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Dicyclic and Tricyclic Diaminopyrimidine Derivatives as Potent Inhibitors of Cryptosporidium parvum Dihydrofolate Reductase: Structure-Activity and Structure-Selectivity Correlations

机译：双环状和三环二氨基嘧啶衍生物作为密码孢子酰亚氢醇的有效抑制剂还原酶还原酶：结构 - 活性和结构选择性相关性

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Richard G. Nelson; Andre Rosowsky;
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年度 2002
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1. Dicyclic and tricyclic diaminopyrimidine derivatives as potent inhibitors of Cryptosporidium parvum dihydrofolate reductase: structure-activity and structure-selectivity correlations. [J] . Nelson RG, Rosowsky A Antimicrobial agents and chemotherapy. . 2001,第12期

机译：二环和三环二氨基嘧啶衍生物作为小隐隐孢子虫二氢叶酸还原酶的有效抑制剂：结构活性和结构选择性的相关性。
2. Three-dimensional quantitative structure-activity and structure-selectivity relationships of dihydrofolate reductase inhibitors [J] . Sutherland JJ, Weaver DF Journal of Computer-Aided Molecular Design . 2004,第5期

机译：二氢叶酸还原酶抑制剂的三维定量结构-活性和结构-选择性关系
3. Identification of Cryptosporidium parvum dihydrofolate reductase inhibitors by complementation in Saccharomyces cerevisiae. [J] . Brophy VH, Vasquez J, Nelson RG, Antimicrobial agents and chemotherapy. . 2000,第4期

机译：通过酿酒酵母中的互补鉴定小隐隐孢子虫二氢叶酸还原酶抑制剂。
4. Biological Evaluation of Some Uracil Derivatives as Potent Glutathione Reductase Inhibitors [C] . Murat GüNEY, Deniz EK?NC?, Huseyin ?AVDAR, International Conference on Advances in Natural and Applied Sciences . 2016

机译：一些尿嘧啶衍生物作为有效谷胱甘肽还原酶抑制剂的生物学评价
5. Biochemical Characterization of FIKK Kinase from Cryptosporidium parvum and Discovery of Potent Inhibitors. [D] . Osman, Khan Tanjid. 2016

机译：小隐隐孢子虫FIKK激酶的生化特征和有效抑制剂的发现。
6. Dicyclic and Tricyclic Diaminopyrimidine Derivatives as Potent Inhibitors of Cryptosporidium parvum Dihydrofolate Reductase: Structure-Activity and Structure-Selectivity Correlations [O] . Richard G. Nelson, Andre Rosowsky 2002

机译：二环和三环二氨基嘧啶衍生物作为隐孢子虫二氢叶酸还原酶的强抑制剂：结构活性和结构选择性的相关性。
7. Dicyclic and Tricyclic Diaminopyrimidine Derivatives as Potent Inhibitors of Cryptosporidium parvum Dihydrofolate Reductase: Structure-Activity and Structure-Selectivity Correlations [O] . Nelson, Richard G., Rosowsky, Andre 2002

机译：二环和三环二氨基嘧啶衍生物作为隐孢子虫二氢叶酸还原酶的强抑制剂：结构活性和结构选择性的相关性。

Dicyclic and Tricyclic Diaminopyrimidine Derivatives as Potent Inhibitors of Cryptosporidium parvum Dihydrofolate Reductase: Structure-Activity and Structure-Selectivity Correlations

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