6-Chloropurine riboside, 98%
6-Chloropurine riboside, 98%
6-Chloropurine riboside, 98%
Thermo Scientific Chemicals

6-Chloropurine riboside, 98%

CAS: 5399-87-1 | C10H11ClN4O4 | 286.67 g/mol
製品番号(カタログ番号) H59634.06
または、製品番号H59634-06
価格(JPY)
-
数量:
5 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS5399-87-1
IUPAC Name2-(6-chloro-9H-purin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
Molecular FormulaC10H11ClN4O4
InChI KeyXHRJGHCQQPETRH-UHFFFAOYNA-N
SMILESOCC1OC(C(O)C1O)N1C=NC2=C(Cl)N=CN=C12
さらに表示
Assay (HPLC)>97.5%
6-Chloropurine riboside is used to study the kinetics and substrate specificity of adenosine deaminase. 6-Chloropurine riboside is benzoylated to facilitate synthesis of nucleoside derivatives such as 9-(2,3-Di-deoxy-2-fluoro-β-D-threo-pentofuranosyl)adenine. It , especially after phosphorylation to NMP, NDP or NTP, is used as a purine substrate analogue in studies with enzymes such as Inosine monophosphate dehydrogenase (IMPDH); bacteriophage T4 RNA-ligase (EC 6.5.1.3) and pancreatic fibonuclease A.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
6-Chloropurine riboside is used to study the kinetics and substrate specificity of adenosine deaminase. 6-Chloropurine riboside is benzoylated to facilitate synthesis of nucleoside derivatives such as 9-(2,3-Di-deoxy-2-fluoro-β-D-threo-pentofuranosyl)adenine. It , especially after phosphorylation to NMP, NDP or NTP, is used as a purine substrate analogue in studies with enzymes such as Inosine monophosphate dehydrogenase (IMPDH); bacteriophage T4 RNA-ligase (EC 6.5.1.3) and pancreatic fibonuclease A.

Solubility
Soluble in water. (10.6 mg/mL)

Notes
Keep away from heat and humidity. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Juli Alonso.; M.Victòria Nogués.; Claudi M. Cuchillo. Modification of bovine pancreatic ribonuclease A with 6-chloropurine riboside. Arch. Biochem. Biophys. 1986, 246 (2),681-689.
  2. Michal Hocek .; Antonín Holý.; Ivan Votruba.; Hana Dvořáková. Synthesis and Cytostatic Activity of Substituted 6-Phenylpurine Bases and Nucleosides: Application of the Suzuki-Miyaura Cross-Coupling Reactions of 6-Chloropurine Derivatives with Phenylboronic Acids.J. Med. Chem. 2000, 43 (9),1817-1825.