Basic information Safety Supplier Related

5'-O-Tritylthymidine

Basic information Safety Supplier Related

5'-O-Tritylthymidine Basic information

Product Name:
5'-O-Tritylthymidine
Synonyms:
  • 5''-O-TRITYLTHYMIDINE(5-OTT)
  • 5-Methyl-5'-O-trityl-2'-deoxyuridine
  • 5'-O-Triphenylmethylthymidine
  • Thymidine, 5'-o-(triphenylmethyl)-
  • Trt-dT
  • 1-[5-[[2-(diphenylmethyl)phenoxy]methyl]-4-hydroxy-2-oxolanyl]-5-methylpyrimidine-2,4-dione
  • 5'-Trt-2'-deoxythymidine
  • 5'-O-Trt-deoxythymidine
CAS:
7791-71-1
MF:
C29H28N2O5
MW:
484.54
EINECS:
2017-001-1
Product Categories:
  • Biochemicals and Reagents
  • Nucleoside Analogs
  • Nucleosides, Nucleotides, Oligonucleotides
Mol File:
7791-71-1.mol
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5'-O-Tritylthymidine Chemical Properties

Melting point:
125 °C(Solv: acetone (67-64-1); ethyl ether (60-29-7))
Density 
1.275±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
pka
9.55±0.10(Predicted)
form 
Solid
color 
White to off-white
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3

MSDS

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5'-O-Tritylthymidine Usage And Synthesis

Uses

5'-O-Tritylthymidine is an inhibitor of TK-2 and inhibits angiogenesis[1]. 5'-O-Tritylthymidine targets FAK-Mdm-2 interactions, decreasing cell viability and increasing apoptosis.

Synthesis

76-83-5

50-89-5

7791-71-1

Triphenylchloromethane (15 g, 53.7 mmol) was slowly added to a solution of pyridine (40 mL) containing 1-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methylpyrimidin-2,4(1H,3H)-dione (10 g, 41.3 mmol) under nitrogen protection, and the reaction mixture was kept at room temperature for The reaction mixture was stirred for 21.5 hours at room temperature. Upon completion of the reaction, the reaction was quenched by the addition of saturated aqueous sodium bicarbonate solution to the system, followed by extraction and separation with dichloromethane. The organic phase was washed sequentially with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. The organic solvent was removed by concentration under reduced pressure, and the resulting crude product was purified by silica gel column chromatography (eluent ratio of ethyl acetate:n-hexane=1:1) to afford the target compound 1-((2R,4S,5R)-4-hydroxy-5-((triphenylmethoxy)methyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione (19.4 g, 97.1% yield), as colorless acicular crystals. ), colorless needle-like crystals.

References

[1] Hernández A et al. Acyclic nucleoside analogues as novel inhibitors of human mitochondrial thymidine kinase. J Med Chem. 2002 Sep 12;45(19):4254-63. DOI:10.1021/jm011128+
[2] Golubovskaya V et al. A small-molecule inhibitor, 5'-O-tritylthymidine, targets FAK and Mdm-2 interaction, and blocks breast and colon tumorigenesis in vivo. Anticancer Agents Med Chem. 2013 May;13(4):532-45. DOI:10.2174/1871520611313040002

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