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PreviewIssue DateTitleAuthor(s)
2006Gas-phase synthesis and reactivity of binuclear gold hydride cations, (R3PAu)(2)H+ (R = Me and Ph)Khairallah, G.; O'Hair, R.; Bruce, M.
2006High-resolution EXAFS of the active site of human sulfite oxidase: Comparison with density functional theory and X-ray crystallographic resultsHarris, H.; George, G.; Rajagopalan, K.
2004Novel endoperoxide antimalarials: Synthesis, heme binding, and antimalarial activityTaylor, D.; Avery, T.; Greatrex, B.; Tiekink, E.; Macreadie, I.; Macreadie, P.; Humphries, A.; Kalkanidis, M.; Fox, E.; Klonis, N.; Tilley, L.
2005Developments in the design and synthesis of calpain inhibitorsNeffe, A.; Abell, A.
2017Reaction mechanism of the metallohydrolase CpsB from Streptococcus pneumoniae, a promising target for novel antimicrobial agentsMonteiro Pedroso, M.; Selleck, C.; Bilyj, J.; Harmer, J.; Gahan, L.; Mitić, N.; Standish, A.; Tierney, D.; Larrabee, J.; Schenk, G.
2019Sulfonamide-based inhibitors of biotin protein ligase as new antibiotic leadsLee, K.J.; Tieu, W.; Blanco-Rodriguez, B.; Paparella, A.S.; Yu, J.; Hayes, A.; Feng, J.; Marshall, A.C.; Noll, B.; Milne, R.; Cini, D.; Wilce, M.C.J.; Booker, G.W.; Bruning, J.B.; Polyak, S.W.; Abell, A.D.
2021Inhibition of Mycobacterium tuberculosis dethiobiotin synthase (MtDTBS): toward next-generation antituberculosis agentsSchumann, N.C.; Lee, K.J.; Thompson, A.P.; Salaemae, W.; Pederick, J.L.; Avery, T.; Gaiser, B.I.; Hodgkinson-Bean, J.; Booker, G.W.; Polyak, S.W.; Bruning, J.B.; Wegener, K.L.; Abell, A.D.
2008Meriolins (3-(pyrimidin-4-yl)-7-azaindoles): synthesis, kinase inhibitory activity, cellular effects, and structure of a CDK2/cyclin A/Meriolin complexEchalier, A.; Bettayeb, K.; Ferandin, Y.; Lozach, O.; Clement, M.; Valette, A.; Liger, F.; Marquet, B.; Morris, J.; Endicott, J.; Joseph, B.; Meijer, L.
2007Modified active site coordination in a clinical mutant of sulfite oxidaseDoonan, C.; Wilson, H.; Rajagopalan, K.; Garrett, R.; Bennett, B.; Prince, R.; George, G.
2014Discovery of (E)-3-((Styrylsulfonyl) methyl) pyridine and (E)-2-((Styrylsulfonyl) methyl) pyridine Derivatives as Anticancer Agents: Synthesis, Structure–Activity Relationships, and Biological ActivitiesLu, T.; Goh, A.W.; Yu, M.; Adams, J.; Lam, F.; Teo, T.; Li, P.; Noll, B.; Zhong, L.; Diab, S.; Chahrour, O.; Hu, A.; Abbas, A.; Liu, X.; Huang, S.; Sumby, C.; Milne, R.; Midgley, C.; Wang, S.