1、

Azole and triazole drugs are cytochrome P 450 inhibitors widely used as fungal antibiotics and antimycobacterial actiity.

唑类和三氮唑类药物作为细胞色素P450抑制剂广泛被作为抗真菌药物和抗微生物药物使用.

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2、

Including, thiabendazole, or mycophenolate triazole, Prochloraz amines, malathion, and so IPRODIONE.

其中包括多菌灵, 噻菌灵, 抑霉唑, 咪鲜胺, 马拉硫磷, 异菌脲等.

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3、

Organochlorine and triazole pesticide residues were stabile in processing of farm induce.

有机氯类、有机唑类农药较为稳定,加工操作很难得到较好的去除效果.

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4、

Objective : To study the antifungal activity of the new triazole compounds against candida species.

目的: 研究一类新型的三氮唑化合物对念珠菌属真菌的抗真菌活性.

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5、

Azoles are the largest class of antifungal agents in clinical use. 1,2,3-Triazole moieties are attractive connecting units, as they are stable to metabolic degradation and capable of hydrogen bonding, which can be favorable in binding of biomolecular targets and solubility.

唑类是临床上应用最广泛的抗菌药物。1,2,3-三氮唑由于其不容易被生物降解和容易形成氢键增加了其与生物大分子的结合能力,被作为一个极具吸引力的连接单元广泛应用。

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6、

Azole and triazole drugs are cytochrome P450 inhibitors widely used as fungal antibiotics and possessing potent antimycobacterial actiity.

唑类和三氮唑类药物作为细胞色素P450抑制剂广泛被作为抗真菌药物和抗微生物药物使用。

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7、

We present here the crystal structure of Mycobacterium tuberculosis cytochrome P450 CYP121 in complex with the triazole drug fluconazole, revealing a new azole heme ligation mode.

我们提出了肺结核分支杆菌细胞色素P450CYP121与三氮唑类药物氟康唑的复合物的晶体结构,揭示了唑类与亚铁血红素新的结合模式。

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8、

Each triazole group of fluconazole links two SBUs and the compound 9 exhibits a chain-like architecture with strong antiferromagnetism.

氟康唑中的每个三唑基连接两个单元格,磁性研究表明配合物9存在强的反铁磁性。

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9、

In this paper PAHMT chelating resin having symmetrical triazole AHMT as the function group was synthesized by means of macroporous polystyrene backbone and the structure of resin was characterized.

本文以大孔聚苯乙烯树脂为骨架合成了含有对称三唑AHMT功能基的螯合树脂PAHMT,并对其结构进行了表征;

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