Therapeutic inhibition of Myc in cancer. Structural bases and computer-aided drug discovery approaches
LA Carabet, PS Rennie, A Cherkasov - International journal of molecular …, 2018 - mdpi.com
Myc (avian myelocytomatosis viral oncogene homolog) represents one of the most sought
after drug targets in cancer. Myc transcription factor is an essential regulator of cell growth …
after drug targets in cancer. Myc transcription factor is an essential regulator of cell growth …
Ligand design to acquire specificity to intended G‐quadruplex structures
S Asamitsu, T Bando… - Chemistry–A European …, 2019 - Wiley Online Library
AG‐quadruplex is a nucleic acid secondary structure that is adopted by guanine‐rich
sequences, and is considered to be relevant in various pharmacological and biological …
sequences, and is considered to be relevant in various pharmacological and biological …
Digitizing chemistry using the chemical processing unit: from synthesis to discovery
Conspectus The digitization of chemistry is not simply about using machine learning or
artificial intelligence systems to process chemical data, or about the development of ever …
artificial intelligence systems to process chemical data, or about the development of ever …
[HTML][HTML] Small molecules targeting c-Myc oncogene: promising anti-cancer therapeutics
BJ Chen, YL Wu, Y Tanaka, W Zhang - International journal of …, 2014 - ncbi.nlm.nih.gov
The nuclear transcription factor c-Myc is a member of the Myc gene family with multiple
functions and located on band q24. 1 of chromosome 8. The c-Myc gene is activated by …
functions and located on band q24. 1 of chromosome 8. The c-Myc gene is activated by …
Drug repositioning by structure-based virtual screening
DL Ma, DSH Chan, CH Leung - Chemical Society Reviews, 2013 - pubs.rsc.org
Approved drugs have favourable or validated pharmacokinetic properties and toxicological
profiles, and the repositioning of existing drugs for new indications can potentially avoid …
profiles, and the repositioning of existing drugs for new indications can potentially avoid …
Conjugating a groove-binding motif to an Ir (III) complex for the enhancement of G-quadruplex probe behavior
In this study, the reported G-quadruplex groove binder benzo [d, e] isoquinoline was linked
to a cyclometallated Ir (III) complex to generate a highly selective DNA probe 1 that retains …
to a cyclometallated Ir (III) complex to generate a highly selective DNA probe 1 that retains …
Cell penetrating thiazole peptides inhibit c-MYC expression via site-specific targeting of c-MYC G-quadruplex
The structural differences among different G-quadruplexes provide an opportunity for site-
specific targeting of a particular G-quadruplex structure. However, majority of G-quadruplex …
specific targeting of a particular G-quadruplex structure. However, majority of G-quadruplex …
Structural insight for the recognition of G-quadruplex structure at human c-myc promoter sequence by flavonoid Quercetin
Small molecule ligands that could stabilize G-quadruplex structure formed at the promoter
region of human c-myc oncogene will regulate its expression in cancer cells. Flavonoids, a …
region of human c-myc oncogene will regulate its expression in cancer cells. Flavonoids, a …
Selective, disruptive luminescent Ru (II) polypyridyl probes of G-quadruplex
Sensors capable of transducing G-quadruplex DNA binding are important both in solution
and for imaging and interrogation in cellulo. Ru (II)-based light switches incorporating …
and for imaging and interrogation in cellulo. Ru (II)-based light switches incorporating …
G-quadruplex virtual drug screening: A review
RC Monsen, JO Trent - Biochimie, 2018 - Elsevier
Over the past two decades biologists and bioinformaticians have unearthed substantial
evidence supporting a role for G-quadruplexes as important mediators of biological …
evidence supporting a role for G-quadruplexes as important mediators of biological …