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From Single-to Multi-Target Drugs in Cancer Therapy : When Aspecificity Becomes an Advantage

Author
PETRELLI, A1 ; GIORDANO, S1
[1] Division of Molecular Oncology, Institute for Cancer Research and Treatment (IRCC), University of Turin Medical School, Str. Provinciale 142, 10060, Candiolo (Torino), Italy
Source

Current medicinal chemistry. 2008, Vol 15, Num 5, pp 422-432, 11 p ; ref : 165 ref

ISSN
0929-8673
Scientific domain
Biochemistry, molecular biology, biophysics; Pharmacology drugs
Publisher
Bentham Science, Schiphol
Publication country
Netherlands
Document type
Article
Language
English
Author keyword
Tyrosine kinase receptors cancer therapy monoclonal antibodies small molecules targeted therapy tyrosine kinase inhibitors
Keyword (fr)
Activité biologique Anticancéreux Anticorps monoclonal Bévacizumab Cétuximab Erlotinib Géfitinib Imatinib Immunomodulateur Inhibiteur enzyme Lapatinib Molécule petite Mécanisme action Médicament ciblé Pertuzumab Recherche et développement Récepteur facteur croissance Sorafénib Sunitinib Thérapeutique ciblée Traitement Transduction signal Transferases Trastuzumab Tumeur maligne Vandétanib Protein-tyrosine kinases Receptor protein-tyrosine kinase Cancer Enzyme
Keyword (en)
Biological activity Antineoplastic agent Monoclonal antibody Bevacizumab Cetuximab Erlotinib Gefitinib Imatinib Immunomodulator Enzyme inhibitor Lapatinib Small molecule Mechanism of action Targeted drug Pertuzumab Research and development Growth factor receptor Sorafenib Sunitinib Targeted therapy Treatment Signal transduction Transferases Trastuzumab Malignant tumor Vandetanib Cancer Enzyme
Keyword (es)
Actividad biológica Anticanceroso Anticuerpo monoclonal Bevacizumab Cetuximab Erlotinib Gefitinib Imatinib Inmunomodulador Inhibidor enzima Lapatinib Molécula pequeña Mecanismo acción Medicamento dirigido Pertuzumab Investigación desarrollo Receptor factor crecimiento Sorafenib Sunitinib Terapéutica dirigida Tratamiento Transducción señal Transferases Trastuzumab Tumor maligno Vandetanib Cáncer Enzima
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
20128427

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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