1965
DOI: 10.1007/bf02138474
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The taste ofl- andd-amino acids

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1969
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Cited by 119 publications
(45 citation statements)
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“…5) Aromatic side chains generally increase bitter taste intensity. L-phenylalanine and Ltryptophan, for instance, are among the most bitter amino acids; in fact tryptophan is the most hydrophobie of ail common amino acids and is approximately half as bitter as caffeine (Solms et al, 1965). According to Okai (1976) the hydrophobie side group of these aromatic amino acids may act as one of the bitter taste binding sites (fig 11).…”
Section: Bitterness Of Amino Acidsmentioning
confidence: 99%
“…5) Aromatic side chains generally increase bitter taste intensity. L-phenylalanine and Ltryptophan, for instance, are among the most bitter amino acids; in fact tryptophan is the most hydrophobie of ail common amino acids and is approximately half as bitter as caffeine (Solms et al, 1965). According to Okai (1976) the hydrophobie side group of these aromatic amino acids may act as one of the bitter taste binding sites (fig 11).…”
Section: Bitterness Of Amino Acidsmentioning
confidence: 99%
“…Solms, Vuataz and Egli (1965) have investigated the taste of eighteen amino acids in water, at a concentration of 3 mg/ml. Nine of the L-acids (arginine, aspartic acid, histidine, isoleucine, lysine, proline, serine, threonine and valine) were found to be practically devoid of taste.…”
Section: Discussionmentioning
confidence: 99%
“…Solms et al (1965) ont montré qu'à une faible concentration (0,3 % dans H20, pH = 6), un jury décrit le goût des acides aminés (énantiomères D et L). En solution aqueuse, Meister (1965) et Birch et Kemp (1989) les ont également caractérisés.…”
Section: Le Goût Des Acides Aminésunclassified