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Synthesis and biological evaluation of new symmetrical derivatives as cytotoxic agents and apoptosis inducers

Author
SANMARTIN, Carmen1 ; ECHEVERRIA, Mikel1 ; MENDIVIL, Beatriz1 ; CORDEU, Lucia2 ; CUBEDO, Elena2 ; GARCIA-FONCILLAS, Jesus2 ; FONT, Maria3 ; PALOP, Juan Antonio1
[1] Sección de Síntesis, Departamento de Quimica Orgânica y Farmacéutica, Universidad de Navarra, Irunlarrea, 1, 31008 Pamplona, Spain
[2] Laboratorio de Bioternología y Genómica, Área de Terapia Celulur, Clínica Universitaria de Navarra, Pamplona, Spain
[3] Sección de Modelización Molecular, Departamento de Quimica Orgânica y Farmacéutica, Universidad de Navarra, Pamplona, Spain
Source

Bioorganic & medicinal chemistry. 2005, Vol 13, Num 6, pp 2031-2044, 14 p

ISSN
0968-0896
Scientific domain
Biochemistry, molecular biology, biophysics; Pharmacology drugs
Publisher
Elsevier Science, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Author keyword
Amides and amines Apoptosis Carbamates: Ureas Caspase-3 Cytotoxics Symmetrical ethers
Keyword (fr)
Activité biologique Amide Amine Anticancéreux Apoptose Biphényle dérivé Carbamate organique Caspase Cellule tumorale Cytotoxicité Côlon DNA Ether Homme In vitro Isozyme Lignée cellulaire Lymphocyte T Modulation Mécanisme action Naphtalène dérivé Relation dose réponse Synthèse chimique Urées Vessie urinaire Caspase 3 Lignée HT29 Lignée T24 Pyrido[2,3-d]pyrimidine dérivé Pyridopyrimidine Enzyme Hydrolases Peptidases
Keyword (en)
Biological activity Amides Amine Antineoplastic agent Apoptosis Biphenyl derivatives Organic carbamate Caspase Tumor cell Cytotoxicity Colon DNA Ether Human In vitro Isozyme Cell line T-Lymphocyte Modulation Mechanism of action Naphthalene derivatives Dose activity relation Chemical synthesis Ureas Urinary bladder Enzyme Hydrolases Peptidases
Keyword (es)
Actividad biológica Amina Anticanceroso Apoptosis Bifenilo derivado Carbamato orgánico Caspase Célula tumoral Citotoxicidad Colón DNA Eter Hombre In vitro Isozima Línea celular Linfocito T Modulación Mecanismo acción Naftaleno derivado Relación dosis respuesta Síntesis química Ureas Vejiga Enzima Hydrolases Peptidases
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02R Antineoplastic agents / 002B02R01 General aspects

Discipline
Pharmacological treatments
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
16568002

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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