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  • Alizapride-13C-d3 (hydrochloride)
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Alizapride-13C-d3 (hydrochloride)

An internal standard for the quantification of alizapride

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Alizapride-13C-d3 (hydrochloride)的二维码
  • 库存: 现货
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  • 包装
    价格
    促销价
    数量
  • 500ug
    ¥2037.00
    1630.00
    - +
  • 1mg
    ¥3862.00
    3090.00
    - +
  • 5mg
    ¥15100.00
    12080.00
    - +
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金额: ¥0.00
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  • 货号: ajcx25118
  • CAS: N/A
  • 别名:
  • 分子式: C15[13C]H18D3N5O2·HCl
  • 分子量: 355.9
  • 纯度: >98%
  • 溶解度: DMSO: soluble,Methanol: soluble,Water: soluble
  • 储存: -20°C
  • 库存: 现货

Background

Alizapride-13C-d3 is intended for use as an internal standard for the quantification of alizapride by GC- or LC-MS. Alizapride is a dopamine D2 receptor antagonist (Ki = 66-340 nM in radioligand binding assays).1 It is selective for dopamine D2 over α1-, α2-, and β-adrenergic receptors (IC50s = >10 µM for all). It reduces decreases in gastrointestinal transit induced by dopamine , apomorphine, or bromocriptine in rats when administered at a dose of 5 mg/kg.2 Formulations containing alizapride have been used in the treatment of pre- and postoperative nausea.



1.Chivers, J.K., Gommeren, W., Leysen, J.E., et al.Comparison of the in-vitro receptor selectivity of substituted benzamide drugs for brain neurotransmitter receptorsJ. Pharm. Pharmacol.40(6)415-421(1988) 2.Dhasmana, K.M., Villalón, C.M., Zhu, Y.N., et al.The role of dopamine (D2), α and β-adrenoceptor receptors in the decrease in gastrointestinal transit induced by dopamine and dopamine-related drugs in the ratPharmacol. Res.27(4)335-347(1993)

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