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2-Chloroadenosine Chemical Structure 2-Chloroadenosine

Catalog NO.: NS-009 | CAS NO.: 146-77-0 | Brand: BIOCAXIS

Category

Nucleosides & Nucleotides, nucleobase

Synonyms:

AT-265-B; AT-265B; 6-Amino-2-chloropurine riboside; (2R,3R,4S,5R)-2-(6-amino-2-chloro-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol; 2-Chloro-9-(beta-D-ribofuranosyl)adenine; 2-Chlor-9-(β-D-ribofuranosyl)-9H-purin-6-amine; 2'-Chloroadenosine

2-CADO, 6-Amino-2-chloropurine riboside

Molecular Formula

C10H12ClN5O4

Molecular Weight

301.69

General description

2-Chloroadenosine is a nucleoside antibiotic produced by Streptomyces rishiensis. It has anti-gram-positive and negative bacteria activity.

2-Chloroadenosine, a stable adenosine analogue, protects against long term development of ischaemic cell loss in the rat hippocampus. 2-Chloroadenosine is an apparent competitive inhibitor of uridine influx (apparent Ki=33 μM) and high-affinity nitrobenzylthioinosine binding (apparent Ki=0.18 mM). 2-Chloroadenosine is a transported permeant for the nucleoside transporter in human erythrocytes.

2-Chloroadenosine has been used:

as an agonist of adenosine receptors (A1R) in dorsal hippocampus (DH) and ventral hippocampus (VH) of mice

as a component of artificial cerebrospinal fluid (aCSF) for electrophysiological experiments using hippocampal slices

as an internal standard in solid phase extraction coupled with liquid chromatography-tandem mass spectrometry (XLC-MS/MS) for the quantification of certain metabolites from axonal lysates and dorsal root ganglia (DRG) neurons

 

Biochem/physiol Actions

2-Chloroadenosine is an analog of adenosine.[4] It is an adenosine A1 receptor agonist.[5] It might possess anti-oxidant property.[6]

 

 

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