About: Pyrazolopyridines as Cyclin-Dependent Kinase Inhibitors     Goto   Sponge   NotDistinct   Permalink

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  • In its many embodiments, the present invention provides a novel class of pyrazolo[1,5-a]pyridine compds. I [R = (un)substiuted-alkyl, -aryl, -heteroaryl, -heteroarylalkyl, etc.; R1 = H, alkyl or aryl; R2 = H, (un)substituted-alkyl, -alkenyl, -alkynyl, -aryl, etc.; R3 = H, halo, CF3, (un)substituted-alkyl, -aryl, etc.; R4 = H, halo, CF3, (un)substituted-alkyl, -cycloalkyl, -aryl, -heteroaryl, etc.] as inhibitors of cyclin dependent kinases, methods of prepg. such compds., pharmaceutical compns. contg. one or more such compds., methods of prepg. pharmaceutical formulations comprising one or more such compds., and methods of treatment, prevention, inhibition, or amelioration of one or more diseases assocd. with the CDKs using such compds. or pharmaceutical compns. Thus, e.g., II was prepd. by condensation of 7-amino-5-phenylpyrazolo[1,5-a]pyridine (prepn. given) with 3-formylpyridine. I possessed excellent CDK inhibitory properties as demonstrated by the IC50 value for III of 0.078 .mu.
  • In its many embodiments, the present invention provides a novel class of pyrazolo[1,5-a]pyridine compds. I [R = (un)substiuted-alkyl, -aryl, -heteroaryl, -heteroarylalkyl, etc.; R1 = H, alkyl or aryl; R2 = H, (un)substituted-alkyl, -alkenyl, -alkynyl, -aryl, etc.; R3 = H, halo, CF3, (un)substituted-alkyl, -aryl, etc.; R4 = H, halo, CF3, (un)substituted-alkyl, -cycloalkyl, -aryl, -heteroaryl, etc.] as inhibitors of cyclin dependent kinases, methods of prepg. such compds., pharmaceutical compns. contg. one or more such compds., methods of prepg. pharmaceutical formulations comprising one or more such compds., and methods of treatment, prevention, inhibition, or amelioration of one or more diseases assocd. with the CDKs using such compds. or pharmaceutical compns. Thus, e.g., II was prepd. by condensation of 7-amino-5-phenylpyrazolo[1,5-a]pyridine (prepn. given) with 3-formylpyridine. I possessed excellent CDK inhibitory properties as demonstrated by the IC50 value for III of 0.078 .mu. (en)
Title
  • Pyrazolopyridines as Cyclin-Dependent Kinase Inhibitors
  • Pyrazolopyridines as Cyclin-Dependent Kinase Inhibitors (en)
skos:prefLabel
  • Pyrazolopyridines as Cyclin-Dependent Kinase Inhibitors
  • Pyrazolopyridines as Cyclin-Dependent Kinase Inhibitors (en)
skos:notation
  • RIV/00216224:14310/04:00035989!RIV10-MSM-14310___
http://linked.open...tracePatentuVzoru
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • N
http://linked.open...cisloPatentuVzoru
  • WO 2004/026872 A1
http://linked.open...eleniPatentuVzoru
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
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  • 583270
http://linked.open...ai/riv/idVysledku
  • RIV/00216224:14310/04:00035989
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • cyclin dependent kinase; inhibitor; pyrazolopyrimidine (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...ontrolniKodProRIV
  • [FC37D832B078]
http://linked.open.../licencniPoplatek
http://linked.open...ydaniPatentuVzoru
  • USA
http://linked.open...atelePatentuVzoru
  • World Intellectual Property Organization
http://linked.open...in/vavai/riv/obor
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http://linked.open...ydaniPatentuVzoru
http://linked.open...iv/tvurceVysledku
  • Dwyer, Michael
  • Guzi, Timothy
  • Paruch, Kamil
  • Doll, Ronald
  • Girijavallabhan, Viyyoor
  • Keertikar, Kartik
http://linked.open...mniOchranaPatentu
http://linked.open...avai/riv/vlastnik
http://linked.open...itiJinymSubjektem
http://linked.open...uzitiPatentuVzoru
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  • Schering-Plough
http://localhost/t...ganizacniJednotka
  • 14310
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