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Gunther Bal, Ph.D.

Affiliations: 
2002 Universitaire Instelling Antwerpen (Belgium) 
Area:
Pharmaceutical Chemistry, Pharmacy, Organic Chemistry
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K Augustyns grad student 2002 Universitaire Instelling Antwerpen (Belgium)
 (Dipeptidyl peptides IV and prolyl oligopeptidase: Design, synthesis and evaluation of substrates and inhibitors.)

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Publications

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Berg M, Bal G, Goeminne A, et al. (2009) Synthesis of bicyclic N-arylmethyl-substituted iminoribitol derivatives as selective nucleoside hydrolase inhibitors. Chemmedchem. 4: 249-60
Goeminne A, Berg M, McNaughton M, et al. (2008) N-Arylmethyl substituted iminoribitol derivatives as inhibitors of a purine specific nucleoside hydrolase. Bioorganic & Medicinal Chemistry. 16: 6752-63
Goeminne A, McNaughton M, Bal G, et al. (2008) Synthesis and biochemical evaluation of guanidino-alkyl-ribitol derivatives as nucleoside hydrolase inhibitors. European Journal of Medicinal Chemistry. 43: 315-26
Goeminne A, McNaughton M, Bal G, et al. (2007) 1,2,3-Triazolylalkylribitol derivatives as nucleoside hydrolase inhibitors. Bioorganic & Medicinal Chemistry Letters. 17: 2523-6
Pil J, Van der Veken P, Bal G, et al. (2004) Synthesis and electrophysiological characterization of cyclic morphiceptin analogues. Biochemical Pharmacology. 67: 1887-95
Bal G, Van der Veken P, Antonov D, et al. (2003) Prolylisoxazoles: potent inhibitors of prolyloligopeptidase with antitrypanosomal activity. Bioorganic & Medicinal Chemistry Letters. 13: 2875-8
Senten K, Van der Veken P, Bal G, et al. (2002) Development of potent and selective dipeptidyl peptidase II inhibitors. Bioorganic & Medicinal Chemistry Letters. 12: 2825-8
Amssoms K, Oza SL, Augustyns K, et al. (2002) Glutathione-like tripeptides as inhibitors of glutathionylspermidine synthetase. Part 2: substitution of the glycine part. Bioorganic & Medicinal Chemistry Letters. 12: 2703-5
Amssoms K, Oza SL, Ravaschino E, et al. (2002) Glutathione-like tripeptides as inhibitors of glutathionylspermidine synthetase. Part 1: Substitution of the glycine carboxylic acid group. Bioorganic & Medicinal Chemistry Letters. 12: 2553-6
Lambeir AM, Proost P, Durinx C, et al. (2001) Kinetic investigation of chemokine truncation by CD26/dipeptidyl peptidase IV reveals a striking selectivity within the chemokine family. The Journal of Biological Chemistry. 276: 29839-45
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