[go: up one dir, main page]

MA29634B1 - Heterocycles condenses avec la 1,4-dihydropyridine, procede pour preparer ceux-ci, utilisation et compositions contenant ceux-ci - Google Patents

Heterocycles condenses avec la 1,4-dihydropyridine, procede pour preparer ceux-ci, utilisation et compositions contenant ceux-ci

Info

Publication number
MA29634B1
MA29634B1 MA30580A MA30580A MA29634B1 MA 29634 B1 MA29634 B1 MA 29634B1 MA 30580 A MA30580 A MA 30580A MA 30580 A MA30580 A MA 30580A MA 29634 B1 MA29634 B1 MA 29634B1
Authority
MA
Morocco
Prior art keywords
same
dihydropyridine
preparing
compositions containing
heterocycles
Prior art date
Application number
MA30580A
Other languages
English (en)
Inventor
Jacques Mauger
Anil Nair
Nina Ma
Kirsten Bjergarde
Bruno Filoche-Romme
Odile Angouillant-Boniface
Serge Mignani
Cecile Combeau
Jean-Christophe Carry
Francois Clerc
Herve Minoux
Laurent Schio
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 MA29634B1 publication Critical patent/MA29634B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/12Heterocyclic 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
    • C07D471/14Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Dermatology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

La présente invention concerne des hétérocycles condensés avec la 1,4-dihydropyridine, un procédé pour préparer ceux-ci, l'utilisation et des compositions contenant ceux-ci. L'invention concerne des hétérocycles condensés avec la dihydropyridine substitués utiles pour le traitement d'une maladie cancéreuse, en particulier pour empêcher des cellules cancéreuses de se diviser. Ces composés agissent en tant qu'inhibiteurs des kinases Aurora A et/ou B.
MA30580A 2005-07-20 2008-01-16 Heterocycles condenses avec la 1,4-dihydropyridine, procede pour preparer ceux-ci, utilisation et compositions contenant ceux-ci MA29634B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP05291558A EP1746097B1 (fr) 2005-07-20 2005-07-20 Héterocyles à fusion1,4-dihydropyridineprocédé de préparation, utilisation et compositions de celles-ci

Publications (1)

Publication Number Publication Date
MA29634B1 true MA29634B1 (fr) 2008-07-01

Family

ID=35510894

Family Applications (1)

Application Number Title Priority Date Filing Date
MA30580A MA29634B1 (fr) 2005-07-20 2008-01-16 Heterocycles condenses avec la 1,4-dihydropyridine, procede pour preparer ceux-ci, utilisation et compositions contenant ceux-ci

Country Status (37)

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

Families Citing this family (14)

* 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.
TR201807023T4 (tr) 2012-05-15 2018-06-21 Novartis Ag Abl1, abl2 ve bcr- abl1 aktivitesinin inhibe edilmesi için benzamid türevleri.
EP2861576B1 (fr) 2012-05-15 2018-01-10 Novartis AG Dérivés de benzamide pour inhiber l'activité d'abl1, d'abl2 et de bcr-abl2
EP2858988B1 (fr) 2012-05-15 2018-02-28 Novartis AG Dérivés de benzamide pour inhiber l'activité d'abl1, d'abl2 et de bcr-abl2
KR102190848B1 (ko) 2012-05-15 2020-12-15 노파르티스 아게 Abl1, abl2 및 bcr-abl1의 활성을 억제하기 위한 화합물 및 조성물
CA2887701C (fr) 2012-10-12 2020-12-15 The Broad Institute, Inc. Inhibiteurs de gsk3 et leurs procedes d'utilisation
AU2015360416A1 (en) 2014-12-10 2017-06-08 Massachusetts Institute Of Technology Fused 1,3-azole derivatives useful for the treatment of proliferative diseases
CA2983314C (fr) 2015-04-30 2024-11-12 Memorial Sloan-Kettering Cancer Center Analogues de la mitragynine et leurs utilisations
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
WO2017124087A1 (fr) 2016-01-15 2017-07-20 Memorial Sloan-Kettering Cancer Center Composés antiparasitaires et leurs utilisations
CA3012846A1 (fr) 2016-02-16 2017-08-24 Massachusetts Institute Of Technology Liants de max comme modulateurs de myc et leurs utilisations
CA3058198A1 (fr) 2017-04-05 2018-10-11 The Broad Institute, Inc. Composes tricycliques en tant qu'inhibiteurs de glycogene synthase kinase 3 (gsk3) et leurs utilisations
WO2018209030A1 (fr) 2017-05-12 2018-11-15 Rti International Diarylurées en tant que modulateurs allostériques de cb1

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002508324A (ja) * 1997-12-13 2002-03-19 ブリストル−マイヤーズ スクイブ カンパニー サイクリン依存性キナーゼ阻害剤としてのピラゾロ[3,4−b]ピリジンの使用
JP2003529552A (ja) 1999-11-19 2003-10-07 アボット・ラボラトリーズ 三環性ジヒドロピリミジンカリウムチャンネル開口剤
US6538004B2 (en) 2000-03-03 2003-03-25 Abbott Laboratories Tricyclic dihydropyrazolone and tricyclic dihydroisoxazolone potassium channel openers
EP1259510B1 (fr) 2000-03-03 2004-06-02 Abbott Laboratories Agents ouvrant les canaux potassium a base de dihydropyrazolone tricyclique et de dihydroisoxazolone tricyclique
CN1630656A (zh) 2001-02-02 2005-06-22 三菱制药株式会社 二氢吡唑并吡啶化合物及其制药用途
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
BRPI0411364A (pt) * 2003-06-13 2006-07-25 Zentaris Gmbh compostos tendo atividade inibidora de fosfatidilinositol 3-cinase e métodos de uso dos mesmos

Also Published As

Publication number Publication date
EA016815B1 (ru) 2012-07-30
BRPI0614002A2 (pt) 2011-03-01
ATE521611T1 (de) 2011-09-15
TWI386411B (zh) 2013-02-21
US20080261969A1 (en) 2008-10-23
UA98928C2 (ru) 2012-07-10
CR9663A (es) 2008-02-21
DK1746097T3 (da) 2010-05-25
HN2008000088A (es) 2011-05-31
EP1746097B1 (fr) 2010-01-13
CN101243087B (zh) 2013-07-24
TNSN08020A1 (en) 2009-07-14
IL188861A0 (en) 2008-04-13
ATE455115T1 (de) 2010-01-15
EP1746097A1 (fr) 2007-01-24
AU2006273692B2 (en) 2012-11-22
KR20080026658A (ko) 2008-03-25
CA2615700C (fr) 2013-06-18
CY1109964T1 (el) 2014-09-10
NO20080831L (no) 2008-04-03
ECSP078062A (es) 2008-01-23
HRP20100195T1 (hr) 2010-05-31
CN101243087A (zh) 2008-08-13
PL1746097T3 (pl) 2010-06-30
PE20070212A1 (es) 2007-03-21
SI1746097T1 (sl) 2010-05-31
JP2009501778A (ja) 2009-01-22
US8163768B2 (en) 2012-04-24
TW200740812A (en) 2007-11-01
RS51351B (sr) 2011-02-28
EA200800374A1 (ru) 2008-08-29
UY29685A1 (es) 2007-02-28
AU2006273692A8 (en) 2012-12-13
AU2006273692A1 (en) 2007-02-01
AU2006273692B8 (en) 2012-12-13
PT1746097E (pt) 2010-04-15
MY148617A (en) 2013-05-15
NZ592766A (en) 2012-12-21
JP2013063987A (ja) 2013-04-11
EP1910366B1 (fr) 2011-08-24
ES2339676T3 (es) 2010-05-24
ZA200800542B (en) 2010-02-24
WO2007012972A2 (fr) 2007-02-01
KR101286796B1 (ko) 2013-07-17
MX2008000902A (es) 2008-03-26
CA2615700A1 (fr) 2007-02-01
AR054845A1 (es) 2007-07-18
PE20100718A1 (es) 2010-10-20
WO2007012972A3 (fr) 2007-04-05
DE602005018911D1 (de) 2010-03-04
EP1910366A2 (fr) 2008-04-16
DOP2006000175A (es) 2007-03-31

Similar Documents

Publication Publication Date Title
MA29634B1 (fr) Heterocycles condenses avec la 1,4-dihydropyridine, procede pour preparer ceux-ci, utilisation et compositions contenant ceux-ci
TN2009000450A1 (fr) Derives de pyridine
TNSN07022A1 (fr) Derives de pyridine
MXPA03011484A (es) Heteroarilos multiciclicos sustituidos con quinuclidinas para el tratamiento de enfermedades.
MA29652B1 (fr) 7-aza-indazoles substitues, compositions les contenant, procede de fabrication et utilisation
MA33450B1 (fr) Dérivés d'oxazine et leur utilisation en tant qu'inhibiteurs de bace pour le traitement de troubles neurologiques
BG108650A (en) Azabicyclic-substituted fused-heteroaryl compounds for the treatment of disease
MA47079A (fr) Composés amino-triazolopyidines et leur utilisation pour traiter le cancer
TN2011000316A1 (fr) Derives de sulfonamides
MA29926B1 (fr) Derives de pyrazine
EP1423111A4 (fr) Composes de liaison au recepteur nucleaire fxr nr1h4
EP1841426A4 (fr) Carbinamines tertiaires incluant des heterocycles substitues, agissant en tant qu'inhibiteurs de la beta-secretase et utilisees dans le traitement de la maladie d'alzheimer
MA29480B1 (fr) Pyrrolopyridines substitues, compositions les contenant, procede de fabrication et utilisation
MXPA04004464A (es) Compuestos de heteroarilo sustituido con azabiciclo para el tratamiento de enfermedades.
MY148479A (en) Piperidinyl-substituted isoquinolone derivatives
EP1819674A4 (fr) Aminopiperidines fusionnees utilisees comme inhibiteurs de la dipeptidyle peptidase-iv permettant de traiter ou de prevenir le diabete
TW200635918A (en) Pharmaceutical compounds
UA103198C2 (en) Squaramide derivatives as cxcr2 antagonists
MA30351B1 (fr) Composes de tetrahydropyridothienopyrimidine et leurs procedes d'utilisation
EP1673078A4 (fr) Inhibiteurs de type benzylether et benzylamino de beta-secretase pour le traitement de la maladie d'alzheimer
MA31586B1 (fr) Dérivés d'alcools alkyliques de 1-phényl-2-pyridinyle en tant qu'inhibiteurs de la phosphodiestérase
TNSN07167A1 (fr) Indoles substitues, compositions les contenant, procede de fabrication et utilisation
MY146644A (en) Cyclohexylamin isoquinolone derivatives
TN2010000130A1 (fr) Derives de quinazolinedione, leur preparation et leurs applications therapeutiques
MA30405B1 (fr) Derives de 4-benzylphtalazinone substitues en 2 en tant qu'antagonistes des histamines hl et h3