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    Amitriptyline hydrochloride 549-18-8

    簡(jiǎn)要描述:Amitriptyline hydrochloride 549-18-8
    描述
    Amitriptyline Hydrochloride is the hydrochloride salt of the tricyclic dibenzocycloheptadiene amitriptyline with antidepressant and antinociceptive activities.

    • 產(chǎn)品型號(hào):abs47027243
    • 廠商性質(zhì):生產(chǎn)廠家
    • 更新時(shí)間:2025-12-03
    • 訪  問(wèn)  量:875

    詳細(xì)介紹

    品牌absinCAS549-18-8
    分子式C20H24ClN純度99%
    分子量313.86貨號(hào)abs47027243
    規(guī)格50mg供貨周期現(xiàn)貨
    主要用途is the hydrochloride salt of the tricycl應(yīng)用領(lǐng)域化工,生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥,綜合

    Amitriptyline hydrochloride 549-18-8

    產(chǎn)品描述
    描述
    Amitriptyline Hydrochloride is the hydrochloride salt of the tricyclic dibenzocycloheptadiene amitriptyline with antidepressant and antinociceptive activities.
    純度
    99%
    儲(chǔ)存/保存方法
    Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
    基本信息
    別名
    鹽酸阿米ti林
    外觀
    白色結(jié)晶性粉末
    可溶性/溶解性
    DMSO : 59 mg/mL (188 mM)

    Ethanol : 59 mg/mL (188 mM)

    Water : 12 mg/mL (38.2 mM)
    生物活性
    靶點(diǎn)
    Serotonin receptor,5-HT4,Norepinephrine receptor,5-HT2,Sigma 1 receptor
    In vitro(體外研究)
    Amitriptyline inhibits Forskolin-stimulated cyclic AMP accumulation with EC50 values of 16.2 μM in intact CHO/DOR cells. Amitriptyline causes a concentration-dependent stimulation of ERK1/2 and GSK-3β phosphorylation with EC50 values of 9.0 μM in CHO/DOR cells. Amitriptyline (15 μM) causes a stimulation of ERK1/2 phosphorylation in C6 cells. Amitriptyline (30 μM) inhibits Forskolin-stimulated adenylyl cyclase activity and antagonizes (?)-U50,488 inhibitory effect in rat nucleus accumbens. Amitriptyline binds the extracellular domain of both TrkA and TrkB and promotes TrkA-TrkB receptor heterodimerization. Amitriptyline (
    In vivo(體內(nèi)研究)
    Amitriptyline (15 mg/kg, i.p.) activates TrkA and TrkB receptors and significantly reduces kainic acid-triggered neuronal cell death in mice. Amitriptyline (15 mg/kg and 30 mg/kg, i.p.) dose-dependently decreases the immobility time in the forced swimming test (FST) of mice. Amitriptyline (15 mg/kg, i.p.) shows a significant 24-h rhythm in the immobility time in the forced swimming test (FST) of mice. Amitriptyline (1 mg/kg and 3 mg/kg) significantly increases the total distance travelled of mice in novel cages. Amitriptyline (10 mg/kg p.o., twice daily) considerably attenuates the hypothermic response to 8-OHDPAT and mCPP in mice. Amitriptyline (10 mg/kg p.o., twice daily) significantly reduces serotonin transporter density by approximately 20% in cortex of mice.
    參考文獻(xiàn)
    參考文獻(xiàn)
    • 1. Vaishnavi SN, et al. Biol Psychiatry. 2004 Feb 1;55(3):320-2.

    • 2. Gould GG, et al. Biol Psychiatry. 2006 Mar 1;59(5):408-14.

    • 3. Cusack B, et al. 1994 May;114(4):559-65.

    • 4. Onali P, et al. J Pharmacol Exp Ther. 2010 Jan;332(1):255-65.

    • 5. Jang SW, et al. Chem Biol. 2009 Jun 26;16(6):644-56.

    研究領(lǐng)域
    研究領(lǐng)域
    MetabolismTypes of diseaseObesity
    NeuroscienceProcesses
    NeuroscienceNeurology processMetabolism
    NeuroscienceNeurotransmissionReceptors / ChannelsGPCRSerotonin Receptors
    Signal TransductionSignaling PathwayG Protein SignalingGPCR
    Drug DiscoverySmall Molecule DrugLead Compound Discovery
    Amitriptyline hydrochloride 549-18-8溫馨提示:本產(chǎn)品僅作科研實(shí)驗(yàn)使用,不支持臨床等研究

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