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Matthias Heydenreich

Researcher at University of Potsdam

Publications -  158
Citations -  2625

Matthias Heydenreich is an academic researcher from University of Potsdam. The author has contributed to research in topics: Nuclear magnetic resonance spectroscopy & Conformational isomerism. The author has an hindex of 26, co-authored 147 publications receiving 2301 citations. Previous affiliations of Matthias Heydenreich include University of Nairobi & University of Mainz.

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Phosphorylation of C6- and C3-positions of glucosyl residues in starch is catalysed by distinct dikinases

TL;DR: Re‐examination of the specificity of the dikinases using an improved method demonstrates that C6‐ and C3‐phosphorylation is selectively catalysed by GWD and PWD, respectively.
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Self-Assembly into Multicompartment Micelles and Selective Solubilization by Hydrophilic−Lipophilic−Fluorophilic Block Copolymers

TL;DR: In this paper, a tri-phiphilic linear ternary block copolymers (ABC, ACB, and BAC) were synthesized in three consecutive steps by the reversible addition-fragmentation chain transfer (RAFT) method.
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Anti-plasmodial flavonoids from the stem bark of Erythrina abyssinica

TL;DR: From the ethyl acetate extract of the stem bark of Erythrina abyssinica, a new chalcone, 2',3,4,4'-tetrahydroxy-5-prenylchalcone (trivial name 5- prenylbutein) and a new flavanone along with known flavonoids have been isolated as the anti-plasmodial principles.
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Hyperphosphorylation of Glucosyl C6 Carbons and Altered Structure of Glycogen in the Neurodegenerative Epilepsy Lafora Disease

TL;DR: This work shows that glycogen phosphorylation is not due to a glycogen synthase side reaction, that C6 is a major glycogenosphorylation site, and that C 6 monophosphates predominate near centers of glycogen molecules and positively correlate with glycogen chain lengths.
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Anti-plasmodial activities and X-ray crystal structures of rotenoids from Millettia usaramensis subspecies usaramensis

TL;DR: The dichloromethane extract of the stem bark of Millettia usaramensis subspecies usaramense showed anti-plasmodial activity against the chloroquine sensitive (D6) andchloroquine resistant (W2) strains of Plasmodium falciparum.