ORA - Oxford University Research Archive

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1

Journal article

Synthesis and evaluation of 3-(dihydroxyboryl)benzoic acids as D,D-carboxypeptidase R39 inhibitors.

Inglis, SR, Zervosen, A, Woon, EC, et al.
2009-10-05

2

Journal article

N-O-isopropyl sulfonamido-based hydroxamates: design, synthesis and biological evaluation of selective matrix metalloproteinase-13 inhibitors as potential therapeutic agents for osteoarthritis.

Nuti, E, Casalini, F, Avramova, SI, et al.
2009-08-05

3

Journal article

SALMON: solvent accessibility, ligand binding, and mapping of ligand orientation by NMR spectroscopy.

Ludwig, C, Michiels, PJ, Wu, X, et al.
2008-01-05

4

Journal article

Structurally simple inhibitors of lanosterol 14alpha-demethylase are efficacious in a rodent model of acute Chagas disease.

Suryadevara, PK, Olepu, S, Lockman, JW, et al.
2009-06-05

5

Journal article

Structural basis of inhibitor specificity of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM-1) kinase.

Bullock, AN, Debreczeni, JE, Fedorov, OY, et al.
2005-12-05

6

Journal article

Relationship of potency and resilience to drug resistant mutations for GW420867X revealed by crystal structures of inhibitor complexes for wild-type, Leu100Ile, Lys101Glu, and Tyr188Cys mutant HIV-1 reverse transcriptases.

Ren, J, Nichols, CE, Chamberlain, PP, et al.
2007-05-05

7

Journal article

Inhibitor scaffolds for 2-oxoglutarate-dependent histone lysine demethylases.

Rose, NR, Ng, SS, Mecinović, J, et al.
2008-11-05

8

Journal article

Rational design and synthesis of highly potent pharmacological chaperones for treatment of N370S mutant Gaucher disease.

Wang, GN, Reinkensmeier, G, Zhang, SW, et al.
2009-05-05

9

Journal article

Ligand docking in the gastric H+/K+-ATPase: homology modeling of reversible inhibitor binding sites.

Kim, CG, Watts, JA, Watts, A
2005-11-05

10

Journal article

2'-deoxy cyclic adenosine 5'-diphosphate ribose derivatives: importance of the 2'-hydroxyl motif for the antagonistic activity of 8-substituted cADPR derivatives.

Zhang, B, Wagner, GK, Weber, K, et al.
2008-03-05

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