| Cat.No. | Name | Information |
|---|---|---|
| M2489 | Carbachol chloride | Carbachol is a cholinomimetic compound that binds and activates the acetylcholine receptor. |
| 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. |
| M2368 | Aclidinium Bromide | Aclidinium Bromide is a novel long-acting muscarinic antagonist that binds to the human muscarinic receptors AChR M1, M2, M3, M4, and M5 with Ki values of 0.1 nM, 0.14 nM, 0.14 nM, 0.21 nM, and 0.16 nM, respectively. It can be used in chronic obstructive pulmonary disease (COPD) studies. |
| M2366 | Aceclidine hydrochloride | Aceclidine is a parasympathomimetic miotic agent used to decreases intraocular pressure. |
| M2268 | Rocuronium bromide | Rocuronium bromide is an aminosteroid non-depolarizing neuromuscular blocker or muscle relaxant used in modern anaesthesia. |
| M2257 | Levetiracetam | Levetiracetam (UCB L059) is an antiepileptic, it is also a selective M2 muscarinic acetylcholine receptors (mAChR) inhibitor. |
| M2244 | Biperiden hydrochloride | Biperiden hydrochloride is a muscarinic receptor antagonist that displays some selectivity for the M1 subtype. |
| M2243 | Aniracetam | Aniracetam is a compound that promotes intellectual development and neuroprotection. |
| M2170 | SVT-40776 | SVT-40776 is a novel M3 muscarinic receptor antagonist. |
| M2037 | Fesoterodine fumarate | Fesoterodine fumarate (Toviaz) is a novel muscarinic receptor antagonist. |
| M1866 | VU 0255035 | VU 0255035 is a highly selective M1 muscarinic acetylcholine receptor (mAChR) antagonist (Ki = 14.87 nM). |
| M1364 | 1-Benzyl-1H-indole-2,3-dione | 1-Benzyl-1H-indole-2,3-dione |
| M54823 | THRX-160209 | THRX-160209 is a potent antagonist at the M(2) muscarinic acetylcholine (ACh) receptor subtype that was designed using a multivalent strategy, simultaneously targeting the orthosteric site and a nearby site known to bind allosteric ligands. |
| M54437 | Catestatin | Catestatin is a 21-amino acid residue, cationic and hydrophobic peptide. |
| M54385 | α-Conotoxin MII | α-Conotoxin MII (α-CTxMII), a 16-amino acid peptide from the venom of the marine snail Conus magus, potently blocks nicotinic acetylcholine receptors (nAChRs) composed of α3β2 subunits, with an IC50 of 0.5 nM. |
| M54173 | COG 133 TFA | COG 133 TFA is a fragment of Apolipoprotein E (APOE) peptide. |
| M53102 | G-Protein antagonist peptide | G-Protein antagonist peptide is the substance P-related peptide that inhibits binding of G proteins to their receptors. |
| M53101 | α-Conotoxin M I | α-Conotoxin M I is a potent and selective inhibitor of mAChR and α1β1γδ nAChR, but has no effect on nicotine-stimulated dopamine release. |
| M52776 | α-Conotoxin AuIB | α-Conotoxin AuIB, a potent and selective α3β4 nicotinic acetylcholine receptor (nAChR) antagonist, blocks α3β4 nAChRs expressed in Xenopus oocytes with an IC50 of 0.75 μM. |
| M52775 | α-Conotoxin PnIA | α-Conotoxin PnIA, a potent and selective antagonist of the mammalian α7 nAChR, has the potential for the research of neurological conditions such as neuropathic pain and Alzheimer’s disease. |
| M52774 | κ-Bungarotoxin | κ-Bungarotoxin (κ-Bgt) is a potent, selective, and slowly reversible antagonist of α3β2 neuronal nicotinic acetylcholine receptors with an IC50 of 2.30 nM. |
| M52773 | Rabies Virus Matrix Protein Fragment(RV-MAT) | Rabies Virus Matrix Protein Fragment (RV-MAT) is a polypeptide. |
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