NO20074853L - Smamolekylinhibitorer av MDM2 og anvendelser derav - Google Patents

Smamolekylinhibitorer av MDM2 og anvendelser derav

Info

Publication number
NO20074853L
NO20074853L NO20074853A NO20074853A NO20074853L NO 20074853 L NO20074853 L NO 20074853L NO 20074853 A NO20074853 A NO 20074853A NO 20074853 A NO20074853 A NO 20074853A NO 20074853 L NO20074853 L NO 20074853L
Authority
NO
Norway
Prior art keywords
mdm2
inhibitors
smamolecule
applications
relates
Prior art date
Application number
NO20074853A
Other languages
English (en)
Norwegian (no)
Inventor
Shaomeng Wang
Ke Ding
Yipin Lu
Zaneta Nikolovska-Coleska
Su Qiu
Guoping Wang
Dongguang Qin
Sanjeev Kumar
Original Assignee
Universtity Of Michigan
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 Universtity Of Michigan filed Critical Universtity Of Michigan
Publication of NO20074853L publication Critical patent/NO20074853L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/54—Spiro-condensed
    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/10—Spiro-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10—Spiro-condensed systems
    • C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Indole Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
NO20074853A 2005-02-22 2007-09-24 Smamolekylinhibitorer av MDM2 og anvendelser derav NO20074853L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US65513505P 2005-02-22 2005-02-22
PCT/US2006/006221 WO2006091646A2 (en) 2005-02-22 2006-02-22 Small molecule inhibitors of mdm2 and uses thereof

Publications (1)

Publication Number Publication Date
NO20074853L true NO20074853L (no) 2007-11-21

Family

ID=36927977

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20074853A NO20074853L (no) 2005-02-22 2007-09-24 Smamolekylinhibitorer av MDM2 og anvendelser derav

Country Status (11)

Country Link
EP (1) EP1856123B1 (pt)
JP (2) JP5248866B2 (pt)
KR (1) KR100944301B1 (pt)
CN (2) CN101160314B (pt)
AU (2) AU2006216780B8 (pt)
BR (1) BRPI0609172A2 (pt)
CA (2) CA2752738C (pt)
EA (2) EA019566B1 (pt)
MX (1) MX2007010272A (pt)
NO (1) NO20074853L (pt)
WO (1) WO2006091646A2 (pt)

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US8222288B2 (en) 2006-08-30 2012-07-17 The Regents Of The University Of Michigan Small molecule inhibitors of MDM2 and the uses thereof
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US8217051B2 (en) 2009-02-17 2012-07-10 Hoffmann-La Roche Inc. Spiroindolinone derivatives
US8076482B2 (en) 2009-04-23 2011-12-13 Hoffmann-La Roche Inc. 3,3′-spiroindolinone derivatives
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US8017607B2 (en) * 2009-10-14 2011-09-13 Hoffmann-La Roche Inc. N-substituted-pyrrolidines as inhibitors of MDM2-P-53 interactions
MY165579A (en) 2009-10-14 2018-04-05 Xenon Pharmaceuticals Inc Synthetic methods for spiro-oxindole compounds
MX2012005507A (es) * 2009-11-12 2012-07-03 Univ Michigan Antagonistas de espiro-oxindol de mdm2.
US20110118283A1 (en) * 2009-11-17 2011-05-19 Qingjie Ding Substituted Pyrrolidine-2-Carboxamides
US8088815B2 (en) 2009-12-02 2012-01-03 Hoffman-La Roche Inc. Spiroindolinone pyrrolidines
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KR20130050938A (ko) * 2010-04-09 2013-05-16 더 리젠츠 오브 더 유니버시티 오브 미시건 질환 치료시 사용하기 위한 ｍｄｍ2 억제제에 대한 바이오마커
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US20120046306A1 (en) * 2010-08-18 2012-02-23 David Joseph Bartkovitz Substituted Heteroaryl Spiropyrrolidine MDM2 Antagonists
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US20120071499A1 (en) * 2010-09-20 2012-03-22 Xin-Jie Chu Substituted Spiro[3H-Indole-3,6'(5'H)-[1H]Pyrrolo[1,2c]Imidazole-1',2(1H,2'H)-diones
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ES2624808T3 (es) * 2011-05-11 2017-07-17 The Regents Of The University Of Michigan Antagonistas de MDM2 espirooxindólicos
CN102627650B (zh) * 2012-03-08 2015-07-08 徐州师范大学 手性四氢吡咯-3,2′-氧化吲哚螺环化合物及其合成方法
TWI586668B (zh) 2012-09-06 2017-06-11 第一三共股份有限公司 二螺吡咯啶衍生物之結晶
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CN103435622B (zh) * 2013-07-31 2015-11-18 陕西科技大学 一种螺环吲哚二酮哌嗪类生物碱及其合成方法和应用
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HUE046057T2 (hu) * 2014-08-21 2020-02-28 Boehringer Ingelheim Int Új spiro[3H-indol-3,2'-pirrolidin]-2(1H)-on vegyületek és származékok, mint MDM2-P53-inhibitorok
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TWI711452B (zh) * 2015-02-20 2020-12-01 日商第一三共股份有限公司 癌症的倂用治療法
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CN108486041A (zh) * 2018-03-28 2018-09-04 华南农业大学 PI3K/Akt信号通路在鸡胚成纤维细胞内对马立克氏病毒增殖的应用及其检测方法
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Also Published As

Publication number Publication date
CA2752738C (en) 2014-05-27
WO2006091646A3 (en) 2006-11-30
CA2752738A1 (en) 2006-08-31
BRPI0609172A2 (pt) 2010-02-23
EA200701771A1 (ru) 2008-06-30
KR20070108917A (ko) 2007-11-13
CA2598690A1 (en) 2006-08-31
JP5638023B2 (ja) 2014-12-10
AU2010202759A1 (en) 2010-07-22
JP2012162550A (ja) 2012-08-30
EP1856123B1 (en) 2016-02-17
CN101160314B (zh) 2012-05-23
MX2007010272A (es) 2008-03-12
EP1856123A4 (en) 2010-12-29
JP5248866B2 (ja) 2013-07-31
WO2006091646A2 (en) 2006-08-31
CN101160314A (zh) 2008-04-09
EA019566B1 (ru) 2014-04-30
KR100944301B1 (ko) 2010-02-24
EA201001255A1 (ru) 2011-02-28
EA014445B1 (ru) 2010-12-30
AU2006216780B2 (en) 2010-04-01
AU2006216780B8 (en) 2010-04-22
CN102627649A (zh) 2012-08-08
CN102627649B (zh) 2015-03-25
JP2008531504A (ja) 2008-08-14
AU2006216780A1 (en) 2006-08-31
EP1856123A2 (en) 2007-11-21
CA2598690C (en) 2011-11-15
AU2010202759B2 (en) 2012-07-19

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