41382-35-8Relevant articles and documents
Naphthalimide intercalators with chiral amino side chains: Effects of chirality on DNA binding, photodamage and antitumor cytotoxicity
Yang, Qing,Yang, Peng,Qian, Xuhong,Tong, Lianpeng
scheme or table, p. 6210 - 6213 (2009/07/18)
Several novel heterocyclic-fused naphthalimides intercalators with chiral amino side chains were investigated. Their side chains' chiral configuration determines DNA binding activities in the order: S-enantiomers > R-enantiomers. And their DNA photodamagi
Thio-heterocylic naphthalimides with aminoalkyl side chains: Novel alternative tools for photodegradation of genomic DNA without impairment on bioactivities of proteins
Yang, Qing,Qian, Xuhong,Xu, Jianqiang,Sun, Yuanshe,Li, Yonggang
, p. 1615 - 1622 (2007/10/03)
Thio-heterocylic naphthalimides (R1-R5) were designed, synthesized and evaluated as nonmetallic and long-wavelength photocleavers. Some of them showed highly efficient abilities in the degradation of plasmid and genomic DNA under the mild conditions witho
OLIGOMERIC DYES AND PREPARATION THEREOF
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Page 25, (2010/02/06)
The invention provides a method for preparing an oligomeric dye by reacting a first component oligomer, having a carbon-carbon backbone, comprising a plurality of polymerized monomer units comprising pendant reactive nucleophilic or electrophilic functional groups; and a dye component having a co-reactive functional group.These oligomeric dyes are suitable for use as additives to impart coloration or fluorescence to thermoplastic polymers, particularly olefinic polymers. The oligomeric dyes of the present invention advantageously are compatible in polymers where conventional dyes often have poor compatibility or solubility.