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Ulrike Holzgrabe

Researcher at University of Würzburg

Publications -  591
Citations -  11158

Ulrike Holzgrabe is an academic researcher from University of Würzburg. The author has contributed to research in topics: Allosteric regulation & Capillary electrophoresis. The author has an hindex of 45, co-authored 566 publications receiving 9806 citations. Previous affiliations of Ulrike Holzgrabe include Jagiellonian University & University of Illinois at Chicago.

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Routine quality control of medicines in developing countries: Analytical challenges, regulatory infrastructures and the prevalence of counterfeit medicines in Tanzania

TL;DR: In this paper, the authors collected information on the prevalence of counterfeit and substandard pharmaceuticals in Tanzania and discussed suitable analytical approaches for their analysis, e.g. non-sophisticated HPLC, low-field NMR, capillary electrophoresis, or vibrational spectroscopy.
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Atypical Muscarinic Allosteric Modulation: Cooperativity between Modulators and Their Atypical Binding Topology in Muscarinic M2 and M2/M5 Chimeric Receptors

TL;DR: The atypical actions of tacrine and Duo3 involve different modes of receptor interaction, but their sites of attachment seem to be the “common” allosteric binding domain at the entrance to the orthosteric ligand binding pocket of the M2-receptor.
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A Photoswitchable Dualsteric Ligand Controlling Receptor Efficacy

TL;DR: BQCAAI proved to be an unprecedented molecular tool; it is the first photoswitchable dualsteric ligand, and its activity can be regulated by light, and it was applied to investigate the time course of several receptor activation processes.
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Composition of OSCS-contaminated heparin occurring in 2008 in batches on the German market.

TL;DR: Analysis of a representative set of heparin samples proves the suitability of 1H NMR spectroscopy for the quality control ofheparin of both glycosaminoglycans and residual solvents.
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Search for dual function inhibitors for Alzheimer’s disease: Synthesis and biological activity of acetylcholinesterase inhibitors of pyridinium-type and their Aβ fibril formation inhibition capacity

TL;DR: The anti-Abeta fibril formation property of AChE inhibitors of pyridinium- and bispyrid inium-type was evaluated to expand their activity profile and to reveal potential additive pharmacological effects which may reinforce their therapeutic application besides their capacity of increasing acetylcholine levels.