review Open AccessTop 1% cited
Metal-based antitumour drugs in the post genomic era
Dalton Transactions · 2006 · pp. 1929–1929
Paul J. Dyson✉(École Polytechnique Fédérale de Lausanne)Gianni Sava(University of Trieste)
Abstract
The discovery of new metal-based antitumour drugs, whether cisplatin derivatives or those based on other metals, has been largely based on cell viability assays (IC50 values) and compounds that bind to DNA. This approach has been applied for more than 30 years during which time very few new drugs have entered clinical use. In this article we discuss what the future holds for metal-based drugs, in particular anti-metastasis drugs, in these enlightened times of the post genomic era.
Ferrocene Chemistry and ApplicationsMetal complexes synthesis and propertiesRadiopharmaceutical Chemistry and ApplicationsCisplatinComputational biologyPharmacologyChemistryViability assayDrug discoverygenomic DNADNACombinatorial chemistryMedicine
MeSH terms
AnimalsAntineoplastic AgentsCell SurvivalDNAHumansNeoplasm MetastasisNeoplasmsOrganometallic CompoundsStructure-Activity RelationshipMetals, HeavyGenomics
Funding
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Ligue Contre le Cancer
- Krebsliga Schweiz
Citations
760
FWCI
32.47
field-weighted impact
References
39
Percentile
100%
vs. same field & year
Citations per year
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Journal of Medicinal Chemistry · 2005 · 769 citations
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Chemical Communications · 2005 · 752 citations
A Phase I and Pharmacological Study with Imidazolium-<b> <i>trans-</i> </b>DMSO-imidazole-tetrachlororuthenate, a Novel Ruthenium Anticancer Agent
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