Intramolecular π-stacks in mixed-ligand copper(II) complexes formed by heteroaromatic amines and antivirally active acyclic nucleotide analogs carrying a hydroxy-2-(phosphonomethoxy)propyl residue‡-Reference-Cited by-同舟云学术

Intramolecular π-stacks in mixed-ligand copper(II) complexes formed by heteroaromatic amines and antivirally active acyclic nucleotide analogs carrying a hydroxy-2-(phosphonomethoxy)propyl residue‡

Published:2018-07-03 Issue:11-13 Volume:71 Page:1910-1934
ISSN:0095-8972
Container-title:Journal of Coordination Chemistry
language:en
Short-container-title:Journal of Coordination Chemistry

Author:

Blindauer Claudia A.¹²,Griesser Rolf¹,Holý Antonín³,Operschall Bert P.¹,Sigel Astrid¹,Song Bin¹⁴,Sigel Helmut¹

Affiliation:

1. Department of Chemistry, Inorganic Chemistry, University of Basel, Basel, Switzerland;

2. Department of Chemistry, University of Warwick, Coventry, UK;

3. Institute of Organic Chemistry and Biochemistry, Centre of Novel Antivirals and Antineoplastics, Academy of Sciences, Prague, Czech Republic;

4. Vertex Pharmaceuticals Inc., Boston, MA, USA

Funder

Department of Chemistry of the University of Basel

University of Warwick

Publisher

Informa UK Limited

Subject

Materials Chemistry,Physical and Theoretical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00958972.2018.1490019

Reference107 articles.

1. Extent of intramolecular π stacks in aqueous solution in mixed-ligand copper(II) complexes formed by heteroaromatic amines and the anticancer and antivirally active 9-[2-(phosphonomethoxy)ethyl]guanine (PMEG). A comparison with related acyclic nucleotide analogues

2. Extent of Intramolecular π Stacks in Aqueous Solution in Mixed-Ligand Copper(II) Complexes Formed by Heteroaromatic Amines and 1-[2-(Phosphonomethoxy)ethyl]cytosine (PMEC), a Relative of Antivirally Active Acyclic Nucleotide Analogues (Part 72)[1, 2]

3. Organic Chemist Whose Inventions Reshaped the Antiviral Drug World

4. The clinical potential of the acyclic (and cyclic) nucleoside phosphonates. The magic of the phosphonate bond

5. Solution properties of antiviral adenine-nucleotide analogues. The acid–base properties of 9-[2-(phosphonomethoxy)ethyl]adenine (PMEA) † and of its N1, N3 and N7 deaza derivatives in aqueous solution

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1. Coordination Chemistry of Nucleotides and Antivirally Active Acyclic Nucleoside Phosphonates, including Mechanistic Considerations;Molecules;2022-04-19

2. Acid–base properties of an antivirally active acyclic nucleoside phosphonate: (S)-9-[3-hydroxy-2-(phosphonomethoxy)propyl]adenine (HPMPA);New Journal of Chemistry;2022

3. Early Metal Di(pyridyl) Pyrrolide Complexes with Second Coordination Sphere Arene−π Interactions: Ligand Binding and Ethylene Polymerization;ACS Omega;2019-09-19

4. Metal Ion‐Coordinating Properties in Aqueous Solutions of the Antivirally Active Nucleotide Analogue ( S )‐9‐[3‐Hydroxy‐2‐(phosphonomethoxy)propyl]adenine (HPMPA) – Quantification of Complex Isomeric Equilibria;European Journal of Inorganic Chemistry;2019-09-11