BRPI0508364A - derivados de 4-benzimidazol-2-ilpiridazin-3-ona - Google Patents

derivados de 4-benzimidazol-2-ilpiridazin-3-ona

Info

Publication number
BRPI0508364A
BRPI0508364A BRPI0508364-8A BRPI0508364A BRPI0508364A BR PI0508364 A BRPI0508364 A BR PI0508364A BR PI0508364 A BRPI0508364 A BR PI0508364A BR PI0508364 A BRPI0508364 A BR PI0508364A
Authority
BR
Brazil
Prior art keywords
benzimidazol
compounds
derivatives
ylpyridazin
kinase inhibitors
Prior art date
Application number
BRPI0508364-8A
Other languages
English (en)
Inventor
Swen Hoelder
Karl Schoenafinger
David William Will
Hans Matter
Guenther Mueller
Cecile Combeau
Christine Delaisi
Anke Steinmetz
Ingrid Sassoon
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 BRPI0508364A publication Critical patent/BRPI0508364A/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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 containing three or more hetero rings
    • 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
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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 containing two hetero rings
    • C07D401/04—Heterocyclic 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 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

DERIVADOS DE 4-BENZIMIDAZOL-2-ILPIRIDAZIN-3-ONA. A presente invenção refere-se a compostos da fórmula geral (l), onde a definição dos substituintes A, B, D, E, R¬ 1¬ e R¬ 2¬ são detalhadas na descrição, e os seus sais fisioligicamente tolerados, a um processo para a preparação destes compostos e a seu uso como produtos farmacêuticos. Estes compostos são inibidores de quinase, em particular inibidores da quinase CDK2 (quinase 2 dependente de ciclina).
BRPI0508364-8A 2004-03-02 2005-02-18 derivados de 4-benzimidazol-2-ilpiridazin-3-ona BRPI0508364A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102004010207A DE102004010207A1 (de) 2004-03-02 2004-03-02 Neue 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate
PCT/EP2005/002569 WO2005085231A1 (en) 2004-03-02 2005-02-18 Novel 4-benzimidazol-2-ylpyridazin-3-one derivatives

Publications (1)

Publication Number Publication Date
BRPI0508364A true BRPI0508364A (pt) 2007-07-24

Family

ID=34853913

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0508364-8A BRPI0508364A (pt) 2004-03-02 2005-02-18 derivados de 4-benzimidazol-2-ilpiridazin-3-ona

Country Status (14)

Country Link
US (2) US7470689B2 (pt)
EP (1) EP1723137A1 (pt)
JP (1) JP4792455B2 (pt)
KR (1) KR20070008582A (pt)
CN (1) CN101061108A (pt)
AR (1) AR047987A1 (pt)
AU (1) AU2005219563A1 (pt)
BR (1) BRPI0508364A (pt)
CA (1) CA2555161A1 (pt)
DE (1) DE102004010207A1 (pt)
IL (1) IL177204A0 (pt)
TW (1) TW200538452A (pt)
UY (1) UY28783A1 (pt)
WO (1) WO2005085231A1 (pt)

Cited By (1)

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WO2013075199A1 (pt) 2011-11-25 2013-05-30 Universidade Federal De Santa Catarina "compostos acil-hidrazonas e oxadiazóis, composições farmacêuticas compreendendo os mesmos e seus usos

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DE102004010194A1 (de) * 2004-03-02 2005-10-13 Aventis Pharma Deutschland Gmbh 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate, ihre Herstellung und Verwendung in Arzneimitteln
EP1604988A1 (en) * 2004-05-18 2005-12-14 Sanofi-Aventis Deutschland GmbH Pyridazinone derivatives, methods for producing them and their use as pharmaceuticals
EP1598348A1 (en) 2004-05-18 2005-11-23 Aventis Pharma Deutschland GmbH Novel pyridazinone derivatives as inhibitors of CDK2
US8629147B2 (en) 2005-11-03 2014-01-14 Chembridge Corporation Heterocyclic compounds useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders
EP2069312B1 (en) * 2006-07-25 2012-11-07 Cephalon, Inc. Pyridizinone derivatives
CN101538245B (zh) 2008-03-18 2011-02-16 中国科学院上海药物研究所 一类哒嗪酮类化合物及其制备方法和制备药物的用途
US9212146B2 (en) 2008-03-18 2015-12-15 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Substituted pyridazinones for the treatment of tumors
US20150051208A1 (en) * 2013-08-14 2015-02-19 Boehringer Ingelheim International Gmbh Pyridinones
WO2016057931A1 (en) 2014-10-10 2016-04-14 The Research Foundation For The State University Of New York Trifluoromethoxylation of arenes via intramolecular trifluoromethoxy group migration
CA2982664A1 (en) * 2015-04-16 2016-10-20 Merck Patent Gmbh 3-(1h-benzimidazol-2-yl)-1h-pyridin-2-one derivatives
WO2017151409A1 (en) 2016-02-29 2017-09-08 University Of Florida Research Foundation, Incorporated Chemotherapeutic methods
CN111393374A (zh) * 2020-05-08 2020-07-10 张建蒙 氧代二氢哒嗪类衍生物及其在抗肿瘤药物中的应用
CN115650968B (zh) * 2022-12-27 2023-03-21 英矽智能科技(上海)有限公司 作为cdk选择性抑制剂的新型哒嗪酮化合物

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US6727102B1 (en) * 1997-06-20 2004-04-27 Leuven Research & Development Vzw Assays, antibodies, and standards for detection of oxidized and MDA-modified low density lipoproteins
CA2294548A1 (en) * 1997-08-22 1999-03-04 Abbott Laboratories Pyridazinones as prostaglandin endoperoxide h synthase biosynthesis inhibitors
TWI241295B (en) 1998-03-02 2005-10-11 Kowa Co Pyridazine derivative and medicine containing the same as effect component
PL200674B1 (pl) * 1999-06-28 2009-01-30 Janssen Pharmaceutica Nv Pochodna benzoimidazolu lub imidazopirydyny i sposób jej otrzymywania oraz kompozycja farmaceutyczna i sposób jej otrzymywania
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US7232897B2 (en) * 2001-04-24 2007-06-19 Harvard University, President And Fellows Of Harvard College Compositions and methods for modulating NH2-terminal Jun Kinase activity
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EP1298125A1 (en) 2001-09-26 2003-04-02 Aventis Pharma S.A. Substituted benzimidazole compounds and their use for the treatment of cancer
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DE102004010194A1 (de) 2004-03-02 2005-10-13 Aventis Pharma Deutschland Gmbh 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate, ihre Herstellung und Verwendung in Arzneimitteln
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BRPI0609685A2 (pt) * 2005-04-06 2010-04-20 Hoffmann La Roche compostos, processo para a sua manufatura, composições farmacêuticas que os compreendem, método para tratamento e/ou profilaxia de enfermidades que estão associados com a modulação de receptores de cb1, e utilização dos mesmos
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013075199A1 (pt) 2011-11-25 2013-05-30 Universidade Federal De Santa Catarina "compostos acil-hidrazonas e oxadiazóis, composições farmacêuticas compreendendo os mesmos e seus usos

Also Published As

Publication number Publication date
US20070173503A1 (en) 2007-07-26
IL177204A0 (en) 2006-12-10
AR047987A1 (es) 2006-03-15
AU2005219563A1 (en) 2005-09-15
JP2007531712A (ja) 2007-11-08
EP1723137A1 (en) 2006-11-22
US7470689B2 (en) 2008-12-30
UY28783A1 (es) 2005-09-30
US20090042880A1 (en) 2009-02-12
WO2005085231A1 (en) 2005-09-15
DE102004010207A1 (de) 2005-09-15
JP4792455B2 (ja) 2011-10-12
CN101061108A (zh) 2007-10-24
US7754713B2 (en) 2010-07-13
TW200538452A (en) 2005-12-01
KR20070008582A (ko) 2007-01-17
CA2555161A1 (en) 2005-09-15

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Legal Events

Date Code Title Description
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 6A ANUIDADE(S).

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: REFERENTE A 8.6 NA RPI 2099 DE 29/03/2011.