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  1. GPCR/G Protein Neuronal Signaling Autophagy Metabolic Enzyme/Protease
  2. Dopamine Receptor Autophagy Cytochrome P450 5-HT Receptor
  3. Chlorpromazine hydrochloride

Chlorpromazine hydrochloride  (Synonyms: 鹽酸氯丙嗪)

目錄號(hào): HY-B0407A 純度: 99.88%
COA 產(chǎn)品使用指南

Chlorpromazine hydrochloride 是一種口服有效的、可透過血腦屏障的抗精神病劑,能有效拮抗 D2 多巴胺受體和 5-HT2A,已廣泛用于精神分裂癥和其他精神疾病。Chlorpromazine hydrochloride 可通過多種途徑發(fā)揮抗癌活性,包括抗增殖、誘導(dǎo)自噬和周期停滯 (G2-M 期)、抑制細(xì)胞色素 c 氧化酶 (CcO)、抑制腫瘤生長(zhǎng)和轉(zhuǎn)移以及抑制腫瘤免疫逃逸等。Chlorpromazine hydrochloride 還能阻斷 hNav1.7 通道 (IC50=25.9 μM; 濃度依賴的方式) 和 HERG 鉀通道 (IC50=21.6 μM) ,其在止痛以及心律失常方面也具有較好的研究潛力。Chlorpromazine hydrochloride 也能抑制網(wǎng)格蛋白介導(dǎo)的內(nèi)吞作用。

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Chlorpromazine hydrochloride Chemical Structure

Chlorpromazine hydrochloride Chemical Structure

CAS No. : 69-09-0

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Customer Review

Other Forms of Chlorpromazine hydrochloride:

MCE 顧客使用本產(chǎn)品發(fā)表的 61 篇科研文獻(xiàn)

IF

    Chlorpromazine hydrochloride purchased from MCE. Usage Cited in: Commun Biol. 2022 Nov 14;5(1):1248.  [Abstract]

    Chlorpromazine (CPZ) (10 μM; 30 min) remarkably decreases the cellular internalization of FITC-P-LPK in HCT116 cells. Chlorpromazine can inhibit clathrin-mediated endocytosis. The fluorescence intensity is observed by confocal microscopy and detected using a multi-well plate reader.
    • 生物活性

    • 純度 & 產(chǎn)品資料

    • 參考文獻(xiàn)

    生物活性

    Chlorpromazine hydrochloride is an orally active, blood-brain barrier-transparent antipsychotic agent that effectively antagonises D2 dopamine receptors and 5-HT2A, which is widely used in schizophrenia and other psychiatric disorders. Chlorpromazine hydrochloride exerts anti-cancer activity through a variety of pathways, including anti-proliferation, induction of autophagy and cycle arrest (G2-M phase), inhibition of cytochrome c oxidase (CcO), inhibition of tumour growth and metastasis, and inhibition of tumour immune escape. Chlorpromazine hydrochloride also blocks hNav1.7 channels (IC50=25.9 μM; concentration-dependent) and HERG potassium channels (IC50=21.6 μM), which has potential for analgesic and cardiac arrhythmic studies. Chlorpromazine hydrochloride also can inhibit clathrin-mediated endocytosis[1][2][3][4][5].

    IC50 & Target

    D2 dopamine receptors; 5-HT2A[1][6].

    體外研究
    (In Vitro)

    Chlorpromazine hydrochloride (0,10,20,40 μM;0,24,48 h) 以劑量和時(shí)間依賴的方式抑制 U-87MG 神經(jīng)膠質(zhì)瘤細(xì)胞的生長(zhǎng)[2]。
    Chlorpromazine hydrochloride (20 μM;0、12、24、48 小時(shí)) 降低 U-87MG 神經(jīng)膠質(zhì)瘤細(xì)胞中細(xì)胞周期蛋白 A 和細(xì)胞周期蛋白 B1 的水平,12 小時(shí)后[2]。
    Chlorpromazine hydrochloride (20 μM) 抑制細(xì)胞周期進(jìn)程[2]
    Chlorpromazine hydrochloride (10 μM;1 h) 顯著抑制 sEV 內(nèi)化并顯著減少經(jīng) sEV 處理的骨骼中的 MDSCs骨髓細(xì)胞 (MDSCs可顯著抑制免疫細(xì)胞反應(yīng),引起癌細(xì)胞免疫抑制)[3]。
    Chlorpromazine hydrochloride (3,10,20,40,60 μM) 阻斷hNa v1.7 電流呈濃度依賴性[4]。
    Chlorpromazine hydrochloride 阻斷 HERG 鉀通道,IC50 值為21.6 μM,希爾系數(shù)為 1.11[5]

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

    Cell Proliferation Assay[2]

    Cell Line: U-87MG glioma cells
    Concentration: 0, 10, 20, 40 μM
    Incubation Time: 0, 24, 48 h
    Result: Showed anti-proliferative activity in a dose- and time-dependent manner.

    Immunofluorescence[3]

    Cell Line: Bone marrow cells (sEV-treated)
    Concentration: 10 μM
    Incubation Time: 1 h
    Result: Reduced MDSCs and suppressed the sEV internalization.

    Western Blot Analysis[2]

    Cell Line: U-87MG glioma cells
    Concentration: 20 μM
    Incubation Time: 0, 12, 24, 48 h
    Result: Decreased the levels of cyclin A and cyclin B1 12 h later, whereas levels of cyclin D1, proliferating cell nuclear antigen and GAPDH remained unchanged.
    體內(nèi)研究
    (In Vivo)

    Chlorpromazine(20 mg/kg;腹腔注射;每天一次,連續(xù) 7 天)hydrochloride 可抑制裸鼠異種移植腫瘤的生長(zhǎng)[2]

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

    Animal Model: 5- to 6-week-old athymic nude mice bearing intracranial U-87MG xenograft tumors[2].
    Dosage: 20 mg/kg
    Administration: Injected intraperitoneally; single daily for 7 days
    Result: Inhibited tumor growth on day 17.
    分子量

    355.33

    Formula

    C17H20Cl2N2S

    CAS 號(hào)
    性狀

    固體

    顏色

    White to off-white

    中文名稱

    鹽酸氯丙嗪

    運(yùn)輸條件

    Room temperature in continental US; may vary elsewhere.

    儲(chǔ)存方式

    4°C, sealed storage, away from moisture and light

    *該產(chǎn)品在溶液狀態(tài)不穩(wěn)定,建議您現(xiàn)用現(xiàn)配,即刻使用。

    溶解性數(shù)據(jù)
    細(xì)胞實(shí)驗(yàn): 

    H2O 中的溶解度 : 100 mg/mL (281.43 mM; 超聲助溶)

    DMSO 中的溶解度 : ≥ 60 mg/mL (168.86 mM; 吸濕的 DMSO 對(duì)產(chǎn)品的溶解度有顯著影響,請(qǐng)使用新開封的 DMSO)

    * "≥" means soluble, but saturation unknown.

    配制儲(chǔ)備液
    濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg
    1 mM 2.8143 mL 14.0714 mL 28.1429 mL
    5 mM 0.5629 mL 2.8143 mL 5.6286 mL
    查看完整儲(chǔ)備液配制表

    * 請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度,選擇合適的溶劑配制儲(chǔ)備液;該產(chǎn)品在溶液狀態(tài)不穩(wěn)定,建議您現(xiàn)用現(xiàn)配,即刻使用。

    * 備注:如您選擇水作為儲(chǔ)備液,請(qǐng)稀釋至工作液后,再用 0.22 μm 的濾膜過濾除菌后使用。

    • 摩爾計(jì)算器

    • 稀釋計(jì)算器

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    質(zhì)量
    =
    濃度
    ×
    體積
    ×
    分子量 *

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    濃度 (start)

    C1

    ×
    體積 (start)

    V1

    =
    濃度 (final)

    C2

    ×
    體積 (final)

    V2

    動(dòng)物實(shí)驗(yàn):

    以下溶解方案,請(qǐng)直接配制工作液。建議現(xiàn)用現(xiàn)配,在短期內(nèi)盡快用完。 以下溶劑前顯示的百分比是指該溶劑在您配制終溶液中的體積占比; 如在配制過程中出現(xiàn)沉淀、析出現(xiàn)象,可以通過加熱和/或超聲的方式助溶。

    • 方案 一

      請(qǐng)依序添加每種溶劑: PBS

      Solubility: ≥ 200 mg/mL (562.86 mM); 澄清溶液

    動(dòng)物溶解方案計(jì)算器
    請(qǐng)輸入動(dòng)物實(shí)驗(yàn)的基本信息:

    給藥劑量

    mg/kg

    動(dòng)物的平均體重

    g

    每只動(dòng)物的給藥體積

    μL

    動(dòng)物數(shù)量

    由于實(shí)驗(yàn)過程有損耗,建議您多配一只動(dòng)物的量
    計(jì)算結(jié)果
    工作液所需濃度 : mg/mL
    該產(chǎn)品水溶性佳,請(qǐng)具體參考實(shí)測(cè) 水 / PBS / Saline 中的溶解度數(shù)據(jù)。
    您所需的儲(chǔ)備液濃度超過該產(chǎn)品的實(shí)測(cè)溶解度,如有需要,請(qǐng)與 MCE 中國(guó)技術(shù)支持聯(lián)系。
    純度 & 產(chǎn)品資料

    純度: 99.90%

    參考文獻(xiàn)

    完整儲(chǔ)備液配制表

    * 請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度,選擇合適的溶劑配制儲(chǔ)備液;該產(chǎn)品在溶液狀態(tài)不穩(wěn)定,建議您現(xiàn)用現(xiàn)配,即刻使用。

    可選溶劑 濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg 25 mg
    DMSO / H2O 1 mM 2.8143 mL 14.0714 mL 28.1429 mL 70.3571 mL
    5 mM 0.5629 mL 2.8143 mL 5.6286 mL 14.0714 mL
    10 mM 0.2814 mL 1.4071 mL 2.8143 mL 7.0357 mL
    15 mM 0.1876 mL 0.9381 mL 1.8762 mL 4.6905 mL
    20 mM 0.1407 mL 0.7036 mL 1.4071 mL 3.5179 mL
    25 mM 0.1126 mL 0.5629 mL 1.1257 mL 2.8143 mL
    30 mM 0.0938 mL 0.4690 mL 0.9381 mL 2.3452 mL
    40 mM 0.0704 mL 0.3518 mL 0.7036 mL 1.7589 mL
    50 mM 0.0563 mL 0.2814 mL 0.5629 mL 1.4071 mL
    60 mM 0.0469 mL 0.2345 mL 0.4690 mL 1.1726 mL
    80 mM 0.0352 mL 0.1759 mL 0.3518 mL 0.8795 mL
    100 mM 0.0281 mL 0.1407 mL 0.2814 mL 0.7036 mL

    * 備注:如您選擇水作為儲(chǔ)備液,請(qǐng)稀釋至工作液后,再用 0.22 μm 的濾膜過濾除菌后使用。

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    產(chǎn)品名稱:
    Chlorpromazine hydrochloride
    目錄號(hào):
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