PL2144909T3 - [2,6]-Naftyrydyny użyteczne jako inhibitory kinaz białkowych - Google Patents

[2,6]-Naftyrydyny użyteczne jako inhibitory kinaz białkowych

Info

Publication number
PL2144909T3
PL2144909T3 PL08735845T PL08735845T PL2144909T3 PL 2144909 T3 PL2144909 T3 PL 2144909T3 PL 08735845 T PL08735845 T PL 08735845T PL 08735845 T PL08735845 T PL 08735845T PL 2144909 T3 PL2144909 T3 PL 2144909T3
Authority
PL
Poland
Prior art keywords
protein kinase
kinase inhibitors
inhibitors
naphthyridines
useful
Prior art date
Application number
PL08735845T
Other languages
English (en)
Inventor
Markus Rolf Dobler
Jr Charles Francis Jewell
Erik Meredith
Lauren G Monovich
Sarah Siska
Matt Anette Von
Eis Maurice Van
Taeyoung Yoon
Christoph Gaul
Michael Paul Capparelli
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of PL2144909T3 publication Critical patent/PL2144909T3/pl

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
    • A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10—Antioedematous agents; Diuretics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Diabetes (AREA)
  • Immunology (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Obesity (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Transplantation (AREA)
  • Child & Adolescent Psychology (AREA)
  • Endocrinology (AREA)
  • Hospice & Palliative Care (AREA)
  • Emergency Medicine (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Cephalosporin Compounds (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
PL08735845T 2007-04-06 2008-04-04 [2,6]-Naftyrydyny użyteczne jako inhibitory kinaz białkowych PL2144909T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US91051907P 2007-04-06 2007-04-06
EP08735845A EP2144909B1 (en) 2007-04-06 2008-04-04 [2,6]naphthyridines useful as protein kinase inhibitors
PCT/EP2008/054105 WO2008122615A1 (en) 2007-04-06 2008-04-04 [2, 6] naphthyridines useful as protein kinase inhibitors

Publications (1)

Publication Number Publication Date
PL2144909T3 true PL2144909T3 (pl) 2011-08-31

Family

ID=39590973

Family Applications (1)

Application Number Title Priority Date Filing Date
PL08735845T PL2144909T3 (pl) 2007-04-06 2008-04-04 [2,6]-Naftyrydyny użyteczne jako inhibitory kinaz białkowych

Country Status (16)

Country Link
US (1) US20120142685A1 (pl)
EP (1) EP2144909B1 (pl)
JP (1) JP2010523530A (pl)
KR (1) KR20100016291A (pl)
CN (1) CN101679418A (pl)
AT (1) ATE502940T1 (pl)
AU (1) AU2008235456B2 (pl)
BR (1) BRPI0810661A2 (pl)
CA (1) CA2682340A1 (pl)
DE (1) DE602008005729D1 (pl)
EA (1) EA016108B1 (pl)
ES (1) ES2363831T3 (pl)
MX (1) MX2009010697A (pl)
PL (1) PL2144909T3 (pl)
PT (1) PT2144909E (pl)
WO (1) WO2008122615A1 (pl)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA201100136A1 (ru) * 2008-06-13 2011-08-30 Новартис Аг 2,4'-бипиридинилы в качестве ингибиторов протеинкиназы d, применимые для лечения сердечной недостаточности и рака
WO2011082268A2 (en) * 2009-12-30 2011-07-07 Arqule Inc. Substituted naphthalenyl-pyrimidine compounds
EP2495244A1 (en) * 2011-03-02 2012-09-05 NovaSaid AB Piperidinyl benzoimidazole derivatives as mPGEs-1 inhibitors
ES2761587T3 (es) 2013-08-07 2020-05-20 Friedrich Miescher Institute For Biomedical Res Nuevo método de cribado para el tratamiento de la ataxia de Friedreich
PH12019500056B1 (en) 2016-07-12 2024-01-31 Revolution Medicines Inc 2,5-disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines as allosteric shp2 inhibitors
BR112019015075A2 (pt) 2017-01-23 2020-03-10 Revolution Medicines, Inc. Compostos bicíclicos como inibidores de shp2 alostéricos
SG11201906412SA (en) 2017-01-23 2019-08-27 Revolution Medicines Inc Pyridine compounds as allosteric shp2 inhibitors
JP7356414B2 (ja) 2017-09-07 2023-10-04 レヴォリューション・メディスンズ,インコーポレイテッド がんを治療するためのshp2阻害剤組成物および方法
SG11202002941WA (en) 2017-10-12 2020-04-29 Revolution Medicines Inc Pyridine, pyrazine, and triazine compounds as allosteric shp2 inhibitors
CA3084058A1 (en) 2017-12-15 2019-06-20 Revolution Medicines, Inc. Polycyclic compounds as allosteric shp2 inhibitors
KR102890015B1 (ko) 2020-06-30 2025-11-25 제넨테크, 인크. 치환된 페닐 또는 피리디닐 모이어티를 갖는 serd 트리시클릭 화합물의 제조 방법
AU2022284188A1 (en) * 2021-06-04 2023-11-30 Genentech, Inc. 2, 8-diazaspiro [4.5] decane compounds
KR20240130693A (ko) * 2021-12-16 2024-08-29 트랜스테라 사이언시즈 (난징), 인크. Cdk9 억제제 및 이의 용도

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3928367A (en) * 1969-04-14 1975-12-23 Schering Corp 1-Amino naphthyridines
US7550589B2 (en) * 2004-09-21 2009-06-23 Hoffman-La Roche Inc. 6-(2-alkyl-phenyl)-pyrido[2,3-D]pyrimidines useful as protein kinase inhibitors
WO2008122614A1 (en) * 2007-04-06 2008-10-16 Novartis Ag 2, 6-naphthyridine derivatives as protein kinase modulators

Also Published As

Publication number Publication date
JP2010523530A (ja) 2010-07-15
WO2008122615A1 (en) 2008-10-16
DE602008005729D1 (en) 2011-05-05
EP2144909A1 (en) 2010-01-20
CN101679418A (zh) 2010-03-24
US20120142685A1 (en) 2012-06-07
ATE502940T1 (de) 2011-04-15
ES2363831T3 (es) 2011-08-17
BRPI0810661A2 (pt) 2019-04-30
PT2144909E (pt) 2011-06-29
EA200901325A1 (ru) 2010-04-30
AU2008235456A1 (en) 2008-10-16
AU2008235456B2 (en) 2011-12-08
MX2009010697A (es) 2009-12-11
EA016108B1 (ru) 2012-02-28
CA2682340A1 (en) 2008-10-16
EP2144909B1 (en) 2011-03-23
KR20100016291A (ko) 2010-02-12

Similar Documents

Publication Publication Date Title
PT2144909E (pt) [2,6]naftiridinas úteis como inibidores de proteínas quinases
BRPI0720525B8 (pt) inibidores de mapk/erk quinase
TW200740761A (en) Histone deacetylase inhibitors
WO2010009139A3 (en) Imidazolylpyrimidine compounds as hdac and / or cdk inhibitors
TW200612913A (en) Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase
EA200701257A1 (ru) Пирролопиразолы в качестве сильнодействующих ингибиторов киназы
WO2010009155A3 (en) Fused heterocyclyc inhibitors of histone deacetylase and/or cyclin-dependent kinases
WO2010014930A3 (en) Piperidine derivatives as jak3 inhibitors
WO2008039359A3 (en) Bicyclic pyrimidine kinase inhibitors
MY148634A (en) Pyridazinone derivatives
MX2009004716A (es) Compuestos y composiciones en la forma de inhibidores de quinasa de proteina.
MY146989A (en) Kinase inhibitors
EA200970207A1 (ru) Соединения пиридо[2,3-d]пиримидинона и их применение в качестве pi3 ингибиторов
ATE479687T1 (de) Kinaseinhibitoren
MX2010009207A (es) Compuestos y composiciones heterociclicos como inhibidores de c-kit y pdgfr cinasa.
WO2006036395A3 (en) Inhibitors of akt activity
PL1981874T3 (pl) Pochodne aminofenylowe jako nowe inhibitory deacetylazy histonowej
MY148107A (en) Kinase inhibitor
WO2006122319A3 (en) Histone deacetylase inhibitors
MX2014014803A (es) Derivados de imidazo[1,2-b]piridazina como inhibidores de cinasa.
BRPI0809542A8 (pt) Compostos derivados de indol tendo atividade de inibição de cpla2, composição farmacêutica, e métodos de produção dos referidos compostos
GEP20166481B (en) (crystalline forms of hydrochloride salt of (4a-r, 9a-s)-1-(1h-benzoimidazole-5-carbonyl)-2, 3, 4, 4a, 9, 9a-hexa- hydro-1h-indeno [2, 1-b] pyridine-6-carbonitrile and their use as hsd 1 inhibitors
WO2008054956A3 (en) Kinase inhibitors
EA200700143A1 (ru) Производные замещенного пропенилпиперазина в качестве новых ингибиторов гистондеацетилазы
WO2009129401A8 (en) Kinase inhibitors