Literature DB >> 22421021

Identification of novel telomeric G-quadruplex-targeting chemical scaffolds through screening of three NCI libraries.

Khondaker M Rahman1, Karolina Tizkova, Anthony P Reszka, Stephen Neidle, David E Thurston.   

Abstract

Thirteen compounds with diverse chemical structures have been identified as selective telomeric G-quadruplex-binding ligands through screening the NCI Diversity Set II, the NCI Natural Products Set II and the NCI Mechanistic Diversity Set libraries containing a total of 2307 members against a human telomeric G-quadruplex using a FRET-based DNA melting assay. These compounds show significant selectivity towards a telomeric G-quadruplex compared to duplex DNA, fall within a molecular weight range of 327-533, and are generally consistent with the Lipinski Rule of Five for drug-likeness. Thus they provide new chemical scaffolds for the development of novel classes of G-quadruplex-targeting agents.
Copyright © 2012 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22421021     DOI: 10.1016/j.bmcl.2012.02.020

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  9 in total

Review 1.  A practical guide to studying G-quadruplex structures using single-molecule FRET.

Authors:  Parastoo Maleki; Jagat B Budhathoki; William A Roy; Hamza Balci
Journal:  Mol Genet Genomics       Date:  2017-02-01       Impact factor: 3.291

2.  A single molecule study of a fluorescently labeled telomestatin derivative and G-quadruplex interactions.

Authors:  Parastoo Maleki; Yue Ma; Keisuke Iida; Kazuo Nagasawa; Hamza Balci
Journal:  Nucleic Acids Res       Date:  2016-11-29       Impact factor: 16.971

3.  Identification, synthesis and evaluation of substituted benzofurazans as inhibitors of CREB-mediated gene transcription.

Authors:  Fuchun Xie; Bingbing X Li; Candice Broussard; Xiangshu Xiao
Journal:  Bioorg Med Chem Lett       Date:  2013-07-31       Impact factor: 2.823

4.  Finding and characterizing the complexes of drug like molecules with quadruplex DNA: combined use of an enhanced hydroxyl radical cleavage protocol and NMR.

Authors:  Harikrushan Ranpura; Dobroslawa Bialonska; Philip H Bolton
Journal:  PLoS One       Date:  2014-04-24       Impact factor: 3.240

Review 5.  Target-Directed Approaches for Screening Small Molecules against RNA Targets.

Authors:  Hafeez S Haniff; Laurent Knerr; Jonathan L Chen; Matthew D Disney; Helen L Lightfoot
Journal:  SLAS Discov       Date:  2020-05-18       Impact factor: 3.341

6.  Characterization of clinically used oral antiseptics as quadruplex-binding ligands.

Authors:  David R Calabrese; Katherine Zlotkowski; Stephanie Alden; William M Hewitt; Colleen M Connelly; Robert M Wilson; Snehal Gaikwad; Lu Chen; Rajarshi Guha; Craig J Thomas; Beverly A Mock; John S Schneekloth
Journal:  Nucleic Acids Res       Date:  2018-04-06       Impact factor: 16.971

7.  Quantifying the impact of small molecule ligands on G-quadruplex stability against Bloom helicase.

Authors:  Parastoo Maleki; Golam Mustafa; Prabesh Gyawali; Jagat B Budhathoki; Yue Ma; Kazuo Nagasawa; Hamza Balci
Journal:  Nucleic Acids Res       Date:  2019-11-18       Impact factor: 16.971

8.  In Silico Design, Synthesis, and Biological Evaluation of Anticancer Arylsulfonamide Endowed with Anti-Telomerase Activity.

Authors:  Giulia Culletta; Mario Allegra; Anna Maria Almerico; Ignazio Restivo; Marco Tutone
Journal:  Pharmaceuticals (Basel)       Date:  2022-01-10

Review 9.  Major Achievements in the Design of Quadruplex-Interactive Small Molecules.

Authors:  Eduarda Mendes; Israa M Aljnadi; Bárbara Bahls; Bruno L Victor; Alexandra Paulo
Journal:  Pharmaceuticals (Basel)       Date:  2022-02-28
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.