Biosynthesis of isonorargemonine, eschscholtzidine and 4-hydroxyeschscholtzidine in Thalictrum minus
1Faculty of Chemistry, University of Sofia, 1 James Bourchier Avenue, 1126 Sofia, Bulgaria.
Abstract:
Feeding experiments with (14)C-labelled reticuline have shown that reticuline is an efficient precursor of isonorargemonine, eschscholtzidine, and 4-hydroxyeschscholtzidine in Thalictrum minus (Ranunculaceae). Feeding experiments using (14)C-labelled isonorargemonine and eschscholtzidine led to the conclusion that the substitution pattern of 4-hydroxyeschscholtzidine can be formed at the pavine stage.
More Related Videos
09:36Applications of Liquid-Chromatography Tandem Mass Spectrometry in Natural Products Research: Tropane Alkaloids as a Case Study
Published on: March 8, 2024
09:04A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products
Published on: September 9, 2016
Related Concept Videos
Biosynthesis of Nucleic Acids
Drugs Affecting Neurotransmitter Synthesis
Phase II Reactions: Miscellaneous Conjugation Reactions
A key example involves the conjugation of cyanide ions, which impair cellular respiration and alter hemoglobin into non-oxygen-carrying cyanmethemoglobin. To neutralize this threat, a sulfur atom from thiosulphate is transferred to the cyanide ion, catalyzed by the enzyme rhodanese, resulting in an inactive compound called thiocyanate. The production of...
Antiprotozoal Agents
Amino Acid Biosynthetic Pathways
