抑制剂

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

抗雌激素。选择性PKC。诱导凋亡。

Highly active inhibitor of fibrinolysin and chymotrypsin.

溶纤维蛋白酶和胰凝乳蛋白酶高活性。

Fumagillin is among the most potent natural product inhibitors of angiogenesis.

马洁林是目前已知最有潜力天然血管生成之一。

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，主要作用于中枢神经系统。

In addition,DNJ is also a potent inhibites of a-glucoamy-lase, trehalase.

另外,DNJ还是α-葡萄糖淀粉酶有效。

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-引更烈性比阿昔洛韦及其衍生物.

I also use a medicine called Trental or Pentoxifylline as a phosphodiesterase inhibitor.

我也使用磷酸二酯酶如巡能泰或己酮可可碱进行疗。

Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.

显示细胞生长和细胞活性。EGFR激酶。有抗血管生成活性。

Application of newtype immunodepressant and new therapeutic regimen had achieved success in organ transplantation.

新型免疫应用以及新疗方案使用,使器官移植取得了不断成功。

The terbutaline effect was partly blocked by amiloride and ouabain,which were inhibitors of sodium transport.

钠转运特异性——阿咪洛利或哇巴因能部分特普他林刺激肺泡内液体清除作用。

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。也羧肽酶Y类外肽酶。

This article reviews study progresses of neotype immunodepressant of myasthenia gravis by collecting its lastest related information.

本文收集新近相关进展信息,对疗MG新型免疫研究进展进行综述。

Pyridazinone derivatives have considerable kinds of biological activities such as those cardiotonic,platelet aggregation inhibitory,anti-inflammatory,aldose reductase inhibitory,antifungal and so on.

哒嗪酮类化合物具有多种重要生物活性,根据作用机不同,可分为钙增敏、磷酸二酯酶、环氧合酶等,并可用于相关疾病疗。

The synthesis of epalrestat,an aldose reductase inhibitor, was improved. The yield of its intermediate 3-carboxymethyl rhodanine was raised to 76.4%.

对醛搪还原酶依帕司他合成工艺作了改进，使中间体绕丹宁乙酸收率提高到76．4％。

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酶可逆竞争性。也鼠肝细胞中磷酸酯酶D和C活化。

If allopurinol toxicity occurs, options include other xanthine oxidase inhibitors, a uricosuric agent, or allopurinol desensitisation (the latter only in cases of mild rash).

如出现药物性，其他选择包括其他黄嘌呤氧化酶、促进尿酸排泄药或脱敏疗法（后者仅适于轻度皮疹者）。

Objective To disclose the changes in pathophysiology of cardiovascular deconditioning(CVD) induced by tail-suspension(TS) and to explore the effects of NOS inhibitor on CVD in TS rats.

目揭示模拟微重力大鼠心血管脱锻炼(CVD)病理生理学变化;探索一氧化氮合酶对抗模拟微重力大鼠CVD效应。

After the tolerizing regimen, the host is withdrawn from the suppressive agents, but is able to maintain specific immune tolerance to the immunogenic epitopes present on the toleragen.

在致耐受方案后，将免疫从宿主撤离，宿主仍能保持对存在于耐受原上免疫原性表位特异性免疫耐受。