N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide

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Company Name: Tianjin Kailiqi Biotechnology Co., Ltd.  Gold
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N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide manufacturers

  • PNU-282987
  • PNU-282987 pictures
  • $40.00
  • 2026-07-15
  • CAS:123464-89-1
  • Purity: 99.97%
  • Supply Ability: 10g
N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide Basic information
Product Name:N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide
Synonyms:PNU 282987;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;PNU282987 HCl;PNU 282987(PNU 282987 hydrochloride);CS-1012;PNU 282987 - CAS 123464-89-1 - Calbiochem;SKL843
CAS:123464-89-1
MF:C14H17ClN2O
MW:264.75058
EINECS:
Product Categories:Inhibitors;Acetylcholine receptor
Mol File:123464-89-1.mol
N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide Structure
N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide Chemical Properties
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.
InChIInChI=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
InChIKeyWECKJONDRAUFDD-VHLFKADZNA-N
SMILESC(=O)(C1=CC=C(C=C1)Cl)N[C@@H]1[C@]2([H])CCN(CC2)C1 |&1:10,11,r|
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide Usage And Synthesis
DescriptionPNU 282987 (CAS 123464-89-1) is a selective α7 nicotinic acetylcholine receptor (nAChR) agonist (Ki= 26 nM).1 Thea7 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
UsesPNU 282987 is used as an activator of α-7 nicotinic acetylcholine receptor.
General DescriptionA 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 ActivityHighly 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 ActionsPrimary Targetα7 nAChRs
References[1] ALICE L. BODNAR. Discovery and Structure−Activity Relationship of Quinuclidine Benzamides as Agonists of α7 Nicotinic Acetylcholine Receptors[J]. Journal of Medicinal Chemistry, 2005, 48 4: 905-908. DOI:10.1021/jm049363q
[2] VANESSA STUCKENHOLZ. The α7 nAChR agonist PNU-282987 reduces inflammation and MPTP-induced nigral dopaminergic cell loss in mice.[J]. Journal of Parkinson’s disease, 2013: 161-172. DOI:10.3233/jpd-120157
[3] PALOMA VICENS. Motor and anxiety effects of PNU-282987, an alpha7 nicotinic receptor agonist, and stress in an animal model of Alzheimer’s disease.[J]. Current Alzheimer research, 2013, 10 5: 516-523. DOI:10.2174/15672050113109990130
[4] ELISA NAVARRO . Alpha7 nicotinic receptor activation protects against oxidative stress via heme-oxygenase I induction[J]. Biochemical pharmacology, 2015, 97 4: Pages 473-481. DOI:10.1016/j.bcp.2015.07.022
[5] SAMANTHA L. MCLEAN . Nicotinic α7 and α4β2 agonists enhance the formation and retrieval of recognition memory: Potential mechanisms for cognitive performance enhancement in neurological and psychiatric disorders[J]. Behavioural Brain Research, 2016, 302: Pages 73-80. DOI:10.1016/j.bbr.2015.08.037
N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide Preparation Products And Raw materials
Tag:N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide(123464-89-1) Related Product Information
Thip hydrochloride (E)-3-[[[3-[2-(7-Chloro-2-quinolinyl)ethenyl]phenyl]-[[(3-dimethylamino)-3-oxopropyl]thio]methyl]thio]-propanoic acid, sodium salt Tamoxifen citrate REVERSINE PNU-282987 S enantiomer hydrochloride Benzamide, N-(3R)-1-azabicyclo[2.2.2]oct-3-yl-4-chloro- PNU-282987 (S enantiomer free base) N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chloro-benzamide monohydrochloride hydrate N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide 2-amino-N-1-azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide 3-amino-N-1-azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide 2-amino-N-1-azabicyclo[2.2.2]oct-3-yl-5-chlorobenzamide N1-(1-azabicyclo[2.2.2]oct-3-yl)-3-chlorobenzamide 5-amino-N-1-azabicyclo[2.2.2]oct-3-yl-2-chlorobenzamide 4-amino-N-1-azabicyclo[2.2.2]oct-3-yl-2-chlorobenzamide