3 Phenylisopropylamine藥物之aryl-CH 2-CH(CH 3 )-NR 1 R 2結構中,R 1及R 2為何種取代基時,其amphetamine-like作用最強?
(A) R1 = CH3 , R2 = H
(B) R1 = C3 H7 , R2 = C3H7
(C) R1 = C3 H7 , R2 = H
(D) R1 = H, R2 = H
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統計: A(41), B(14), C(17), D(11), E(0) #457246
統計: A(41), B(14), C(17), D(11), E(0) #457246
詳解 (共 3 筆)
#3833115
中樞活性↑
1. alpha碳上有低烷基的支鏈
2. N-methylation
中樞活性↓
1. N上單取代大於甲基 (保留厭食活性)
2. 芳香環或beta碳上羥基化
1
0
#5758048
Phenylisopropylamine
1
0