P6499
PNU-282987 hydrate
solid, ≥98% (HPLC)
Synonym(s):
N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chloro-benzamide monohydrochloride hydrate
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About This Item
Empirical Formula (Hill Notation):
C14H17ClN2O · HCl · xH2O
Molecular Weight:
301.21 (anhydrous basis)
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
SMILES string
Cl[H].[H]O[H].Clc1ccc(cc1)C(=O)N[C@H]2CN3CCC2CC3
InChI
1S/C14H17ClN2O.ClH.H2O/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);1H;1H2/t13-;;/m0../s1
InChI key
OCWLMMBVXIESNP-GXKRWWSZSA-N
assay
≥98% (HPLC)
form
solid
storage condition
desiccated
solubility
DMSO: >10 mg/mL
storage temp.
2-8°C
Quality Level
Related Categories
Application
PNU-282987 hydrate has been used to check its activity in wound repair by inhibiting AGE (advanced glycation end products)-mediated tumor necrosis factor-α (TNF-α) production in a streptozotocin (STZ)-induced diabetic mouse model. It has also been used to evaluate the effects of nicotinic α-7 acetylcholine receptor (nAChRα7) activation on non-diabetic wound healing.
Biochem/physiol Actions
Decreased expression of a homomeric alpha7 nicotinic acetylcholine receptor (nAChR) is connected with inability to process sensory information in schizophrenia. PNU-282987 is a novel selective agonist of the alpha7 nAChR that evoked whole-cell currents from cultured rat hippocampal neurons that were sensitive to the selective alpha7 nAChR antagonist methyllycaconitine (MLA) and enhanced GABAergic synaptic activity. The alpha7 nAChR agonist PNU-282987 improves auditory gating and enhances hippocampal oscillatory activity. These results provide further support for the concept that drugs that selectively activate alpha7 nAChRs may offer a novel, potential pharmacotherapy in treatment of schizophrenia.
PNU-282987 is an agonist of nicotinic α-7 acetylcholine receptor (nAChRα7). It helps to decrease acute lung injury (ALI), stimulated by lipopolysaccharide (LPS). PNU-282987 can increase GABAergic synaptic activity in brain slices and helps to bring back auditory gating deficits in anesthetized rats.
Selective α7 nicotinic receptor agonist. Ki = 27 nM; displays negligible blockade of α1β1γδ and α3β4 nAChRs (IC50 = 60 mM); enhances GABAergic synaptic activity in the hippocampus in vitro and enhances amphetamine-induced hippocampal theta wave activity.
Features and Benefits
This compound is featured on the Acetylcholine Receptors (Nicotinic) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
Disclaimer
Air sensitive
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Activation of alpha7nAChR promotes diabetic wound healing by suppressing AGE-induced TNF-alpha production
Dong M W, et al.
Inflammation, 39(2), 687-699 (2016)
alpha7-nAChR Activation Has an Opposite Effect on Healing of Covered and Uncovered Wounds
Li J Y, et al.
Inflammation, 41(2), 474-484 (2018)
Acute lung injury is reduced by the alpha7nAChR agonist PNU-282987 through changes in the macrophage profile
Pinheiro N M, et al.
Faseb Journal, 31(1), 320-332 (2016)
Zhenzhen Shao et al.
Molecular medicine reports, 19(5), 3791-3798 (2019-03-14)
The cholinergic anti‑inflammatory pathway is considered an attractive approach for the alleviation of inflammatory diseases. Sepsis is characterized by systemic inflammation and widespread organ injury, especially that in the lung. In the present study, we explored the effects of an
The selective alpha7 nicotinic acetylcholine receptor agonist PNU-282987 [N-[(3R)-1-azabicyclo [2.2. 2] oct-3-yl]-4-chlorobenzamide hydrochloride] enhances GABAergic synaptic activity in brain slices and restores auditory gating deficits in anesthetized rats
Hajos M, et al.
Journal of Pharmacology and Experimental Therapeutics, 312(3), 1213-1222 (2005)
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