Structure-based Design, Synthesis, and Evaluation of 2′-(2-Hydroxyethyl)-2′-Deoxyadenosine and Its 5′-Diphosphate as Novel Ribonucleotide Reductase Inhibitors

Por Sun, Dianqing, Xu, Hai, Wijerathna, Sanath, R., Dealwis, Chris, Lee, Richard E.
Publicado em 2009

Role of Arginine 293 and Glutamine 288 in Communication between Catalytic and Allosteric Sites in Yeast Ribonucleotide Reductase

Por Ahmad, Md. Faiz, Kaushal, Prem Singh, Wan, Qun, Wijerathna, Sanath R., An, Xiuxiang, Huang, Mingxia, Dealwis, Chris Godfrey
Publicado em 2012

The Structural Basis for Peptidomimetic Inhibition of Eukaryotic Ribonucleotide Reductase: a Conformationally Flexible Pharmacophore

Por Xu, Hai, Fairman, James W., Wijerathna, Sanath R., Kreischer, Nathan R., LaMacchia, John, Helmbrecht, Elizabeth, Cooperman, Barry S., Dealwis, Chris
Publicado em 2008

Inhibition of yeast ribonucleotide reductase by Sml1 depends on the allosteric state of the enzyme

Por Misko, Tessianna A., Wijerathna, Sanath R., Radivoyevitch, Tomas, Berdis, Anthony J., Ahmad, Md. Faiz, Harris, Michael E., Dealwis, Chris G.
Publicado no FEBS Lett (2016)

Targeting the Large Subunit of Human Ribonucleotide Reductase for Cancer Chemotherapy

Por Wijerathna, Sanath R., Ahmad, Md. Faiz, Xu, Hai, Fairman, James W., Zhang, Andrew, Kaushal, Prem Singh, Wan, Qun, Kiser, Jianying, Dealwis, Chris G.
Publicado em 2011