S. aureus dihydrofolate reductase co-crystallized with 1-ethylpropyl-dihydropthalazine inhibitor and NADP(H)
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S. aureus dihydrofolate reductase co-crystallized with 1-ethylpropyl-dihydropthalazine inhibitor and NADP(H) Descriptor: (2E)-3-{5-[(2,4-diaminopyrimidin-5-yl)methyl]-2,3-dimethoxyphenyl}-1-[(1S)-1-(pentan-3-yl)-3,4-dihydrophthalazin-2(1H)-yl]prop-2-en-1-one, Dihydrofolate reductase, GLYCEROL, ... Authors: Bourne, C.R, Thomas, L.M. Deposit date: 2019-07-10 Release date: 2020-06-17 Last modified: 2023-10-11 Method: X-RAY DIFFRACTION (2.01 Å) Cite: Inhibitor design to target a unique feature in the folate pocket of Staphylococcus aureus dihydrofolate reductase. Eur.J.Med.Chem., 200, 2020
金黄色葡萄球菌(Staphylococcus aureus)二氢叶酸还原酶(dihydrofolate reductase)与1-乙基丙基二氢酞嗪抑制剂及烟酰胺腺嘌呤二核苷酸磷酸(还原型)(NADP(H))共结晶。 描述项:(2E)-3-{5-[(2,4-二氨基嘧啶-5-基)甲基]-2,3-二甲氧基苯基}-1-[(1S)-1-(3-戊基)-3,4-二氢酞嗪-2(1H)-基]丙-2-烯-1-酮、二氢叶酸还原酶、甘油(GLYCEROL)…… 作者:Bourne C.R.、Thomas L.M. 提交日期:2019-07-10 发布日期:2020-06-17 最近修改日期:2023-10-11 实验方法:X射线衍射(X-RAY DIFFRACTION,分辨率2.01埃) 引用文献:《靶向金黄色葡萄球菌二氢叶酸还原酶叶酸口袋独特特征的抑制剂设计》,《欧洲药物化学杂志》(Eur.J.Med.Chem.),2020,第200卷
创建时间:
2019-07-10



