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  1. GPCR/G Protein Neuronal Signaling
  2. 5-HT Receptor Dopamine Receptor
  3. Metoclopramide hydrochloride

Metoclopramide hydrochloride  (Synonyms: 鹽酸甲氧氯普胺)

目錄號: HY-17382B
產(chǎn)品使用指南

Metoclopramide hydrochloride 是一種有效和具有口服活性的 5-HT3 和多巴胺 D2 受體拮抗劑,IC50 值分別為 308 nM 和 483 nM。Metoclopramide hydrochloride 可用于惡心嘔吐、胃食管反流和胃輕癱的研究。

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Metoclopramide hydrochloride Chemical Structure

Metoclopramide hydrochloride Chemical Structure

CAS No. : 7232-21-5

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Metoclopramide hydrochloride 的其他形式現(xiàn)貨產(chǎn)品:

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  • 生物活性

  • 純度 & 產(chǎn)品資料

  • 參考文獻

生物活性

Metoclopramide hydrochloride is a potent and orally active antagonist of 5-HT3 and dopamine D2 receptor, with IC50s of 308 nM and 483 nM, respectively. Metoclopramide hydrochloride can be used for the research of nausea and vomiting, gastro-oesophageal reflux, and gastroparesis[1][2].

IC50 & Target[1]

5-HT3 Receptor

308 nM (IC50)

D2 Receptor

483 nM (IC50)

細胞效力
(Cellular Effect)
Cell Line Type Value Description References
HEK293 IC50
94.8 μM
Compound: Methoclopramide
Inhibition of 4-(4-(dimethylamino)styryl)-N-methylpyridinium uptake at human OCT1 expressed in HEK293 cells by confocal microscopy
Inhibition of 4-(4-(dimethylamino)styryl)-N-methylpyridinium uptake at human OCT1 expressed in HEK293 cells by confocal microscopy
[PMID: 18788725]
NHDF IC50
> 50 μM
Compound: 43
Cytotoxicity against NHDF assessed as reduction in cell viability after 72 hrs by MTT assay
Cytotoxicity against NHDF assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 28671460]
體外研究
(In Vitro)

Metoclopramide (0.01-10 μM) hydrochloride stimulates aldosterone release in isolated perfused rat zona glomerulosa cells[3].
Metoclopramide hydrochloride results in prokinesis by four mechanisms: inhibition of presynaptic D2 receptors and stimulation of presynaptic excitatory 5-HT4 receptors, thereby allowing acetylcholine (ACh) release from intrinsic cholinergic motor neurons; inhibition of D2 postsynaptic receptors; and antagonism of the presynaptic inhibition of muscarinic receptors, leading to further augmentation of ACh release[2].

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

體內研究
(In Vivo)

Metoclopramide (6.7 μg/g; s.c. daily for 50 days) hydrochloride significantly increases the number and the volume of lactotroph cells of the pituitary gland during all phases of the estrous cycle[4].
Metoclopramide (5-40 mg/kg; i.p.) hydrochloride induces catalepsy and antagonizes Apomorphine induced cage climbing behaviour in mice[5].
Metoclopramide (1.25-2.5 mg/kg; i.p.) hydrochloride induces stereotyped cage climbing behaviour in mice[5].

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

Animal Model: Adult, virgin female mice of the Swiss EPM-1 strain[4]
Dosage: 6.7 μg/g
Administration: S.c. daily for 50 days
Result: Increased the number but also stimulated the metabolic activity of lactotrophs.
分子量

336.26

Formula

C14H23Cl2N3O2

CAS 號
中文名稱

鹽酸甲氧氯普胺;鹽酸胃復安

運輸條件

Room temperature in continental US; may vary elsewhere.

儲存方式

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

純度 & 產(chǎn)品資料
參考文獻
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Help & FAQs
  • 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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產(chǎn)品名稱:
Metoclopramide hydrochloride
目錄號:
HY-17382B
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