PMID

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Understanding the binding of 5-substituted 2'-deoxyuridine substrates to thymidine kinase of herpes simplex virus type-1.

Katholieke Universiteit Leuven

New derivatives of kanamycin B obtained by combined modifications in positions 1 and 6". Synthesis, microbiological properties, and in vitro and computer-aided toxicological evaluation.

Katholieke Universiteit Leuven

Synthesis and evaluation of 5-substituted 2'-deoxyuridine monophosphate analogues as inhibitors of flavin-dependent thymidylate synthase in Mycobacterium tuberculosis.

Katholieke Universiteit Leuven

Synthesis and biological evaluation of (11)C-labeled beta-galactosyl triazoles as potential PET tracers for in vivo LacZ reporter gene imaging.

Katholieke Universiteit Leuven

Synthesis and biological evaluation of an 123I-labeled bicyclic nucleoside analogue (BCNA) as potential SPECT tracer for VZV-tk reporter gene imaging.

Katholieke Universiteit Leuven

New approaches toward anti-HIV chemotherapy.

Katholieke Universiteit Leuven

Aminoacyl-tRNA synthetase inhibitors as potential antibiotics.

Katholieke Universiteit Leuven

Preclinical evaluation of 1H-benzylindole derivatives as novel human immunodeficiency virus integrase strand transfer inhibitors.

Katholieke Universiteit Leuven

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Katholieke Universiteit Leuven

Synthesis and evaluation of three 18F-labeled aminophenylbenzothiazoles as amyloid imaging agents.

Katholieke Universiteit Leuven

Substrate based peptide aldehyde inhibits bacterial type I signal peptidase.

Katholieke Universiteit Leuven

Synthesis and anti-HIV studies of 2- and 3-adamantyl-substituted thiazolidin-4-ones.

Katholieke Universiteit Leuven

Synthesis and evaluation of 18F-labeled 2-phenylbenzothiazoles as positron emission tomography imaging agents for amyloid plaques in Alzheimer's disease.

Katholieke Universiteit Leuven

Synthesis and anti-HIV studies of 2-adamantyl-substituted thiazolidin-4-ones.

Katholieke Universiteit Leuven

Identification of potent and selective neuropeptide Y Y(1) receptor agonists with orexigenic activity in vivo.

Schering-Plough Research Institute

Synthesis and structure-activity relationships of amide derivatives of (4,4-difluoro-1,2,3,4-tetrahydro-5H-1-benzazepin-5-ylidene)acetic acid as selective arginine vasopressin V2 receptor agonists.

Astellas Pharma