Results 11 to 20 of about 32,953 (312)

GW-2974 and SCH-442416 modulators of tyrosine kinase and adenosine receptors can also stabilize human telomeric G-quadruplex DNA.

open access: yesPLoS ONE, 2022
GW-2974 is a potent tyrosine kinase receptor inhibitor while SCH-442416 is a potent adenosine receptors' antagonist with high selectivity towards human adenosine A2A receptor over other adenosine receptors. The two compounds were reported to possess anti-
Alaa A Salem   +2 more
doaj   +3 more sources

Structured Waters Mediate Small Molecule Binding to G-Quadruplex Nucleic Acids

open access: yesPharmaceuticals, 2021
The role of G-quadruplexes in human cancers is increasingly well-defined. Accordingly, G-quadruplexes can be suitable drug targets and many small molecules have been identified to date as G-quadruplex binders, some using computer-based design methods and
Stephen Neidle
doaj   +1 more source

Binding-Induced Diversity of a Human Telomeric G-Quadruplex Stability Phase Space

open access: yesPharmaceuticals, 2022
The structural polymorphism of G-quadruplex nucleic acids is an important factor in their recognition by proteins and small-molecule ligands. However, it is not clear why the binding of several ligands alters G-quadruplex topology.
Domen Oblak   +3 more
doaj   +1 more source

G-quadruplexes and helicases [PDF]

open access: yesNucleic Acids Research, 2016
Guanine-rich DNA strands can fold in vitro into non-canonical DNA structures called G-quadruplexes. These structures may be very stable under physiological conditions. Evidence suggests that G-quadruplex structures may act as 'knots' within genomic DNA, and it has been hypothesized that proteins may have evolved to remove these structures.
Mendoza, Oscar   +4 more
openaire   +3 more sources

Structural insights and shedding light on preferential interactions of dietary flavonoids with G-quadruplex DNA structures: A new horizon

open access: yesHeliyon, 2023
G-quadruplex, a structurally unique structure in nucleic acids present all throughout the human genome, has sparked great attention in therapeutic investigations. Targeting G-quadruplex structure is a new strategy for the drug development. Flavonoids are
Sagar Bag   +2 more
doaj   +1 more source

G‐Quadruplex Nucleic Acids [PDF]

open access: yesJournal of Nucleic Acids, 2010
Peer ...
ERITJA R.   +4 more
openaire   +5 more sources

Polyelectrolyte effects in G-quadruplexes [PDF]

open access: yesBiophysical Chemistry, 2013
The role of counterion condensation as a dominant force governing the stability of DNA duplexes and triplexes is well established. In contrast, the effect of counterion condensation on the stability of G-quadrupex conformations is poorly understood. Unlike other ordered nucleic acid structures, G-quadruplexes exhibit a specific binding of counterions ...
Kim, Byul   +2 more
openaire   +2 more sources

Duplex DNA from Sites of Helicase-Polymerase Uncoupling Links Non-B DNA Structure Formation to Replicative Stress [PDF]

open access: yes, 2020
BACKGROUND: Replication impediments can produce helicase-polymerase uncoupling allowing lagging strand synthesis to continue for as much as 6 kb from the site of the impediment.
Abdelhamid, Mahmoud A S   +9 more
core   +2 more sources

G-Quadruplex Structures and G-Quadruplex-Interactive Compounds [PDF]

open access: yes, 2011
G-quadruplexes are noncanonical secondary structures formed in DNA sequences containing consecutive runs of guanines. DNA G-quadruplexes have recently emerged as attractive cancer therapeutic targets. It has been shown that the 3' G-rich single-stranded overhangs of human telomeres can form G-quadruplex structures.
Raveendra I, Mathad, Danzhou, Yang
openaire   +2 more sources

Aminoglycosylation can enhance the G-quadruplex binding activity of epigallocatechin. [PDF]

open access: yesPLoS ONE, 2013
With the aim of enhancing G-quadruplex binding activity, two new glucosaminosides (16, 18) of penta-methylated epigallocatechin were synthesized by chemical glycosylation.
Li-Ping Bai   +5 more
doaj   +1 more source

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