| Cat.No. | Name | Information |
|---|---|---|
| M3470 | Oxybutynin | Oxybutynin is an anticholinergic medication used to relieve urinary and bladder difficulties. |
| M3190 | PNU-282987 | PNU-282987 is a highly selective α7 nAChR agonist with Ki of 27 nM. |
| M56529 | (±)-Epibatidine | (±)-Epibatidine is a nicotinic agonist. |
| M56528 | SSR180711 hydrochloride | SSR180711 hydrochloride is an orally active, selective and reversible α7 acetylcholine nicotinic receptor (n-AChRs) partial agonist. |
| M56527 | PHA-543613 hydrochloride | PHA-543613 hydrochloride is an oral or active α7 nAChR agonist with brain permeability, For α3β4, α1β1γδ, α4β2 and 5-HT3 receptors selective. |
| M56526 | RJR-2429 dihydrochloride | RJR 2429 hydrochloride is a α4β2 and α7 nAChR agonist. |
| M56525 | PHA-543613 dihydrochloride | PHA-543613 dihydrochloride is a potent, orally active, brain-penetrant and selective α7 nAChR agonist with a Ki value of 8.8 nM. |
| M56524 | Tebanicline dihydrochloride | Tebanicline dihydrochloride (Ebanicline dihydrochloride) is a nAChR modulator with potent, orally effective analgesic activity. |
| M56523 | (±)-Anatoxin A fumarate | (±)-Anatoxin A fumarate is a potent nicotinic receptor agonist and exhibits Ki values of 1.25 nM and 1.84 μM for binding to putative α4β2-type nAChR and α7-type nAChR in rat brain membranes, respectively. |
| M56522 | 5-Iodo-A-85380 dihydrochloride | 5-Iodo-A-85380 dihydrochloride is a selective ligand of nAChR. |
| M56255 | AC-42 | AC-42 is a poent M1 muscarinic selective allosteric agonist with EC50s of 805 nM and 220 nM for human wild-type and Y381A mutated M1 receptors, respectively. |
| M56254 | ASP8302 | ASP8302 is a positive allosteric modulator of muscarinic M3 Receptor. |
| M56253 | VU6019650 | VU6019650 is a potent and selective orthosteric antagonist of M5 mAChR (IC50=36 nM), can be used for opioid use disorder (OUD) relief. |
| M56252 | LY 2033298 | LY 2033298 is a selective positive allosteric modulator of the muscarinic M4 receptor. |
| M56251 | mAChR-IN-1 | mAChR-IN-1 is a potent muscarinic cholinergic receptor (mAChR) antagonist, with an IC50 of 17 nM. |
| M56250 | Zamifenacin | Zamifenacin (UK-76654) is a potent gut-selective muscarinic M3 receptor antagonist. |
| M56249 | Tolterodine | Tolterodine(PNU-200583) is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo. |
| M56248 | N-Demethyl MK-6884 | N-Demethyl MK-6884 is a potent M4 mAChR allosteric modulator. |
| M56247 | AC-42 hydrochloride | AC-42 hydrochloride is the hydrochloride salt form of AC-42. |
| M56246 | Rapacuronium bromide | Rapacuronium bromide (Org 9487), a non-depolarizing neuromuscular blocker, is an allosteric modulator of muscarinic acetylcholine receptor (mAChR). |
| M56245 | Zamifenacin fumarate | Zamifenacin fumarate (UK-76654 fumarate) is a potent gut-selective muscarinic M3 receptor antagonist. |
| M56244 | mAChR-IN-1 hydrochloride | mAChR-IN-1 hydrochloride is a potent muscarinic cholinergic receptor (mAChR) antagonist, with an IC50 of 17 nM. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
