1. GPCR/G Protein Neuronal Signaling
  2. Opioid Receptor
  3. Naldemedine

Naldemedine  (Synonyms: S-297995)

目录号: HY-19627
产品使用指南

Naldemedine (S-297995) 是一种具有口服活性的 μ-阿片受体拮抗剂 (PAMORA)。Naldemedine 对重组人源 μ-、δ- 和 κ- 阿片受体表现出强大的亲和作用 (Ki 分别为 0.34,0.43,0.94 nM) 和拮抗作用 (IC50 分别为 25.57,7.09,16.1 nM) 。Naldemedine 可用于阿片类化合物引起的便秘 (OIC) 研究。Naldemedine 预测可能与 SARS-CoV2 基因组编码的 3CLpro 结合。

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Naldemedine Chemical Structure

Naldemedine Chemical Structure

CAS No. : 916072-89-4

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  • 生物活性

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生物活性

Naldemedine (S-297995) is an orally active μ-opioid receptor antagonist (PAMORA)[1]. Naldemedine shows potent binding affinities (Ki=0.34, 0.43, 0.94 nM, respectively) and antagonist activities (IC50=25.57, 7.09, 16.1 nM, respectively) for recombinant human μ-, δ-, and κ- opioid receptors[2]. Naldemedine can be used in opioid-induced constipation (OIC) research[2]. Naldemedine is predicted to bind to 3CLpro encoded by SARS-CoV2 genome[3].

体内研究
(In Vivo)

Naldemedine (oral gavage; 0.03-10 mg/kg; once) represses the opioid-induced inhibition of small intestinal transit in rats by subcutaneous morphine and oxycodone[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 6-week-old Wistar and SD male rats[2]
Dosage: 0.03-10 mg/kg
Administration: Oral gavage; 0.03-10 mg/kg; once
Result: Repressed the subcutaneous morphine-induced inhibition of small intestinal transit in rats with an ED50 of 0.03 mg/kg, and the oxycodone-induced inhibition model with an ED50 of 0.02 mg/kg.
Clinical Trial
分子量

570.64

Formula

C32H34N4O6

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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