Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffolds. Sainas, S., Pippione, A. C., Giorgis, M., Lupino, E., Goyal, P., Ramondetti, C., Buccinnà, B., Piccinini, M., Braga, R. C., Andrade, C. H., Andersson, M., Moritzer, A., Friemann, R., Mensa, S., Al-Karadaghi, S., Boschi, D., & Lolli, M. L. European Journal of Medicinal Chemistry, 129:287–302, Elsevier BV, mar, 2017.
Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffolds [link]Paper  doi  bibtex   
@article{Sainas_2017,	doi = {10.1016/j.ejmech.2017.02.017},	url = {https://doi.org/10.1016%2Fj.ejmech.2017.02.017},	year = 2017,	month = {mar},	publisher = {Elsevier {BV}},	volume = {129},	pages = {287--302},	author = {Stefano Sainas and Agnese C. Pippione and Marta Giorgis and Elisa Lupino and Parveen Goyal and Cristina Ramondetti and Barbara Buccinn{\`{a}} and Marco Piccinini and Rodolpho C. Braga and Carolina H. Andrade and Mikael Andersson and Ann-Christin Moritzer and Rosmarie Friemann and Stefano Mensa and Salam Al-Karadaghi and Donatella Boschi and Marco L. Lolli},	title = {Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffolds},	journal = {European Journal of Medicinal Chemistry}}

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