97606-26-3Relevant articles and documents
One small molecule as a theranostic agent: Naphthalimide dye for subcellular fluorescence localization and photodynamic therapy: In vivo
Zhang, Lei,Lei, Kecheng,Zhang, Jingwen,Song, Wenlin,Zheng, Yuanhong,Tan, Shaoying,Gao, Yuwei,Xu, Yufang,Liu, Jianwen,Qian, Xuhong
supporting information, p. 1171 - 1175 (2016/07/06)
A novel single and small molecular theranostic agent (1a) based on a naphthalimide dye has been developed and characterized. The agent (1a) displays excellent fluorescence for cell imaging (fluorescent quantum yields of 0.81) and photodynamic effects for
Five-member thio-heterocyclic fused naphthalimides with aminoalkyl side chains: Intercalation and photocleavage to DNA
Xu, Yufang,Qu, Baoyuan,Qian, Xuhong,Li, Yonggang
, p. 1139 - 1142 (2007/10/03)
Novel five-member thio-heterocyclic fused naphthalimides with aminoalkyl side chains were designed, synthesized and evaluated. These compounds have high Scatchard binding constants. They could damage DNA (supercoiled pBR322) from form I (closed) to II (ni
Novel naphthalimide hydroperoxide photonucleases: The role of thiocyclic-Fused area and the difference in spectra, photochemistry and photobiological activity
Xu, Yufang,Qian, Xuhong,Yao, Wei,Mao, Ping,Cui, Jingnan
, p. 5427 - 5433 (2007/10/03)
Novel five- and six-membered thiocyclic-fused naphthalimide hydroperoxides (7, 8) as photonucleases were designed, synthesized via unusual isomerization in Pschorr cyclization and photooxygenation. The five-membered 7 was able to induce single-strand nick
