Evaluation of by disubstituted acridone derivatives as telomerase inhibitors: the importance of G-quadruplex binding
- 1 December 2004
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 14 (23) , 5845-5849
- https://doi.org/10.1016/j.bmcl.2004.09.037
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Crystal structure of parallel quadruplexes from human telomeric DNANature, 2002
- Telomerase inhibition, oligonucleotides, and clinical trialsOncogene, 2002
- Telomerase inhibitorsPublished by Elsevier ,2001
- NMR-Based Model of a Telomerase-Inhibiting Compound Bound to G-Quadruplex DNABiochemistry, 1998
- Specific Association of Human Telomerase Activity with Immortal Cells and CancerScience, 1994
- Inhibition of telomerase by G-quartet DMA structuresNature, 1991
- Potential antitumor agents. 36. Quantitative relationships between experimental antitumor activity, toxicity, and structure for the general class of 9-anilinoacridine antitumor agentsJournal of Medicinal Chemistry, 1982
- Potential antitumor agents. 24. Dicationic analogs of the 4'-(9-acridinylamino)alkanesulfonanilidesJournal of Medicinal Chemistry, 1977
- 29. Synthesis of diaminoacridines. Part IJournal of the Chemical Society, 1946
- THE SYNTHESIS OF CERTAIN ACRIDINE COMPOUNDSJournal of the American Chemical Society, 1929