
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)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1191 | 有现货 |
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10MG | ¥1847 | 有现货 |
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25MG | ¥3151 | 有现货 |
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50MG | ¥4641 | 有现货 |
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100MG | 获取报价 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称beta-Eudesmol
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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
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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。
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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.
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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%.
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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.
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同义词——
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通路Others
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靶点Other Targets
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受体nAChR| TRPA1| TRPV3| TRPM8
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研究领域——
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适应症——
化学信息
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CAS Number473-15-4
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分子量222.37
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分子式C15H26O
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (449.70 mM)
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SMILESCC(C)(O)[C@@H]1CC[C@@]2(C)CCCC(=C)[C@@H]2C1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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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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