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S81431

SB 271046 (Hydrochloride)

源葉(MedMol) ≥99%
  • 英文名:
  • SB 271046 (Hydrochloride)
  • 別名:
  • CAS號(hào):
  • 209481-24-3
  • 分子式:
  • C20H23Cl2N3O3S2
  • 分子量:
  • 488.4509
品牌貨號(hào)產(chǎn)品規(guī)格價(jià)格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計(jì)量單位 加入購(gòu)物車...
源葉(MedMol) S81431-5mg ≥99% ¥530.00元 10 - - - EA 加入購(gòu)物車
源葉(MedMol) S81431-10mg ≥99% ¥696.00元 10 - - - EA 加入購(gòu)物車
源葉(MedMol) S81431-25mg ≥99% ¥1524.00元 6 - - - EA 加入購(gòu)物車
源葉(MedMol) S81431-50mg ≥99% ¥2591.00元 7 - - - EA 加入購(gòu)物車
源葉(MedMol) S81431-100mg ≥99% ¥4405.00元 6 - - - EA 加入購(gòu)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(jì)算器

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  • 提示:詳情請(qǐng)下載說明書。
  • 產(chǎn)品描述: SB 271046 Hydrochloride (SB 271046A) is a potent, selective and orally active 5-HT6 receptor antagonist with pKi of 9.02, 8.55, and 8.81 for rat, pig and human, respectively. SB 271046 Hydrochloride is over 200 fold selective for the 5-HT6 receptor vs 55 other receptors, binding sites and ion channels. Anticonvulsant activity (EC50=0.16 μM)
  • 靶點(diǎn): 5-HT6 Receptor:8.92-9.02 (pKi);5-HT1D Receptor:6.55 (pKi);5-HT1A Receptor:6.35 (pKi);5-HT1B Receptor;6.05 (pKi);5-HT1F Receptor:5.95 (pKi);5-HT2A Receptor:5.62 (pKi);5-HT2B Receptor:5.41 (pKi);5-HT7 Receptor:5.39 (pKi);5-HT4 Receptor:5.27 (pKi);5-HT1E Receptor:<4.99 (pKi);Human 5-HT2C Receptor:5.73 (pKi);5-HTReceptor
  • 體外研究:
    SB 271046 Hydrochloride (SB 271046A) shows pKi values of 6.55, 6.35, 6.27, 6.05, 5.95, 5.76, 5.73, 5.62, 5.55, 5.41, 5.39, 5.27 and < 4.99 at 5-HT1D, 5-HT1A, D3, 5-HT1B, 5-HT1F, α1B, 5-HT2C, 5-HT2A, D2, 5-HT2B, 5-HT7, 5-HT4 and 5-HT1E respectively. SB-271046 Hydrochloride competitively antagonizes 5-HT-induced stimulation of adenylyl cyclase activity with a pA2 of 8.71
  • 體內(nèi)研究:
    SB 271046 Hydrochloride (10?mg/kg; p.o.) produces an increase in seizure threshold over a wide-dose range in the rat maximal electroshock seizure threshold (MEST) test, with a minimum effective dose of ?0.1?mg/kg p.o. and maximum effect at 4?h post-dose Animal Model: Male Sprague Dawley rats Dosage: 10?mg/kg Administration: P.o. Result: Produced an increase in seizure threshold over a wide-dose range in the rat maximal electroshock seizure threshold (MEST) test, with a minimum effective dose of ?0.1?mg?kg?1 p.o. and maximum effect at 4?h post-dose. The level of anticonvulsant activity achieved correlated well with the blood concentrations of SB-271046 (EC50 of 0.16?μM) and brain concentrations of 0.01-0.04?μM at Cmax.
  • 參考文獻(xiàn):
    1. Routledge C, et al. Characterization of SB-271046: a potent, selective and orally active 5-HT(6) receptor antagonist. Br J Pharmacol. 2000;130(7):1606-1612.
  • 溶解性: Soluble  in  DMSO、H2O
  • 保存條件: 2-8℃;干燥
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.047 ml 10.236 ml 20.473 ml
    5 mM 0.409 ml 2.047 ml 4.095 ml
    10 mM 0.205 ml 1.024 ml 2.047 ml
    50 mM 0.041 ml 0.205 ml 0.409 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
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