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S82144

Basmisanil

源葉(MedMol) 99%
  • 英文名:
  • Basmisanil
  • 別名:
  • (1,1-dioxo-1λ6-thiomorpholin-4-yl)-{6-[3-(4-fluoro-phenyl)-5-methyl-isoxazol-4-ylmethoxy]-pyridin-3-yl}-methanone; (1,1-dioxo-1λ6-thiomorpholin-4-yl)-{6-[3-(4-fluoro-phenyl)-5-methyl-isoxazol
  • CAS號:
  • 1159600-41-5
  • 分子式:
  • C21H20FN3O5S
  • 分子量:
  • 445.464
  • 核磁/質(zhì)譜:
品牌貨號產(chǎn)品規(guī)格價格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計量單位 加入購物車...
源葉(MedMol) S82144-1mg 99% ¥230.00元 10 - - - EA 加入購物車
源葉(MedMol) S82144-5mg 99% ¥530.00元 5 - - - EA 加入購物車
源葉(MedMol) S82144-10mg 99% ¥780.00元 6 - - - EA 加入購物車
源葉(MedMol) S82144-25mg 99% ¥1290.00元 6 - - - EA 加入購物車
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產(chǎn)品介紹

參考文獻(xiàn)

質(zhì)檢證書(COA)

摩爾濃度計算器

相關(guān)產(chǎn)品

  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: Basmisanil (RG1662) is a highly selective orally active α subunit-containing GABAA receptors (GABAAα5) negative allosteric modulator (NAMs). Basmisanil can inhibit GABAA-α5 with a Ki value of 5 nM and IC50 value of 8 nM, respectively. Basmisanil can be used for the research of multiple cognitive and psychiatric disorders
  • 靶點: IC50: 8 nM (GABAAα5) Ki: 5 nM (GABAAα5); 1031 nM (GABAAα1); 458 nM (GABAAα2); 510 nM (GABAAα3);GABAReceptor
  • 體外研究:
    Basmisanil (0.1 nM-100 μM) has high affinity for bounding to recombinant human GABAA-α5 receptors with a Ki value of 5 nM and more than 90-fold selectivity versus α1 (Ki = 1031 nM), α2 (Ki = 458 nM), and α3 (Ki = 510 nM) subunit-containing receptors. Basmisanil (1 nM-1 μM) shows a highly selective inhibition of GABAA-α5 with a IC50 value of 8 nM. Basmisanil (1 μM) inhibits GABA-induced currents at GABAA-α5 yet had little or no effect at the other receptor subtypes
  • 體內(nèi)研究:
    Basmisanil (3-100 mg/kg, p.o.) occupies GABAA-α receptor in dose-dependent in rat brain. Basmisanil (3-600 mg/kg p.o.) improves cognition in rats and non.human primates and not show anxiogenic or proconvulsant effects. Animal Model: Sprague Dawley rats(180 g; female) Dosage: 3-100 mg/kg Administration: p.o. Result: Decreased the binding of [3H]-Ro 15-4513 in a dose-dependent manner.Reduced specific binding in the hippocampus by 70% at the highest dose (100 mg/kg). Animal Model: Lister Hooded rats, Wistar rats and F-344 Fischer rats(Lister Hooded rats: 220-250 g; male)(Wistar rats: 200-220 g; male and female)(F-344 Fischer rats: 170-180 g; male) Dosage: 3-600 mg/kg Administration: p.o. Result: Significantly attenuated the diazepam-induced deficit.Showed plasma concentrations in dose- and time-dependent manner and reached a maximal level of 903 ng/mL (379 nM free plasma) 30 min after the administration at 10 mg/kg. Animal Model: Male cynomolgus macaques(Macaca fascicularis; 7-10 kg) Dosage: 1-600 mg/kg Administration: p.o. Result: Significantly improved the percentage of correct first reaches during difficult trials of the object retrieval task at the 3 and 10 mg/kg doses.Exhibited an inverted U-shaped dose response in this paradigm with the 1 and 30 mg/kg doses producing no marked improvement on performance.Increased the total plasma exposure in dose-dependent.
  • 參考文獻(xiàn):
    1. Joerg F Hipp, et al. Basmisanil, a highly selective GABA A-α5 negative allosteric modulator: preclinical pharmacology and demonstration of functional target engagement in man. Sci Rep. 2021 Apr 8;11(1):7700.
  • 溶解性: soluble  in  DMSO
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.245 ml 11.224 ml 22.449 ml
    5 mM 0.449 ml 2.245 ml 4.49 ml
    10 mM 0.224 ml 1.122 ml 2.245 ml
    50 mM 0.045 ml 0.224 ml 0.449 ml
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質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)


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