scispace - formally typeset
Open AccessJournal ArticleDOI

Anticancer activity expressed by a library of 2,9-diazaperopyrenium dications.

Reads0
Chats0
TLDR
Investigations reveal that a number of 2,9-diazaperopyrenium dications show similar activities as doxorubicin toward a variety of cancer cell lines, and reports the solid-state structures of these dications, and relates their tendency to aggregate in solution to their toxicity profiles.
Abstract
Polyaromatic compounds are well-known to intercalate DNA. Numerous anticancer chemotherapeutics have been developed upon the basis of this recognition motif. The compounds have been designed such t...

read more

Citations
More filters
Journal ArticleDOI

ExTzBox: A Glowing Cyclophane for Live-Cell Imaging

TL;DR: A simple, yet effective, strategy is introduced based on well-established chemistry for designing a new class of fluorescent probes for live-cell imaging that is non-cytotoxic to RAW 264.7 macrophages and allows the cells to glow brightly with blue laser excitation without any hint of photobleaching or disruption of normal cell behavior under the imaging conditions.
Journal ArticleDOI

Intramolecular Energy and Electron Transfer within a Diazaperopyrenium-Based Cyclophane

TL;DR: The synthesis, characterization, and photophysical properties of a rationally designed multichromophoric tetracationic cyclophane, DAPPBox4+, containing a diazaperopyrenium (DAPP2+) unit and an extended viologen (ExBIPY2%) unit, which are linked together by two p-xylylene bridges are reported on.
Journal ArticleDOI

Donor-acceptor single cocrystal of coronene and perylene diimide: molecular self-assembly and charge-transfer photoluminescence

TL;DR: In this paper, a successful molecular self-assembly design for the perylene-3,4,9,10-tetracarboxylic (PTCDI) cocrystal with a donor molecule, coronene, was reported.
Journal ArticleDOI

Toward a Charged Homo[2]catenane Employing Diazaperopyrenium Homophilic Recognition

TL;DR: It is shown that irradiation of the DAPPHC8+ catenane at 330 nm in acetonitrile solution results in simultaneous energy and electron transfer and the generation of a temporary charge-separated state within a rigid and robust homo[2]catenane.
Journal ArticleDOI

Concurrent Covalent and Supramolecular Polymerization.

TL;DR: A concurrent covalent and supramolecular polymerization strategy-namely, one which utilizes a bis-azide-functionalized diazaperopyrenium dication that undergoes polymeriation covalently with a Bis-alkyne- functionalized biphenyl derivative in one dimension, resulting in an extended polymer network in an orthogonal dimension is described.
References
More filters
Journal ArticleDOI

A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics adriamycin and daunorubicin

TL;DR: The potential role of DNA synthesis inhibition, free radical formation and lipid peroxidation, DNA binding and alkylation, DNA cross-linking, interference with DNA strand separation and helicase activity, direct membrane effects, and the initiation of DNA damage via the inhibition of topoisomerase II in the interaction of these drugs with the tumor cell are addressed.
Journal ArticleDOI

Structural considerations in the interaction of DNA and acridines.

TL;DR: The proposed structural change is compatible with the normal restrictions on bond lengths, angles, and non-bonded contacts, and maintenance of the hydrogen- bonded base pairs perpendicular to the axis of the molecule.
Journal ArticleDOI

Perylene bisimide dyes as versatile building blocks for functional supramolecular architectures

TL;DR: Perylene bisimide dyes and their organization into supramolecular architectures through hydrogen-bonding, metal ion coordination and pi-pi-stacking is discussed; further self-assembly leading to nano- and meso-scopic structures and liquid-crystalline compounds is also addressed.
Journal ArticleDOI

Adriamycin-induced DNA damage mediated by mammalian DNA topoisomerase II

TL;DR: In studies in vitro, mammalian DNA topoisomerase II mediates DNA damage by adriamycin and other related antitumor drugs, and has been shown to induce single- and double-strand breaks in DNA.
Journal ArticleDOI

DNA and its associated processes as targets for cancer therapy

TL;DR: A new generation of agents that target DNA-associated processes are anticipated to be far more specific and effective in cancer therapeutics.
Related Papers (5)