ATE445604T1 - Neue 2,6-diaminopyridin-3-on-derivate - Google Patents

Neue 2,6-diaminopyridin-3-on-derivate

Info

Publication number
ATE445604T1
ATE445604T1 AT05759728T AT05759728T ATE445604T1 AT E445604 T1 ATE445604 T1 AT E445604T1 AT 05759728 T AT05759728 T AT 05759728T AT 05759728 T AT05759728 T AT 05759728T AT E445604 T1 ATE445604 T1 AT E445604T1
Authority
AT
Austria
Prior art keywords
diaminopyridine
derivatives
new
Prior art date
Application number
AT05759728T
Other languages
English (en)
Inventor
David Bartkovitz
Xin-Jie Chu
Allen Lovey
Peter Wovkulich
Original Assignee
Hoffmann La Roche
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35385535&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ATE445604(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Application granted granted Critical
Publication of ATE445604T1 publication Critical patent/ATE445604T1/de

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/73—Unsubstituted amino or imino radicals
    • 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • 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
    • C07D401/12—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 linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Mobile Radio Communication Systems (AREA)
AT05759728T 2004-07-15 2005-07-08 Neue 2,6-diaminopyridin-3-on-derivate ATE445604T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US58812204P 2004-07-15 2004-07-15
PCT/EP2005/007432 WO2006005548A1 (en) 2004-07-15 2005-07-08 Novel 2,6-diaminopyridine-3-one derivatives

Publications (1)

Publication Number Publication Date
ATE445604T1 true ATE445604T1 (de) 2009-10-15

Family

ID=35385535

Family Applications (1)

Application Number Title Priority Date Filing Date
AT05759728T ATE445604T1 (de) 2004-07-15 2005-07-08 Neue 2,6-diaminopyridin-3-on-derivate

Country Status (16)

Country Link
US (1) US7423051B2 (de)
EP (1) EP1771420B1 (de)
JP (1) JP2008505955A (de)
KR (1) KR100853973B1 (de)
CN (1) CN1980893B (de)
AR (1) AR050427A1 (de)
AT (1) ATE445604T1 (de)
AU (1) AU2005261899A1 (de)
BR (1) BRPI0513366A (de)
CA (1) CA2573604A1 (de)
DE (1) DE602005017152D1 (de)
ES (1) ES2330765T3 (de)
MX (1) MX2007000574A (de)
RU (1) RU2385866C2 (de)
TW (1) TW200612929A (de)
WO (1) WO2006005548A1 (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007137196A2 (en) * 2006-05-19 2007-11-29 Threshold Pharmaceuticals, Inc. Tubulin binding anti cancer compounds and prodrugs thereof
EP1900727A1 (de) * 2006-08-30 2008-03-19 Cellzome Ag Aminopyridinderivate als Kinase-Inhibitoren
US8017607B2 (en) 2009-10-14 2011-09-13 Hoffmann-La Roche Inc. N-substituted-pyrrolidines as inhibitors of MDM2-P-53 interactions
US20230115907A1 (en) * 2019-12-20 2023-04-13 Evopoint Biosciences Co., Ltd. Heterocyclic compound and pharmaceutical composition, preparation method, intermediate and use thereof
EP4289835A4 (de) * 2021-02-05 2024-08-28 Shanghai Qilu Pharmaceutical Research and Development Centre Ltd. Cdk-hemmer
CN113117077B (zh) * 2021-03-04 2022-08-09 西南民族大学 一种用于肿瘤联合治疗的铂基单原子纳米酶及其制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2306082A1 (en) 1997-10-27 1999-05-06 Agouron Pharmaceuticals, Inc. Substituted 4-amino-thiazol-2-y compounds as cdks inhibitors
US6262096B1 (en) 1997-11-12 2001-07-17 Bristol-Myers Squibb Company Aminothiazole inhibitors of cyclin dependent kinases
WO2000076980A1 (en) * 1999-06-10 2000-12-21 Yamanouchi Pharmaceutical Co., Ltd. Novel nitrogen-contaiing heterocyclic derivatives or salts thereof
MXPA02001108A (es) 1999-09-15 2002-08-20 Warner Lambert Co Pieridinonas como inhibidores de la cinasa.
CA2386955A1 (en) 1999-11-22 2001-05-31 Warner-Lambert Company Quinazolines and their use for inhibiting cyclin-dependent kinase enzymes
MXPA02010222A (es) 2000-04-18 2003-05-23 Agouron Pharma Pirazoles para inhibir proteina cinasa.
FR2832148B1 (fr) * 2001-11-14 2004-05-21 Oreal Nouvelles bases d'oxydation 2,5-diaminopyridine utiles pour la teinture des fibres keratiniques
JP2006518368A (ja) 2003-02-21 2006-08-10 ファイザー・インク プロテインキナーゼ阻害剤としてのｎ−ヘテロシクリル置換アミノチアゾール誘導体
KR20060123330A (ko) * 2003-11-19 2006-12-01 얀센 파마슈티카 엔.브이. 키나제 장애의 치료에 유용한 아미노치환 피리디닐 메타논화합물

Also Published As

Publication number Publication date
DE602005017152D1 (de) 2009-11-26
ES2330765T3 (es) 2009-12-15
WO2006005548A1 (en) 2006-01-19
CN1980893B (zh) 2011-01-19
CA2573604A1 (en) 2006-01-19
AU2005261899A1 (en) 2006-01-19
EP1771420A1 (de) 2007-04-11
EP1771420B1 (de) 2009-10-14
RU2007105558A (ru) 2008-08-20
KR100853973B1 (ko) 2008-08-25
JP2008505955A (ja) 2008-02-28
US7423051B2 (en) 2008-09-09
RU2385866C2 (ru) 2010-04-10
KR20070028539A (ko) 2007-03-12
TW200612929A (en) 2006-05-01
MX2007000574A (es) 2007-03-07
CN1980893A (zh) 2007-06-13
BRPI0513366A (pt) 2008-05-06
AR050427A1 (es) 2006-10-25
US20060014708A1 (en) 2006-01-19

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Legal Events

Date Code Title Description
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