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- W2950898807 abstract "Abstract A series of (R)- and (S)-3-aminomethyl-1-tetralones, conformationally constrained analogues of haloperidol, have been obtained by enzymatic resolution of the corresponding racemic 3-hydroxymethyl-1-tetralones using Pseudomonas fluorescens lipase. Their binding affinities at dopamine D2 and serotonin 5-HT2A and 5-HT2C receptors were determined showing in some cases an atypical antipsychotic profile with Meltzer's ratio higher than 1.30." @default.
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- W2950898807 date "2004-06-15" @default.
- W2950898807 modified "2023-10-03" @default.
- W2950898807 title "Chemoenzymatic Synthesis and Binding Affinity of Novel (R)- and (S)-3-Aminomethyl-1-tetralones, Potential Atypical Antipsychotics." @default.
- W2950898807 cites W2174544994 @default.
- W2950898807 doi "https://doi.org/10.1002/chin.200424106" @default.
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