Date published: 2025-9-10

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mAChR M4 Inhibitors

The class of mAChR M4 inhibitors encompasses a diverse array of chemical compounds that exert their inhibitory effects on the receptor through various mechanisms. Tropicamide, an example within this class, directly interferes with mAChR M4 by binding to its acetylcholine binding site, preventing the receptor's normal activation. This direct inhibition disrupts downstream signaling pathways associated with mAChR M4, modulating cellular responses. Additionally, methoctramine acts as a selective mAChR M4 antagonist, achieving inhibition through binding to the receptor's allosteric site, inducing conformational changes that hinder its interaction with acetylcholine. Scopolamine, another member of this class, competitively binds to the orthosteric site of mAChR M4, impeding the receptor's interaction with acetylcholine and disrupting downstream signaling pathways. These inhibitors, including pirenzepine, darifenacin, and himbacine, further contribute to the specificity of mAChR M4 modulation by targeting the receptor directly and interfering with its normal functioning. Notably, telenzepine achieves inhibition through binding to the receptor, showcasing the versatility within this chemical class.AF-DX 384, a potent and selective mAChR M4 antagonist, distinguishes itself by targeting the receptor's allosteric site, inducing conformational changes that impede acetylcholine binding. Ipratropium bromide competitively binds to the orthosteric site, disrupting the normal activation of mAChR M4 and modulating downstream signaling pathways. AQRA 741, with its selectivity for mAChR M4, binds to the receptor and interferes with acetylcholine binding, providing a targeted means of influencing receptor function. Pilocarpine introduces an indirect mechanism within this class, stimulating muscarinic receptors M1 and M3, leading to increased acetylcholine release. This, in turn, activates negative feedback mechanisms inhibiting acetylcholine release at the M4 receptor. The indirect inhibition of mAChR M4 by pilocarpine showcases the diversity of approaches within this class.

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