Relationship between the conformation of the cyclopeptides isolated from the fungus Amanita phalloides (Vaill. Ex Fr.) Secr. and its toxicity

Molecules

Volumn 5, Issue 3, 2000, Pages 489-490

  Battista, M E ^a   Vitale, A A ^a   Pomilio, A B ^a  

^a UNIVERSIDAD DE BUENOS AIRES   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPEPTIDE; FUNGAL PROTEIN; TOXIC SUBSTANCE;

AB INITIO CALCULATION; AMANITA PHALLOIDES; CARBON NUCLEAR MAGNETIC RESONANCE; CONFERENCE PAPER; EMPIRICISM; HYDROGEN BOND; MOLECULAR INTERACTION; NONHUMAN; PROTEIN CONFORMATION; PROTEIN ISOLATION; PROTEIN STRUCTURE; STEREOCHEMISTRY; STRUCTURE ACTIVITY RELATION; STRUCTURE ANALYSIS; TOXICITY;

EID: 0006384880     PISSN: 14203049     EISSN: None     Source Type: Journal    
DOI: 10.3390/50300489     Document Type: Conference Paper

References (2)

1. 17O NMR study of aromatic compounds with dicoordinate oxygen atoms. 2. Intramolecular hydrogen bonding in hydroxy- and methoxybenzene derivatives. J. Phys. Chem. 1991, 95, 6179-6181.
2. 13C NMR and AM1 study on intramolecular interactions defining the methoxy group conformation in unhindered anisole derivatives. J. Mol. Structure 1995, 344, 143-150.