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PE20020959A1 - Derivados quimicos y su aplicacion como agentes antitelomerasa - Google Patents

Derivados quimicos y su aplicacion como agentes antitelomerasa

Info

Publication number
PE20020959A1
PE20020959A1 PE2002000227A PE2002000227A PE20020959A1 PE 20020959 A1 PE20020959 A1 PE 20020959A1 PE 2002000227 A PE2002000227 A PE 2002000227A PE 2002000227 A PE2002000227 A PE 2002000227A PE 20020959 A1 PE20020959 A1 PE 20020959A1
Authority
PE
Peru
Prior art keywords
amino
nil
methyl
triazine
quinoli
Prior art date
Application number
PE2002000227A
Other languages
English (en)
Inventor
Patrick Mailliet
Abdelazize Laoui
Gilles Doerflinger
Francois Hamy
Thomas Caulfield
Jean-Louis Mergny
Jean-Francois Riou
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
Priority claimed from FR0103916A external-priority patent/FR2822468B1/fr
Application filed by Aventis Pharma Sa filed Critical Aventis Pharma Sa
Publication of PE20020959A1 publication Critical patent/PE20020959A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems

Landscapes

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

Abstract

SE REFIERE A UN AGENTE REPARTIDOR LIGADO A GRUPOS AMINO AROMATICOS DE FORMULA: CICLOAROMATICO NITROGENADO-NR3-DISTRIBUIDOR-NR'3-CICLO AROMATICO; DONDE CICLOAROMATICO NITROGENADO ES QUINOLEINA, ISOQUINOLEINA, BENZAMIDINA, PIRIDINA; CICLO AROMATICO REPRESENTA QUINOLEINA SUSTITUIDO POR N(Ra)(Rb); BENZAMIDINA, PIRIDINA, FENILO, HETEROCICLO MONO, BI, TRICICLICO; Ra, Rb SON H, ALQUILO C1-C4, ALCOXI C1-C4. R3, R'3 SON TRIAZINA SUSTITUDO, DIAZINA SUSTITUIDO. SON COMPUESTOS PREFERIDOS 2,4-BIS-(4-DIMETILAMINO-2-METIL-QUINOLI-6-NIL)AMINO-6-(3-DIMETILAMINO-PROPIL)AMINO-[1,3,5]TRIAZINA; 2,4,6-TRIS-(4-AMINO-2-METIL-QUINOLI-6-NIL)AMINO-[1,3,5]TRIAZINA, 2,4-BIS-(4-AMINO-2-METIL-QUINOLI-6-NIL)AMINO-6-(4-DIMETILAMINO-2-METIL-QUINOLI-6-NIL)-AMINO-[1,3,5]TRIAZINA, 2,4-BIS-(4-DIMETILAMINO-2-METIL-QUINOLI-6-NIL)AMINO-6-((1-METIL-PIPERIDI-4-NIL)-[1,3,5]TRIAZINA, ENTRE OTROS. LOS COMPUESTOS NO NUCLEOTIDOS INTERACTUAN CON ESTRUCTURAS ESPECIFICAS DEL ADN O ARN, SON INHIBIDORES DE TELOMERASA VIA LA ESTABILIZACION DE G-CUADRUPLEXAS, Y PUEDEN SER UTILES PARA EL TRATAMIENTO DE CANCER
PE2002000227A 2001-03-23 2002-03-22 Derivados quimicos y su aplicacion como agentes antitelomerasa PE20020959A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0103916A FR2822468B1 (fr) 2001-03-23 2001-03-23 Derives chimiques et leur application comme agent anti-telomerase
FR0110370 2001-08-02

Publications (1)

Publication Number Publication Date
PE20020959A1 true PE20020959A1 (es) 2002-12-17

Family

ID=26212933

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2002000227A PE20020959A1 (es) 2001-03-23 2002-03-22 Derivados quimicos y su aplicacion como agentes antitelomerasa

Country Status (11)

Country Link
EP (1) EP1373252A1 (es)
JP (1) JP2004524349A (es)
AR (1) AR034297A1 (es)
AU (1) AU2002251140B2 (es)
CA (1) CA2442012A1 (es)
CO (1) CO5380035A1 (es)
IL (2) IL158056A0 (es)
MX (1) MXPA03008269A (es)
MY (1) MY130957A (es)
PE (1) PE20020959A1 (es)
WO (1) WO2002076975A1 (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1401833A2 (fr) 2001-05-28 2004-03-31 Aventis Pharma S.A. Derives chimiques et leur application comme agent antitelomerase
US7173032B2 (en) * 2001-09-21 2007-02-06 Reddy Us Therapeutics, Inc. Methods and compositions of novel triazine compounds
WO2003055866A1 (en) * 2001-12-21 2003-07-10 Bayer Pharmaceuticals Corporation Quinazoline and quinoline derivative compounds as inhibitors of prolylpeptidase, inducers of apoptosis and cancer treatment agents
WO2004001018A2 (en) * 2002-06-25 2003-12-31 The Center For Blood Research, Inc. Vacuolins
FR2850970B1 (fr) * 2003-02-07 2006-07-07 Aventis Pharma Sa Derives chimiques se liant de maniere tres specifique aux structures d'adn en g-quadruplexe et leur application comme agent anticancereux specifique
AU2004253967B2 (en) 2003-07-03 2010-02-18 Cytovia, Inc. 4-arylamino-quinazolines as activators of caspases and inducers of apoptosis
US8309562B2 (en) 2003-07-03 2012-11-13 Myrexis, Inc. Compounds and therapeutical use thereof
CA2592900A1 (en) 2005-01-03 2006-07-13 Myriad Genetics Inc. Nitrogen containing bicyclic compounds and therapeutical use thereof
US8258145B2 (en) 2005-01-03 2012-09-04 Myrexis, Inc. Method of treating brain cancer
WO2006122431A1 (en) * 2005-05-19 2006-11-23 Prometic Biosciences Inc. Triazine compounds and compositions thereof for the treatment of cancers
EP2046763A2 (en) * 2006-07-31 2009-04-15 Praecis Pharmaceuticals Incorporated Aurora kinase inhibitors from an encoded small molecule library
JP5282091B2 (ja) * 2007-07-25 2013-09-04 ブリストル−マイヤーズ スクイブ カンパニー トリアジンキナーゼ阻害剤
FR2948686B1 (fr) * 2009-07-30 2011-08-19 Biomerieux Sa Nouveaux substrats de peptidase
US20210024455A1 (en) * 2018-03-20 2021-01-28 Hiroshima University Compound which inhibits telomere-binding protein, and telomere-binding protein inhibitor containing same

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9206768D0 (en) * 1992-03-27 1992-05-13 Jarman Michael New compounds for use in the treatment of cancer
JPH1160573A (ja) * 1997-08-22 1999-03-02 Nippon Kayaku Co Ltd トリアジン誘導体及びテロメラーゼ阻害剤
US6262053B1 (en) * 1999-06-23 2001-07-17 Parker Hughes Institute Melamine derivatives as potent anti-cancer agents
DK1244650T3 (da) * 1999-11-29 2003-10-20 Aventis Pharma Sa Arylaminderivater og deres anvendelse som antitelomerasemidler
ATE511858T1 (de) * 2002-02-05 2011-06-15 Astellas Pharma Inc 2,4,6-triamino-1,3,5-triazin-derivat

Also Published As

Publication number Publication date
EP1373252A1 (fr) 2004-01-02
MXPA03008269A (es) 2004-10-15
CO5380035A1 (es) 2004-03-31
IL158056A0 (en) 2004-03-28
MY130957A (en) 2007-07-31
AU2002251140B2 (en) 2007-03-15
AR034297A1 (es) 2004-02-18
IL158056A (en) 2010-02-17
CA2442012A1 (fr) 2002-10-03
WO2002076975A1 (fr) 2002-10-03
JP2004524349A (ja) 2004-08-12

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Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed