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 Number473-15-4
-
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)
-
SMILESCC(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
关联产品
-
UNC6934
UNC6934 是一种针对 NSD2 N 端 PWWP (PWWP1) 结构域的化学探针。
-
INCA-6
INCA-6 是活化 T 细胞核因子 (NFAT) 和钙调神经磷酸酶-NFAT 信号传导的抑制剂。
-
Anantin (linear sequ...
Anantin binds competitively to the receptor of atrial natriuretic factor (ANF) from bovine adrenal cortex (Kd = 0.6 μM) and acts as natriuretic peptide receptor A antagonist.
021-51111890
购物车()
sales@molnova.cn

