STRUCTURE‐ACTIVITY RELATIONSHIPS OF N‐β‐PHENYLPROPIONYL‐l‐TYROSINE AND ITS DERIVATIVES ON THE INHIBITION OF AN IDENTIFIABLE GIANT NEURONE OF AN AFRICAN GIANT SNAIL

Abstract

1 Inhibitory effects of N-β-phenylpropionyl-l-tyrosine, N-β-phenylpropionyl-l-tryptophan and their derivatives on an identifiable giant neurone, TAN (tonically autoactive neurone) of an African giant snail (Achatina fulica Férussac) were examined in an attempt to elucidate which structural features are necessary to produce the effect. 2 Of the compounds examined, N-β-cyclohexylpropionyl-l-tyrosine showed the strongest effect. Its critical concentration (c.c.) was 3 × 10⁻⁸-10⁻⁷m, about ten times lower than that of N-β-phenylpropionyl-l-tyrosine (c.c, 3 × 10⁻⁷-10⁻⁶m). N-β-cyclohexylpropionyl-l-tryptophan (c.c, 10⁻⁶m) had an effect almost similar to that of N-β-phenylpropionyl-l-tryptophan (c.c, 10⁻⁶m). 3 N-β-Phenylpropionyl-N-methyl-l-tyrosine had no effect at a high concentration. 4 Effects of N-β-phenylpropionyl-l-tyrosine amide (c.c, 3 × 10⁻⁷-10⁻⁶m) and N-β-phenylpropionyl-l-tryptophan amide (c.c, 10⁻⁶m) were very similar to those of N-β-phenylpropionyl-l-tyrosine and N-β-phenylpropionyl-l-tryptophan respectively. 5 N-β-Phenylpropionyl-p-amino-l-phenylalanine (c.c, 3 × 10⁻⁵-10⁻⁴m) and N-β-phenylpropionyl-p-chloro-l-phenylalanine (c.c, 10⁻⁴m) had only a weak effect. 6 It is proposed that the structural features producing the effect are as follows: the active compound has a phenyl or a cyclohexyl group (hydrophobic binding group), after a suitable distance a peptide bond (proton donor and proton acceptor), adjacently a carbonyl group (proton acceptor), and a phenolic hydroxyl or an indolyl imino group (proton donor) in the molecule.