9.Highly active inhibitor of fibrinolysin and chymotrypsin.
溶纤维蛋白和胰凝乳蛋白的高活性剂。
10.Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC剂。诱导凋亡。
11.Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长和细胞毒活性。EGFR激剂。有抗血管生成活性。
12.I also use a medicine called Trental or Pentoxifylline as a phosphodiesterase inhibitor.
我也使用磷酸二酯剂如巡能泰或己酮可可碱进行治疗。
13.The synthetic method and performance testing of BH series acidulate corrosion inhibitor were introduced.
介绍了BH系列酸化缓蚀剂的合成方法及性能测试。
14.Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.
酯、脂肪和N-甲酰甲硫氨酸氨基肽无毒的剂。也羧肽Y类外肽。
15.The ability of the gas phase inhibitor—cyclohexylamine carbonate (CHC)for chemical equipment was studied.
研究了气相缓蚀剂碳酸环己胺(CHC)用于化工装备保护的可能性。
16.The transportability through BBB and bioavailability of the inhibitors will be the focus by the systemafic bioassay in vivo.
指出以后的工作重点是进行系统深入的生物体内评价,解决药物透过血脑屏障和生物利用度等问题。
17.And quercetin(QU), one of inhibitors of lipoxygenase pathway, was observed on procedure from preneoplastic foci into nodules in rat liver.
方法利用大白鼠复肝癌前病变发生的动物模型,然后将带有癌前病灶的大鼠分组。
18.Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.
三肽醛。丝氨酸和半胱氨酸蛋白可逆的竞争性剂。也鼠肝细胞中磷酸酯D和C的活化。
19.The synthesis of epalrestat,an aldose reductase inhibitor, was improved. The yield of its intermediate 3-carboxymethyl rhodanine was raised to 76.4%.
对醛搪还原剂依帕司他的合成工艺作了改进,使中间体绕丹宁乙酸的收率提高到76.4%。
20.A new paint remover was synthesized with chloroalkane as primary solvent,organic acid as accelerator and organic compound containing N and S as inhibitor.