Year |
Citation |
Score |
2023 |
Maji A, Soutar CP, Zhang J, Lewandowska A, Uno BE, Yan S, Shelke Y, Murhade G, Nimerovsky E, Borcik CG, Arango AS, Lange JD, Marin-Toledo JP, Lyu Y, Bailey KL, et al. Tuning sterol extraction kinetics yields a renal-sparing polyene antifungal. Nature. PMID 37938782 DOI: 10.1038/s41586-023-06710-4 |
0.654 |
|
2018 |
Uno BE, Dicken RD, Redfern LR, Stern CM, Krzywicki GG, Scheidt KA. Calcium(ii)-catalyzed enantioselective conjugate additions of amines. Chemical Science. 9: 1634-1639. PMID 29675209 DOI: 10.1039/C7Sc05205G |
0.444 |
|
2017 |
Beniah G, Chen X, Uno BE, Liu K, Leitsch EK, Jeon J, Heath WH, Scheidt KA, Torkelson JM. Combined Effects of Carbonate and Soft-Segment Molecular Structures on the Nanophase Separation and Properties of Segmented Polyhydroxyurethane Macromolecules. 50: 3193-3203. DOI: 10.1021/Acs.Macromol.6B02513 |
0.483 |
|
2017 |
Beniah G, Uno BE, Lan T, Jeon J, Heath WH, Scheidt KA, Torkelson JM. Tuning nanophase separation behavior in segmented polyhydroxyurethane via judicious choice of soft segment Polymer. 110: 218-227. DOI: 10.1016/J.Polymer.2017.01.017 |
0.413 |
|
2014 |
Anderson TM, Clay MC, Cioffi AG, Diaz KA, Hisao GS, Tuttle MD, Nieuwkoop AJ, Comellas G, Maryum N, Wang S, Uno BE, Wildeman EL, Gonen T, Rienstra CM, Burke MD. Amphotericin forms an extramembranous and fungicidal sterol sponge. Nature Chemical Biology. 10: 400-6. PMID 24681535 DOI: 10.1038/Nchembio.1496 |
0.777 |
|
2013 |
Wilcock BC, Endo MM, Uno BE, Burke MD. C2'-OH of amphotericin B plays an important role in binding the primary sterol of human cells but not yeast cells. Journal of the American Chemical Society. 135: 8488-91. PMID 23718627 DOI: 10.1021/Ja403255S |
0.69 |
|
2012 |
Wilcock BC, Uno BE, Bromann GL, Clark MJ, Anderson TM, Burke MD. Electronic tuning of site-selectivity. Nature Chemistry. 4: 996-1003. PMID 23174979 DOI: 10.1038/Nchem.1495 |
0.705 |
|
2012 |
Gray KC, Palacios DS, Dailey I, Endo MM, Uno BE, Wilcock BC, Burke MD. Amphotericin primarily kills yeast by simply binding ergosterol. Proceedings of the National Academy of Sciences of the United States of America. 109: 2234-9. PMID 22308411 DOI: 10.1073/Pnas.1117280109 |
0.546 |
|
2009 |
Uno BE, Gillis EP, Burke MD. Vinyl MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis Tetrahedron. 65: 3130-3138. DOI: 10.1016/j.tet.2008.11.010 |
0.721 |
|
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