A New Type of Potent Inhibitors of HIV-1 TAR RNA−Tat Peptide Binding by Zinc(II)−Macrocyclic Tetraamine Complexes
Author:
Affiliation:
1. Department of Medicinal Chemistry Faculty of Medicine, Hiroshima University Kasumi 1-2-3, Minami-ku, Hiroshima 734-8551, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja0108335
Reference28 articles.
1. Inhibition of Tat-Mediated Transactivation of HIV-1 LTR Transcription by Polyamide Nucleic Acid Targeted to TAR Hairpin Element
2. A New Class of HIV-1 Tat Antagonist Acting through Tat−TAR Inhibition
3. Synthesis and Antiviral Activity of Ethidium−Arginine Conjugates Directed Against the TAR RNA of HIV-1
4. 1,10-phenanthroline-copper, a footprinting reagent for single-stranded regions of RNAs
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