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PE20061198A1 - Derivados de pirazol como inhibidores de cdk y gsk - Google Patents

Derivados de pirazol como inhibidores de cdk y gsk

Info

Publication number
PE20061198A1
PE20061198A1 PE2006000081A PE2006000081A PE20061198A1 PE 20061198 A1 PE20061198 A1 PE 20061198A1 PE 2006000081 A PE2006000081 A PE 2006000081A PE 2006000081 A PE2006000081 A PE 2006000081A PE 20061198 A1 PE20061198 A1 PE 20061198A1
Authority
PE
Peru
Prior art keywords
piperidin
ester
amino
acid
pirazol
Prior art date
Application number
PE2006000081A
Other languages
English (en)
Inventor
Valerio Berdini
Eva Figueroa Navarro
Gary Trewartha
Paul Graham Wyatt
Theresa Rachel Phillips
Andrew James Woodhead
Adrian Liam Gill
Michael Alistair O'brien
Original Assignee
Astex Therapeutics Ltd
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
Priority claimed from GB0501480A external-priority patent/GB0501480D0/en
Priority claimed from GB0501748A external-priority patent/GB0501748D0/en
Application filed by Astex Therapeutics Ltd filed Critical Astex Therapeutics Ltd
Publication of PE20061198A1 publication Critical patent/PE20061198A1/es

Links

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic 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
    • C07D231/14Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • C07D231/14Heterocyclic 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
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    • 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
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    • C07D405/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
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    • C07D417/14Heterocyclic 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 three or more hetero rings

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Abstract

SE REFIERE A UN COMPUESTO DE FORMULA I, DONDE R1 ES 2,6-DICLOROFENILO, 2,6-DIFLUOROFENILO, FENILO 2,3,6-TRISUSTITUIDO, ENTRE OTROS; R2a Y R2b SON CADA UNO H, METILO; R3 ES DE PREFERENCIA ISOBUTIL-ESTER DEL ACIDO PIPERIDIN-1-CARBOXILICO, 2-MORFOLIN-4-IL-ETIL-ESTER DEL ACIDO PIPERIDIN-1-CARBOXILICO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: ISOBUTIL-ESTER DEL ACIDO 4-{[4-(2,6-DICLORO-BENZOIL-AMINO)-1H-PIRAZOL-3-CARBONIL]-AMINO}-PIPERIDIN-1-CARBOXILICO; CICLOPROPIL-METIL-ESTER DEL ACIDO 4-{[4-(2,6-DICLORO-BENZOIL-AMINO)-1H-PIRAZOL-3-CARBONIL]-AMINO}-PIPERIDIN-1-CARBOXILICO; ACETOXI-METIL-ESTER DEL ACIDO 4-{[4-(2,6-DICLORO-BENZOIL-AMINO)-1H-PIRAZOL-3-CARBONIL]-AMINO}-PIPERIDIN-1-CARBOXILICO; ENTRE OTROS. REFERIDA TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE QUINASAS DEPENDIENTES DE CICLINA (CDK) Y QUINASAS DE SINTASA DE GLICOGENO (GSK) UTILES EN EL TRATAMIENTO DE TRASTORNOS PROLIFERATIVOS, CONDICIONES VIRALES, ENFERMEDADES AUTOINMUNES, ENTRE OTROS
PE2006000081A 2005-01-21 2006-01-20 Derivados de pirazol como inhibidores de cdk y gsk PE20061198A1 (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US64621705P 2005-01-21 2005-01-21
GB0501480A GB0501480D0 (en) 2005-01-22 2005-01-22 Pharmaceutical compounds
GB0501748A GB0501748D0 (en) 2005-01-27 2005-01-27 Pharmaceutical compounds
US65133905P 2005-02-09 2005-02-09

Publications (1)

Publication Number Publication Date
PE20061198A1 true PE20061198A1 (es) 2006-12-19

Family

ID=35967182

Family Applications (3)

Application Number Title Priority Date Filing Date
PE2006000081A PE20061198A1 (es) 2005-01-21 2006-01-20 Derivados de pirazol como inhibidores de cdk y gsk
PE2006000079A PE20060876A1 (es) 2005-01-21 2006-01-20 Derivados de pirazol como inhibidores de quinasa dependientes de ciclina
PE2006000080A PE20061073A1 (es) 2005-01-21 2006-01-20 Compuestos derivados de piperidinilamida como agentes inhibidores de quinasas

Family Applications After (2)

Application Number Title Priority Date Filing Date
PE2006000079A PE20060876A1 (es) 2005-01-21 2006-01-20 Derivados de pirazol como inhibidores de quinasa dependientes de ciclina
PE2006000080A PE20061073A1 (es) 2005-01-21 2006-01-20 Compuestos derivados de piperidinilamida como agentes inhibidores de quinasas

Country Status (15)

Country Link
US (2) US20080306069A1 (es)
EP (3) EP1853584A1 (es)
JP (3) JP2008528467A (es)
KR (3) KR20070098928A (es)
AR (3) AR052660A1 (es)
AU (3) AU2006207311A1 (es)
BR (2) BRPI0606107A2 (es)
CA (3) CA2593656A1 (es)
IL (3) IL184499A0 (es)
MA (3) MA29255B1 (es)
MX (3) MX2007008782A (es)
NO (3) NO20073955L (es)
PE (3) PE20061198A1 (es)
TN (3) TNSN07279A1 (es)
WO (3) WO2006077419A1 (es)

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* Cited by examiner, † Cited by third party
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TW200533657A (en) 2004-02-17 2005-10-16 Esteve Labor Dr Substituted pyrazoline compounds, their preparation and use as medicaments
AR052660A1 (es) * 2005-01-21 2007-03-28 Astex Therapeutics Ltd Derivados de pirazol para inhibir la cdk's y gsk's
AR054425A1 (es) 2005-01-21 2007-06-27 Astex Therapeutics Ltd Sales de adicion de piperidin 4-il- amida de acido 4-(2,6-dicloro-benzoilamino) 1h-pirazol-3-carboxilico.
RU2007131101A (ru) * 2005-01-21 2009-02-27 Астекс Терапьютикс Лимитед (Gb) Комбинации пиразольных ингибиторов киназы и других средств против злокачественных новообразований
JP5475234B2 (ja) * 2005-01-21 2014-04-16 アステックス・セラピューティクス・リミテッド 医薬化合物
US8404718B2 (en) 2005-01-21 2013-03-26 Astex Therapeutics Limited Combinations of pyrazole kinase inhibitors
ES2552338T3 (es) * 2005-01-21 2015-11-27 Astex Therapeutics Limited Compuestos farmacéuticos
US20080139620A1 (en) * 2005-01-21 2008-06-12 Astex Therapeutics Limited Pyrazole Derivatives For The Inhibition Of Cdk's And Gsk's
EP1862478B1 (en) * 2005-03-03 2012-01-25 Mitsubishi Rayon Co., Ltd. Polymer particle, resin composition containing same, and molded body
EP1743892A1 (en) 2005-07-15 2007-01-17 Laboratorios del Dr. Esteve S.A. Substituted pyrazoline compounds, their preparation and use as medicaments
EP1743890A1 (en) 2005-07-15 2007-01-17 Laboratorios Del Dr. Esteve, S.A. 4,5-Dihydro-1H-pyrazole derivatives, their preparation and use as medicaments
US7897589B2 (en) 2005-07-15 2011-03-01 Laboratorios Del Dr. Esteve, S.A. Substituted pyrazoline compounds, their preparation and use as medicaments
EP2027109A1 (en) * 2006-05-05 2009-02-25 Astex Therapeutics Limited 4- (2, 6-dichloro-benzoylamino) -1h-pyrazole-s-carboxylic acid (1-methanesulph0nyl-piperidin-4-yl) -amide for the treatment of cancer
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