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

无论研究小组断定-制剂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.

显示细胞生长制和细胞毒活性。EGFR激酶制剂。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剂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剂，全粉末直接压片的干燥粘合剂，胶囊填充剂,崩解剂，湿法造粒粘合剂和着色的延展剂。

Conclusion The cream has therapeutic effect on pudendum leukoplakia,and it is safe and convenient.

结论该制剂治疗外阴白斑疗效确切,使用安全方便。

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

也使用磷酸二酯酶制剂如巡能泰或己酮可可碱进行治疗。

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

抗雌激素。选择性PKC制剂。诱导凋亡。

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

钠转运特异性制剂——阿咪洛利或哇巴因能部分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制剂。也制羧肽酶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剂中维生素A的含量。

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

夫马洁林已知的最有潜力的天然血管生成制剂之一。

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

盐酸芬氟拉明一种食欲制剂，主要作用于中枢神经系统。

Mixing phoxim and phorate produces the emulsifiable mixure of phoxim and phorate.

辛、甲混合制剂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α-葡萄糖淀粉酶的有效的制剂。

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

新型免疫制剂的应用以及新的治疗方案的使用,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制剂。

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剂的抗郁疗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剂中利血生的测定。

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,对治疗MG的新型免疫制剂研究进展进行综述。

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,对制剂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。

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

无论研究小组断旋-引抑剂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.

显示细胞生长抑和细胞毒活性。EGFR激抑剂。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,采用络合滴法剂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剂，全粉末直接压片的干燥粘合剂，胶囊填充剂,崩解剂，湿法造粒粘合剂和着色的延展剂。

Conclusion The cream has therapeutic effect on pudendum leukoplakia,and it is safe and convenient.

结论该剂治疗外阴白斑疗效确切,使用安全方便。

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

也使用磷酸二酯抑剂如巡能泰或己酮可可碱进行治疗。

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

抗雌激素。选择性PKC抑剂。诱导凋亡。

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

钠转运特异性抑剂——阿咪洛利或哇巴因能部分抑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、和N-甲酰甲硫氨酸氨基肽无毒的抑剂。也抑羧肽Y类外肽。

A novel method,fluorophotometry, was used to determine Vitamin A in galactosyl ceramide liposomes.

用荧光法了半乳糖神经酰胺质体剂中维生素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剂，主要作用于中枢神经系统。

Mixing phoxim and phorate produces the emulsifiable mixure of phoxim and phorate.

辛、甲混合剂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-葡萄糖淀粉的有效的抑剂。

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

新型免疫抑剂的应用以及新的治疗方案的使用,使器官移植取得了不断的成功。

Highly active inhibitor of fibrinolysin and chymotrypsin.

溶纤维蛋白和胰凝乳蛋白的高活性抑剂。

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剂的抗抑郁疗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剂中利血生的。

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,对治疗MG的新型免疫抑剂研究进展进行综述。

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,对剂中所含熊果酸成分进行含量,结果含量的标准品线性关系好,检数据稳。

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.

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。

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剂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剂，全粉末直的干燥粘合剂，胶囊填充剂,崩解剂，湿法造粒粘合剂和着色的延展剂。

Conclusion The cream has therapeutic effect on pudendum leukoplakia,and it is safe and convenient.

结论该制剂治疗外阴白斑疗效确切,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剂如巡能泰或己酮可可碱进行治疗。

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

抗雌激素。选择性PKC抑制剂。诱导凋亡。

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

钠转运特异性抑制剂——阿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。

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剂中维生素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。

Mixing phoxim and phorate produces the emulsifiable mixure of phoxim and phorate.

辛、甲混合制剂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剂。

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治疗方案的使用,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剂。

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剂的抗抑郁疗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剂中血生的测定。

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,对治疗MG的新型免疫抑制剂研究进展进行综述。

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,对制剂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。

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.

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。

The samples were ignited, then bismuth subcarbonate in residue was determined by compleximetry.

供试品经有机破坏后,采用定法测定制剂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剂，全粉末直接压片的干燥粘剂，胶囊填充剂,崩解剂，湿法造粒粘剂和着色的延展剂。

Conclusion The cream has therapeutic effect on pudendum leukoplakia,and it is safe and convenient.

结论该制剂治疗外阴白斑疗效确切,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剂如巡能泰或己酮可可碱进行治疗。

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

抗雌激素。选择性PKC抑制剂。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-硫氨酸氨基肽酶无毒的抑制剂。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胺脂质体制剂中维生素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。

Mixing phoxim and phorate produces the emulsifiable mixure of phoxim and phorate.

辛、混制剂是由辛硫磷与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剂。

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治疗方案的使用,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剂。

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剂的抗抑郁疗效优于传统化学成药物，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剂中利血生的测定。

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,对治疗MG的新型免疫抑制剂研究进展进行综述。

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,对制剂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。

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.

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酶抑制剂。有抗血管生成活性。

The samples were ignited, then bismuth subcarbonate in residue was determined by compleximetry.

供试经有机破坏后,采用络合滴定法测定制剂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.

要用作药物固体制剂，全粉末直接压片的干燥粘合剂，胶囊填充剂,崩解剂，湿法造粒粘合剂和着色的延展剂。

Conclusion The cream has therapeutic effect on pudendum leukoplakia,and it is safe and convenient.

结论该制剂治疗外阴白斑疗效确切,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剂如巡能泰或己酮可可碱进行治疗。

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

抗雌素。选择性PKC抑制剂。诱导凋亡。

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

钠转运特异性抑制剂——阿咪洛利或哇巴因能部分抑制特普他林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。

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剂中维生素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，要作用于中枢神经系统。

Mixing phoxim and phorate produces the emulsifiable mixure of phoxim and phorate.

辛、甲混合制剂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剂。

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治疗方案的使用,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剂。

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剂的抗抑郁疗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剂中利血生的测定。

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

文收集新近的相关进展信息,对治疗MG的新型免疫抑制剂研究进展进行综述。

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,对制剂中所含熊果酸成分进行含量测定,结果含量测定的标准线性关系好,检测数据稳定。

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.

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。

The samples were ignited, then bismuth subcarbonate in residue was determined by compleximetry.

供试品经有机破坏后,采络合滴定法测定制剂中碱式碳铋的含量。

That is a padhesive with the powder Diecty,Compress tablets and replenisher,Disinteante,adhesive of the capsula.

本品主要作药物固体制剂，粉末直接压片的干燥粘合剂，胶囊填充剂,崩解剂，湿法造粒粘合剂和着色的延展剂。

Conclusion The cream has therapeutic effect on pudendum leukoplakia,and it is safe and convenient.

结论该制剂治疗外阴白斑疗效确切,使方便。

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

也使二酯酶抑制剂如巡能泰或己酮可可碱进行治疗。

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

抗雌激素。选择性PKC抑制剂。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。

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

酯酶、脂肪酶和N-甲酰甲硫氨氨基肽酶无毒的抑制剂。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.

荧光法测定了半乳糖神经酰胺脂质体制剂中维生素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剂之一。

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

盐芬氟拉明是一种食欲抑制剂，主要作于中枢神经系统。

Mixing phoxim and phorate produces the emulsifiable mixure of phoxim and phorate.

辛、甲混合制剂是由辛硫与甲拌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剂。

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治疗方案的使,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剂。

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剂的抗抑郁疗效优于传统化学合成药物，具有较好的耐受性与性。

An indirect atomic absorption spectroscopic method (AAS) was proposed for the determination of leucogen in pharmaceutical preparations.

该法可成功地于药物制剂中利血生的测定。

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,对治疗MG的新型免疫抑制剂研究进展进行综述。

Silica gel column separation method and spectrophotography were used to determine the content of urson in the preparation.

采硅胶柱分离分光光度法,对制剂中所含熊果成分进行含量测定,结果含量测定的标准品线性关系好,检测数据稳定。

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.

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。

The samples were ignited, then bismuth subcarbonate in residue was determined by compleximetry.

供试品经有机破坏后,采络合滴定法测定制剂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.

本品作药物固体制剂，全粉末直接压片的干燥粘合剂，胶囊填充剂,崩解剂，湿法造粒粘合剂和着色的延展剂。

Conclusion The cream has therapeutic effect on pudendum leukoplakia,and it is safe and convenient.

结论该制剂治疗外阴白斑疗效确切,使安全方便。

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

也使磷酸二酯酶抑制剂如巡能泰或己酮可可碱进行治疗。

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

抗雌激素。选择性PKC抑制剂。诱导凋亡。

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

钠转运特异性抑制剂——阿咪洛利或哇巴因能部分抑制特普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无毒的抑制剂。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.

荧光法测定了半乳糖神经酰胺脂质体制剂中维生素A的含量。

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

夫马洁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，作于中枢神经系统。

Mixing phoxim and phorate produces the emulsifiable mixure of phoxim and phorate.

辛、甲混合制剂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剂。

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治疗方案的使,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剂。

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剂的抗抑郁疗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.

该法可成功地于药物制剂中利血生的测定。

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,对治疗MG的新型免疫抑制剂研究进展进行综述。

Silica gel column separation method and spectrophotography were used to determine the content of urson in the preparation.

采硅胶柱分离分光光度法,对制剂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。

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.

结论该制治疗外阴白斑疗效确切,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泰或己酮可可碱进行治疗。

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。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。

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

盐酸芬氟拉明是种食欲抑制，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治疗方案的使用,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疗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,对治疗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。

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.

显示细胞生长和细胞毒活。EGFR激酶剂。有抗血管生成活。

The samples were ignited, then bismuth subcarbonate in residue was determined by compleximetry.

供试品经有机破坏后,采用络滴定法测定剂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剂，全粉末直接压片的干剂，胶囊填充剂,崩解剂，湿法造粒剂和着色的延展剂。

Conclusion The cream has therapeutic effect on pudendum leukoplakia,and it is safe and convenient.

结论该剂治疗外阴白斑疗效确切,使用安全方便。

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

也使用磷酸二酯酶剂如巡能泰或己酮可可碱进行治疗。

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

抗雌激素。选择PKC剂。诱导凋亡。

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

钠转运特异剂——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剂。也羧肽酶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剂中维生素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。

Mixing phoxim and phorate produces the emulsifiable mixure of phoxim and phorate.

辛、甲混剂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剂。

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治疗方案的使用,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剂。

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剂的抗郁疗效优于传统化学成药物，具有较好的耐受与安全。

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剂中利血生的测定。

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,对治疗MG的新型免疫剂研究进展进行综述。

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,对剂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关系好,检测数据稳定。