Photo-induced cytotoxicity of malonic acid [C60]fullerene derivatives and its mechanism
- 21 January 2002
- journal article
- Published by Elsevier in Toxicology in Vitro
- Vol. 16 (1) , 41-46
- https://doi.org/10.1016/s0887-2333(01)00102-3
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Synthesis of oligoadducts of malonic acid C 60 and their scavenging effects on hydroxyl radicalJournal of Physics and Chemistry of Solids, 2000
- Hydroxyl Radical Scavenging and Producing Activities of Water-Soluble Malonic Acid C60Fullerene Science and Technology, 2000
- Activity of water-soluble fullerenes towards OH-radicals and molecular oxygenRadiation Physics and Chemistry, 1999
- Carboxyfullerenes as neuroprotective agentsProceedings of the National Academy of Sciences, 1997
- Sequence-specific modification of guanosine in DNA by a C60-linked deoxyoligonucleotide: Evidence for a non-singlet oxygen mechanismTetrahedron, 1996
- Fullerene–Oligonucleotide Conjugates: Photoinduced Sequence‐Specific DNA CleavageAngewandte Chemie International Edition in English, 1995
- Free radical scavenging activity of water-soluble fullerenolsJournal of the Chemical Society, Chemical Communications, 1995
- Inhibition of the HIV-1 protease by fullerene derivatives: model building studies and experimental verificationJournal of the American Chemical Society, 1993
- A new class of proteinase inhibitor. Cyclopropenone-containing inhibitor of papainJournal of the American Chemical Society, 1993
- Photophysical properties of sixty atom carbon molecule (C60)The Journal of Physical Chemistry, 1991