CAS: 66335-37-3; 5’-Deoxy-2’,3’-O-Isopropylidene-5-Fluorocytidine

该化合物是一个经过修改的细胞碘核素类比,该化合物在5'位置上具有氟原子特征,与天然核素相比,这增强了其稳定性并改变了其生物活动.2'和3'位置上的异丙基乙酰胺组为氢氧基组提供保护,使其更能抗酶降解.这一改变在核素类比中意义重大,因为它可以影响化合物作为抗病毒或抗癌剂的能力.氟原子的存在还可能影响化合物与核素酸和酶的相互作用,有可能导致药性特性的改变.

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362-42-5 61787-04-0 66335-39-5

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    上下游产品

    2,3-O-isopropylidene-3-O-acetyl-5-deoxy-D-ribose 2-trimethylsilyloxy-4-trimethylsilylamino-5-fluoropyrimidine 5'-deoxy-5-fluor°Cytidine

    合成工艺路线路线简述

      📜5'-脱氧-5-氟-5'-碘-2',3'-O-异亚丙基胞苷 反应生成 5'-脱氧-2',3'-O-异亚丙基-5-氟-D-胞啶
      参考文献:Cook,A. F.
      标题:Cook,A. F.

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      ✅ COA系统入驻 | 共享模式

      主要参考文献

      参考标题:Synthesis Of Thiol Derivatives Of Biological Active Compounds For Nanotechnology Application
      作者:Katarzyna Sidoryk,Olga Michalak,Marek Kubiszewski,Andrzej Leś,Marcin Cybulski,Elżbieta U. Stolarczyk,Jan Doubsky
      摘要:In Obtaining Different Compounds From Those Designed. Nevertheless, In All Above Cases We Were Able To Obtain Thiol-Containing Derivatives Of Selected Biological Active Compounds. Moreover, A Modelling Study For The Two-Step Thiolation Of Genistein And Some Of Its Derivatives Was Accomplished Using The Density Functional Theory (B3Lp). A Hypothesis On A Possible Reason For The Unsuccessful Deprotection
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