Both research groups conclude that helicase-primase inhibitors are more potent than acyclovir and its derivatives.
无论研究小组断定旋-引抑制更烈性比阿昔洛韦及其衍生物.
Both research groups conclude that helicase-primase inhibitors are more potent than acyclovir and its derivatives.
无论研究小组断定旋-引抑制更烈性比阿昔洛韦及其衍生物.
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激酶抑制。有抗血管生成活性。
The samples were ignited, then bismuth subcarbonate in residue was determined by compleximetry.
供试品经有机破坏后,采用络合滴定法测定制中碱式碳酸铋的含量。
That is a padhesive with the powder Diecty,Compress tablets and replenisher,Disinteante,adhesive of the capsula.
本品主要用作药物固体制,全粉末直接压片的干燥粘合
,胶囊填充
,崩解
,湿法造粒粘合
和着色的延展
。
Conclusion The cream has therapeutic effect on pudendum leukoplakia,and it is safe and convenient.
结论该制外阴白斑
效确切,使用安全方便。
I also use a medicine called Trental or Pentoxifylline as a phosphodiesterase inhibitor.
也使用磷酸二酯酶抑制
如巡能
酮可可碱进行
。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制。诱导凋亡。
The terbutaline effect was partly blocked by amiloride and ouabain,which were inhibitors of sodium transport.
钠转运特异性抑制——阿咪洛利
哇巴因能部分抑制特普他林刺激肺泡内液体清除的作用。
Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.
酯酶、脂肪酶和N-甲酰甲硫氨酸氨基肽酶无毒的抑制。也抑制羧肽酶Y类外肽酶。
A novel method,fluorophotometry, was used to determine Vitamin A in galactosyl ceramide liposomes.
用荧光法测定了半乳糖神经酰胺脂质体制中维生素A的含量。
Fumagillin is among the most potent natural product inhibitors of angiogenesis.
夫马洁林是目前已知的最有潜力的天然血管生成抑制之一。
Fenfluramine Hydrochloride is an appetite inhibitor, a major role in the central nervous system.
盐酸芬氟拉明是一种食欲抑制,主要作用于中枢神经系统。
Mixing phoxim and phorate produces the emulsifiable mixure of phoxim and phorate.
辛、甲混合制是由辛硫磷与甲拌磷两种农药复配而成的。
In addition,DNJ is also a potent inhibites of a-glucoamy-lase, trehalase.
另外,DNJ还是α-葡萄糖淀粉酶的有效的抑制。
Application of newtype immunodepressant and new therapeutic regimen had achieved success in organ transplantation.
新型免疫抑制的应用以及新的
方案的使用,使器官移植取得了不断的成功。
Highly active inhibitor of fibrinolysin and chymotrypsin.
溶纤维蛋白酶和胰凝乳蛋白酶的高活性抑制。
The clinical trials indicated that this galenical was superior to the traditional synthetic drugs for antidepression.
临床试验表明该植物制的抗抑郁
效优于传统化学合成药物,具有较好的耐受性与安全性。
An indirect atomic absorption spectroscopic method (AAS) was proposed for the determination of leucogen in pharmaceutical preparations.
该法可成功地用于药物制中利血生的测定。
This article reviews study progresses of neotype immunodepressant of myasthenia gravis by collecting its lastest related information.
本文收集新近的相关进展信息,对MG的新型免疫抑制
研究进展进行综述。
Silica gel column separation method and spectrophotography were used to determine the content of urson in the preparation.
采用硅胶柱分离分光光度法,对制中所含熊果酸成分进行含量测定,结果含量测定的标准品线性关系好,检测数据稳定。
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