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Phosphodiesterase II

Base Information
  • Chemical Name:Phosphodiesterase II
  • CAS No.:9068-54-6
  • Molecular Formula:
  • Molecular Weight:0
  • Hs Code.:
Phosphodiesterase II

Synonyms:3'-Exonuclease;3'-Nucleotide phosphodiesterase; 3'-Phosphodiesterase; DNA3'-phosphodiesterase; E.C. 3.1.16.1; E.C. 3.1.4.18

Suppliers and Price of Phosphodiesterase II
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • Phosphodiesterase II from bovine spleen lyophilized powder, ≥5.0?units/mg protein
  • 25 units
  • $ 337.00
  • Sigma-Aldrich
  • Phosphodiesterase II from bovine spleen lyophilized powder, ≥5.0 units/mg protein
  • 25un
  • $ 325.00
  • Sigma-Aldrich
  • Phosphodiesterase II from bovine spleen lyophilized powder, ≥5.0?units/mg protein
  • 10 units
  • $ 169.00
  • Sigma-Aldrich
  • Phosphodiesterase II from bovine spleen lyophilized powder, ≥5.0 units/mg protein
  • 10un
  • $ 163.00
Total 17 raw suppliers
Chemical Property of Phosphodiesterase II
Chemical Property:
  • PSA:0.00000 
  • LogP:0.00000 
  • Storage Temp.:−20°C 
Purity/Quality:

98%,99%, *data from raw suppliers

Phosphodiesterase II from bovine spleen lyophilized powder, ≥5.0?units/mg protein *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses The product has been used in the characterization of polynucleotide chain length, base composition, and identity of terminal nucleotide. The enzyme has also been used in excision of pyridyloxobutyl (POB) base adducts from DNA. Furthermore, it has been used along with micrococcal endonuclease to hydrolyze purified DNA to 3 -nucleoside monophosphates.
Refernces

NUCLEOSIDE PHOSPHONODITHIOATES AS INTERMEDIATES IN THE PREPARATION OF DINUCLEOSIDE PHOSPHORODITHIOATES AND PHOSPHOROTHIOATES

10.1016/S0040-4039(01)80782-6

The research focuses on the synthesis of dinucleoside phosphorodithioates and phosphorothioates, which are analogues of oligonucleotides with potential applications as antiviral agents and in studies involving interactions with nucleic acids and proteins. The purpose of the study is to develop an alternative and convenient approach to synthesizing these analogues using protected nucleoside 3'-phosphonodithioates as starting materials. The researchers successfully converted 5'-O-(9-phenylxanthen-9-yl)thymidine into its 3'-phosphonodithioate derivative and further into dinucleoside phosphonothioate and dinucleoside phosphorodithioate with good overall yields. Key chemicals used in the process include triethylammonium salt, 3'-O-acetylthymidine, pivaloyl chloride, and sulfur. The study concludes that the procedure is potentially applicable to the synthesis of phosphorodithioate analogues of oligodeoxyribo- and oligoribo-nucleotides, both in solution and on solid supports, and that the synthesized dinucleoside phosphorodithioate (6a) is resistant to digestion by snake venom phosphodiesterase, bovine spleen phosphodiesterase, and nuclease PI.

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