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  1. GPCR/G Protein Neuronal Signaling Membrane Transporter/Ion Channel Anti-infection Autophagy
  2. Dopamine Receptor Adrenergic Receptor P-glycoprotein CaMK Influenza Virus Autophagy
  3. Trifluoperazine

Trifluoperazine 是一種抗精神病藥物,通過阻斷中樞多巴胺受體 (dopamine receptors) 起作用。Trifluoperazine 是一種有效的 α1-adrenergic 受體拮抗劑。Trifluoperazine 是一種有效的 NUPR1 抑制劑,具有抗癌活性。Trifluoperazine是一種鈣調(diào)蛋白 (calmodulin) 抑制劑,還可抑制 P-糖蛋白 (P-glycoprotein),可用于精神分裂癥的研究。Trifluoperazine 是流感病毒 (influenza virus) 形態(tài)發(fā)生的可逆抑制劑。

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Trifluoperazine Chemical Structure

Trifluoperazine Chemical Structure

CAS No. : 117-89-5

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

Customer Review

Other Forms of Trifluoperazine:

查看 Dopamine Receptor 亞型特異性產(chǎn)品:

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  • 生物活性

  • 純度 & 產(chǎn)品資料

  • 參考文獻(xiàn)

生物活性

Trifluoperazine, an antipsychotic agent, acts by blocking central dopamine receptors. Trifluoperazine is a potent α1-adrenergic receptor antagonist. Trifluoperazine is a potent NUPR1 inhibitor exerting anticancer activity. Trifluoperazine is a calmodulin inhibitor, and also inhibits P-glycoprotein. Trifluoperazine can be used for the research of schizophrenia. Trifluoperazine acts as a reversible inhibitor of influenza virus morphogenesis[1][2][3][4][5].

體外研究
(In Vitro)

Trifluoperazine is a long-established, widely used 'conventional' antipsychotic agent. Trifluoperazine has been an extensively studied drug molecule that has been used as a calmodulin inhibitor[3][4].
Trifluoperazine acts as a reversible inhibitor of influenza virus morphogenesis, but not budding, by disturbing cellular CaM and/or CaM-dependent functions[5].

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

分子量

407.50

Formula

C21H24F3N3S

CAS 號
中文名稱

三氟拉嗪

運(yùn)輸條件

Room temperature in continental US; may vary elsewhere.

儲(chǔ)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(xiàn)
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產(chǎn)品名稱:
Trifluoperazine
目錄號:
HY-B0532
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