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L-701,324

    
99.3%

L-701,324

源葉(MedMol)
S83248 一鍵復制產品信息
142326-59-8
C21H14ClNO3
363.794
7-氯-4-羥基-3-(3-苯氧基)苯基-2(1H)-喹啉;Sulprostone; L-701,324;
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S83248-10mg
99.3% ¥552.00 10 - - -
S83248-25mg
99.3% ¥770.00 6 - - -
S83248-50mg
≥98% ¥1310.00 貨期:2-3天 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

L-701324 is a potent, orally active NMDA receptor antagonist that antagonizes the activity of the NMDA receptor by blocking its glycine B binding site. L-701324 binds with high affinity to rat brain membranes (IC50=2 nM). L-701324 has antidepressant activity

產品描述: L-701324 is a potent, orally active NMDA receptor antagonist that antagonizes the activity of the NMDA receptor by blocking its glycine B binding site. L-701324 binds with high affinity to rat brain membranes (IC50=2 nM). L-701324 has antidepressant activity
靶點: iGluR;NMDAR;?iGluR
體內研究: L-701324 (5-10 mg/kg; i.p.; once) exhibits antidepressant-like potential in the forced swim test (FST) and tail suspension test (TST) without affecting the locomotor activity of mice. L-701324 (5-10 mg/kg; i.p.; daily, for 2 weeks) produces strong antidepressant-like effects in the chronic unpredictable mild stress (CUMS) model of depression and prevents the CUMS-induced decreases in eurogenesis and the BDNF signaling cascade in the hippocampus. L-701324 (2.5-5 mg/kg; p.o.; once) inhibits NMDA receptor activity via a blockade of the NMDA/glycine-sensitive site at the NMDA receptor is accompanied by a reduction of anxiety-like behavior in both non-conditioned and conditioned conflict behavior situations
參考文獻: 1. Liu L, et, al. Antidepressant-like activity of L-701324 in mice: A behavioral and neurobiological characterization. Behav Brain Res. 2021 Feb 5;399:113038. 2. Kotlinska J, et, al. A characterization of anxiolytic-like actions induced by the novel NMDA/glycine site antagonist, L-701,324. Psychopharmacology (Berl). 1998 Jan;135(2):175-81. 3. Hutson PH, et, al. L-701,324, a glycine/NMDA receptor antagonist, blocks the increase of cortical dopamine metabolism by stress and DMCM. Eur J Pharmacol. 1997 May 20;326(2-3):127-32.
溶解性: DMSO  :  ≥  34  mg/mL  (93.46  mM)
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.749 ml 13.744 ml 27.488 ml
5 mM 0.55 ml 2.749 ml 5.498 ml
10 mM 0.275 ml 1.374 ml 2.749 ml
50 mM 0.055 ml 0.275 ml 0.55 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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