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  • Demethylzeylasteral
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Demethylzeylasteral

A nortriterpenoid with diverse biological activities

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Demethylzeylasteral的二维码
  • 库存: 现货
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  • 5mg
    ¥425.00
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  • 10mg
    ¥675.00
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  • 20mg
    ¥1200.00
    960.00
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  • 货号: ajcn4564
  • CAS: 107316-88-1
  • 别名: 去甲泽拉木醛
  • 分子式: C29H36O6
  • 分子量: 480.59
  • 纯度: >98%
  • 溶解度: DMSO: 250 mg/mL (520.19 mM)
  • 储存: Store at 2-8°C,protect from light
  • 库存: 现货

Background

Demethylzeylasteral is a nortriterpenoid originally isolated from T. wilfordii that has diverse biological activities, including enzyme inhibitory, anti-angiogenic, antiproliferative, anti-inflammatory, and immunosuppressive properties.1,2,3,4 Demethylzeylasteral inhibits the UDP-glucuronosyltransferase (UGT) isoforms UGT1A6 and UGT2B7 (Kis = 0.6 and 17.3 μM, respectively).2 It inhibits growth of bovine aortic endothelial cells (BAEs) and U251 human glioma cancer cells in vitro (IC50s = 0.21 and ~6.2 μM, respectively), as well as inhibits tumor growth and neovascularization in vivo in a B16/F10 melanoma mouse allograft model when administered at a dose of 30 mg/kg per day.1 Demethylzeylasteral (0.12 mg/kg per day) decreases renal proteinuria, lesions, immune cell infiltration, and protein levels of TNF-α, COX-2, and ICAM-1 in lupus-prone MRL/lpr mice.3 Demethylzeylasteral (10 mg/kg per day) also increases survival of recipient rats in a model of kidney transplant.4


1.Ushiro, S., Ono, M., Nakayama, J., et al.New nortriterpenoid isolated from anti-rheumatoid arthritic plant, Tripterygium wilfordii, modulates tumor growth and neovascularizationInt. J. Cancer72(4)657-663(1997) 2.Zhao, J.-W., Wang, G.-H., Chen, M., et al.Demethylzeylasteral exhibits strong inhibition towards UDP-glucuronosyltransferase (UGT) 1A6 and 2B7Molecules17(8)9469-9475(2012) 3.Hu, Q., Yang, C., Wang, Q., et al.Demethylzeylasteral (T-96) Treatment Ameliorates Mice Lupus Nephritis Accompanied by Inhibiting Activation of NF-κB PathwayPLoS One10(7)e0133724(2015) 4.Xu, W., Lin, Z., Yang, C., et al.Immunosuppressive effects of demethylzeylasteral in a rat kidney transplantation modelInt. Immunopharmacol.9(7-8)996-1001(2009)

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