124842-39-3Relevant articles and documents
Pseudopeptidic ligands: Exploring the self-assembly of isophthaloylbisglycine (H2IBG) and divalent metal ions
Dokorou, Vassiliki N.,Milios, Constantinos J.,Tsipis, Athanassios C.,Haukka, Matti,Weidler, Peter G.,Powell, Annie K.,Kostakis, George E.
, p. 12501 - 12513 (2012)
We present a systematic study of the complexation of the new pseudopeptidic ligand isophthaloylbisglycine (H2IBG) with divalent metal ions of varying ionic radius. This work represents the initial employment of H 2IBG in the coordina
DNA binding, solubility, and partitioning characteristics of extended lexitropsins
Fishleigh,Fox,Khalaf,Pitt,Scobie,Suckling,Urwin,Waigh,Young
, p. 3257 - 3266 (2007/10/03)
Four new ligands that bind to the minor groove of DNA have been designed, synthesized, and evaluated by DNA footprinting. Two of the ligands are polyamides containing central regions with five or six N-methylpyrrole units, conferring hydrophobicity and go
Platelet aggregation inhibiting and anticoagulant effects of oligoamines, XVIII: Oligoamines with fluorescent properties, Part B: Fluorophores in the molecular periphery
Rehse,Seidel
, p. 399 - 404 (2007/10/02)
Seventeen N,N'-benzene-1,3-dimethane and nine N,N',N''-benzene-1,3,5-trimethane derivatives with fluorescent properties have been synthesized. Three of them show antiplatelet activities (inducer collagen, IC50 Borntest) in concentrations 10 μmol/L. They are suitable for interaction studies with biological macromolecules and synthetical and biological membranes. Structure activity relationships demonstrate that heteropolycyclic fluorophores i.e. quinoline, dibenzofurane, or carbazole are favorable substituents for this purpose.