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beta-Eudesmol

CAS No. 473-15-4

beta-Eudesmol ( —— )

产品货号. M18588 CAS No. 473-15-4

β-Eudesmol 是烟碱型乙酰胆碱受体 (nAChR) 的非竞争性拮抗剂。它是一种倍半萜烯,已在包括大麻在内的多种植物中发现,并具有多种生物活性。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1191 有现货
10MG ¥1847 有现货
25MG ¥3151 有现货
50MG ¥4641 有现货
100MG 获取报价 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    beta-Eudesmol
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    β-Eudesmol 是烟碱型乙酰胆碱受体 (nAChR) 的非竞争性拮抗剂。它是一种倍半萜烯,已在包括大麻在内的多种植物中发现,并具有多种生物活性。
  • 产品描述
    β-Eudesmol is a noncompetitive antagonist of nicotinic acetylcholine receptors (nAChRs). It is a sesquiterpene that has been found in a variety of plants, including Cannabis, and has diverse biological activities.
  • 体外实验
    Western Blot Analysis Cell Line:HL-60Concentration:40 μM, 80 μM Incubation Time:4 h Result:Increased the expression of caspase-3 protein at 80 μM.Cell Viability Assay Cell Line:HL-60 Concentration:10 μM, 20 μM, 40 μM, 60 μM, 80 μM, 120 μM Incubation Time:4 h Result:Didn’t affect cell activity at a dose of 40 μM, but decreased cell activity at a dose of 80 μM, and cell viability decreased by 51.6%.Apoptosis Analysis Cell Line:HL-60 Concentration:40 μM, 80 μM Incubation Time:4 hResult:Had no effect on apoptosis at the dose of 40 μM, but induced apoptosis at the dose of 80 μM, and the apoptosis rate was 31.7%.
  • 体内实验
    Animal Model:Male KM mice modelDosage:1.25 mg/kg, 2.5mg/kg, 5 mg/kg Administration:Intraperitoneal injection (i.p.); Once daily for 7 days Result:Inhibited the growth of H22 tumor cells with inhibition rates of 39.9% (2.5 mg/kg) and 49.3%(5 mg/kg), respectively.Inhibited the growth of S108 tumor cells with inhibition rates of 22.4% (2.5 mg/kg) and 42.2%(5 mg/kg), respectively.Significantly decreased vascular index with inhibition rates of 34.4% (2.5 mg/kg) and 44.3% (5 mg/kg).Animal Model: Male C57BL/6 mice model Dosage:50 mg/kg, 100 mg/kg Administration:Intraperitoneal injection (i.p.); Single dose. 2 h before the cecal ligation and puncture (CLP) operation. Result:Increased the expression of TNF-α, IL-1β and IL-6 in a dose-dependent manner.Increased the levels of superoxide dismutase (SOD) and glutathione (GSH), and decreased the levels of malondialdehyde (MDA) and myeloperoxidase (MPO).Inhibit the phosphorylation of p65.
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    nAChR| TRPA1| TRPV3| TRPM8
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    473-15-4
  • 分子量
    222.37
  • 分子式
    C15H26O
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (449.70 mM)
  • SMILES
    CC(C)(O)[C@@H]1CC[C@@]2(C)CCCC(=C)[C@@H]2C1
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Kimura M, et al. Mechanism of the blocking action of beta-eudesmol on the nicotinic acetylcholine receptor channel in mouse skeletal muscles[J]. Neuropharmacology, 1991, 30(8):835-41.
产品手册
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