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mAChR

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mAChR

Chemical Structure Cat. No. Product Name CAS No.
Difenidol hydrochloride Chemical Structure
BCP13983 Difenidol hydrochloride 3254-89-5
Diphenidol hydrochloride is a muscarinic antagonist employed as an antiemetic and as an antivertigo agent.
Benzetimide Hydrochloride Chemical Structure
BCP28424 Benzetimide Hydrochloride 5633-14-7 
Benzetimide hydrochloride is a muscarinic acetylcholine receptor antagonist.
Fesoterodine fumarate Chemical Structure
BCP27699 Fesoterodine fumarate 286930-03-8
Fesoterodine Fumarate is an antimuscarinic agent and is rapidly de-esterified to its active metabolite 5-hydroxymethyl tolterodine that is a muscarinic receptor antagonist.
Piperidolate hydrochloride Chemical Structure
BCP29729 Piperidolate hydrochloride 129-77-1
Piperidolate hydrochloride is an antimuscarinic, inhibits intestinal cramp induced by acetylcholine (rats and dogs).
TD-4208 Chemical Structure
BCP15793 TD-4208 864750-70-9
Revefenacin (TD-4208; GSK1160724) is a potent mAChR antagonist; has a high affinity on M3 receptor with a Ki of 0.18 nM
Scopolamine hydrobromide Chemical Structure
BCP29441 Scopolamine hydrobromide 114-49-8
Scopolamine hydrobromide is a high affinity (nM) muscarinic antagonist. 5-HT3 receptor-responses are reversibly inhibited by Scopolamine with an IC50 of 2.09 μM.
Batefenterol succinate Chemical Structure
BCP19637 Batefenterol succinate 945905-37-3
Batefenterol, also known as GSK961081 and TD-5959, is a Muscarinic Antagonist and β2-Agonist possessing both muscarinic antagonist (MA) and β2-adrenoceptor agonist (BA) properties (MABA).
Tolterodine Chemical Structure
BCP24952 Tolterodine 124937-51-5
Tolterodine is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo.
Batefenterol Chemical Structure
BCP19636 Batefenterol 743461-65-6
Batefenterol (GSK961081;TD-5959) is a novel muscarinic receptor antagonist and β2-adrenoceptor agonist; displays high affinity for hM2, hM3 muscarinic and hβ2-adrenoceptor with Ki values of 1.4, 1.3 and 3.7 nM, respectively.
AVex-73 Chemical Structure
BCP23552 AVex-73 195615-83-9
AVex-73 acts as a muscarinic receptor and a moderate sigma1 receptor agonist.
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