| Identification | Back Directory | [Name]
N-(3R)-1-AZABICYCLO[2.2.2]OCT-3-YL-4-CHLOROBENZAMIDE | [CAS]
123464-89-1 | [Synonyms]
CS-1012
PNU 282987
PNU282987 HCl
PNU 282987(PNU 282987 hydrochloride)
PNU 282987 - CAS 123464-89-1 - Calbiochem
N-(3R)-1-AZABICYCLO[2.2.2]OCT-3-YL-4-CHLOROBENZAMIDE
N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide hydrochloride
N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide hydrochloride PNU 282987 | [Molecular Formula]
C14H17ClN2O | [MDL Number]
MFCD08703110 | [MOL File]
123464-89-1.mol | [Molecular Weight]
264.751 |
| Chemical Properties | Back Directory | [Melting point ]
240-242℃ | [storage temp. ]
Inert atmosphere,2-8°C | [solubility ]
Soluble in DMSO (up to 25 mg/ml) | [form ]
Off-white solid | [color ]
White | [Water Solubility ]
water: 100mM | [Stability:]
Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months. | [InChI]
InChI=1/C14H17ClN2O/c15-12-3-1-11(2-4-12)14(18)16-13-9-17-7-5-10(13)6-8-17/h1-4,10,13H,5-9H2,(H,16,18)/t13-/s3 | [InChIKey]
WECKJONDRAUFDD-VHLFKADZNA-N | [SMILES]
C(=O)(C1=CC=C(C=C1)Cl)N[C@@H]1[C@]2([H])CCN(CC2)C1 |&1:10,11,r| |
| Hazard Information | Back Directory | [Description]
PNU 282987 (CAS 123464-89-1) is a selective α7 nicotinic acetylcholine receptor (nAChR) agonist (Ki?= 26 nM).1? The?a7 nAChR is a potential therapeutic target of cognitive deficits in diseases such as Alzheimer’s, Parkinson’s, schizophrenia, and attention deficit disorders – agonism of this receptor with PNU 282987 has shown potential to ameliorate these deficits.2-5 | [Uses]
PNU 282987 is used as an activator of α-7 nicotinic acetylcholine receptor. | [General Description]
A potent agonist highly selective for α7 nAChRs (Ki = 26 nM). Used in investigating the roles of α7 nAChRs in sensory gating, learning and memory, cognitive functions, and treatment of Schizophrenia. | [Biological Activity]
Highly selective α 7 nAChR agonist (K i = 26 nM) displaying negligible blockade of α 1 β 1 γ δ and α 3 β 4 nAChRs (IC 50 ≥ 60 μ M). Found to be inactive against a panel of 32 receptors at 1 μ M, except 5-HT 3 receptors (K i = 930 nM). | [Biochem/physiol Actions]
Primary Targetα7 nAChRs | [References]
1) Bodnar?et al.?(2005),?Discovery and structure-activity relationship of quinuclidine benzamides as agonists of α7 nicotinic acetylcholine receptors; J. Med. Chem.?48?905
2) Stuckenholz?et al.?(2013),?The α7 nAChR agonist PNU-282987 reduces inflammation and MPTP-induced nigral dopaminergic cell loss in mice; J. Parkinsons Dis.?3?161
3) Vicens?et al. (2013),?Motor and anxiety effects of PNU-282987, an alpha7 nicotinic receptor agonist, and stress in an animal model of Alzheimer’s disease; Curr. Alzheimer Res.?10?516
4) Navarro?et al.?(2015),?Alpha7 nicotinic receptor activation protects against oxidative stress via heme-oxygenase I induction; Biochem. Pharmacol.?97?473
5) McLean?et al.?(2016),?Nicotinic α7 and α4β2 agonists enhance the formation and retrieval of recognition memory: Potential mechanisms for cognitive performance enhancement in neurological and psychiatric disorders; Behav. Brain Res.?302?73 |
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