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nAChR

nAChR

Nicotinic acetylcholine receptors, or nAChRs, are proteins on neurons that signal when a chemical stimulus causes muscles to contract. On the presynaptic and postsynaptic sides of the neuromuscular junction, as well as in the plasma membranes of some neurons, they are cholinergic receptors that create ligand-gated ion channels. The most extensively researched ionotropic receptors are those for nicotinic acetylcholine. The neurotransmitter acetylcholine (ACh) binds to the nAChR, just like it does with the other type of acetylcholine receptor, the muscarinic acetylcholine receptor (mAChR). Nicotinic receptors can be opened by both acetylcholine and nicotine, hence the name "nicotinic," just as muscarinic receptors are so named because they are also activated by muscarine.

nAChR related products

Structure Cat No. Product Name CAS No. Product Description
nAChR agonist CMPI hydrochloride V70724 nAChR agonist CMPI hydrochloride 2250025-94-4 nAChR agonist CMPI HCl is a potent and specific PAM (positive allosteric modulator) of nAChR containing an α4:α4 subunit interface.
nAChR-IN-1 hydrochloride V70700 nAChR-IN-1 hydrochloride 849461-91-2 nAChR-IN-1 ( HCl), a tetramethylpiperidinyl enanthate, is a selective inhibitor of the nicotinic acetylcholine receptor (nAChR) lacking the α5, α6, or β3 subunits.
nAChRagonist 2 V70725 nAChRagonist 2 252870-46-5 nAChR agonist 2 (compound 8) is a selective α4β2 nAChR (nicotinic acetylcholine receptor) agonist (Kd=26 nM).
Nelonicline V4407 Nelonicline 1026134-63-3 Nelonicline (aslo known as ABT-126) is a novel, potent and selectiveneuronal nicotinicreceptor agonist.
Nelonicline citrate (ABT-126 citrate) V70745 Nelonicline citrate (ABT-126 citrate) 1026136-84-4 Nelonicline (ABT-126) citrate is a potent and specific α7 nicotinic receptor (α7 nAChR) agonist/activator with high affinity (Ki=12.3 nM) to α7 nAChRs in the human brain.
Nereistoxin (Nereistoxine) V70757 Nereistoxin (Nereistoxine) 1631-58-9 Nereistoxin (Nereistoxine) is a neurotoxin extracted from the marine annelid Lumbriconereis heteropoda that acts by blocking nicotinic acetylcholine receptors.
NS 1738 (NSC 213859) V5093 NS 1738 (NSC 213859) 501684-93-1 NS 1738 (also known as NSC 213859) is a novel and potent positive allosteric modulator of the α7 nAChR, with respect to positive modulation of nicotinic alpha7 receptor (α7 nAChR) with EC50of 3.4 μM in oocyte experiments.
NS3861 V26678 NS3861 216853-60-0 NS-3861 is a novel and potent α3β2 nAChRfull agonist and an α3β4 partial agonist (Ki = 0.62 nM).
NS3861 V70712 NS3861 216853-59-7 NS3861 is an agonist of nicotinic acetylcholine receptors (nAChRs) with high affinity for α3β4 nAChR.
PHA 568487 V70754 PHA 568487 527680-57-5 PHA 568487 is a selective agonist of the alpha-7 nicotinic acetylcholine receptor (α-7 nAchR).
PHA 568487 free base V70748 PHA 568487 free base 527680-56-4 PHA 568487 free base is a selective α-7 nicotinic acetylcholine receptor (α-7 nAchR) agonist.
PHA-543613 dihydrochloride V70722 PHA-543613 dihydrochloride 478148-58-2 PHA-543613 di-HCl is a potent, orally bioactive, BBB (blood-brain barrier) crossing, and selective α7 nAChR agonist/activator with Ki of 8.8 nM.
PHA-543613 hydrochloride V84558 PHA-543613 hydrochloride 1586767-92-1
PNU-282987 S enantiomer free base V29474 PNU-282987 S enantiomer free base 737727-12-7 PNU-282987 S enantiomer free base is the S-enantiomer of PNU-282987.
PNU282987 freebase V2411 PNU282987 freebase 711085-63-1 PNU282987 isa novel selective agonist of the alpha7 nAChR, 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 when applied to hippocampal slices.
Proadrenomedullin (N-20) (bovine, porcine) (ProADM N20(bovine, porcine); PAMP-20(bovine, porcine)) V81202 Proadrenomedullin (N-20) (bovine, porcine) (ProADM N20(bovine, porcine); PAMP-20(bovine, porcine)) Proadrenomedullin (N-20) (ProADM N20) (bovine, porcine) is a potent, noncompetitive antihypertensive and catecholamine release inhibitory peptide released from chromaffin cells.
PSEM 89S TFA V70727 PSEM 89S TFA 1336913-03-1 PSEM 89S TFA is a selective, BBB (blood-brain barrier) permeable (penetrable) agonist of ion channels produced.
Pyrantel tartrate V30868 Pyrantel tartrate 33401-94-4 Pyrantel tartrate, thetartrate salt of pyrantel, is a potent antinematodal and anthelmintic agentwith a broad spectrum of activities.
R-(+)-Cotinine (R-(+)-Cotinine; (+)-Cotinine; (R)-Cotinine; (R)-NIH-10498) V70771 R-(+)-Cotinine (R-(+)-Cotinine; (+)-Cotinine; (R)-Cotinine; (R)-NIH-10498) 32162-64-4 R-(+)-Cotinine ((+)-Cotinine) is a nicotine metabolite that lacks significant activity across a broad range of pharmacological targets.
Rabies Virus Matrix Protein Fragment(RV-MAT) V70770 Rabies Virus Matrix Protein Fragment(RV-MAT) 1023648-37-4 Rabies Virus Matrix Protein Fragment (RV-MAT) is a bioactive peptide.
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