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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T9787 | Suvn-911 | AChR | |
suvn-911 is a potent and selective antagonist of neuronal nicotinic acetylcholine α4β2 receptor (Ki = 1.5 nM) with antidepressant activity. | |||
T9076 | Spinosad | Others | |
Spinosad is a naturally-occurring insecticide found in the the soil bacterium S. spinosa. It is a mixture of the macrocyclic lactones spinosyn A and spinosyn D, which act as agonists of insect nicotinic acetylcholinester... | |||
T60080 | TMPH | 2,2,6,6-Tetramethylpiperidin-4-yl heptanoate | AChR |
TMPH is an inhibitor of nAChR and inhibits nAChRs lacking α5, α6, or β3 subunits. TMPH can be used in studies about nAChR dysfunction or neurological disorders. | |||
T2285 | Encenicline hydrochloride | EVP-6124 (hydrochloride),EVP-6124 hydrochloride | AChR |
Encenicline hydrochloride (EVP-6124 hydrochloride) is a new-type partial agonist of α7 neuronal nicotinic acetylcholine receptors (nAChRs). | |||
T7884 | NS 1738 | NSC 213859 | AChR |
NS 1738 (NSC-213859) is a positive allosteric modulator of the α7-containing neuronal nicotinic acetylcholine receptors (nAChRs) | |||
TP2063 | α-Conotoxin MII | AChR | |
α-Conotoxin MII is a highly potent and selective competitive antagonist for α3β2 subunit-containing nicotinic receptors (IC50 = 0.5 - 3.5 nM at α3β2 expressed in Xenopus oocytes). Also potently blocks β3-containing neuro... | |||
T22735 | DMAB-anabaseine dihydrochloride | N,N-dimethyl-4-[(E)-(6-pyridin-3-yl-3,4-dihydro-2H-pyridin-5-ylidene)methyl]aniline;dihydrochloride | AChR |
DMAB-anabaseine dihydrochloride (N,N-dimethyl-4-[(E)-(6-pyridin-3-yl-3,4-dihydro-2H-pyridin-5-ylidene)methyl]aniline;dihydrochloride) is an α7-containing neuronal nicotinic receptor partial agonist and an antagonist at α... | |||
TP2063L | α-Conotoxin MII acetate | α-Conotoxin MII acetate (175735-93-0 Free base) | AChR |
α-Conotoxin MII acetate is a 16-amino acid peptide from the venom of the marine snail Conus magus. α-Conotoxin MII acetate potently blocks nicotinic acetylcholine receptors composed of α3β2 subunits, with an IC50 of 0.5 ... | |||
T0086 | Galanthamine hydrobromide | Galantamine hydrobromide,Galanthamine HBr | AChR , AChE |
Galanthamine hydrobromide (Galantamine hydrobromide), a long-acting and centrally active AChE inhibitor (IC50:410 nM), is an allosteric potentiator at neuronal nicotinic ACh receptors. | |||
T30248 | AZD 3043 | TD 4756,THRX 918661,AZD-3043,AZD3043 | GABA Receptor |
AZD 3043 (THRX 918661) is a variant modulator of the γ-aminobutyric acid type A receptor, a novel sedative-hypnotic and a potential short-acting anesthetic that produces hypnosis and EEG suppression in rats.AZD 3043 pote... | |||
T16281 | Nelonicline | ABT-126 | Adenosine Receptor |
Nelonicline is a selective agonist of neuronal nicotinic receptors. | |||
T23462 | TMPH hydrochloride | Others | |
neuronal nicotinic ACh receptors (nAChRs) antagonist | |||
T29916 | Altinicline | ||
Altinicline can bine with neuronal nicotinic acetylcholine receptors; SIB-1765F - fumarate. | |||
T12738L | Rivanicline | RJR-2403,(E)-Metanicotine | Others |
Rivanicline is a neuronal nicotinic receptor agonist, showing high selectivity for the α4β2 subtype (Ki=26 nM). It show > 1,000 fold selectivity than α7 receptors(Ki= 36000 nM and IC50 : 26 nM). | |||
T11041 | Dihydro-β-erythroidine hydrobromide | DHβE hydrobromide | Others |
Dihydro-β-erythroidine hydrobromide(DHβE) is a potent, oral active and competitive antagonist of neuronal nicotinic acetylcholine receptors (nAChRs). Dihydro-β-carotene hydrobromide showed selectivity to α4β4 and α4β2nAC... | |||
T22401 | PNU-282987 S enantiomer hydrochloride | (S)-PNU-282987 HCl | Others |
(S)-PNU-282987 is the absolute stereochemistry form of PNU-282987. PNU 282987, a potent agonist of α7-containing neuronal nicotinic acetylcholine receptors (nAChRs) with Ki of 26 nM for the rat receptor, has negligible a... | |||
T23235 | RJR-2403 hemioxalate | Others | |
RJR-2403 hemioxalate is a neuronal nicotinic receptor agonist, showing high selectivity for the α4β2 subtype (Ki=26 nM). RJR-2403 hemioxalate > 1,000 fold selectivity than α7 receptors(Ki= 36000 nM). | |||
T75927 | α-Conotoxin MII TFA | ||
α-Conotoxin MII TFA (α-CTxMII TFA), a peptide consisting of 16 amino acids derived from the venom of Conus magus, selectively inhibits nicotinic acetylcholine receptors (nAChRs) that are composed of α3β2 subunits, demons... | |||
T80466 | κ-Bungarotoxin | κ-Bgt | |
κ-Bungarotoxin (κ-Bgt) is a selective and potent antagonist of α3β2 neuronal nicotinic acetylcholine receptors, exhibiting slow reversibility and an IC50 of 2.30 nM [1]. | |||
T80481 | α-Conotoxin Bt1.8 | ||
α-Conotoxin Bt1.8 is a potent inhibitor of both rat α6/α3β2β3 and α3β2 neuronal nicotinic acetylcholine receptors (nAChRs), exhibiting half-maximal inhibitory concentrations (IC50s) of 2.1 nM for α6/α3β2β3 and 9.4 nM for... |