Explore: Amanitins

hepatotoxic substances such as paracetamol and amanitins. Based on a 2002 crystal structure analysis, α-amanitin interacts with the bridge helix in RNA polymerase

γ-Amanitin ε-Amanitin Amatoxin, a class of toxic compounds that include the amanitins Amanin, another amatoxin This set index article lists chemical compounds

destroying angel amanitins liver Deciduous woodland Guangdong province, China; India Amanita fuliginea Hongo East Asian brown death cap amanitins liver Woodland

occurrence of γ-amanitin and β-amanitin in German specimens of G. autumnalis and G. marginata and revealed the presence of the three amanitins in the fruit

ISSN 0264-6021. PMC 1138336. PMID 2467661. Vetter, János (2023-08-07). "Amanitins: The Most Poisonous Molecules of the Fungal World". Molecules (Basel,

the University of Munich. Of the amatoxins, α-Amanitin is the chief component and along with β-amanitin is likely responsible for the toxic effects. Their

currently ten named amatoxins: δ-Amanitin has been reported, but its chemical structure has not been determined. Amanitin is very closely related to phalloidins

transcribing polymerase. RNA polymerase II is inhibited by α-Amanitin and other amatoxins. α-Amanitin is a highly poisonous substance found in many mushrooms

β-Amanitin (beta-Amanitin) is a cyclic peptide comprising eight amino acids. It is part of a group of toxins called amatoxins, which can be found in several

ε-Amanitin (epsilon-Amanitin) is a cyclic peptide. It is an amatoxin, all of which are found in several members of the mushroom genus Amanita. The oral