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• W2029168180 abstract "Our model of the active site of the sweet taste receptor is shown to be consistent with the aspartame analogues in which the L-Phe2 residue is replaced by L-(αMe)Phg, L-(αMe)Phe or L-(αMe)Hph. The analogues containing either the first or the third Cα-methylated, phenyl-containing residue in the second position of the dipeptide were synthesized and found to be approximately as sweet as aspartame itselfand its L-(αMe)Phe2 analogue." @default.
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• W2029168180 date "1997-04-01" @default.
• W2029168180 modified "2023-09-23" @default.
• W2029168180 title "Aspartame dipeptide analogues: effect of number of side-chain methylene group spacers and Cα-methylation in the second position" @default.
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• W2029168180 doi "https://doi.org/10.1016/s0957-4166(97)00127-4" @default.
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