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A. Haemers

Researcher at University of Antwerp

Publications -  20
Citations -  555

A. Haemers is an academic researcher from University of Antwerp. The author has contributed to research in topics: Diaminopimelic acid & Ames test. The author has an hindex of 8, co-authored 20 publications receiving 538 citations. Previous affiliations of A. Haemers include National Health Research Institutes.

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4'-Hydroxy-3-methoxyflavones with potent antipicornavirus activity.

TL;DR: The most interesting compound was 4',7-dihydroxy-3-methoxy-5,6-dimethylflavone possessing in vitro TI99 values of greater than 1000 and greater than 200 against poliovirus type 1 and rhinovirus type 15, respectively, and showed to be not mutagenic in concentrations up to 2.5 mg in the Ames test.
Journal Article

The unique properties of dipeptidyl-peptidase IV (DPP IV / CD26) and the therapeutic potential of DPP IV inhibitors.

TL;DR: In this paper, the properties and functions of dipeptidyl peptidase IV (DPP IV, EC 3.4.14.5) were discussed, and the role of CD26 in the intestinal and renal handling of proline containing peptides, in cell adhesion, in peptide metabolism, in the immune system and in HIV infection.
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The Unique Properties of Dipeptidyl-Peptidase IV (DPP IV / CD26) and the Therapeutic Potential of DPP IV Inhibitors

TL;DR: The latest developments in the search for new inhibitors will be reported as well as the discovery of new natural substrates for DPP IV such as the glucagon-like peptides and the chemokines.
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Irreversible Inhibition of Dipeptidyl Peptidase 8 by Dipeptide-Derived Diaryl Phosphonates

TL;DR: Dipeptide-derived compounds, bearing various P2 residues and a diaryl pyrrolidin-2-yl phosphonate at the P1 position, were evaluated as dipeptidyl peptidase 8 (DPP8) inhibitors and compound 2e was shown to be a potent, irreversible inhibitor of DPP8, demonstrating very low affinity for DPP IV and DPP II.
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Synthesis and antibacterial evaluation of phosphonic acid analogues of diaminopimelic acid

TL;DR: In this paper, the synthesis of a series of phosphonic acid analogues of this diamino-dicarboxylic acid is described: mono- and diphosphonic acid derivatives as well as their homologues, N -alkyl analogues and some peptidyl derivatives.