The former consists of glutathione, glutathione reductase and glutaredoxin, while the later consists of thioredoxin and thioredoxin reductase.

谷氧蛋白属于硫氧蛋白超家族，广分布在各种生物体内。

An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.

的一个经历一个单电子转移黄蛋白的例子是与微粒NADPH -细胞色P450酶。

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、磷二酯酶抑制剂、环氧合酶抑制剂等,并可用于相关疾病的治疗。

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，使中间体绕丹宁乙的收率提高到76．4％。

The main body of a book is adopt to follow different condition of admeasurement in vitro to active effect of stem tumour mustard hydrogen nitrate reductase.

本文采用离体法测定不同条件对于茎瘤芥酶活性的影响。

The former consists of glutathione, glutathione reductase and glutaredoxin, while the later consists of thioredoxin and thioredoxin reductase.

谷还蛋白属于硫还蛋白超家族，广布在各种生物体内。

An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.

的一个经历一个单电子转移黄素蛋白的例子是与微粒NADPH -细胞色素P450还原。

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

哒嗪酮类合物具有多种重要的生物活性,根据作用机制的不同,可增敏剂、磷酸二酯抑制剂、环合抑制剂等,并可用于相关疾病的治疗。

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％。

The main body of a book is adopt to follow different condition of admeasurement in vitro to active effect of stem tumour mustard hydrogen nitrate reductase.

本文采用离体法测定不同条件对于茎瘤芥硝酸还原活性的影响。

The former consists of glutathione, glutathione reductase and glutaredoxin, while the later consists of thioredoxin and thioredoxin reductase.

氧还蛋白属于硫氧还蛋白超家族，广分布在各种生物体内。

An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.

的一经历一子转移黄素蛋白的例子是与微粒NADPH -细胞色素P450还原酶。

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治疗。

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％。

The main body of a book is adopt to follow different condition of admeasurement in vitro to active effect of stem tumour mustard hydrogen nitrate reductase.

本文采用离体法测定不同条件对于茎瘤芥硝酸还原酶活性的影响。

The former consists of glutathione, glutathione reductase and glutaredoxin, while the later consists of thioredoxin and thioredoxin reductase.

谷还蛋白属于硫还蛋白超家族，广分布在各种生物体内。

An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.

的一个经历一个单电子转移黄素蛋白的例子是与微粒NADPH -细胞色素P450还原。

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

哒嗪酮类合物具有多种重要的生物活性,根据作用机制的不同,可分敏剂、磷酸二酯抑制剂、环合抑制剂等,并可用于相关疾病的治疗。

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％。

The main body of a book is adopt to follow different condition of admeasurement in vitro to active effect of stem tumour mustard hydrogen nitrate reductase.

本文采用离体法测定不同条件对于茎瘤芥硝酸还原活性的影响。

The former consists of glutathione, glutathione reductase and glutaredoxin, while the later consists of thioredoxin and thioredoxin reductase.

谷氧还蛋白属于硫氧还蛋白超家族，广分布在各种生物体内。

An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.

的一个经历一个单电转移黄素蛋白的例微粒NADPH -细胞色素P450还。

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、磷酸酯抑制剂、环氧合抑制剂等,并可用于相关疾病的治疗。

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％。

The main body of a book is adopt to follow different condition of admeasurement in vitro to active effect of stem tumour mustard hydrogen nitrate reductase.

本文采用离体法测定不同条件对于茎瘤芥硝酸还活性的影响。

The former consists of glutathione, glutathione reductase and glutaredoxin, while the later consists of thioredoxin and thioredoxin reductase.

谷氧还蛋白属于硫氧还蛋白超家族，广分布在各种体内。

An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.

一个经历一个单电子转移黄素蛋白例子是与微粒NADPH -细胞色素P450还原酶。

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

哒嗪酮类化具有多种重要活性,根据作用不同,可分为钙增敏剂、磷酸二酯酶抑剂、环氧酶抑剂等,并可用于相关疾病治疗。

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

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

The main body of a book is adopt to follow different condition of admeasurement in vitro to active effect of stem tumour mustard hydrogen nitrate reductase.

本文采用离体法测定不同条件对于茎瘤芥硝酸还原酶活性影响。

The former consists of glutathione, glutathione reductase and glutaredoxin, while the later consists of thioredoxin and thioredoxin reductase.

谷氧还蛋白属于硫氧还蛋白超家族，广分布在各种生物体内。

An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.

的一个经历一个单电子转移黄素蛋白的例子是与微粒NADPH -细胞色素P450还原。

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

酮类化合物具有多种重要的生物活性,根据作机制的不同,可分为钙增敏剂、磷酸二酯抑制剂、环氧合抑制剂等,并可于相关疾病的治疗。

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％。

The main body of a book is adopt to follow different condition of admeasurement in vitro to active effect of stem tumour mustard hydrogen nitrate reductase.

本文采离体法测定不同条件对于茎瘤芥硝酸还原活性的影响。

The former consists of glutathione, glutathione reductase and glutaredoxin, while the later consists of thioredoxin and thioredoxin reductase.

谷氧还蛋白属于硫氧还蛋白超家族，广分布在各种生物体内。

An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.

的一个经历一个单电转移黄素蛋白的与微粒NADPH -细胞色素P450还原。

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、磷酸酯抑制剂、环氧合抑制剂等,并可用于相关疾病的治疗。

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％。

The main body of a book is adopt to follow different condition of admeasurement in vitro to active effect of stem tumour mustard hydrogen nitrate reductase.

本文采用离体法测定不同条件对于茎瘤芥硝酸还原活性的影响。

The former consists of glutathione, glutathione reductase and glutaredoxin, while the later consists of thioredoxin and thioredoxin reductase.

谷氧还蛋白属于硫氧还蛋白超家族，广分布在各种物体内。

An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.

一个经历一个单电子转移黄素蛋白例子是与微粒NADPH -细胞色素P450还原。

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物活性,根据作用机制,可分为钙增敏剂、磷酸二酯抑制剂、环氧合抑制剂等,并可用于相关疾病治疗。

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

对醛搪还原抑制剂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％。

The main body of a book is adopt to follow different condition of admeasurement in vitro to active effect of stem tumour mustard hydrogen nitrate reductase.

本文采用离体法测定条件对于茎瘤芥硝酸还原活性影响。