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Tracking antitumor metallodrugs: promising agents with the Ru(II)- and Fe(II)-cyclopentadienyl scaffolds.
- Source :
-
Future medicinal chemistry [Future Med Chem] 2016 Apr; Vol. 8 (5), pp. 527-44. Date of Electronic Publication: 2016 Apr 20. - Publication Year :
- 2016
-
Abstract
- Research on the field of metal complexes for the treatment of cancer diseases has attracted increasing interest due to the urgency in finding more efficient and selective treatments. Owing to their wide structural diversity, organometallic complexes appear as potential alternatives to the design of new anticancer candidates. Herein, we review recent progress in our work toward the development of new drugs based on Ru(II)- and Fe(II)-cyclopentadienyl scaffolds. Their design and chemical properties are reviewed and correlated with their biological effects, in particular the key role that coligands play in the overall behavior of the complex.
- Subjects :
- Antineoplastic Agents therapeutic use
Cell Line, Tumor
Coordination Complexes chemistry
Coordination Complexes therapeutic use
Cyclopentanes chemistry
Dimethyl Sulfoxide analogs & derivatives
Dimethyl Sulfoxide chemistry
Dimethyl Sulfoxide pharmacology
Dimethyl Sulfoxide therapeutic use
Drug Discovery
Ferrous Compounds chemistry
Ferrous Compounds therapeutic use
Humans
Indazoles chemistry
Indazoles pharmacology
Indazoles therapeutic use
Molecular Targeted Therapy
Organometallic Compounds chemistry
Organometallic Compounds pharmacology
Organometallic Compounds therapeutic use
Protein Binding
Ruthenium chemistry
Ruthenium therapeutic use
Ruthenium Compounds
Antineoplastic Agents chemistry
Antineoplastic Agents pharmacology
Coordination Complexes pharmacology
Ferrous Compounds pharmacology
Neoplasms drug therapy
Ruthenium pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1756-8927
- Volume :
- 8
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Future medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 27096164
- Full Text :
- https://doi.org/10.4155/fmc.16.7