MA30018B1 - Derives de 1-orthofluorophenyl substitues 1, 2, 5-thiazolidinedione utilises comme inhibiteurs de la ptp-ase - Google Patents

Derives de 1-orthofluorophenyl substitues 1, 2, 5-thiazolidinedione utilises comme inhibiteurs de la ptp-ase

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Publication number
MA30018B1
MA30018B1 MA30986A MA30986A MA30018B1 MA 30018 B1 MA30018 B1 MA 30018B1 MA 30986 A MA30986 A MA 30986A MA 30986 A MA30986 A MA 30986A MA 30018 B1 MA30018 B1 MA 30018B1
Authority
MA
Morocco
Prior art keywords
compounds
diseases
inhibitors
ptpases
formula
Prior art date
Application number
MA30986A
Other languages
English (en)
Inventor
David Barnes
Gary Mark Coppola
Travis Stams
Sidney Wolf Topiol
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.)
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37903424&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA30018(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of MA30018B1 publication Critical patent/MA30018B1/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic 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
    • C07D417/02—Heterocyclic 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 two hetero rings
    • C07D417/10—Heterocyclic 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 two hetero rings linked by a carbon chain containing aromatic rings
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/433—Thidiazoles
    • A—HUMAN NECESSITIES
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    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • 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
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    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01—Five-membered rings
    • C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/10—1,2,5-Thiadiazoles; Hydrogenated 1,2,5-thiadiazoles

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
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  • Life Sciences & Earth Sciences (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Cardiology (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Psychology (AREA)
  • Hospice & Palliative Care (AREA)
  • Vascular Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Oncology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Psychiatry (AREA)
  • Communicable Diseases (AREA)
  • Ophthalmology & Optometry (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pulmonology (AREA)

Abstract

Les composés de formule : sont des inhibiteurs des protéine-tyrosine-phosphatases (PTPases) et peuvent ainsi être utilisés pour le traitement d'affections induites par l'activité des PTPases. Les composés de la présente invention peuvent également être utilisés comme inhibiteurs d'autres enzymes caractérisées par une région de liaison à la phosphotyrosine, comme le domaine SH2. Par conséquent, les composés de formule (I) peuvent être utilisés pour la prévention et/ou le traitement d'une résistance à l'insuline associée à l'obésité, d'une intolérance au glucose, du diabète sucré, de l'hypertension et de maladies ischémiques des gros et des petits vaisseaux sanguins, d'affections qui accompagnent le diabète de type 2, y compris une hyperlipidémie, une hypertriglycéridémie, l'athérosclérose, une resténose vasculaire, le syndrome du côlon irritable, la pancréatite, des tumeurs et carcinomes à cellules adipeuses, tels que le liposarcome, une dyslipidémie et d'autres affections dans lesquelles est indiquée une résistance à l'insuline. De plus, les composés de la présente invention peuvent être utilisés pour traiter et/ou prévenir un cancer, l'ostéoporose, des maladies neurodégénératives et infectieuses, et des maladies impliquant une inflammation et le système immunitaire.
MA30986A 2005-12-08 2008-06-02 Derives de 1-orthofluorophenyl substitues 1, 2, 5-thiazolidinedione utilises comme inhibiteurs de la ptp-ase MA30018B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US74849205P 2005-12-08 2005-12-08

Publications (1)

Publication Number Publication Date
MA30018B1 true MA30018B1 (fr) 2008-12-01

Family

ID=37903424

Family Applications (1)

Application Number Title Priority Date Filing Date
MA30986A MA30018B1 (fr) 2005-12-08 2008-06-02 Derives de 1-orthofluorophenyl substitues 1, 2, 5-thiazolidinedione utilises comme inhibiteurs de la ptp-ase

Country Status (23)

Country Link
US (1) US8252820B2 (fr)
EP (1) EP1963293A1 (fr)
JP (1) JP2009518419A (fr)
KR (1) KR20080075218A (fr)
CN (1) CN101336235A (fr)
AR (1) AR058285A1 (fr)
AU (1) AU2006321902B2 (fr)
BR (1) BRPI0619567A2 (fr)
CA (1) CA2631007A1 (fr)
CR (1) CR10047A (fr)
EC (1) ECSP088509A (fr)
GT (1) GT200800093A (fr)
IL (1) IL191711A0 (fr)
MA (1) MA30018B1 (fr)
NO (1) NO20083030L (fr)
NZ (1) NZ568663A (fr)
PE (2) PE20100470A1 (fr)
RU (1) RU2008127262A (fr)
TN (1) TNSN08248A1 (fr)
TW (1) TW200800928A (fr)
UA (1) UA94921C2 (fr)
WO (1) WO2007067612A1 (fr)
ZA (1) ZA200804489B (fr)

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BRPI0619547A2 (pt) * 2005-12-08 2011-10-04 Novartis Ag 1,1,3-trioxo-1,2,5-tiadiazolidinas, composição farmacêutica e uso das mesmas
AU2007233251A1 (en) 2006-03-31 2007-10-11 Novartis Ag Thiadiazolidinone inhibitors of PTPase
DE102007015169A1 (de) * 2007-03-27 2008-10-02 Universität des Saarlandes Campus Saarbrücken 17Beta-Hydroxysteroid-Dehydrogenase-Typ1-Inhibitoren zur Behandlung hormonabhängiger Erkrankungen
EP2025674A1 (fr) 2007-08-15 2009-02-18 sanofi-aventis Tetrahydronaphthaline substituée, son procédé de fabrication et son utilisation en tant que médicament
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US8710050B2 (en) 2011-03-08 2014-04-29 Sanofi Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
EP2683704B1 (fr) 2011-03-08 2014-12-17 Sanofi Dérivés oxathiazine ramifiés, procédé pour leur préparation, utilisation en tant que médicament, agents pharmaceutiques contenant ces dérivés et leur utilisation
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CN116802177A (zh) 2021-01-27 2023-09-22 巴斯夫欧洲公司 二氨基三嗪化合物
CN117279913A (zh) * 2021-03-11 2023-12-22 金橘生物科技公司 杂环化合物及其用途
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CN119790052A (zh) * 2022-09-13 2025-04-08 金橘生物科技公司 苯并稠合的n-杂环及其用途
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US8252820B2 (en) 2012-08-28
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