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

Imidazoline Receptor (咪唑啉受体)

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 (23):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-101380A
    BU226 hydrochloride 98.93%
    BU226 hydrochloride 是一种具有选择性的咪唑啉 2 (I2) 受体配体,对 I2Ki 为 1.4 nM,对 I1IC50 为 534.5 nM。BU226 hydrochloride 可用于抗抑郁研究。
    BU226 hydrochloride
  • 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>
  • HY-B0374AS
    Moxonidine-13C,d3 hydrochloride

    盐酸莫索尼定-13C,d3

    Agonist
    Moxonidine-13C,d3 hydrochloride 是 13C 和氘代标记的 Moxonidine hydrochloride (HY-B0374A)。Moxonidine (BDF5895) 盐酸盐是咪唑啉1型受体(I1-R)选择性激动剂,为降压剂。
    Moxonidine-<sup>13</sup>C,d<sub>3</sub> hydrochloride