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，广泛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。

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,据作用机的不同,可分为钙增敏剂、磷酸二酯剂、环氧合剂等,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，广泛分布在各种体内。

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.

哒嗪酮类化合具有多种重要活性,据作不同,可分为钙增敏剂、磷酸二酯酶抑剂、环氧合酶抑剂等,并可于相关疾病治疗。

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，广泛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.

哒嗪酮物具有多种重要的生物活性,据作用机制的不同,可分为钙、磷酸二酯酶抑制、环氧酶抑制等,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，广泛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,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.

谷氧蛋白属于硫氧蛋白超家族，广泛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P450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,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％。

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，广泛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.

哒嗪酮物具有多种重要的生物活性,据作用机制的不同,可分为钙、磷酸二酯酶抑制、环氧酶抑制等,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.

谷氧还白属硫氧还白超家族，广泛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白的例子是与微粒NADPH -细胞色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,据作机制的不同,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.

本文采离体法测定不同条件对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，广泛分布在各种体内。

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.

哒嗪酮类化合具有多种重要活性,据作不同,可分为钙增敏剂、磷酸二酯酶抑剂、环氧合酶抑剂等,并可于相关疾病治疗。

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，广泛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黄素蛋白的例是与微粒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,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。