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PreviewIssue DateTitleAuthor(s)
2005Design and synthesis of aromatic inhibitors of anthranilate synthasePayne, R.; Bulloch, E.; Abell, A.; Abell, C.
2004Identification and specificity studies of small-molecule ligands for SH3 protein domainsInglis, S.; Stojkoski, C.; Branson, K.; Cawthray, J.; Fritz, D.; Wiadrowski, E.; Pyke, S.; Booker, G.
2007Interaction of product analogues with the active site of Rhodobacter sphaeroides dimethyl sulfoxide reductaseGeorge, G.; Nelson, K.; Harris, H.; Doonan, C.; Rajagopalan, K.
2008Synthesis, biological evaluation and molecular modelling of N-heterocyclic dipeptide aldehydes as selective calpain inhibitorsJones, M.; Morton, J.; Coxon, J.; McNabb, S.; Lee, H.; Aitken, S.; Mehrtens, J.; Robertson, L.; Neffe, A.; Miyamoto, S.; Bickerstaffe, R.; Gately, K.; Wood, J.; Abell, A.
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.
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.
2007Investigation into the P3 binding domain of m-calpain using photoswitchable diazo- and triazene-dipeptide aldehydes: New anticataract agentsAbell, A.; Jones, M.; Neffe, A.; Aitken, S.; Cain, T.; Payne, R.; McNabb, S.; Coxon, J.; Stuart, B.; Pearson, D.; Lee, H.; Morton, J.

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