1. Signaling Pathways
  2. Neuronal Signaling
  3. Imidazoline Receptor

Imidazoline Receptor (咪唑啉受体)

咪唑啉受体 (Imidazoline Receptor) 是可乐定和其他咪唑啉类药物作用的主要受体。咪唑啉受体有三类:I1 受体 - 介导咪唑啉类药物的交感神经抑制作用以降低血压(NISCH 或 IRAS,咪唑啉受体抗血清选择);I2 受体 - 单胺氧化酶的变构结合位点,参与疼痛调节和神经保护;I3 受体 - 调节胰腺 β 细胞的胰岛素分泌。激活的 I1-咪唑啉受体触发磷脂酰胆碱水解为 DAG。升高的 DAG 水平反过来会触发第二信使花生四烯酸和下游二十烷酸的合成。此外,钠氢反向转运体受到抑制,儿茶酚胺合成酶受到诱导。I1-咪唑啉受体可能属于神经细胞因子受体家族,因为其信号通路与白细胞介素相似。

Imidazoline receptors are the primary receptors on which clonidine and other imidazolines act. There are three classes of imidazoline receptors: I1 receptor – mediates the sympatho-inhibitory actions of imidazolines to lower blood pressure, (NISCH or IRAS, imidazoline receptor antisera selected), I2 receptor - an allosteric binding site of monoamine oxidase and is involved in pain modulation and neuroprotection, I3 receptor - regulates insulin secretion from pancreatic beta cells. Activated I1-imidazoline receptors trigger the hydrolysis of phosphatidylcholine into DAG. Elevated DAG levels in turn trigger the synthesis of second messengers arachidonic acid and downstreameicosanoids. In addition, the sodium-hydrogen antiporter is inhibited, and enzymes of catecholamine synthesis are induced. The I1-imidazoline receptor may belong to the neurocytokine receptorfamily, since its signaling pathways are similar to those of interleukins.

Imidazoline Receptor 相关产品 (42):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-N0543R
    Allantoin (Standard)

    尿囊素 (Standard)

    Agonist
    Allantoin (Standard) 是 Allantoin 的分析标准品。本产品用于研究及分析应用。Allantoin是促进皮肤健康,刺激新鲜健康组织生长的皮肤调理剂。
    Allantoin (Standard)
  • HY-B0374S
    Moxonidine-d4

    莫索尼定 d4

    Agonist
    Moxonidine-d4 是 Moxonidine 的氘代物。Moxonidine(BDF5895)是咪唑啉1型受体(I1-R)选择性激动剂,为降压剂。
    Moxonidine-d<sub>4</sub>