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性,根据作机制的不同,可分为钙增敏剂、磷酸二酯酶抑制剂、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%.

对搪还原酶抑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％。

Transketolase is the key enzyme of pentose-phophate pathway, catalyses transfer of a two-carbon fragment from a ketolase (donor substance) to an aldose (acceptor substance).

摘要转酮醇酶是磷酸戊糖途径的关键酶，催化二碳单元在酮糖（供体）和糖（受体）间的转移。

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性,根据作机制的不同,分为钙增敏剂、磷酸二酯酶抑制剂、环氧合酶抑制剂等,并相关疾病的治疗。

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％。

Transketolase is the key enzyme of pentose-phophate pathway, catalyses transfer of a two-carbon fragment from a ketolase (donor substance) to an aldose (acceptor substance).

摘要转酮醇酶是磷酸戊糖途径的关键酶，催化二碳单元在酮糖（供体）和醛糖（受体）间的转移。

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性,根据作机制的不同,可分为钙增敏剂、磷酸二酯酶抑制剂、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%.

对搪还原酶抑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％。

Transketolase is the key enzyme of pentose-phophate pathway, catalyses transfer of a two-carbon fragment from a ketolase (donor substance) to an aldose (acceptor substance).

摘要转酮醇酶是磷酸戊糖途径的关键酶，催化二碳单元在酮糖（供体）和糖（受体）间的转移。

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生物性,根据作用机制不同,可分为钙增敏剂、磷酸二酯抑制剂、环氧抑制剂等,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成工艺作了改进，使中间体绕丹宁乙酸收率提高到76．4％。

Transketolase is the key enzyme of pentose-phophate pathway, catalyses transfer of a two-carbon fragment from a ketolase (donor substance) to an aldose (acceptor substance).

摘要转酮醇是磷酸戊糖途径关键，催化二碳单元在酮糖（供体）和醛糖（受体）间转移。

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性,根据作用机的不同,可分为钙增敏、磷酸二酯酶抑、环氧合酶抑,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％。

Transketolase is the key enzyme of pentose-phophate pathway, catalyses transfer of a two-carbon fragment from a ketolase (donor substance) to an aldose (acceptor substance).

摘要转酮醇酶是磷酸戊途径的关键酶，催化二碳单元在酮（供体）和醛（受体）间的转移。

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重要生物性,根据作用不同,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合成工艺作了改进，使中间体绕丹宁乙酸收率提高到76．4％。

Transketolase is the key enzyme of pentose-phophate pathway, catalyses transfer of a two-carbon fragment from a ketolase (donor substance) to an aldose (acceptor substance).

摘要转酮醇酶是磷酸戊糖途径关键酶，催化二碳单元在酮糖（供体）和醛糖（受体）间转移。

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的生物性,根据制的不同,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了改进，使中间体绕丹宁乙酸的收率提高到76．4％。

Transketolase is the key enzyme of pentose-phophate pathway, catalyses transfer of a two-carbon fragment from a ketolase (donor substance) to an aldose (acceptor substance).

摘转酮醇酶是磷酸戊糖途径的关键酶，催化二碳单元在酮糖（供体）和醛糖（受体）间的转移。

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要的生物性,根据作的不同,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％。

Transketolase is the key enzyme of pentose-phophate pathway, catalyses transfer of a two-carbon fragment from a ketolase (donor substance) to an aldose (acceptor substance).

摘要转酮醇酶是磷酸戊糖途径的关键酶，催化二碳单元在酮糖（供体）和醛糖（受体）间的转移。

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性,根据作用机制不同,可分为钙增敏、磷酸二酯酶抑制、环氧合酶抑制等,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％。

Transketolase is the key enzyme of pentose-phophate pathway, catalyses transfer of a two-carbon fragment from a ketolase (donor substance) to an aldose (acceptor substance).

摘要转酮醇酶是磷酸戊糖途径关键酶，催化二碳单元在酮糖（供体）和醛糖（受体）间转移。