1. Neuronal Signaling Membrane Transporter/Ion Channel
  2. Sigma Receptor iGluR
  3. MS-377

MS-377 是一种选择性且具有口服活性的 σ-1 受体配体 (Ki=73 nM),对 σ-2 受体的亲和力较弱 (Ki=6900 nM),且对包括多巴胺、血清素、PCP位点、谷氨酸、γ-氨基丁酸、腺苷、肾上腺素受体等在内的其他受体没有亲和力 (Ki: >10 μM)。MS-377 间接调节 NMDA 受体离子通道复合物。MS-377 是一种抗精神病化合物。MS-377 通过抑制大鼠内侧前额叶皮层中多巴胺和血清素释放的增加来抑制 PCP 诱导的行为。MS-377 可用于精神分裂症研究。

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MS-377

MS-377 Chemical Structure

CAS No. : 206862-30-8

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生物活性

MS-377 is a selective and orally active sigma-1 receptor ligand (Ki=73 nM) with weak affinity for sigma-2 receptor (Ki=6900 nM) and no affinity for any other receptors including dopamine, serotonin, PCP site, glutamate, γ-aminobutylic acid, adenosine, adrenergic receptors, etc. (Ki: >10 μM). MS-377 indirectly modulates the NMDA receptor ion-channel complex. MS-377 is a antipsychotic agent. MS-377 inhibits PCP-induced behaviors by inhibition of the increase in dopamine and serotonin release in the rat medial prefrontal cortex. MS-377 can be used for research of schizophrenia[1][2].

IC50 & Target[1]

Sigma 1 Receptor

73 nM (Ki)

Sigma 2 Receptor

6900 nM (Ki)

分子量

351.87

Formula

C18H26ClN3O2

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
MS-377
目录号:
HY-120155
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