| Literature DB >> 11674719 |
Helmut H. Zepik1, Steven A. Benner.
Abstract
A set of substituted bisguanidines have been prepared and examined for their ability to bind and catalyze the hydrolysis of uridylyl-3',5'-uridine (UpU), an unactivated RNA substrate in water. The unexpected result is that this set includes both catalysts (binding the transition state better than the ground state) and anticatalysts (binding the ground state better than the transition state), each with respectable rate enhancements and/or affinities, despite the fact that these molecules all have very similar structures. These results therefore show the level of sophistication that must be achieved in the conformational theory of small molecules if we hope to truly "design" supramolecular structures that bind preferentially to a transition state over the ground state.Entities:
Year: 1999 PMID: 11674719 DOI: 10.1021/jo982418+
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354