The synthesis of epalrestat,an aldose reductase inhibitor, was improved. The yield of its intermediate 3-carboxymethyl rhodanine was raised to 76.4%.
对醛搪还原酶抑制依帕司他的合成工艺作
改进,使中间体绕丹宁乙酸的收率提高到76.4%。
The synthesis of epalrestat,an aldose reductase inhibitor, was improved. The yield of its intermediate 3-carboxymethyl rhodanine was raised to 76.4%.
对醛搪还原酶抑制依帕司他的合成工艺作
改进,使中间体绕丹宁乙酸的收率提高到76.4%。
If allopurinol toxicity occurs, options include other xanthine oxidase inhibitors, a uricosuric agent, or allopurinol desensitisation (the latter only in cases of mild rash).
如出现药物毒性,其他选择包括其他黄嘌呤化酶抑制
、促进尿酸排泄药或脱敏疗法(后者仅适于轻度皮疹者)。
A new paint remover was synthesized with chloroalkane as primary solvent,organic acid as accelerator and organic compound containing N and S as inhibitor.
以氯代烷为主溶、烷基醇为助溶
、有机酸为促进
、
和硫的有机化合物为缓蚀
合成
一种新的脱漆
。
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.
The synthetic method and performance testing of BH series acidulate corrosion inhibitor were introduced.
介绍BH系列酸化缓蚀
的合成方法及性能测试。
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。
The ability of the gas phase inhibitor—cyclohexylamine carbonate (CHC)for chemical equipment was studied.
研究气相缓蚀
碳酸环己胺(CHC)用于化工装备保护的可能性。
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.
目的揭示模拟微重力大鼠心血管脱锻炼(CVD)病理生理学变化;探索一化
合酶抑制
对
模拟微重力大鼠CVD的效应。
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的竞争性抑制。也抑制鼠肝细胞中磷酸酯酶D和C的活化。
Surfactants used in gathering transportation,include demulsifier,defoamer,deoiler,scale inhibitor,corrosion inhibitor,bactericide etc.
在原油集输中,表面活性用作破乳
、消泡
、除油
、防垢
、缓蚀
、杀菌
等。
The terbutaline effect was partly blocked by amiloride and ouabain,which were inhibitors of sodium transport.
钠转运特异性抑制——阿咪洛利或哇巴因能部分抑制特普他林刺激肺泡内液体清除的作用。
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
血管生成活性。
To improve the anti-corrosion performance of electrocoating,organic andinorganic inhibitors are applied in an anodic electrophoretic-coating.
在电泳涂装工艺中使用缓蚀,可提高阳极电泳涂层的防腐蚀性。
STAT3 is an important inhibitor of apoptosis gene discovered in recent years,with a bifunction of inhibiting apoptosis and getting involved in cell cycle control.
STAT3基因是近年来发现的凋亡抑制基因,具有抑制凋亡和参与细胞周期调控的双重功能。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有肿瘤活性,易
化为Herbimycin A,后者是很好的除草
,并具有一定
菌活性。
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。
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。
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。
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。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
雌激素。选择性PKC抑制
。诱导凋亡。
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