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Complexation of aminoglutethimide with native and modified cyclodextrins

机译:氨基谷氨酰胺与天然和修饰的环糊精的络合

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摘要

Complexations of R(+) and RS(+/-)aminoglutethimide (AGT), the drug used in a treatment of breast and prostate cancer with native and modified cyclodextrins (alpha-CD, beta-CD, gamma-CD, 2,6-di-O-methyl-beta-CD (DM-beta-CD), 2,3,6-tri-O-methyl-beta-CD (TM-beta-CD) and carboxymethyl-beta-CD (CM-beta-CD)) were studied. The stability constants were determined with UV-Vis spectrophotometric method at pH 9.0. The NMR data obtained for TM-beta-CD suggest that the complexation of AGT is possible from both sides of CD molecule. This was confirmed by molecular dynamic simulations.
机译:R(+)和RS(+/-)氨基谷氨酰胺(AGT)与天然和修饰的环糊精(α-CD,β-CD,γ-CD,2,6 -二-O-甲基-β-CD(DM-β-CD),2,3,6-三-O-甲基-β-CD(TM-β-CD)和羧甲基-β-CD(CM-β -CD))。用UV-Vis分光光度法在pH 9.0下测定稳定性常数。从TM-β-CD获得的NMR数据表明,从CD分子的两面都可以进行AGT的络合。分子动力学模拟证实了这一点。

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