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AU4198400A - Neurotrophic thio substituted pyrimidines - Google Patents

Neurotrophic thio substituted pyrimidines

Info

Publication number
AU4198400A
AU4198400A AU41984/00A AU4198400A AU4198400A AU 4198400 A AU4198400 A AU 4198400A AU 41984/00 A AU41984/00 A AU 41984/00A AU 4198400 A AU4198400 A AU 4198400A AU 4198400 A AU4198400 A AU 4198400A
Authority
AU
Australia
Prior art keywords
neurotrophic
substituted pyrimidines
thio substituted
thio
pyrimidines
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
AU41984/00A
Inventor
Lilia M. Beauchamp
James L. Kelley
Thomas A. Krenitsky
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Krenitsky Pharmaceuticals Inc
Original Assignee
Krenitsky Pharmaceuticals Inc
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 Krenitsky Pharmaceuticals Inc filed Critical Krenitsky Pharmaceuticals Inc
Publication of AU4198400A publication Critical patent/AU4198400A/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AU41984/00A 1999-04-06 2000-04-05 Neurotrophic thio substituted pyrimidines Abandoned AU4198400A (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US12792399P 1999-04-06 1999-04-06
US60127923 1999-04-06
US12884299P 1999-04-12 1999-04-12
US60128842 1999-04-12
PCT/US2000/009004 WO2000059893A1 (en) 1999-04-06 2000-04-05 Neurotrophic thio substituted pyrimidines

Publications (1)

Publication Number Publication Date
AU4198400A true AU4198400A (en) 2000-10-23

Family

ID=26826090

Family Applications (1)

Application Number Title Priority Date Filing Date
AU41984/00A Abandoned AU4198400A (en) 1999-04-06 2000-04-05 Neurotrophic thio substituted pyrimidines

Country Status (4)

Country Link
EP (1) EP1165522A1 (en)
AU (1) AU4198400A (en)
CA (1) CA2369945A1 (en)
WO (1) WO2000059893A1 (en)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1217000A1 (en) * 2000-12-23 2002-06-26 Aventis Pharma Deutschland GmbH Inhibitors of factor Xa and factor VIIa
TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
ES2445208T3 (en) 2002-07-29 2014-02-28 Rigel Pharmaceuticals, Inc. 2,4-Pyrimidinediamine compounds for use in methods to treat or prevent autoimmune diseases
US6800652B2 (en) 2002-08-16 2004-10-05 Pfizer Inc. Diaryl compounds
RS53109B (en) 2003-07-30 2014-06-30 Rigel Pharmaceuticals Inc. 2,4-pyrimidinediamine compounds for use in the treatment or prevention of autoimmune diseases
CA2584295C (en) 2004-11-24 2014-08-26 Rigel Pharmaceuticals, Inc. Spiro-2, 4-pyrimidinediamine compounds and their uses
FR2932481B1 (en) 2008-06-13 2010-10-08 Sanofi Aventis 4- {2-4-PHENYL-3,6-DIHYDRO-2H-PYRIDIN-1-YL] -2-OXO-ALKYL} -1-PIPERAZIN-2-ONE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE.
FR2932482B1 (en) 2008-06-13 2010-10-08 Sanofi Aventis NOVEL (PHENYL-3,6-DIHYDRO-2H-PYRIDINYL) - (PIPERAZINYL PONTE) -1-ALKANONE DERIVATIVES AND THEIR USE AS P75 INHIBITORS
EP2467142B1 (en) 2009-08-17 2016-09-21 Memorial Sloan-Kettering Cancer Center 2-(Pyrimidin-5-yl)-thiopyrimidine derivatives as Hsp70 and Hsc70 modulators for the treatment of proliferative disorders
FR2953836B1 (en) 2009-12-14 2012-03-16 Sanofi Aventis NOVEL DERIVATIVES (HETEROCYCLE-TETRAHYDRO-PYRIDINE) - (PIPERAZINYL) -1-ALKANONE AND (HETEROCYCLE-DIHYDRO-PYRROLIDINE) - (PIPERAZINYL) -1-ALKANONE AND THEIR USE AS INHIBITORS OF P75
FR2953839A1 (en) 2009-12-14 2011-06-17 Sanofi Aventis NOVEL (HETEROCYCLE-PIPERIDINE CONDENSEE) - (PIPERAZINYL) -1ALCANONE OR (HETEROCYCLE-PYRROLIDINE CONDENSED) - (PIPERAZINYL) -1ALCANONE DERIVATIVES AND THEIR USE AS INHIBITORS OF P75
EP2606894A1 (en) 2011-12-20 2013-06-26 Sanofi Novel therapeutic use of p75 receptor antagonists
JO3517B1 (en) 2014-01-17 2020-07-05 Novartis Ag N-azaspirocycloalkane substituted n-heteroaryl compounds and compositions for inhibiting the activity of shp2
ES2699354T3 (en) 2014-01-17 2019-02-08 Novartis Ag Derivatives of 1- (triazin-3-yl / pyridazin-3-yl) -piper (-azin) idine and compositions thereof to inhibit the activity of SHP2
WO2015107493A1 (en) 2014-01-17 2015-07-23 Novartis Ag 1 -pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine derivatives and and compositions thereof for inhibiting the activity of shp2
EP3310779B1 (en) 2015-06-19 2019-05-08 Novartis AG Compounds and compositions for inhibiting the activity of shp2
CN112625028B (en) 2015-06-19 2024-10-29 诺华股份有限公司 Compounds and compositions for inhibiting SHP2 activity
ES2824576T3 (en) 2015-06-19 2021-05-12 Novartis Ag Compounds and compositions to inhibit SHP2 activity
MA43821A (en) 2016-03-14 2018-11-28 Afferent Pharmaceuticals Inc PYRIMIDINS AND VARIANTS THEREOF, AND THEIR USES
JP6902045B2 (en) * 2016-03-25 2021-07-14 アファレント ファーマシューティカルズ インコーポレイテッド Pyrimidines and their variants, and their use
EA036446B1 (en) 2016-06-14 2020-11-11 Новартис Аг Compounds and compositions for inhibiting the activity of shp2
KR102571130B1 (en) 2017-01-10 2023-08-28 노파르티스 아게 A pharmaceutical combination comprising an ALK inhibitor and a SHP2 inhibitor

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB951431A (en) * 1959-03-17 1964-03-04 Wellcome Found Pyrimidine derivatives and the manufacture thereof
CA2217034A1 (en) * 1995-04-03 1996-10-10 Sumitomo Pharmaceuticals Company, Limited Novel pyrimidine derivatives effective as psychotropic drug and process for the production thereof

Also Published As

Publication number Publication date
CA2369945A1 (en) 2000-10-12
WO2000059893A1 (en) 2000-10-12
EP1165522A1 (en) 2002-01-02

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Legal Events

Date Code Title Description
MK6 Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase