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65358-15-8
  • names:

    Pseudothymidine

  • CAS號:

    65358-15-8

    MDL Number: MFCD04973713
  • MF(分子式): C10H14N2O5 MW(分子量): 242.23
  • EINECS:No data available Reaxys Number:No data available
  • Pubchem ID:375973985 Brand:BIOFOUNT
偽胸苷
偽胸苷(65358-15-8,Pseudothymidine)是胸苷的C-核苷(C-nucleosid)類似物。
貨品編碼 規(guī)格 純度 價格 (¥) 現(xiàn)價(¥) 特價(¥) 庫存描述 數(shù)量 總計 (¥)
YZM000669-5mg 5mg 99.85% ¥ 6581.00 ¥ 6581.00 2-3天
- +
0.00
YZM000669-1mg 1mg 99.85% ¥ 1852.50 ¥ 1852.50 2-3天
- +
0.00
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中文別名 偽胸苷(65358-15-8);5-(2-脫氧-BETA-D-赤式-呋喃戊糖基)-1-甲基-2,4(1H,3H)-嘧啶二酮;
英文別名 Pseudothymidine(65358-15-8);5-Methyl-2'-Deoxypseudouridin;5-(2-Deoxy-beta-D-erythro-pentofuranosyl)-1-methyl-2,4(1H,3H)-pyrimidinedione;PSEUDOTHYMIDINE;5-Methyl-2'-Deoxypseudouridin;
CAS號 65358-15-8
Inchi No data available
InchiKey No data available
分子式 Formula C10H14N2O5
分子量 Molecular Weight 242.23
溶解度Solubility 生物體外In Vitro:DMSO溶解度≥ 61.17 mg/mL(252.53 mM)*"≥" means soluble可溶, but saturation unknown溶解度未知.
性狀 固體粉末,Power
儲藏條件 Storage conditions -20°C 3 years年 4°C 2 years年 / In solvent溶液中:-80°C 6 months月 -20°C 1 month月

偽胸苷(65358-15-8,Pseudothymidine)實驗注意事項:
1.實驗前需戴好防護眼鏡,穿戴防護服和口罩,佩戴手套,避免與皮膚接觸。
2.實驗過程中如遇到有毒或者刺激性物質及有害物質產生,必要時實驗操作需要手套箱內完成以免對實驗人員造成傷害
3.實驗后產生的廢棄物需分類存儲,并交于專業(yè)生物廢氣物處理公司處理,以免造成環(huán)境污染Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.

Tags:Pseudothymidine試劑,Pseudothymidine雜質,Pseudothymidine中間體,Pseudothymidine密度,Pseudothymidine旋光度,Pseudothymidine溶解度,Pseudothymidine閃點,Pseudothymidine熔點,Pseudothymidine結構式,Pseudothymidine購買,
產品說明 (65358-15-8,Pseudothymidine)偽胸苷是胸苷的C-核苷(C-nucleosid)類似物。
Introduction(偽胸苷,65358-15-8)Pseudothymidine is a Cucleoside analog of thymidine.
Application1
Application2
Application3

偽胸苷(65358-15-8,Pseudothymidine)藥理學:


偽胸苷是胸苷的C-核苷(C-nucleosid)類似物。


S Lutz, et al. An in vitro screening technique for DNA polymerases that can incorporate modified nucleotides. Pseudo-thymidine as a substrate for thermostable polymerases. Nucleic Acids Res. 1999 Jul
Havemann SA, et al. Incorporation of multiple sequential pseudothymidines by DNA polymerases and their impact on DNA duplex structure. Nucleosides Nucleotides Nucleic Acids. 2008 Mar;27(3):261-78.
 
偽胸苷(65358-15-8,Pseudothymidine)參考文獻:
1、Incorporation of multiple sequential pseudothymidines by DNA polymerases and their impact on DNA duplex structure
Stephanie A Havemann , Shuichi Hoshika, Daniel Hutter, Steven A Benner

Abstract:Thermal denaturation and circular dichroism studies suggested that multiple (up to 12), sequential pseudothymidines, a representative C-glycoside, do not perturb the structure of a representative DNA duplex. Further, various Family A and B DNA polymerases were found to extend a primer by incorporating four sequential pseudothymidine triphosphates, and then continue the extension to generate full-length product. Detailed studies showed that Taq polymerase incorporated up to five sequential C-glycosides, but not more. These results constrain architectures for sequencing, quantitating, and analyzing DNA analogs that exploit C-glycosides, and define better the challenge of creating a synthetic biology using these with natural polymerases.

2、An in vitro screening technique for DNA polymerases that can incorporate modified nucleotides. Pseudo-thymidine as a substrate for thermostable polymerases
S Lutz , P Burgstaller, S A Benner

Abstract:DNA polymerases are desired that incorporate modified nucleotides into DNA with diminished pausing, premature termination and infidelity. Reported here is a simple in vitro assay to screen for DNA polymerases that accept modified nucleotides based on a set of primer extension reactions. In combination with the scintillation proximity assay (SPA[trade]), this allows rapid and simple screening of enzymes for their ability to elongate oligonucleotides in the presence of unnatural nucleotides. A proof of the concept is obtained using pseudo-thymidine (psiT), the C-nucleoside analog of thymidine, as the unnatural substrate. The conformational properties of psiT arising from the carbon-carbon bond between the sugar and the base make it an interesting probe for the importance of conformational restraints in the active site of polymerases during primer elongation. From a pool of commercially available thermostable polymerases, the assay identified Taq DNA polymerase as the most suitable enzyme for the PCR amplification of oligonucleotides containing psiT. Subsequent experiments analyzing PCR performance and fidelity of Taq DNA polymerase acting on psiT are presented. This is the first time that PCR has been performed with a C-nucleoside.

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