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Featured researches published by A. Huizing.


Journal of Medicinal Chemistry | 2015

Fighting Malaria: Structure-Guided Discovery of Nonpeptidomimetic Plasmepsin Inhibitors

A. Huizing; Milon Mondal; Anna K. H. Hirsch

Plasmepsins (Plms) are aspartic proteases involved in the degradation of human hemoglobin by Plasmodium falciparum. Given that the parasite needs the resulting amino acid building blocks for its growth and development, plasmepsins are an important antimalarial drug target. Over the past decade, tremendous progress has been achieved in the development of inhibitors of plasmepsin using two strategies: structure-based drug design (SBDD) and structure-based virtual screening (SBVS). Herein, we review the inhibitors of Plms I-IV developed by SBDD or SBVS with a particular focus on obtaining selectivity versus the human Asp proteases cathepsins and renin and activity in cell-based assays. By use of SBDD, the flap pocket of Plm II has been discovered and constitutes a convenient handle to obtain selectivity. In SBVS, activity against Plms I-IV and selectivity versus cathepsins are not always taken into account. A combination of SBVS, SBDD, and molecular dynamics simulations opens up opportunities for future design cycles.


Journal of Medicinal Chemistry | 2014

Synthesis and preclinical evaluation of 2-(2-furanyl)-7-[2-[4-[4-(2-[11C]methoxyethoxy)phenyl]-1-piperazinyl]ethyl]7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine-5-amine ([11C]Preladenant) as a PET tracer for the imaging of cerebral adenosine A2A receptors

Xiaoyun Zhou; Shivashankar Khanapur; A. Huizing; Rolf Zijlma; Marianne Schepers; Rudi A. J. O. Dierckx; Aren van Waarde; Erik F. J. de Vries; Philip H. Elsinga

2-(2-Furanyl)-7-[2-[4-[4-(2-[(11)C]methoxyethoxy)phenyl]-1-piperazinyl]ethyl]7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine-5-amine [(11)C]-3 ([(11)C]Preladenant) was developed for mapping cerebral adenosine A2A receptors (A2ARs) with PET. The tracer was synthesized in high specific activity and purity. Tissue distribution was studied by PET imaging, ex vivo biodistribution (BD), and in vitro autoradiography (ARG) experiments. Regional brain uptake of [(11)C]-3 was consistent with known A2ARs distribution, with highest uptake in striatum. The results indicate that [(11)C]-3 has favorable brain kinetics and exhibits suitable characteristics as an A2AR PET tracer.


Archive | 1995

Business reengineering- Het regisseren van complexe organisatieverandering

W. Bouman; A. Huizing; E. Koster; J. Mink; M. Oliehoek; L.E.J. Pels Rijcken; E.J. de Vries


Business Reengineering op doorreis: tussenstation of eindstation? | 1997

Marktwerking en informatietechnologie.

C. Ciborra; E.J. de Vries; A. Huizing


Tijdschrift voor Bedrijfsadministratie | 1998

Business reengineering: over en uit?

A. Huizing; E.J. de Vries


Business reengineering op doorreis: tussenstation of eindstation? | 1997

Waarom herontwerpprojecten mislukken en wat we daaraan kunnen doen

J.J. Boonstra; E.J. de Vries; A. Huizing


Associatie Nieuwsbrief | 1997

Is business reengineering aan het einde van zijn latijn

A. Huizing; E.J. de Vries


Anticancer Research | 1997

Verstrikt in eigen complexiteit - het relaas van een zorgverzekeraar.

E. Koster; E.J. de Vries; A. Huizing


ACM Sigsoft Software Engineering Notes | 1997

Informatie op het moment van de waarheid.

E.J. de Vries; A. Huizing


Computable | 1995

Betere resultaten bij meerdere veranderingen

E.J. de Vries; A. Huizing

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Aren van Waarde

University Medical Center Groningen

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Erik F. J. de Vries

University Medical Center Groningen

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Marianne Schepers

University Medical Center Groningen

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Milon Mondal

University of Groningen

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Philip H. Elsinga

University Medical Center Groningen

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Rolf Zijlma

University Medical Center Groningen

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Rudi A. J. O. Dierckx

University Medical Center Groningen

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Shivashankar Khanapur

University Medical Center Groningen

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Xiaoyun Zhou

University Medical Center Groningen

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