Efficient inhibition of muscle and liver glycogen phosphorylases by a new glucopyranosylidene-spiro-thiohydantoin

Reaction of C-(1- bromo-1-deoxy-β- d-glucopyranosyl)formamide 2 with thiocyanate ions was the key step of a short synthesis of d-glucopyranosylidene-spiro-thiohydantoin 7 which proved to be a potent inhibitor of muscle and liver glycogen phosphorylases. Graphic

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 1999-05, Vol.9 (10), p.1385-1390
Hauptverfasser: Ősz, Erzsébet, Somsák, László, Szilágyi, László, Kovács, László, Docsa, Tibor, Tóth, Béla, Gergely, Pál
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container_end_page 1390
container_issue 10
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container_title Bioorganic & medicinal chemistry letters
container_volume 9
creator Ősz, Erzsébet
Somsák, László
Szilágyi, László
Kovács, László
Docsa, Tibor
Tóth, Béla
Gergely, Pál
description Reaction of C-(1- bromo-1-deoxy-β- d-glucopyranosyl)formamide 2 with thiocyanate ions was the key step of a short synthesis of d-glucopyranosylidene-spiro-thiohydantoin 7 which proved to be a potent inhibitor of muscle and liver glycogen phosphorylases. Graphic
doi_str_mv 10.1016/S0960-894X(99)00192-4
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Biological and medical sciences
Enzyme Inhibitors - pharmacology
General and cellular metabolism. Vitamins
Kinetics
Liver - drug effects
Liver - enzymology
Medical sciences
Muscle, Skeletal - drug effects
Muscle, Skeletal - enzymology
Pharmacology. Drug treatments
Phosphorylases - antagonists & inhibitors
Rabbits
title Efficient inhibition of muscle and liver glycogen phosphorylases by a new glucopyranosylidene-spiro-thiohydantoin
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