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  • Dihydrosanguinarine (13,14-Dihydrosanguinarine)
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Dihydrosanguinarine (13,14-Dihydrosanguinarine)

A metabolite of sanguinarine with diverse biological activities

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Dihydrosanguinarine (13,14-Dihydrosanguinarine)的二维码
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  • 1mg
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  • 5mg
    ¥1675.00
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  • 10mg
    ¥3212.00
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  • 25mg
    ¥5000.00
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  • 货号: ajce52172
  • CAS: 3606-45-9
  • 别名: 二氢血根碱; 13,14-Dihydrosanguinarine
  • 分子式: C20H15NO4
  • 分子量: 333.34
  • 纯度: >98%
  • 溶解度: DMSO : 5.2 mg/mL (15.60 mM)
  • 储存: Store at -20°C
  • 库存: 现货

Background

Dihydrosanguinarine is an alkaloid and a metabolite of the alkaloid sanguinarine that has diverse biological activities, including anticancer, fungicidal, and antiprotozoal properties.1,2,3 It inhibits proliferation of PANC-1, SW 1990, and HPDE6c7 cancer cells when used at concentrations of 10, 20, and 30 ?M.1 It also reduces the levels of phosphorylated ERK and C-RAF, halts the cell cycle at the G0/G1 and G2/M phases, and induces apoptosis in PANC-1 cells. Dihydrosanguinarine inhibits spore germination of the phytopathogenic fungi B. cinerea and E. graminis in vitro (EC50s = 56.35 and 95.75 ?g/ml, respectively).2 It has protective and curative effects against B. cinerea and E. graminis when applied as a spray to plants either before or after infection, respectively, at concentrations of 100 and 500 ?g/ml. Dihydrosanguinarine is also effective against I. multifiliis infestation in S. curriculus (EC50 = 5.18 mg/L) with an LC50 value of 13.3 mg/L.3


1.Wu, S.-Z., Xu, H.-C., Wu, X.-L., et al.Dihydrosanguinarine suppresses pancreatic cancer cells via regulation of mut-p53/WT-p53 and the Ras/Raf/Mek/Erk pathwayPhytomedicine59152895(2019) 2.Feng, G., Zhang, J., and Liu, Y.-Q.Inhibitory activity of dihydrosanguinarine and dihydrochelerythrine against phytopathogenic fungiNat. Prod. Res.25(11)1082-1089(2011) 3.Yao, J.-Y., Zhou, Z.-M., Li, X.-L., et al.Antiparasitic efficacy of dihydrosanguinarine and dihydrochelerythrine from Macleaya microcarpa against Ichthyophthirius multifiliis in richadsin (Squaliobarbus curriculus)Vet. Parasitol.183(1-2)8-13(2011)

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