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Johan Van hemel

Researcher at University of Antwerp

Publications -  26
Citations -  369

Johan Van hemel is an academic researcher from University of Antwerp. The author has contributed to research in topics: Bicyclic molecule & Pyridine. The author has an hindex of 10, co-authored 26 publications receiving 348 citations.

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Hemin potentiates the anti-hepatitis C virus activity of the antimalarial drug artemisinin

TL;DR: It is reported that the antimalarial drug artemisinin inhibits hepatitis C virus (HCV) replicon replication in a dose-dependent manner in two replicon constructs at concentrations that have no effect on the proliferation of the exponentially growing host cells.
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Structure and X-ray conformation of pseudodesmins A and B, two new cyclic lipodepsipeptides from Pseudomonas bacteria

TL;DR: Two new cyclic lipodepsipeptides named pseudodesmins A and B have been isolated from Pseudomonas bacteria collected from the mucus layer in the skin of the black belly salamander and show moderate antibacterial activity against Gram positive bacteria, including MRSA.
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Spores from two distinct colony types of the strain Bacillus subtilis PB6 substantiate anti-inflammatory probiotic effects in mice

TL;DR: Subtilis strain PB6, provided as a preparation of spores, shows pre-clinical anti-inflammatory effects, suggesting further evaluation in a clinical intervention trial, e.g. with IBD type patients.
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A convergent ring-closing metathesis approach to carbohydrate-based macrolides with potential antibiotic activity.

TL;DR: An efficient convergent approach has been developed for the construction of novel, non-natural, carbohydrate-based macrolides and the obtained macrolide analogues have been screened for biological activity against gram-positive and gram-negative bacteria, including resistant strains, yeasts, and molds.
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Carbohydrate-based macrolides prepared via a convergent ring closing metathesis approach: in search for novel antibiotics.

TL;DR: An efficient convergent approach has been developed for the construction of novel, nonnatural polysubstituted carbohydrate-based macrolides through the formation of the macrocyclic ring via a ring-closing metathesis reaction.