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Cited by 384

The DOI matches its Crossref record; 65 of the 65 references it cites were found in a registry or an index.

The path for metal complexes to a DNA target

Open access
Komor, Alexis C., Barton, Jacqueline K.·2013·Chemical Communications

Abstract

The discovery of cisplatin as a therapeutic agent stimulated a new era in the application of transition metal complexes for therapeutic design. Here we describe recent results on a variety of transition metal complexes targeted to DNA to illustrate many of the issues involved in new therapeutic design. We describe first structural studies of complexes bound covalently and non-covalently to DNA to identify potential lesions within the cell. We then review the biological fates of these complexes, illustrating the key elements in obtaining potent activity, the importance of uptake and subcellular localization of the complexes, as well as the techniques used to delineate these characteristics. Genomic DNA provides a challenging but valuable target for new transition metal-based therapeutics.

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Crossref · 10.1039/c3cc00177f

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Metadata

Authors
Komor, A. C., & Barton, J. K.
Venue
Chemical Communications
Published
2013
Volume
49
Issue
35
Pages
3617
ISSN
  • 1359-7345 (ISSN-L)
  • 1364-548X
OpenAlex
W2095084300
Cited by
384
References
65
FWCI
17.86
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: The path for metal complexes to a DNA target. https://app.cochat.ai/papers/10.1039/c3cc00177f
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Komor, A. C., & Barton, J. K. (2013). The path for metal complexes to a DNA target. Chemical Communications. https://doi.org/10.1039/c3cc00177f

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.