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MA26701A1 - PYRAZOLOPYRIMIDINONES NOUVELLES INHIBITRICES DE PDE-5 GMPc, PROCEDE POUR LEUR PREPARATION ET COMPOSTIONS PHARMACEUTIQUES LES CONTENANT. - Google Patents

PYRAZOLOPYRIMIDINONES NOUVELLES INHIBITRICES DE PDE-5 GMPc, PROCEDE POUR LEUR PREPARATION ET COMPOSTIONS PHARMACEUTIQUES LES CONTENANT.

Info

Publication number
MA26701A1
MA26701A1 MA25821A MA25821A MA26701A1 MA 26701 A1 MA26701 A1 MA 26701A1 MA 25821 A MA25821 A MA 25821A MA 25821 A MA25821 A MA 25821A MA 26701 A1 MA26701 A1 MA 26701A1
Authority
MA
Morocco
Prior art keywords
preparation
pyrazolopyrimidinones
pharmaceutical compositions
inhibitors
gmpc
Prior art date
Application number
MA25821A
Other languages
English (en)
Inventor
Edward Bunnage Mark
Nigel Maw Graham
Wood Anthony
Paul Mathias John
James Rawson David
Derek Albert Street Stephen
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of MA26701A1 publication Critical patent/MA26701A1/fr

Links

Classifications

    • 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
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

DEPOSANT Société dite : PFIZER INC, REVENDICATION DE PRIORITES GB 23/10/1998 9823102.0 Voir en annexe le titre de l'invention et le texte de l'abrégé Pyrazolopyrimidinones nouvelles inhibitrices de PDE-5 GMPc, procédé pour leur préparation et compositions pharmaceutiques les contenant L'invention concerne des composés de formule IA ou IB dans laquelle R1, R2, R3, R4 et A représentent divers radicaux. Elle concerne également un procédé pour leur préparation et des formulations pharmaceutiques les contenant. Application : utilisation de ces composés et formulations pharmaceutiques, inhibant la PDE-5 GMPc, pour le traitement ou la prévention de diverses maladies.
MA25821A 1998-10-23 1999-10-20 PYRAZOLOPYRIMIDINONES NOUVELLES INHIBITRICES DE PDE-5 GMPc, PROCEDE POUR LEUR PREPARATION ET COMPOSTIONS PHARMACEUTIQUES LES CONTENANT. MA26701A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9823102.0A GB9823102D0 (en) 1998-10-23 1998-10-23 Pharmaceutically active compounds

Publications (1)

Publication Number Publication Date
MA26701A1 true MA26701A1 (fr) 2004-12-20

Family

ID=10841068

Family Applications (1)

Application Number Title Priority Date Filing Date
MA25821A MA26701A1 (fr) 1998-10-23 1999-10-20 PYRAZOLOPYRIMIDINONES NOUVELLES INHIBITRICES DE PDE-5 GMPc, PROCEDE POUR LEUR PREPARATION ET COMPOSTIONS PHARMACEUTIQUES LES CONTENANT.

Country Status (7)

Country Link
US (1) US6333330B1 (fr)
GB (1) GB9823102D0 (fr)
GT (1) GT199900183A (fr)
MA (1) MA26701A1 (fr)
PE (1) PE20001114A1 (fr)
TN (1) TNSN99198A1 (fr)
UY (1) UY25795A1 (fr)

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US20090035221A1 (en) * 2002-01-25 2009-02-05 Ramsey Sallis Methods and Compositions for Treatment of Erectile Dysfunction
US20090257956A1 (en) * 2002-01-25 2009-10-15 Ramsey Sallis Treatment Method for Treatment of Erectile Dysfunction and Premature Ejaculation
US20050048573A1 (en) * 2003-02-03 2005-03-03 Plexxikon, Inc. PDE5A crystal structure and uses
US20050079548A1 (en) * 2003-07-07 2005-04-14 Plexxikon, Inc. Ligand development using PDE4B crystal structures
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US7449462B2 (en) 2004-01-22 2008-11-11 Pfizer, Inc. Triazole derivatives which inhibit vasopressin antagonistic activity
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CA2647932C (fr) * 2006-04-04 2011-06-07 Dong A Pharm. Co. Ltd. Agent de prevention et de traitement de l'hyperplasie de la prostate comprenant un compose pyrazolopyrimidinone
TW201811799A (zh) 2016-09-09 2018-04-01 美商英塞特公司 吡唑并嘧啶化合物及其用途
US20180072718A1 (en) 2016-09-09 2018-03-15 Incyte Corporation Pyrazolopyridine compounds and uses thereof
MA46191A (fr) 2016-09-09 2021-04-21 Incyte Corp Dérivés de pyrazolopyridine comme modulateurs de hpk1 et leurs utilisations pour le traitement du cancer
WO2018152220A1 (fr) 2017-02-15 2018-08-23 Incyte Corporation Composés de pyrazolopyridine et leurs utilisations
US10722495B2 (en) 2017-09-08 2020-07-28 Incyte Corporation Cyanoindazole compounds and uses thereof
LT3755703T (lt) 2018-02-20 2022-10-10 Incyte Corporation N-(fenil)-2-(fenil)pirimidin-4-karboksamido dariniai ir susiję junginiai, kaip hpk1 inhibitoriai, skirti vėžio gydymui
US10752635B2 (en) 2018-02-20 2020-08-25 Incyte Corporation Indazole compounds and uses thereof
US10745388B2 (en) 2018-02-20 2020-08-18 Incyte Corporation Indazole compounds and uses thereof
US11299473B2 (en) 2018-04-13 2022-04-12 Incyte Corporation Benzimidazole and indole compounds and uses thereof
US10899755B2 (en) 2018-08-08 2021-01-26 Incyte Corporation Benzothiazole compounds and uses thereof
ES2973117T3 (es) 2018-09-25 2024-06-18 Incyte Corp Compuestos de pirazolo[4,3-d]pirimidina como moduladores de ALK2 y/o FGFR
CR20220097A (es) 2019-08-06 2022-06-01 Incyte Corp Formas sólidas de un inhibidor de hpk1

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Also Published As

Publication number Publication date
TNSN99198A1 (fr) 2005-11-10
UY25795A1 (es) 2000-08-21
GB9823102D0 (en) 1998-12-16
PE20001114A1 (es) 2000-10-28
US6333330B1 (en) 2001-12-25
GT199900183A (es) 2001-04-14

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