PE20100718A1 - Derivados triciclicos de 1, 4-dihidropiridina [b, e]-condensados como inhibidores de aurora quinasas - Google Patents

Derivados triciclicos de 1, 4-dihidropiridina [b, e]-condensados como inhibidores de aurora quinasas

Info

Publication number
PE20100718A1
PE20100718A1 PE2010000153A PE2010000153A PE20100718A1 PE 20100718 A1 PE20100718 A1 PE 20100718A1 PE 2010000153 A PE2010000153 A PE 2010000153A PE 2010000153 A PE2010000153 A PE 2010000153A PE 20100718 A1 PE20100718 A1 PE 20100718A1
Authority
PE
Peru
Prior art keywords
naphthyridin
ona
hexahydro
phenyl
dihydropyridine
Prior art date
Application number
PE2010000153A
Other languages
English (en)
Inventor
Jacques Mauger
Anil Nair
Nina Ma
Kirsten Bjergarde
Bruno Filoche-Romme
Odile Angouillant-Boniface
Serge Mignani
Original Assignee
Aventis Pharma Sa
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 Aventis Pharma Sa filed Critical Aventis Pharma Sa
Publication of PE20100718A1 publication Critical patent/PE20100718A1/es

Links

Classifications

    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07D471/12—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 three hetero rings
    • C07D471/14—Ortho-condensed systems

Abstract

SE REFIERE A COMPUESTOS DE FORMULA (I) DONDE R1 ES H O METILO; R2 ES ARILO O HETEROARILO SUSTITUIDOS; R3 ES H O R4; X ES N O CR7, DONDE R4 Y R7 SON CADA UNO R8, -COOR8, COR8 O CONHR8, EN DONDE R8 ES H, ALQUILO, CICLOALQUILO, ARILO, ENTRE OTROS; Y, Y' E Y'' SON CADA UNO CH2, C=O, O, S, NH, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 4-(4-HIDROXI-3-METIL-FENIL)-2,4,6,7,8,9-HEXAHIDRO-PIRAZOLO[3,4-b]-1,7-NAFTIRIDIN-5-ONA, 4-[5-(4-CLORO-FENIL)-FURAN-2-IL]-2,4,6,7,8,9-HEXAHIDRO-PIRAZOLO[3,4-b]-1,7-NAFTIRIDIN-5-ONA, 4-[3-(4-CLORO-FENOXI)-FENIL]-2,4,6,7,8,9-HEXAHIDRO-PIRAZOLO[3,4-b]-1,7-NAFTIRIDIN-5-ONA, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON MODULADORES DE LAS QUINASAS AURORA A Y B SIENDO UTILES EN EL TRATAMIENTO DE CANCER DE MAMA, CANCER DE COLON, MELANOMA, LEUCEMIA MIELOIDE AGUDA
PE2010000153A 2005-07-20 2006-07-18 Derivados triciclicos de 1, 4-dihidropiridina [b, e]-condensados como inhibidores de aurora quinasas PE20100718A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP05291558A EP1746097B1 (en) 2005-07-20 2005-07-20 1,4-dihydropyridine-fused heterocycles, process for preparing the same, use and compositions containing them

Publications (1)

Publication Number Publication Date
PE20100718A1 true PE20100718A1 (es) 2010-10-20

Family

ID=35510894

Family Applications (2)

Application Number Title Priority Date Filing Date
PE2010000153A PE20100718A1 (es) 2005-07-20 2006-07-18 Derivados triciclicos de 1, 4-dihidropiridina [b, e]-condensados como inhibidores de aurora quinasas
PE2006000862A PE20070212A1 (es) 2005-07-20 2006-07-18 Heterociclos de 1,4-dihidropiridina-condensados, procesos para preparar los mismos, uso y composiciones que los contienen

Family Applications After (1)

Application Number Title Priority Date Filing Date
PE2006000862A PE20070212A1 (es) 2005-07-20 2006-07-18 Heterociclos de 1,4-dihidropiridina-condensados, procesos para preparar los mismos, uso y composiciones que los contienen

Country Status (37)

Country Link
US (1) US8163768B2 (es)
EP (2) EP1746097B1 (es)
JP (2) JP2009501778A (es)
KR (1) KR101286796B1 (es)
CN (1) CN101243087B (es)
AR (1) AR054845A1 (es)
AT (2) ATE455115T1 (es)
AU (1) AU2006273692B8 (es)
BR (1) BRPI0614002A2 (es)
CA (1) CA2615700C (es)
CR (1) CR9663A (es)
CY (1) CY1109964T1 (es)
DE (1) DE602005018911D1 (es)
DK (1) DK1746097T3 (es)
DO (1) DOP2006000175A (es)
EA (1) EA016815B1 (es)
EC (1) ECSP078062A (es)
ES (1) ES2339676T3 (es)
HN (1) HN2008000088A (es)
HR (1) HRP20100195T1 (es)
IL (1) IL188861A0 (es)
MA (1) MA29634B1 (es)
MX (1) MX2008000902A (es)
MY (1) MY148617A (es)
NO (1) NO20080831L (es)
NZ (1) NZ592766A (es)
PE (2) PE20100718A1 (es)
PL (1) PL1746097T3 (es)
PT (1) PT1746097E (es)
RS (1) RS51351B (es)
SI (1) SI1746097T1 (es)
TN (1) TNSN08020A1 (es)
TW (1) TWI386411B (es)
UA (1) UA98928C2 (es)
UY (1) UY29685A1 (es)
WO (1) WO2007012972A2 (es)
ZA (1) ZA200800542B (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2945535B1 (fr) * 2009-05-18 2011-06-10 Sanofi Aventis Compose anticancereux et composition pharmaceutique le contenant
FR2967413A1 (fr) * 2010-11-17 2012-05-18 Sanofi Aventis Compose 8-oxo-9-[3-(1h-benzimidazol-2-yloxy)-phenyl]-4,5,6,7,8,9-hexahydro-2h-pyrrolo[3,4-b]quinoline-3-carboxylate d'ethyle, sel, forme cristalline, co-cristal, formulation, procedes de preparation, application a titre de medicaments, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteur des kinases aurora.
CA2871715A1 (en) 2012-05-15 2013-11-21 Novartis Ag Benzamide derivatives for inhibiting the activity of abl1, abl2 and bcr-abl1
CA2871332A1 (en) 2012-05-15 2013-11-21 Novartis Ag Benzamide derivatives for inhibiting the activity of abl1, abl2 and bcr-abl1
US9315489B2 (en) 2012-05-15 2016-04-19 Novartis Ag Compounds and compositions for inhibiting the activity of ABL1, ABL2 and BCR-ABL1
DK2861579T5 (da) 2012-05-15 2022-10-24 Novartis Ag Benzamidderivater til at hæmme aktiviteten af ABL1, ABL2 og BCR-ABL1
JP6321662B2 (ja) 2012-10-12 2018-05-09 ザ ブロード インスティテュート, インコーポレーテッドThe Broad Institute, Inc. Ｇｓｋ３阻害剤およびその使用の方法
AU2015360416A1 (en) 2014-12-10 2017-06-08 Massachusetts Institute Of Technology Fused 1,3-azole derivatives useful for the treatment of proliferative diseases
EP4212532A3 (en) 2015-04-30 2023-09-27 Memorial Sloan Kettering Cancer Center Mitragynine analogs and uses thereof
RU2619932C1 (ru) * 2015-11-25 2017-05-22 федеральное государственное бюджетное образовательное учреждение высшего образования "Воронежский государственный университет" (ФГБОУ ВО "ВГУ") ЗАМЕЩЕННЫЕ ПИРАЗОЛО[1,5-а]ПИРИДО[3,4-е]ПИРИМИДИНЫ И ИХ ИСПОЛЬЗОВАНИЕ В КАЧЕСТВЕ ИНГИБИТОРОВ ПРОТЕИНКИНАЗ
US11180492B2 (en) 2016-01-15 2021-11-23 University Of Central Florida Research Foundation, Inc. Anti-parasitic compounds and uses thereof
EP3416950A1 (en) 2016-02-16 2018-12-26 Massachusetts Institute of Technology Max binders as myc modulators and uses thereof
JP7157075B2 (ja) 2017-04-05 2022-10-19 ザ ブロード インスティテュート，インコーポレーテッド グリコーゲンシンターゼキナーゼ３（ｇｓｋ３）インヒビターとしての三環式化合物およびそれらの使用

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE355841T1 (de) * 1997-12-13 2007-03-15 Bristol Myers Squibb Co Verwendung von pyrazolo ( 3,4-b) pyridin als cyclin-abhängige kinase hemmer
CA2391291A1 (en) 1999-11-19 2001-05-25 Abbott Laboratories Tricyclic dihydropyrimidine potassium channel openers
MXPA02008615A (es) 2000-03-03 2003-04-14 Abbott Lab Abridores de canales de potasio de dihidropirazolona triciclica y dihidroisoxazolona triciclica.
US6538004B2 (en) 2000-03-03 2003-03-25 Abbott Laboratories Tricyclic dihydropyrazolone and tricyclic dihydroisoxazolone potassium channel openers
KR20030076650A (ko) 2001-02-02 2003-09-26 미쯔비시 웰 파마 가부시키가이샤 디하이드로피라졸로피리딘 화합물 및 그의 약학적 용도
FR2823854A1 (fr) 2001-04-18 2002-10-25 Centre Nat Rech Scient Nouveau procede de criblage d'inhibiteurs de la liaison entre la proteine oxyde nitrique synthase neuronale et la proteine inhibitrice de l'oxyde nitrique synthase neuronale
FR2825091B1 (fr) * 2001-05-23 2003-07-04 Servier Lab Nouveaux derives tricycliques de dihydro-quinnoleines, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
US7037902B2 (en) * 2002-07-03 2006-05-02 Receptron, Inc. Affinity small molecules for the EPO receptor
SE0301371D0 (sv) 2003-05-09 2003-05-09 Astrazeneca Ab New Compounds
JP2007500249A (ja) * 2003-06-13 2007-01-11 ツェンタリス ゲゼルシャフト ミット ベシュレンクテル ハフツング ホスファチジルイノシトール３−キナーゼ阻害活性を有する化合物及びその使用方法

Also Published As

Publication number Publication date
KR20080026658A (ko) 2008-03-25
MA29634B1 (fr) 2008-07-01
SI1746097T1 (sl) 2010-05-31
ECSP078062A (es) 2008-01-23
NZ592766A (en) 2012-12-21
DOP2006000175A (es) 2007-03-31
MX2008000902A (es) 2008-03-26
CA2615700C (en) 2013-06-18
CY1109964T1 (el) 2014-09-10
PT1746097E (pt) 2010-04-15
ES2339676T3 (es) 2010-05-24
ATE455115T1 (de) 2010-01-15
EA016815B1 (ru) 2012-07-30
CR9663A (es) 2008-02-21
WO2007012972A2 (en) 2007-02-01
AU2006273692B2 (en) 2012-11-22
EA200800374A1 (ru) 2008-08-29
TWI386411B (zh) 2013-02-21
ZA200800542B (en) 2010-02-24
UY29685A1 (es) 2007-02-28
CN101243087A (zh) 2008-08-13
US8163768B2 (en) 2012-04-24
AR054845A1 (es) 2007-07-18
BRPI0614002A2 (pt) 2011-03-01
TNSN08020A1 (en) 2009-07-14
ATE521611T1 (de) 2011-09-15
KR101286796B1 (ko) 2013-07-17
CN101243087B (zh) 2013-07-24
NO20080831L (no) 2008-04-03
DE602005018911D1 (de) 2010-03-04
EP1910366A2 (en) 2008-04-16
PE20070212A1 (es) 2007-03-21
EP1910366B1 (en) 2011-08-24
EP1746097A1 (en) 2007-01-24
UA98928C2 (ru) 2012-07-10
AU2006273692A8 (en) 2012-12-13
JP2013063987A (ja) 2013-04-11
RS51351B (en) 2011-02-28
HRP20100195T1 (hr) 2010-05-31
HN2008000088A (es) 2011-05-31
CA2615700A1 (en) 2007-02-01
EP1746097B1 (en) 2010-01-13
US20080261969A1 (en) 2008-10-23
IL188861A0 (en) 2008-04-13
AU2006273692B8 (en) 2012-12-13
WO2007012972A3 (en) 2007-04-05
AU2006273692A1 (en) 2007-02-01
DK1746097T3 (da) 2010-05-25
PL1746097T3 (pl) 2010-06-30
TW200740812A (en) 2007-11-01
MY148617A (en) 2013-05-15
JP2009501778A (ja) 2009-01-22

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