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Biological Data Biological description Analog of adenosine . Adenosine receptor agonist (Ki values are 300, 80 and 1900 nM at A1 , A2A and A3 receptors resepectively. Shows anticonvulsant activity. Active in vivo .
Also inhibits the induction of long-term potentiation (LTP).
Solubility & Handling Storage instructions +4°C
Solubility overview Soluble in water (25mM) and in DMSO (100mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
Chemical Data Chemical name 6-Amino-2-chloropurine riboside
Chemical structure
Molecular Formula C10 H12 ClN5 O4
SMILES C1=NC2=C(N1[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)N=C(N=C2N)Cl
InChi InChI=1S/C10H12ClN5O4/c11-10-14-7(12)4-8(15-10)16(2-13-4)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H2,12,14,15)/t3-,5-,6-,9-/m1/s1
InChiKey BIXYYZIIJIXVFW-UUOKFMHZSA-N
References for 2-Chloroadenosine (CADO) References are publications that support the biological activity of the product
Effects of 2-chloroadenosine on cortical epileptic afterdischarges in immature rats. Pometlova et al (2010) Pharmacol Rep 62(1) : 62-7 The protective effect of 2-chloroadenosine against the development of amygdala kindling and on amygdala-kindled seizures. Abdul-Ghani et al (1997) Eur J Pharmacol. 326(1) : 7-14 Pharmacokinetic-haemodynamic relationships of 2-chloroadenosine at adenosine A1 and A2a receptors in vivo. Mathoot et al (1996) Br J Pharmacol 118(2) : 369-77 2-Chloroadenosine decreases long-term potentiation in the hippocampal CA1 area of the rat. de Mendonca et al (1990) Neurosci Lett 118(1) : 107-11
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Adenosine receptor agonist