Grollman A P
Science. 1967 Jul 7;157(3784):84-5. doi: 10.1126/science.157.3784.84.
A structural model for the inhibition of protein biosynthesis was previously formulated on the basis of a topochemical analogy between the ipecac alkaloids and the glutarimide antibiotics. The structure of tubulosine satisfies the requirements of this model. The prediction that such a compound would exhibit amebicidal activity and act by selectively inhibiting the transfer reaction in protein biosynthesis is confirmed.
先前基于吐根生物碱与戊二酰亚胺抗生素之间的拓扑化学相似性,构建了一个抑制蛋白质生物合成的结构模型。tubulosine的结构符合该模型的要求。这样一种化合物将表现出杀阿米巴活性并通过选择性抑制蛋白质生物合成中的转移反应起作用的预测得到了证实。