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CAS RN: 117946-91-5 | 产品编码: L0316
Luzindole

产品编码 | L0316 |
纯度/分析方法 ![]() |
>98.0%(HPLC) |
分子式/分子量 | C__1__9H__2__0N__2O = 292.38 |
外观与形状(20°C) | 固体 |
储存温度 ![]() |
冷冻 (-20°C) |
应避免的情况 | 加热 |
包装和容器 ![]() |
25MG-Glass Bottle with Plastic Insert (查看图片) |
CAS RN | 117946-91-5 |
Reaxys-RN | 8156010 |
PubChem物质ID | 354335145 |
MDL编号 | MFCD00672498 |
技术规格
Appearance | White to Light yellow to Light orange powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Nonaqueous Titration) | min. 95.0 % |
Melting point | 104.0 to 108.0 °C |
物性(参考值)
熔点 | 106 °C |
GHS
相关法规
RTECS# | AC7765700 |
运输信息
HS编码* | 2933.99-000 |
应用
Luzindole: A Selective MT2 Melatonin Receptor Antagonist
Luzindole (N-0774) is a G protein-coupled melatonin receptors (MT receptors) antagonist.1) Reportedly, luzindole acts as a selective melatonin receptor antagonist with approximately 11- to 25-fold greater affinity for the MT2 over the MT1 receptor.2,3) Therefore, luzindole is used to evaluate the roles of melatonin receptors.4) In addition, it is reported that luzindole has radical scavenging and antioxidant properties due to the chemical nature of the indoleamine.4,5) (cf. a related product: Melatonin [M1105])
References
- 1)Luzindole (N-0774): a novel melatonin receptor antagonist
- 2)Pharmacological characterization of human recombinant melatonin MT1 and MT2 receptors
- 3)Selective MT2 melatonin receptor antagonists block melatonin-mediated phase advances of circadian rhythms
- 4)Molecular tools to study melatonin pathways and actions (a review)
- 5)Melatonin receptor antagonist luzindole is a powerful radical scavenger in vitro
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