E Freisinger, A Schimanski, B Lippert
Index: J. Biol. Inorg. Chem. 6(4) , 378-89, (2001)
Full Text: HTML
Apart from their function as counter ions for the charge neutralization of nucleic acids, alkali metal ions play important roles in stabilizing particular multistranded nucleic acids, e.g. guanine quartets in telomeres and uracil (U) or thymine (T) quartets. Here X-ray crystal structure determinations of a series of alkali metal ions (Na+, K+, Rb+, Cs+) as well as of Mg2+ and H5O2+ adducts with the model bases 1-methylthymine and 1-ethylthymine are reported, which bear relevance to the question of thymine quartet (T4) geometries. The compounds isolated differ in their stoichiometries (T:M = 4:1, 2:1, 1:1), and the ways the metal ions interact with the bases. The two extremes are exclusive metal coordination to exocyclic oxygen atoms of the T bases and exclusive H bonding between M aqua cations and the bases.
Structure | Name/CAS No. | Molecular Formula | Articles |
---|---|---|---|
![]() |
1-METHYLTHYMINE
CAS:4160-72-9 |
C6H8N2O2 |
Thermodynamic, kinetic and structural studies on the ternary...
2000-04-01 [J. Inorg. Biochem. 79(1-4) , 129-38, (2000)] |
Electronic and vibrational spectroscopy of 1-methylthymine a...
2008-08-04 [ChemPhysChem 9 , 1570-1577, (2008)] |
The influence of packing on free radical yields in crystalli...
1994-11-01 [Radiat. Res. 140(2) , 199-214, (1994)] |
Reactivity of substituted charged phenyl radicals toward com...
2003-02-26 [J. Am. Chem. Soc. 125(8) , 2272-81, (2003)] |
On the use of ultraviolet resonance Raman intensities to ela...
1998-01-01 [Biospectroscopy 4(6) , 379-93, (1998)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved