8-hydroxyguanosine and decane

8-hydroxyguanosine has been researched along with decane* in 1 studies

Other Studies

1 other study(ies) available for 8-hydroxyguanosine and decane

Article	Year
The supramolecular helical architecture of 8-oxoinosine and 8-oxoguanosine derivatives. Chemistry (Weinheim an der Bergstrasse, Germany), 2007, Volume: 13, Issue:12 The 8-oxoguanosine derivative 1 and the 8-oxoinosine derivative 2 b, with appropriate substituents on their ribose moieties, form hexagonal lyotropic mesophases in hydrocarbon solvents. Small-angle X-ray scattering analysis of a film of 1 and of the mesophase of 2 b, and NMR and CD spectra of isotropic solutions of 2 b, indicate that in both cases the supramolecular structures adopted are continuous helices formed by a hydrogen-bond network between the heterocyclic bases. Notably, while derivative 2 b, which bears large substituents on its ribose moiety, undergoes self-assembly and mesophase formation, oxoinosine 2 a, with only decanoyl groups on its ribose moiety, does not. This may be ascribed to the reduced amphiphilic properties of the latter and the absence of aromatic groups. Topics: Alkanes; Circular Dichroism; Guanosine; Heterocyclic Compounds; Hydrocarbons; Hydrogen Bonding; Inosine; Liquid Crystals; Magnetic Resonance Spectroscopy; Molecular Structure; Ribose; Scattering, Radiation; Solvents; X-Ray Diffraction	2007

Article

Year

The supramolecular helical architecture of 8-oxoinosine and 8-oxoguanosine derivatives.

Chemistry (Weinheim an der Bergstrasse, Germany), 2007, Volume: 13, Issue:12

The 8-oxoguanosine derivative 1 and the 8-oxoinosine derivative 2 b, with appropriate substituents on their ribose moieties, form hexagonal lyotropic mesophases in hydrocarbon solvents. Small-angle X-ray scattering analysis of a film of 1 and of the mesophase of 2 b, and NMR and CD spectra of isotropic solutions of 2 b, indicate that in both cases the supramolecular structures adopted are continuous helices formed by a hydrogen-bond network between the heterocyclic bases. Notably, while derivative 2 b, which bears large substituents on its ribose moiety, undergoes self-assembly and mesophase formation, oxoinosine 2 a, with only decanoyl groups on its ribose moiety, does not. This may be ascribed to the reduced amphiphilic properties of the latter and the absence of aromatic groups.

Topics: Alkanes; Circular Dichroism; Guanosine; Heterocyclic Compounds; Hydrocarbons; Hydrogen Bonding; Inosine; Liquid Crystals; Magnetic Resonance Spectroscopy; Molecular Structure; Ribose; Scattering, Radiation; Solvents; X-Ray Diffraction

2007