Song DING

Affiliations: 
2010-2015 Chemistry Wake Forest University, Winston-Salem, NC, United States 
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"Song DING"
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Ding S, Hackett CL, Liu F, et al. (2020) Evaluation of a Platinum-Acridine Anticancer Agent and Its Liposomal Formulation in an In Vivo Model of Lung Adenocarcinoma. Chemmedchem
Zheng Y, Fahrenholtz C, Hackett C, et al. (2017) Large-Pore Functionalized Mesoporous Silica Nanoparticles as Drug Delivery Vector for a Highly Cytotoxic Hybrid Platinum-Acridine Anticancer Agent. Chemistry (Weinheim An Der Bergstrasse, Germany)
Fahrenholtz CD, Ding S, Bernish BW, et al. (2016) Design and cellular studies of a carbon nanotube-based delivery system for a hybrid platinum-acridine anticancer agent. Journal of Inorganic Biochemistry
Fahrenholtz CD, Ding S, Bernish BW, et al. (2016) Abstract B05: Self-assembling platinum-acridine loaded carbon nanotubes for triple-negative breast cancer chemotherapy Molecular Cancer Research. 14
Ding S, Bierbach U. (2015) Target-selective delivery and activation of platinum-based anticancer agents. Future Medicinal Chemistry. 7: 911-27
Ding S, Pickard AJ, Kucera GL, et al. (2014) Design of enzymatically cleavable prodrugs of a potent platinum-containing anticancer agent. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 16164-73
Qiao X, Ding S, Liu F, et al. (2014) Investigating the cellular fate of a DNA-targeted platinum-based anticancer agent by orthogonal double-click chemistry. Journal of Biological Inorganic Chemistry : Jbic : a Publication of the Society of Biological Inorganic Chemistry. 19: 415-26
Ding S, Qiao X, Suryadi J, et al. (2013) Using fluorescent post-labeling to probe the subcellular localization of DNA-targeted platinum anticancer agents. Angewandte Chemie (International Ed. in English). 52: 3350-4
Ding S, Qiao X, Kucera GL, et al. (2013) Design of a platinum-acridine-endoxifen conjugate targeted at hormone-dependent breast cancer. Chemical Communications (Cambridge, England). 49: 2415-7
Ding S, Qiao X, Kucera GL, et al. (2012) Using a build-and-click approach for producing structural and functional diversity in DNA-targeted hybrid anticancer agents. Journal of Medicinal Chemistry. 55: 10198-203
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