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.

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.

哒嗪酮类化合具有多种重要的性,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子转移黄素蛋白的例子是与微粒NADPH -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、磷酸二酯抑制剂、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P450。

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子转移黄素蛋白的例子是与微粒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.

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蛋白的例子是与微粒NADPH -细胞色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、磷酸二酯抑制剂、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.

哒嗪酮类化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、磷酸二酯制剂、环氧制剂等,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%.

对醛搪还原制剂依帕司他的成工艺作了改进，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.

的一个经历一个单移黄素蛋白的是与微粒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。