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Bertil Samuelsson

Researcher at Stockholm University

Publications -  201
Citations -  6228

Bertil Samuelsson is an academic researcher from Stockholm University. The author has contributed to research in topics: Protease & HIV-1 protease. The author has an hindex of 40, co-authored 201 publications receiving 6072 citations. Previous affiliations of Bertil Samuelsson include National Institute for Medical Research & Linköping University.

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Novel reagent system for converting a hydroxy-group into an iodo-group in carbohydrates with inversion of configuration. Part 2

TL;DR: In this article, isolated primary and secondary hydroxy-groups in carbohydrate derivatives are transformed into iodo-groups with inversion of configuration on treatment with either triphenylphosphine, iodine, and imidazole or triphensyl-phosphines and 2,4,5-tri-iodoimidazoles at elevated temperatures.
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Regioselective reductive ring-opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protecting-group strategy. Part 1

TL;DR: The 4-methoxybenzyl ether linkage in products containing benzyl ethers or other protective groups is selectively cleaved upon treatment with cerium(IV) ammonium nitrate in aqueous acetonitrile as discussed by the authors.
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Stimulation of renin release from rabbit renal cortex by arachidonic acid and prostaglandin endoperoxides.

TL;DR: Results indicate that stimulation of renin release by C20:4 may depend more specifically on the action of PG endoperoxides than on the primary prostaglandins and raise the possibility of a direct action of the renal cortical PG system on renin secretion.
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In Vitro Activity and Preclinical Profile of TMC435350, a Potent Hepatitis C Virus Protease Inhibitor

TL;DR: TMC435350 is a highly specific and potent inhibitor of NS3/4A protease selected from a series of novel macrocyclic inhibitors that has the potential for combination with other anti-HCV agents and the favorable pharmacokinetic profile.
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Discovery and Development of Simeprevir (TMC435), a HCV NS3/4A Protease Inhibitor

TL;DR: The extensive medicinal chemistry effort to develop novel P2 cyclopentane macrocyclic inhibitors guided by HCV NS3 protease assays, the cellular replicon system, structure-based design, and a panel of DMPK assays are summarized.