Roberts, B. F.; Iyamu, I. D.; Lee, S.; Lee, E.; Ayong, L.; Kyle, D. E.; Yuan, Y.; Manetsch, R.; Chakrabarti, D. Int. J. Parasitol. Drugs Drug Resist. 2016, 6, 85–92.
3-Trifluoromethyl-3-aryldiazirine photolabels with enhanced ambient light stability
Kumar, A. B.; Tipton, J. D.; Manetsch, R. Chem. Commun. 2016, 52, 2729-2732.
SAR refinement of antileishmanial N2,N4-disubstituted quinazoline-2,4-diamines
Zhu, X.; Van Horn, K. S.; Barber, M. M.; Yang, S.; Wang, M. Z.; Manetsch, R.; Werbovetz, K. A. Bioorg. Med. Chem. 2015, 23, 5182–5189.
Monastyrskyi, A.; Namelikonda, N. K.; Manetsch, R. J. Org. Chem. 2015, 4, 2513–2520.
Mahajan, S.; Manetsch, R.; Merkler, D. J.; Stevens Jr., S. M. PLoS One 2015, 10, 1–17.
Cross, R. M.; Flanigan, D. L.; Monastyrskyi, A.; LaCrue, A. N.; Sáenz, F. E.; Maignan, J. R.; Mutka, T. S.; White, K. L.; Shackleford, D. M.; Bathurst, I.; et al. J. Med. Chem. 2014, 57, 8860–8879.
Monastyrskyi, A.; Kyle, D. E.; Manetsch, R. Curr Top Med Chem, 2014; 1693-1705.
Campbell, C. O.; Santiago, D. N.; Guida, W. C.; Manetsch, R.; Adams, J. H. Chem. Biol. Drug Des. 2014, 84, 158–168.
Kumar, A. B.; Manetsch, R. European J. Org. Chem. 2014, 3551–3555.
Antibacterial activity of a series of N2,N4-disubstituted quinazoline-2,4-diamines
Van Horn, K. S.; Burda, W. N.; Fleeman, R.; Shaw, L. N.; Manetsch, R. J. Med. Chem. 2014, 57, 3075–3093.
Antileishmanial activity of a series of N2,N4-disubstituted quinazoline-2,4-diamines
Van Horn, K. S.; Zhu, X.; Pandharkar, T.; Yang, S.; Vesely, B.; Vanaerschot, M.; Dujardin, J.-C.; Rijal, S.; Kyle, D. E.; Wang, M. Z.; et al. J. Med. Chem. 2014, 57, 5141–5156.
Sáenz, F. E.; Lacrue, A. N.; Cross, R. M.; Maignan, J. R.; Udenze, K. O.; Manetsch, R.; Kyle, D. E. Antimicrob. Agents Chemother. 2013, 57, 6187–6195.
Quinolone-3-diarylethers: A new class of drugs for a new era of malaria eradication
Nilsen, A.; LaCrue, A.; White, K. L.; Forquer, I. P.; Cross, R. M.; Marfurt, J.; Mather, M. W.; Delves, M. J.; Shackleford, D. M.; Saenz, F. E.; Morrisey, J. M.; Steuten, J.; Mutka, T.; Li, Y.; Wirjanata, G.; Ryan, E.; Duffy, S.; Kelly, J. X.; Sebayang, B. F.; Zeeman, A-M.; Noviyanti, R.; Sinden, R. E.; Kocken, C. H. M.; Price, R. N.; Avery, V. M.; Angulo-Barturen, I.; Jiménez-Díaz, M. B.; Ferrer, S.; Herreros, E.; Sanz, L. M.; Benito, F. J. G.; Bathurst, I.; Burrows, J.; Siegl, P.; Guy, R. K.; Winter, R. W.; Vaidya, A. B.; Charman, S. A.; Kyle, D. E.; Manetsch, R.; Riscoe, M. K. Sci Transl Med, 2013, 5, 177.
A simple base-mediated amidation of aldehydes with azides
Kulkarni, S. S.; Hu, X.; Manetsch, R. Chem. Commun. (Camb). 2013, 49, 1193–1195.
4(1H)-Quinolones with liver stage activity against Plasmodium berghei
Lacrue, A. N.; Sáenz, F. E.; Cross, R. M.; Udenze, K. O.; Monastyrskyi, A.; Stein, S.; Mutka, T. S.; Manetsch, R.; Kyle, D. E. Antimicrob. Agents Chemother. 2013, 57, 417–424.
Fluorescent properties and resonance energy transfer of 3,4-bis(2,4-difluorophenyl)-maleimide
Nacheva, K. P.; Maza, W. a; Myers, D. Z.; Fronczek, F. R.; Larsen, R. W.; Manetsch, R. Org. Biomol. Chem. 2012, 10, 7840–7846.
Kumar, A. B.; Anderson, J. M.; Melendez, A. L.; Manetsch, R. Bioorg. Med. Chem. Lett. 2012, 22, 4740–4744.
Namelikonda, N. K.; Manetsch, R. Chem. Commun. (Camb). 2012, 48, 1526–1528.
Cross, R. M.; Namelikonda, N. K.; Mutka, T. S.; Luong, L.; Kyle, D. E.; Manetsch, R.; Monastyrskyi, A.; Burrows, J. N. J. Med. Chem. 2011, 54, 8321–8327.
Design, synthesis and photoactivation studies of fluorous photolabels
Kumar, A. B.; Anderson, J. M.; Manetsch, R. Org. Biomol. Chem. 2011, 9, 6284–6292.
Screening of protein-protein interaction modulators via sulfo-click kinetic target-guided synthesis
Kulkarni, S. S.; Hu, X.; Doi, K.; Wang, H.-G.; Manetsch, R. ACS Chem. Biol. 2011, 6, 724–732.
Cross, R. M.; Maignan, J. R.; Mutka, T. S.; Luong, L.; Sargent, J.; Kyle, D. E.; Manetsch, R. J. Med. Chem. 2011, 54, 4399–4426
Divergent route to access structurally diverse 4-quinolones via mono or sequential cross-couplings
Cross, R. M.; Manetsch, R. J. Org. Chem. 2010, 75, 8654–8657.
Cross, R. M.; Monastyrskyi, A.; Mutka, T. S.; Burrows, J. N.; Kyle, D. E.; Manetsch, R. J. Med. Chem. 2010, 53, 7076–7094.
Kinetic target-guided synthesis
Hu, X.; Manetsch, R. Chem. Soc. Rev. 2010, 39, 1316–1324.
Probing gorge dimensions of cholinesterases by freeze-frame click chemistry
Radić, Z.; Manetsch, R.; Fournier, D.; Sharpless, K. B.; Taylor, P. Chem. Biol. Interact. 2008, 175, 161–165.
Hu, X.; Sun, J.; Wang, H.; Manetsch, R. J. Am. Chem. Soc. 2008, 130, 13820–13821.
In situ click chemistry: A powerful means for lead discovery (Review)
Sharpless, B.; Manetsch, R. Expert Opinion on Drug Discovery 2006; 1: 525-538.
Molecular basis of interactions of cholinesterases with tight binding inhibitors
Radić, Z.; Manetsch, R.; Krasiński, A.; Raushel, J.; Yamauchi, J.; Garcia, C.; Kolb, H.; Sharpless, K. B.; Taylor, P. Chem. Biol. Interact. 2005, 157-158, 133–141.
Zheng, L.; Manetsch, R.; Woggon, W.-D.; Baumann, U.; Reymond, J.-L. Bioorg. Med. Chem. 2005, 13, 1021–1029.
Krasiński, A.; Radić, Z.; Manetsch, R.; Raushel, J.; Taylor, P.; Sharpless, K. B.; Kolb, H. C. J. Am. Chem. Soc. 2005, 127, 6686–6692.
A catalytic antibody against a tocopherol cyclase inhibitor
Manetsch, R.; Zheng, L.; Reymond, M. T.; Woggon, W.-D.; Reymond, J.-L. Chemistry 2004, 10, 2487–2506.
In situ click chemistry: enzyme inhibitors made to their own specifications
Manetsch, R.; Krasiński, A.; Radić, Z.; Raushel, J.; Taylor, P.; Sharpless, K. B.; Kolb, H. C. J. Am. Chem. Soc. 2004, 126, 12809–12818 .
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