成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

<button id="vpian"></button>
  • <li id="vpian"></li>
    <code id="vpian"><delect id="vpian"><small id="vpian"></small></delect></code>
  • <button id="vpian"></button>
  • <tfoot id="vpian"><delect id="vpian"></delect></tfoot>
    返回ChemicalBook首頁>CAS數(shù)據(jù)庫列表>479347-85-8

    479347-85-8

    中文名稱 6-CYANO-7-NITROQUINOXALINE-2;3-DIONE DISODIUM
    英文名稱 CNQX disodium salt
    CAS 479347-85-8
    分子式 C9H2N4O4Na2
    分子量 256.15
    MOL 文件 479347-85-8.mol
    更新日期 2025/01/03 13:29:10
    479347-85-8 結(jié)構(gòu)式 479347-85-8 結(jié)構(gòu)式

    基本信息

    中文別名
    CNQX二鈉鹽
    英文別名
    3-dione disodium
    6-Cyano-7-nitroquinoxaline-2

    物理化學(xué)性質(zhì)

    儲存條件Desiccate at RT
    溶解度≥27.6 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O
    形態(tài)固體
    顏色棕色或黃色
    水溶解性Soluble to 20 mM in water

    常見問題列表

    生物活性
    CNQX disodium (FG9065 disodium) 是一種有效的競爭性 AMPA /海藻酸酯受體 (AMPA/kainate receptor) 拮抗劑,IC50 分別為 0.3 μM 和 1.5 μM。CNQX disodium 是一種競爭性的非 NMDA 受體拮抗劑。CNQX disodium 會阻止大鼠恐懼增強(qiáng)的表達(dá)。
    靶點

    IC50: 0.3 μM (AMPA) and 1.5 μM (kainate receptor)

    體外研究

    CNQX disodium (FG9065 disodium; 2-5 μM) reversibly blocks the Schaffer collateral and mossy fibre excitatory postsynaptic potential (EPSP), while sparing the fast and slow GABA-mediated inhibition in superfusion of hippocampal slices.
    CNQX disodium (1-5 μM) produces a selective and dose-dependent reduction in the amplitude of the monosynaptic component of the DR-VRR recorded from lumbar spinal segments.

    體內(nèi)研究

    CNQX disodium (FG9065 disodium; 0.75-3 mg/kg; IP; 20 min before testing) decreased the number of cocaine responses in a dose-dependent manner during the first 15-min cocaine-free interval.
    The bilateral infusion of CNQX disodium (0.5 or 1.25 μg) into the amygdala or dorsal hippocampus 10 min prior to a retention test partially blocks the expression of stepdown inhibitory avoidance in rats 24 h after training. CNQX disodium causes a complete blockade at a dose of 0.5 μg.

    Animal Model: Male Wistar rats weighing 180-200 g
    Dosage: 0.75, 1.5, and 3 mg/kg
    Administration: IP; 20 min before testing
    Result: Decreased the number of cocaine (IV; 0.25 mg/infusion) responses in a dose-dependent manner during the first 15-min cocaine-free interval.
    "479347-85-8" 相關(guān)產(chǎn)品信息