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,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，广泛分布在各种生物内。

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,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素蛋白的例子是与微粒NADPH -细胞色素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，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.

哒嗪酮类化物具有多种重要的生物活性,据作用机制的不同,可为钙增敏剂、磷酸二酯酶抑制剂、环氧酶抑制剂等,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.

的一一单电子转移黄素蛋白的例子是与微粒NADPH -细胞色素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.

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.

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.

哒嗪酮类化合物具有多种重要生物活性,据作用机制不同,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合成工艺作了改进，使中间体绕丹宁乙酸提高到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，广泛分布在各种生物体。

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

个经历个单电子转移黄素蛋白例子是与微粒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.

哒嗪酮类化合物具有多种重要生物活性,据作用机制不同,可分为钙增敏剂、磷酸二酯制剂、环氧合制剂等,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不同条件对于茎瘤芥硝酸还活性影响。

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

还蛋白属于硫还蛋白超家族，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.

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.

哒嗪酮类化合物具有多种重要生物活性,据作用机制不同,可分为钙增敏剂、磷二酯酶抑制剂、环合酶抑制剂等,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%.

对醛搪还原酶抑制剂依帕司他合成工艺作了改进，使中间体绕丹宁乙率提高到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.

的个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,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%.

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于茎瘤芥硝酸还原酶活性的影响。