mAChR

mAChR

The acetylcholine receptors known as mAChRs (muscarinic acetylcholine receptors) are found in the cell membranes of some neurons and other cells. The primary end-receptor stimulated by acetylcholine released from postganglionic fibers in the parasympathetic nervous system is one of their many functions. Because they are more sensitive to muscarine than to nicotine, mAChRs are so named. Nicotinic acetylcholine receptors (nAChRs), receptor ion channels that are also significant in the autonomic nervous system, are their counterparts. Numerous medications and other substances, such as scopolamine and pilocarpine, act as selective agonists or antagonists on these two different receptors. The brain and the autonomic ganglia are both rich sources of the neurotransmitter acetylcholine (ACh).

mAChR related products

Structure Cat No. Product Name CAS No. Product Description
V70511 N-Demethyl MK-6884 2102194-36-3 N-Demethyl MK-6884 (compound 34) is a potent allosteric modulator of M4 mAChR.
V60110 Norarecoline hydrochloride 6197-39-3 Guvacoline hydrochloride is a pyridine alkaloid that can function as a weak full agonist of ileal and atrial muscarinic receptors.
V0462 Norbenzetimide 19315-71-0 Nor-benzetimide is the major metabolite of benzetimide.
V5276 Norclozapine (ACP-104) 6104-71-8 Norclozapine (ACP-104; NDMC; ACP104; N-Desmethylclozapine) is a major active metabolite of the atypical antipsychotic drug clozapine.
V30659 Oxotremorine M iodide 3854-04-4 Oxotremorine M iodide is a novel, potent and selective muscarinic acetylcholine receptor (mAChR) agonist.
V70502 Oxotremorine sesquifumarate 17360-35-9 Oxotremorine sesquifumarate is a mAChR agonist with stronger activation of M2 and may be utilized in neurological research.
V70553 Parapenzolate bromide 5634-41-3 Parapenzolate bromide, an antispasmodic agent, is an orally bioactive mAChR antagonist.
V70509 PD 102807 23062-91-1 PD 102807 is an M4 muscarinic receptor antagonist (inhibitor) with IC50 of 90.7 nM.
V70550 PF-4348235 (β2AR/M-receptor agonist-2) 1017857-38-3 β2AR/M-receptor agonist-2 (compound 15) is a muscarinic antagonist and β2-adrenoceptor agonist (MABA).
V32729 Pilocarpine nitrate 148-72-1 Pilocarpine nitrate, the nitrate salt of pilocarpine, is a potent M3-type muscarinic acetylcholine receptor (M3 muscarinic receptor) agonist used on the eye to treat elevated intraocular pressure, various types of glaucoma, and to induce miosis.
V22201 Piperidolate 82-98-4 Piperidolate is a tertiary amine antimuscarinic.
V3358 Pirmenol (Cl-845) 68252-19-7 Pirmenol (Cl-845) is a potent antiarrhythmic agent that inhibits muscarinic acetylcholine receptor-operated K+ current in the guinea pig heart.
V29911 Pirmenol hydrochloride 61477-94-9 Pirmenol HCl (Cl-845)is a potent antiarrhythmic agent that inhibits muscarinic acetylcholine receptor-operated K+ current in the guinea pig heart.
V70522 Propantheline-d3 bromide (Propantheline-d3 bromide) 64717-35-7 Propantheline-d3 (bromide) is the deuterated form of Propantheline bromide.
V70537 PTACoxalate 201939-40-4 PTAC oxalate is a selective muscarinic receptor ligand.
V32273 Racanisodamine 17659-49-3 Racanisodamine is a racemate of anisodamine and has similar pharmacological effects.
V3863 Revefenacin 864750-70-9 Revefenacin (formerly known as TD-4208; GSK-1160724; trade name: Yupelri) is a long-acting, potent mAChR (muscarinic acetylcholine receptor) antagonist with a high affinity on M3 receptor with a Ki of 0.18 nM.
V14557 Scopolamine HCl 55-16-3 Scopolamine HCl (Hyoscine),the hydrochloride salt ofScopolamine, isa drug approved for the treatment of motion sickness and postoperative nausea and vomiting.
V3721 Solifenacin (YM905) 242478-37-1 Solifenacin (YM-905; Vesikur; Vesicare) is a novel and potent muscarinic receptor antagonist that has beenapproved for the treatment of overactive bladder.
V79282 Solifenacin-d7 hydrochloride Solifenacin-d7 ( HCl) is the deuterated form of Solifenacin HCl.
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