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- W2077798462 abstract "Replacement of the 4-methoxy of mescaline with higher alkyl homologues or with bromine led to increased activity at serotonin receptors in a sheep umbilical artery preparation. This activity appears correlated with lipophilicity, as measured by 1-octanol-water partition coefficients, but drops off when the 4-substituent is about five atoms in length. It is suggested that 3,4,5-trisubhe 2,4,5-substitution pattern." @default.
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- W2077798462 date "1977-02-01" @default.
- W2077798462 modified "2023-10-09" @default.
- W2077798462 title "Lipophilicity and serotonin agonist activity in a series of 4-substituted mescaline analogs" @default.
- W2077798462 doi "https://doi.org/10.1021/jm00212a022" @default.
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