AR040773A1 - Pirazoles utiles como inhibidores de gsk-3 - Google Patents

Pirazoles utiles como inhibidores de gsk-3

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Publication number
AR040773A1
AR040773A1 AR20030102785A ARP030102785A AR040773A1 AR 040773 A1 AR040773 A1 AR 040773A1 AR 20030102785 A AR20030102785 A AR 20030102785A AR P030102785 A ARP030102785 A AR P030102785A AR 040773 A1 AR040773 A1 AR 040773A1
Authority
AR
Argentina
Prior art keywords
independently selected
inhibitors
compounds
pharmaceutically acceptable
aliphatic group
Prior art date
Application number
AR20030102785A
Other languages
English (en)
Inventor
Cornelia J Forster
Larry C Park
Marion W Wannamaker
Yung-Mae Yao
Original Assignee
Vertex Pharma
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 Vertex Pharma filed Critical Vertex Pharma
Publication of AR040773A1 publication Critical patent/AR040773A1/es

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    • 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
    • A—HUMAN NECESSITIES
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    • A—HUMAN NECESSITIES
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    • A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
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    • 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
    • C07D403/14—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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medicinal Chemistry (AREA)
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  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
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Abstract

Compuesto de pirazol o un derivado farmacéuticamente aceptable del mismo. Estos compuestos son inhibidores de las cinasas de proteínas, en particular, inhibidores de la cinasa de proteína de mamífero GSK3. La presente además proporciona composiciones farmacéuticamente aceptables que comprenden los compuestos de la presente; y métodos de utilización de estos compuestos y composiciones en el tratamiento de varios trastornos regulados por cinasas de proteínas, como trastornos neurológicos neurodegenerativos, diabetes, trastornos siquiátricos, esclerosis múltiple, infarto, isquemia, calvicie y apoplejía. Reivindicación 1: Un compuesto de fórmula (1) o una sal farmacéuticamente aceptable del mismo, en donde: W es N o CH; R1 se selecciona entre H o F; y Ry es un grupo alifático C1-4, opcionalmente sustituido con N(R2)2, o un anillo saturado de 5 a 6 miembros que tiene 1 a 2 heteroátomos seleccionados en forma independiente entre N, O, o S, en donde: cada R2 se selecciona de manera independiente entre H o un grupo alifático C1-3 opcionalmente sustituido con -OH, -N(R3)2, o un anillo saturado de 5 a 6 miembros que tiene 1 a 2 heteroátomos seleccionados de manera independiente entre N, O, o S; y en donde: cada R3 se selecciona en forma independiente entre H o un grupo alifático C1-3; siempre que: cuando R1 es H y W es CH, entonces Ry no es metilo.
AR20030102785A 2002-08-02 2003-08-01 Pirazoles utiles como inhibidores de gsk-3 AR040773A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US40096702P 2002-08-02 2002-08-02

Publications (1)

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AR040773A1 true AR040773A1 (es) 2005-04-20

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AR20030102785A AR040773A1 (es) 2002-08-02 2003-08-01 Pirazoles utiles como inhibidores de gsk-3

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US (2) US7491730B2 (es)
EP (1) EP1532145B1 (es)
JP (3) JP4733388B2 (es)
KR (1) KR20050032105A (es)
CN (2) CN1319968C (es)
AR (1) AR040773A1 (es)
AT (1) ATE339419T1 (es)
AU (2) AU2003257078B2 (es)
BR (1) BR0313176A (es)
CA (1) CA2494100C (es)
CO (1) CO5700772A2 (es)
DE (1) DE60308387T2 (es)
DK (1) DK1532145T3 (es)
EA (1) EA200500299A1 (es)
EC (1) ECSP055640A (es)
ES (1) ES2273043T3 (es)
HK (1) HK1081186A1 (es)
IL (1) IL166620A (es)
MX (1) MXPA05001367A (es)
NO (1) NO20051100L (es)
NZ (2) NZ538426A (es)
PL (1) PL374967A1 (es)
PT (1) PT1532145E (es)
TW (1) TWI324157B (es)
WO (1) WO2004013140A1 (es)
ZA (1) ZA200501124B (es)

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