Acetylcholine Recognition by an Aromatic Host: the Role of an All-Hydrogen Topology in Simulations of the Cation-π Interaction
- 1 January 1994
- journal article
- research article
- Published by Wiley in Israel Journal of Chemistry
- Vol. 34 (2) , 159-163
- https://doi.org/10.1002/ijch.199400021
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- The role of aromatic rings as hydrogen-bond acceptors in molecular recognitionPhilosophical Transactions A, 1993
- Quaternary ligand binding to aromatic residues in the active-site gorge of acetylcholinesterase.Proceedings of the National Academy of Sciences, 1993
- The nature of cation-pi binding: interactions between tetramethylammonium ion and benzene in aqueous solutionBiophysical Journal, 1993
- Acetylcholine Binding by a Synthetic Receptor: Implications for Biological RecognitionScience, 1990
- "Hydrophobic" binding of water-soluble guests by high-symmetry, chiral hosts. An electron-rich receptor site with a general affinity for quaternary ammonium compounds and electron-deficient .pi. systemsJournal of the American Chemical Society, 1988
- Aromatic rings act as hydrogen bond acceptorsJournal of Molecular Biology, 1988
- Molecular recognition in aqueous media: donor-acceptor and ion-dipole interactions produce tight binding for highly soluble guestsJournal of the American Chemical Society, 1988
- Tight, oriented binding of an aliphatic guest by a new class of water-soluble molecules with hydrophobic binding sitesJournal of the American Chemical Society, 1986
- Amino‐aromatic interactions in proteinsFEBS Letters, 1986
- Aromatic-Aromatic Interaction: A Mechanism of Protein Structure StabilizationScience, 1985