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

抗雌激素。选择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的高活。

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-葡萄糖淀粉酶的有效的。

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毒活。EGFR激酶。有抗血管生成活。

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

新型免疫的应用以及新的疗方案的使用,使器官移植取得了不断的成功。

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

钠转运特异——咪洛利或哇巴因能部分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。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.

本文收集新近的相关进展信息,对疗MG的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的生物活,根据作用机的不同,可分为钙增敏、磷酸二酯酶、环氧合酶等,并可用于相关疾病的疗。

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％。

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。也鼠肝细胞中磷酸酯酶D和C的活化。

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

如出现药物毒，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;探索一氧化氮合酶对抗模拟微重力大鼠CVD的效应。

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的免疫原表位的特异免疫耐受。

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

抗雌激素。选择性PKC抑制剂。诱导凋亡。

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剂。

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剂之一。

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剂，主要中枢神经系统。

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

另外,DNJ还是α-葡萄糖淀粉酶的有效的抑制剂。

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-引抑制剂更烈性比阿昔韦及其衍生物.

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

我也使磷酸二酯酶抑制剂如巡能泰己酮可可碱进行疗。

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

显示细胞生长抑制和细胞毒活性。EGFR激酶抑制剂。有抗血管生成活性。

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

新型免疫抑制剂的应以及新的疗方案的使,使器官移植取得了不断的成功。

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

钠转运特异性抑制剂——阿咪哇巴因能部分抑制特普他林刺激肺泡内液体清除的。

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剂。也抑制羧肽酶Y类外肽酶。

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

本文收集新近的相关进展信息,对疗MG的新型免疫抑制剂研究进展进行综述。

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的生物活性,根据机制的不同,可分为钙增敏剂、磷酸二酯酶抑制剂、环氧合酶抑制剂等,并可相关疾病的疗。

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

对醛搪还原酶抑制剂依帕司他的合成工艺了改进，使中间体绕丹宁乙酸的收率提高到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的竞争性抑制剂。也抑制鼠肝细胞中磷酸酯酶D和C的活化。

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

如出现药物毒性，其他选择包括其他黄嘌呤氧化酶抑制剂、促进尿酸排泄药脱敏疗法（后者仅适轻度皮疹者）。

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;探索一氧化氮合酶抑制剂对抗模拟微重力大鼠CVD的效应。

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，将免疫抑制剂从宿主撤离，宿主仍能保持对存在耐受原上的免疫原性表位的特异性免疫耐受。

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

抗雌激素。选择性PKC抑制。诱导凋亡。

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。

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-葡萄糖淀粉酶的有效的抑制。

Both research groups conclude that helicase-primase inhibitors are more potent than acyclovir and its derivatives.

研究小组断定旋-引抑制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.

我也磷酸二酯酶抑制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.

显示细胞生长抑制和细胞毒活性。EGFR激酶抑制。有抗血管生成活性。

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

新型免疫抑制的应以及新的疗方案的,官移植取得了不断的成功。

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。

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毒的抑制。也抑制羧肽酶Y类外肽酶。

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

本文收集新近的相关进展信息,对疗MG的新型免疫抑制研究进展进行综述。

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的生物活性,根据作机制的不同,可分为钙增敏、磷酸二酯酶抑制、环氧合酶抑制等,并可于相关疾病的疗。

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

对醛搪还原酶抑制依帕司他的合成工艺作了改进，中间体绕丹宁乙酸的收率提高到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的竞争性抑制。也抑制鼠肝细胞中磷酸酯酶D和C的活化。

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

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

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;探索一氧化氮合酶抑制对抗模拟微重力大鼠CVD的效应。

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，将免疫抑制从宿主撤离，宿主仍能保持对存在于耐受原上的免疫原性表位的特异性免疫耐受。

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的高活性。

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-葡萄糖淀粉酶的有效的。

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毒活性。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.

新型免疫的应用以及新的疗方案的使用,使器官移植取得了不断的成功。

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。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.

本文收集新近的相关进,对疗MG的新型免疫研究进进行综述。

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的生物活性,根据作用机的不同,可分为钙增敏、磷酸二酯酶、环氧合酶等,并可用于相关疾病的疗。

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％。

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。也鼠肝细胞中磷酸酯酶D和C的活化。

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

如出现药物毒性，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;探索一氧化氮合酶对抗模拟微重力大鼠CVD的效应。

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的免疫原性表位的特异性免疫耐受。

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

抗雌激素。选择性PKC抑制剂。诱导凋亡。

Highly active inhibitor of fibrinolysin and chymotrypsin.

溶纤维蛋白酶胰凝乳蛋白酶的高活性抑制剂。

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

夫马洁林是目前已知的有力的天然血管生成抑制剂之一。

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剂，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-葡萄糖淀粉酶的有效的抑制剂。

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-引抑制剂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抑制剂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.

显示细胞生长抑制细胞毒活性。EGFR激酶抑制剂。有抗血管生成活性。

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

新型免疫抑制剂的应用以及新的疗方案的使用,使器官移植取得了不断的成功。

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

钠转运特异性抑制剂——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。

Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

酯酶、脂肪酶N-硫氨酸氨基肽酶无毒的抑制剂。也抑制羧肽酶Y类外肽酶。

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

本文收集新近的相关进展信息,对疗MG的新型免疫抑制剂研究进展进行综述。

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的生物活性,根据作用机制的不同,可分为钙增敏剂、磷酸二酯酶抑制剂、环氧合酶抑制剂等,并可用于相关疾病的疗。

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

对醛搪还原酶抑制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％。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝氨酸半胱氨酸蛋白酶可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酸酯酶DC的活化。

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

如出现药物毒性，其他选择包括其他黄嘌呤氧化酶抑制剂、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;探索一氧化氮合酶抑制剂对抗模拟微重力大鼠CVD的效应。

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，将免疫抑制剂从宿主撤离，宿主仍能保持对存在于耐受原上的免疫原性表位的特异性免疫耐受。

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

抗雌激素。选择性PKC抑制剂。诱导凋亡。

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剂。

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剂之一。

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剂，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-葡萄糖淀粉酶的有效的抑制剂。

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-引抑制剂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抑制剂如巡能泰或己酮可可碱进疗。

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激酶抑制剂。有抗血管生成活性。

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

新型免疫抑制剂的应用以及新的疗方案的使用,使器官移植取得了不断的成功。

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

钠转运特异性抑制剂——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。

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剂。也抑制羧肽酶Y类外肽酶。

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

本文收集新近的相关进展信息,对疗MG的新型免疫抑制剂研究进展进。

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的生物活性,根据作用机制的不同,可分为钙增敏剂、磷酸二酯酶抑制剂、环氧合酶抑制剂等,并可用于相关疾病的疗。

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

对醛搪还原酶抑制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％。

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剂。也抑制鼠肝细胞中磷酸酯酶D和C的活化。

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

如出现药物毒性，其他选择包括其他黄嘌呤氧化酶抑制剂、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;探索一氧化氮合酶抑制剂对抗模拟微重力大鼠CVD的效应。

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，将免疫抑制剂从宿主撤离，宿主仍能保持对存在于耐受原上的免疫原性表位的特异性免疫耐受。

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

抗雌激素。选择性PKC抑制剂。诱导凋亡。

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剂。

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

夫马洁林目前已知的最有潜力的天然血管生成抑制剂之。

Fenfluramine Hydrochloride is an appetite inhibitor, a major role in the central nervous system.

盐酸芬氟拉种食欲抑制剂，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α-葡萄糖淀粉酶的有效的抑制剂。

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-引抑制剂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抑制剂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.

显示细胞生长抑制和细胞毒活性。EGFR激酶抑制剂。有抗血管生成活性。

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

新型免疫抑制剂的应用以及新的疗方案的使用,使器官移植取得了不断的成功。

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

钠转运异性抑制剂——阿咪洛利或哇巴因能部分抑制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剂。也抑制羧肽酶Y类外肽酶。

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

本文收集新近的相关进展信息,对疗MG的新型免疫抑制剂研究进展进行综述。

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的生物活性,根据作用机制的不同,可分为钙增敏剂、磷酸二酯酶抑制剂、环氧合酶抑制剂等,并可用于相关疾病的疗。

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

对醛搪还原酶抑制剂依帕司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％。

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剂。也抑制鼠肝细胞中磷酸酯酶D和C的活化。

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

如出现药物毒性，其选择包括其黄嘌呤氧化酶抑制剂、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;探索氧化氮合酶抑制剂对抗模拟微重力大鼠CVD的效应。

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，将免疫抑制剂从宿主撤离，宿主仍能保持对存在于耐受原上的免疫原性表位的异性免疫耐受。

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

抗雌激素。选择性PKC抑制。诱导凋亡。

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。

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-葡萄糖淀粉酶的有效的抑制。

Both research groups conclude that helicase-primase inhibitors are more potent than acyclovir and its derivatives.

研究小组断定旋-引抑制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.

我也磷酸二酯酶抑制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.

显示细胞生长抑制和细胞毒活性。EGFR激酶抑制。有抗血管生成活性。

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

新型免疫抑制的应以及新的疗方案的,官移植取得了不断的成功。

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。

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毒的抑制。也抑制羧肽酶Y类外肽酶。

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

本文收集新近的相关进展信息,对疗MG的新型免疫抑制研究进展进行综述。

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的生物活性,根据作机制的不同,可分为钙增敏、磷酸二酯酶抑制、环氧合酶抑制等,并可于相关疾病的疗。

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

对醛搪还原酶抑制依帕司他的合成工艺作了改进，中间体绕丹宁乙酸的收率提高到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的竞争性抑制。也抑制鼠肝细胞中磷酸酯酶D和C的活化。

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

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

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;探索一氧化氮合酶抑制对抗模拟微重力大鼠CVD的效应。

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，将免疫抑制从宿主撤离，宿主仍能保持对存在于耐受原上的免疫原性表位的特异性免疫耐受。

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

抗雌激素。选择性PKC剂。诱导凋亡。

Highly active inhibitor of fibrinolysin and chymotrypsin.

溶纤维蛋白酶和胰凝乳蛋白酶的高活性剂。

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剂之一。

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剂，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-葡萄糖淀粉酶的有效的剂。

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-引剂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剂如巡能酮可可碱进行疗。

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

显示细胞生和细胞毒活性。EGFR激酶剂。有抗血管生成活性。

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

新型免疫剂的应用以及新的疗方案的使用,使器官移植取得了不断的成功。

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

钠转运特异性剂——阿咪洛利哇巴因能部分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剂。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.

本文收集新近的相关进展信息,对疗MG的新型免疫剂研究进展进行综述。

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的生物活性,根据作用机的不同,可分为钙增敏剂、磷酸二酯酶剂、环氧合酶剂等,并可用于相关疾病的疗。

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％。

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剂。也鼠肝细胞中磷酸酯酶D和C的活化。

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

如出现药物毒性，其他选择包括其他黄嘌呤氧化酶剂、促进尿酸排泄药脱敏疗法（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;探索一氧化氮合酶剂对抗模拟微重力大鼠CVD的效应。

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，将免疫剂从宿主撤离，宿主仍能保持对存在于耐受原上的免疫原性表位的特异性免疫耐受。