Discovery of Sequence-Selective Peptide Binding by Synthetic Receptors Using Encoded Combinatorial Libraries
- 13 March 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Accounts of Chemical Research
- Vol. 29 (3) , 155-163
- https://doi.org/10.1021/ar950166i
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Engineering of a synthetic receptor to alter peptide binding selectivityChemistry & Biology, 1995
- Cyclooligomeric Receptors Based on Trimesic Acid and 1,2-Diamines. Minimal Structure for Sequence-Selective Peptide BindingThe Journal of Organic Chemistry, 1995
- Peptidomimetic Host That Binds a Peptide Guest Affording a .beta.-Sheet Structure That Subsequently Self-Assembles. A Simple Receptor MimicJournal of the American Chemical Society, 1995
- Expeditious Synthesis of a Novel C3‐Symmetric Receptor that Binds Peptides Sequence‐SelectivelyAngewandte Chemie International Edition in English, 1995
- Remarkable effect of the receptor size in the binding of acetylcholine and related ammonium ions to water-soluble cryptophanesJournal of the American Chemical Society, 1993
- Practical synthesis of a highly enantioselective receptor for peptidesThe Journal of Organic Chemistry, 1993
- An exceptional synthetic receptor for peptidesJournal of the American Chemical Society, 1993
- New molecular complements to imides. Complexation of thymine derivativesJournal of the American Chemical Society, 1991
- The Design of Molecular Hosts, Guests, and Their Complexes (Nobel Lecture)Angewandte Chemie International Edition in English, 1988
- Host-guest complexation. 13. High chiral recognition of amino esters by dilocular hosts containing extended steric barriersJournal of the American Chemical Society, 1978