Borgers M, Thoné F
Histochemistry. 1975 Aug 28;44(3):277-80. doi: 10.1007/BF00491496.
A levamisole analogue, the L-p-bromotetramisole is introduced as a potent inhibitor of non-specific alkaline phosphatase. Complete inhibition is achieved cytochemically at a concentration of 0.1 mM in various rat tissues except the intestine, which is not affected. The D-p-bromotetramisole does not influence the alkaline phosphatase activities. Since no effect of the inhibitor is seen on the activities of specific phosphatases, this drug is recommended also as an additive for specific phosphatase media in order to yield the specific activity only.
左旋咪唑类似物L-对溴四咪唑被作为非特异性碱性磷酸酶的有效抑制剂引入。通过细胞化学方法,在除肠道外的各种大鼠组织中,0.1 mM的浓度可实现完全抑制,而肠道不受影响。D-对溴四咪唑不影响碱性磷酸酶的活性。由于未观察到该抑制剂对特异性磷酸酶的活性有影响,因此该药物也被推荐作为特异性磷酸酶培养基的添加剂,以便仅产生特异性活性。