The enzyme resistant starch formation can be destroyed and inhibited with acetification.
醋酸酯化会破坏和抑制淀粉中抗消化淀粉的形成。
Secondly the enzyme is inhibited by an intermediate lower down the metabolic pathway, usually either phosphoenolpyruvate or citrate.
其次，减缓代谢途径的一个中间体，通常是磷酸烯醇或柠檬酸降低酶的活性。
Enzyme activity decreased with high doses and the growth of Sorghum bicolor was inhibited.
高剂量时酶活下降，会抑制甜高粱的生长。
As the former three substrates were employed, at high substrate concentration, L-Phe inhibited the enzyme uncompetitively and activated the enzyme at low substrate concentration.
在前三种底物条件下，当高底物浓度时，L-苯丙氨酸表现出反竞争性抑制作用；低底物浓度时，则呈现激活作用。
When ABA biosynthesis was inhibited by nordihydroguaiaretic acid (NDGA), an inhibitor of the ABA anabolic enzyme 9-cis-epoxycarotenoid dioxygenase (NCED), rice seed germination showed no response.
当ABA的合成被去甲二氢愈创木酸（NDGA），ABA合成酶9-顺式-环氧类胡萝卜素双加氧酶的抑制因子所抑制，水稻种子萌发无影响。
The enzyme production was strongly inhibited by glycerol, glucose, mannose.
甘油，葡萄糖，甘露糖等对产酶有强的阻遏作用。
The product inhibited the enzyme activity.
反应产物对酶活力的抑制；
CONCLUSION:DZ inhibited the 4 hydroxytative metabolic pathway of AP, suggesting DZ may be a potent and selective microsomal enzyme inhibitor.
结论：DZ选择性地抑制了AP在人体肝脏中的4羟基化代谢途径，提示DZ是一作用较强的、选择性的肝药酶抑制剂。
CONCLUSION:DZ inhibited the 4 hydroxytative metabolic pathway of AP, suggesting DZ may be a potent and selective microsomal enzyme inhibitor.
结论：DZ选择性地抑制了AP在人体肝脏中的4羟基化代谢途径，提示DZ是一作用较强的、选择性的肝药酶抑制剂。
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