CF3 Derivatives of the Anticancer Ru(III) Complexes KP1019, NKP-1339, and Their Imidazole and Pyridine Analogues Show Enhanced Lipophilicity, Albumin Interactions, and Cytotoxicity
Author:
Affiliation:
1. Department of Chemistry, Simon Fraser University, 8888 University Drive, Burnaby, BC Canada, V5A 1S6
2. Department of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC Canada, V5Z 4E6
Funder
Simon Fraser University
Natural Sciences and Engineering Research Council of Canada
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.6b00359
Reference106 articles.
1. Ruthenium metallopharmaceuticals
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4. Classical and Non‐Classical Ruthenium‐Based Anticancer Drugs: Towards Targeted Chemotherapy
5. Antitumour metal compounds: more than theme and variations
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