Sinomenine Hydrochloride
Cat.No:IS0900 Solarbio
CAS:6080-33-7
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:White to off-white Solid
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Sinomenine HydrochlorideCAS:6080-33-7
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:White to off-white Solid
Qty:
Size:
CAS | 6080-33-7 |
Name | Sinomenine Hydrochloride |
Molecular Formula | C19H23NO4·HCl |
Molecular Weight | 365.85 |
Solubility | Soluble in DMSO |
Purity | HPLC≥98% |
Appearance | White to off-white Solid |
Storage | Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year |
MDL | MFCD01714307 |
SMILES | OC(C1=C2C[C@@]3([H])[C@](C=C4OC)([H])[C@@]1(CCN3C)CC4=O)=C(C=C2)OC.Cl |
Target Point | NF-kB |
Passage | NF-κB |
Background | Sinomenine hydrochloride is a blocker of NF-κB activation and an activator of the μ-opioid receptor. |
Biological Activity | Sinomenine hydrochloride 是 NF-κB 活化的阻断剂,也是 μ 阿片受体 (μ-opioid receptor) 的激活剂。[1-3] |
In Vitro | 随着盐酸青藤碱浓度的增加,细胞活力逐渐降低。通过0.25,0.5和1mM的盐酸青藤碱处理,MDA-MB-231细胞的迁移能力显著减弱。伤口愈合测定显示0.25和0.5mM盐酸青藤碱显著抑制伤口愈合。当用0.5mM盐酸青藤碱处理MDA-MB-231细胞时,愈合进程约为50%,但在用0.25mM盐酸青藤碱和未处理对照处理的组中,愈合率为约80%和接近95%,分别。 NF-κB(IκB)抗体IP抑制剂后的IB检测显示,盐酸青藤碱以剂量依赖性方式抑制NF-κB与IκB的结合[1]。 |
In Vivo | Ip青藤碱盐酸盐在雄性大鼠的热板和甩尾试验中以40mg/kg产生抗伤害感受,但在较低剂量(10或20mg/kg)时不产生。 10至40 mg/kg盐酸青藤碱不会产生任何可观察到的副作用,如镇静,过敏或运动障碍。在80mg/kg时,盐酸青藤碱在大鼠中是温和的镇静剂。腹腔注射80mg/kg的盐酸青藤碱在小鼠中不会产生任何可观察到的副作用。 Ip或po盐酸青蒿素40或80mg/kg剂量依赖性地降低神经损伤小鼠的机械超敏反应。 Ip青藤碱盐酸盐40mg/kg,但不低剂量或载体,显著降低机械和冷异常性疼痛持续长达240分钟而不产生运动缺陷或镇静[2]。在剂量为10至40mg/kg时,盐酸青藤碱剂量依赖性地增加缩爪阈值。在非慢性收缩性损伤(CCI)健康大鼠中,剂量范围为10至40mg/kg的盐酸青藤碱不会改变强迫游泳试验中的不动行为[3]。 |
Cell Experiment | 在该研究中使用MDA-MB-231人三阴性和4T1小鼠乳腺癌细胞系。对于实验,细胞以3.5×10 4个细胞/孔在24孔板中生长。在含有不同浓度的盐酸青藤碱的培养基中孵育24或48小时后,根据制造商的说明书[1]用细胞计数试剂盒-8溶液检测细胞的增殖。 |
Animal Experiment | 在该实验中使用重250至300g的雄性Sprague-Dawley大鼠。对于急性盐酸青藤碱研究的作用持续时间,在手术后1天施用不同剂量的盐酸青藤碱(10至40mg/kg),然后每30分钟测量缩爪阈值4小时。对于涉及每日盐酸青藤碱治疗的研究,在每日药物治疗后3小时进行机械痛觉过敏测量。对于拮抗剂研究,在40mg/kg盐酸青藤碱给药前10分钟给予拮抗剂[3]。 |
Data Literature Source | [1]. Song L,et al. Sinomenine inhibits breast cancer cell invasion and migration by suppressing NF-κB activation mediated by IL-4/miR-324-5p/CUEDC2 axis. Biochem Biophys Res Commun. 2015 Aug 28;464(3):705-10. [2]. Gao T,et al. Analgesic effect of sinomenine in rodents after inflammation and nerve injury. Eur J Pharmacol. 2013 Dec 5;721(1-3):5-11. [3]. Zhu Q,et al. Antinociceptive effects of sinomenine in a rat model of neuropathic pain. Sci Rep. 2014 Dec 1;4:7270. |
Unit | Bottle |
Specification | 20mg 10mM*1mL in DMSO 50mg 100mg |
Sinomenine hydrochloride 是 NF-κB 活化的阻断剂,也是 μ 阿片受体 (μ-opioid receptor) 的激活剂。
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
Note:
1. The products are all for scientific research use only. Do not use it for medical, clinical diagnosis or treatment, food and cosmetics, etc. Do not store them in ordinary residential areas.
2. For your safety and health, please wear laboratory clothes, disposable gloves and masks.
3. The experimental results may be affected by many factors, after-sale service is limited to the product itself and does not involve other compensation.
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Sinomenine alleviates lipopolysaccharide-induced acute lung injury via a PPARβ/δ-dependent mechanism
Click to check >>Author:Li Zhao, Mengjie Zhang, Yang-Wuyue Liu, Yan Tan, Jun Yin, Yuanyuan Chen, Dewei Chen, Bing Ni
IF:5.0000
Publish_to:EUROPEAN JOURNAL OF PHARMACOLOGY
PMID:37307937