Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

酯、脂肪和N-甲酰甲硫氨酸氨基肽无毒的抑制剂。也抑制羧肽Y类外肽。

Cutinase is an exteacellular enzyme which catalyses the hydrosis of cutin and belongs to aclass of serine esterases.

角质是一种可以降植物角质的,属于丝氨酸酯。

After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.

本品为前体药,其性代谢产物通过阻碍DNA拓扑异构DNA无法形成超螺旋,导致胞无法分裂繁殖。

The results of biochemical analysis indicated that the difference of the activity of carboxylesterase and esterase isozymes in the larval midguts were the main mechanism of this selective toxicity.

生化分析结果进一步指出,昆虫中肠羧酸酯的性及酯同功的差异是这种选择麻醉作用的重要机制。

Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

酯酶、脂肪酶和N-甲酰甲硫氨酸氨基肽酶无毒抑制剂。也抑制羧肽酶Y类外肽酶。

Cutinase is an exteacellular enzyme which catalyses the hydrosis of cutin and belongs to aclass of serine esterases.

角质酶是一种可以降解植物角质水解酶,属于丝氨酸酯酶。

After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.

本品为前体药,其性代谢产物通过阻碍DNA拓扑异构酶使细菌DNA无法形成超螺旋,导致细菌细胞无法分裂繁殖。

The results of biochemical analysis indicated that the difference of the activity of carboxylesterase and esterase isozymes in the larval midguts were the main mechanism of this selective toxicity.

生化分析结果进一步指出,昆虫中肠羧酸酯酶性及酯酶同功酶差异是这种选择麻醉重要机制。

Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

酯酶、脂肪酶和N-甲酰甲硫氨酸氨基肽酶毒抑制剂。也抑制羧肽酶Y类外肽酶。

Cutinase is an exteacellular enzyme which catalyses the hydrosis of cutin and belongs to aclass of serine esterases.

角酶是一种可以降解植物角解酶,属于丝氨酸酯酶。

After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.

本品为前体药,其性代谢产物通过阻碍DNA拓扑异构酶使细DNA法形成超螺旋,导致细细胞法分裂繁殖。

The results of biochemical analysis indicated that the difference of the activity of carboxylesterase and esterase isozymes in the larval midguts were the main mechanism of this selective toxicity.

生化分析结果进一步指出,昆虫中肠羧酸酯酶性及酯酶同功酶差异是这种选择麻醉作用重要机制。

Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

酯、脂肪和N-甲酰甲硫氨酸氨基无毒的抑制剂。也抑制Y类外。

Cutinase is an exteacellular enzyme which catalyses the hydrosis of cutin and belongs to aclass of serine esterases.

角质是一种可以降解植物角质的水解,属于丝氨酸酯。

After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.

本品为前体药,其性代谢产物通过阻碍DNA拓扑异构使细菌DNA无法形成超螺旋,导致细菌细胞无法裂繁殖。

The results of biochemical analysis indicated that the difference of the activity of carboxylesterase and esterase isozymes in the larval midguts were the main mechanism of this selective toxicity.

析结果进一步指出,昆虫中肠酸酯的性及酯同功的差异是这种选择麻醉作用的重要机制。

Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

酯酶、脂肪酶和N-甲酰甲硫酸基肽酶无毒的抑制剂。也抑制羧肽酶Y类外肽酶。

Cutinase is an exteacellular enzyme which catalyses the hydrosis of cutin and belongs to aclass of serine esterases.

角质酶是一种可以降解植物角质的水解酶,属酸酯酶。

After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.

本品为前体药,其性代谢产物通过阻碍DNA拓酶使细菌DNA无法形成超螺旋,导致细菌细胞无法分裂繁殖。

The results of biochemical analysis indicated that the difference of the activity of carboxylesterase and esterase isozymes in the larval midguts were the main mechanism of this selective toxicity.

生化分析结果进一步指出,昆虫中肠羧酸酯酶的性及酯酶同功酶的差是这种选择麻醉作用的重要机制。

Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

、脂肪和N-甲酰甲硫氨酸氨基肽无毒的抑制剂。也抑制羧肽Y类外肽。

Cutinase is an exteacellular enzyme which catalyses the hydrosis of cutin and belongs to aclass of serine esterases.

角质是一可以降解植物角质的水解,属于丝氨酸。

After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.

本品为前体药,其性代谢产物通过阻碍DNA拓扑异构使细菌DNA无法形成超螺旋,导致细菌细胞无法分裂繁殖。

The results of biochemical analysis indicated that the difference of the activity of carboxylesterase and esterase isozymes in the larval midguts were the main mechanism of this selective toxicity.

生化分析结果进一步指出,昆虫中肠羧酸的性及同功的差异是这麻醉作用的重要机制。

Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

酶、脂肪酶和N-甲酰甲硫氨酸氨基肽酶无毒的抑制剂。也抑制羧肽酶Y类外肽酶。

Cutinase is an exteacellular enzyme which catalyses the hydrosis of cutin and belongs to aclass of serine esterases.

角质酶是一种可以降解植物角质的水解酶,属于丝氨酸酶。

After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.

本品为前体药,其性代谢产物通过阻碍DNA拓扑异构酶使细菌DNA无法形成超螺旋,导致细菌细胞无法分裂繁殖。

The results of biochemical analysis indicated that the difference of the activity of carboxylesterase and esterase isozymes in the larval midguts were the main mechanism of this selective toxicity.

生化分析结果进一步指出,昆虫中肠羧酸酶的性及酶同功酶的差异是这种醉作用的重要机制。

Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

、脂肪和N-酰酸基肽无毒抑制剂。也抑制羧肽Y类外肽。

Cutinase is an exteacellular enzyme which catalyses the hydrosis of cutin and belongs to aclass of serine esterases.

角质是一种可以降解植物角质水解,属于丝酸。

After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.

本品为前体药,其性代谢产物通过阻碍DNA拓扑异构使细菌DNA无法形成超螺旋,导致细菌细胞无法分裂繁殖。

The results of biochemical analysis indicated that the difference of the activity of carboxylesterase and esterase isozymes in the larval midguts were the main mechanism of this selective toxicity.

生化分析结果进一步指出,昆虫中肠羧酸性及同功差异是这种选择麻醉作用重要机制。

Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.

酯酶、脂肪酶和N-甲酰甲硫氨酸氨基肽酶无毒抑制剂。也抑制羧肽酶Y类外肽酶。

Cutinase is an exteacellular enzyme which catalyses the hydrosis of cutin and belongs to aclass of serine esterases.

角质酶是一种可以降解植物角质水解酶,属于丝氨酸酯酶。

After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.

本品为前体药,其性代谢产物通过阻碍DNA拓扑异构酶使细菌DNA无法形成超螺旋,导致细菌细胞无法分裂繁殖。

The results of biochemical analysis indicated that the difference of the activity of carboxylesterase and esterase isozymes in the larval midguts were the main mechanism of this selective toxicity.

生化分析结果进一步指出,昆虫中肠羧酸酯酶性及酯酶同功酶差异是这种选择麻醉重要机制。