1. Signaling Pathways
  2. GPCR/G Protein
    Neuronal Signaling
  3. mAChR

mAChR (毒蕈碱型乙酰胆碱受体)

Muscarinic acetylcholine receptor

mAChR(毒蕈碱乙酰胆碱受体)是乙酰胆碱受体,在某些神经元和其他细胞的细胞膜中形成 G 蛋白受体复合物。它们发挥多种作用,包括充当副交感神经系统中由节后纤维释放的乙酰胆碱刺激的主要终末受体。mAChR 之所以如此命名,是因为它们对毒蕈碱比对尼古丁更敏感。它们的对应物是烟碱乙酰胆碱受体 (nAChR),受体离子通道在自主神经系统中也很重要。许多药物和其他物质(例如毛果芸香碱和东莨菪碱)通过充当选择性激动剂或拮抗剂来操纵这两个不同的受体。乙酰胆碱 (ACh) 是一种广泛存在于大脑和自主神经节中的神经递质。

mAChRs (muscarinic acetylcholine receptors) are acetylcholine receptors that form G protein-receptor complexes in the cell membranes of certainneurons and other cells. They play several roles, including acting as the main end-receptor stimulated by acetylcholine released from postganglionic fibersin the parasympathetic nervous system. mAChRs are named as such because they are more sensitive to muscarine than to nicotine. Their counterparts are nicotinic acetylcholine receptors (nAChRs), receptor ion channels that are also important in the autonomic nervous system. Many drugs and other substances (for example pilocarpineand scopolamine) manipulate these two distinct receptors by acting as selective agonists or antagonists. Acetylcholine (ACh) is a neurotransmitter found extensively in the brain and the autonomic ganglia.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-U00406
    BTM-1086 Modulator
    BTM-1086是一种有效的抗溃疡和胃分泌抑制剂。
    BTM-1086
  • HY-U00104
    YM-46303 Antagonist
    YM-46303是一种毒蕈碱受体拮抗剂,对 M1M3 受体表现出最高的亲和力,对M3受体的选择性较M2受体高。
    YM-46303
  • HY-U00415
    Benzamide Derivative 1 Antagonist
    Benzamide Derivative 1 是来自专利 EP0213775A1,化合物 18,的苯甲酰胺衍生物。Benzamide Derivative 1 有潜力用于胃肠疾病的研究。
    Benzamide Derivative 1
  • HY-U00184
    Timepidium bromide

    噻哌溴铵

    Inhibitor
    Timepidium bromide (Sesden; SA504) 是一种抗胆碱剂。
    Timepidium bromide
  • HY-U00316
    Vinconate Activator
    Vinconate 是一种吲哚萘啶衍生物,可以刺激毒蕈碱乙酰胆碱受体 (muscariic acetylcholine receptor)。
    Vinconate
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