4-(Piperazin-1-yl)-1H-Benzimidazoles as 5-Hydroxytryptamine-6 Ligands
AU2003267063A1 (en) 2,4-substituted indoles and their use as 5-ht6 modulators

Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed