INHIBITION BY BETA-PHENYLETHYLAMINE AND SIMILAR COMPOUNDS OF GLYCINE TRANSPORT BY PIGEON RED CELLS

被引:3
作者
KITTAMS, DW
VIDAVER, GA
机构
[1] Department of Chemistry, University of Nebraska, Lincoln
基金
美国国家科学基金会;
关键词
D O I
10.1016/0005-2736(69)90018-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
1. 1. β-Phenylethylamine gave first-order inhibition of Na+-dependent glycine entry (Ki = 5.35 mM). The ion rather than the free amine was the inhibitor. Inhibition was reversible and (as a first approximation) noncompetitive to both glycine and Na+. 2. 2. β-Phenylethylamine also inhibited Na+-independent glycine entry and 22Na+ entry, but less strongly. 3. 3. Specificity was low but present; e.g., n-hexylamine and α-phenylethylamine were as effective as β-phenylethylamine as inhibitors of Na+-dependent glycine entry, benzylamine and tyramine were about half as effective, and N,N,N-trimethyl-β-phenylethylammonium ion was ineffective. © 1969.
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页码:540 / &
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