Protonated rubyrin and C-Tips: Co-carriers for the transport of guanosine 5′-monophosphate at neutral pH
- 1 December 1993
- journal article
- research article
- Published by Taylor & Francis in Supramolecular Chemistry
- Vol. 3 (1), 5-8
- https://doi.org/10.1080/10610279308029830
Abstract
At neutral and near-neutral pH, rubyrin, a readily protonated, hexapyrrolic expanded porphyrin, and triisopropylsilyl-protected cytidine (C-Tips) act cooperatively to effect the efficient through-transport of guanosine 5′-monophosphate (GMP) in a model three-phase H2O-CH2Cl2-H2O bulk liquid membrane system.Keywords
This publication has 8 references indexed in Scilit:
- Synthetic sapphyrin-cytosine conjugates: carriers for selective nucleotide transport at neutral pH.Journal of the American Chemical Society, 1992
- Rubyrin: A New Hexapyrrolic Expanded PorphyrinAngewandte Chemie International Edition in English, 1991
- Phosphate anion binding: enhanced transport of nucleotide monophosphates using a sapphyrin carrierJournal of the American Chemical Society, 1991
- Enhanced transport of nucleosides and nucleoside analogs with complementary base-pairing agentsJournal of the American Chemical Society, 1991
- Molecular recognition via base pairing: amine-containing, cytosine-based ditopic receptors that complex guanosine monophosphateJournal of the American Chemical Society, 1991
- Phosphonylmethyl Ethers of Nucleosides and Their Acyclic AnaloguesPublished by American Chemical Society (ACS) ,1989
- Supramolecular Chemistry—Scope and Perspectives Molecules, Supermolecules, and Molecular Devices (Nobel Lecture)Angewandte Chemie International Edition in English, 1988
- Sapphyrins: novel aromatic pentapyrrolic macrocyclesJournal of the American Chemical Society, 1983