Vasicinone
CAS No. 486-64-6
Vasicinone ( —— )
产品货号. M24440 CAS No. 486-64-6
Vasicinone 可作为肝脏保护剂。 (±)-Vasicinone 具有显着的镇咳、祛痰和支气管扩张活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1891 | 有现货 |
|
| 10MG | ¥2993 | 有现货 |
|
| 25MG | ¥4622 | 有现货 |
|
| 50MG | ¥6501 | 有现货 |
|
| 100MG | ¥8478 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥1691 | 有现货 |
|
生物学信息
-
产品名称Vasicinone
-
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Vasicinone 可作为肝脏保护剂。 (±)-Vasicinone 具有显着的镇咳、祛痰和支气管扩张活性。
-
产品描述Vasicinone may act as a hepatoprotective agent. (±)-Vasicinone has significant antitussive, expectorant, and bronchodilating activities, which can be used to treat respiratory disease.(S)-Vasicinone exhibits antiproliferative activity against human gastric cancer cells MCG-803.
-
体外实验Vasicinone (1~30 μM; 24 hours; SH-SY5Y cells) significantly reverses the paraquat-induced reduction in cell viability.Vasicinone (10 and 15 μM; 24 hours; SH-SY5Y cells) abates the paraquat-induced injury of SH-SY5Y cells by suppressing the MAPK signaling pathway, dose-dependently reduces the percentage of apoptotic cells and is capable of rescuing paraquat-induced apoptotic death.Vasicinone (10 and 15 μM; SH-SY5Y cells) attenuates the paraquat-induced accumulation of reactive oxygen species (ROS) and attenuates the paraquat-induced expression of apoptotic proteins.Cell Viability Assay Cell Line:SH-SY5Y cells Concentration:1~30 μM Incubation Time:24 hours Result:Significantly reversed the paraquat-induced reduction in cell viability.Western Blot Analysis Cell Line:SH-SY5Y cells Concentration:10 and 15 μM Incubation Time:24 hours Result:Abated the paraquat-induced injury of SH-SY5Y cells by suppressing the MAPK signaling pathway.Apoptosis Analysis Cell Line:SH-SY5Y cells Concentration:10 and 15 μM Incubation Time:24 hours Result:Dose-dependently reduced the percentage of apoptotic cells.
-
体内实验——
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体Others
-
研究领域——
-
适应症——
化学信息
-
CAS Number486-64-6
-
分子量202.21
-
分子式C11H10N2O2
-
纯度>98% (HPLC)
-
溶解度DMSO:10 mM
-
SMILESC1CN2C(=NC3=CC=CC=C3C2=O)[C@H]1O
-
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.Antitussive, expectorant, and bronchodilating effects of quinazoline alkaloids (±)-vasicine, deoxyvasicine, and (±)-vasicinone from aerial parts of Peganum harmala L. Phytomedicine. 2015 Nov 15;22(12):1088-95.
产品手册
关联产品
-
Murepavadin TFA
Murepavadin (TFA) is a 14-amino acid cyclic peptide that is a potent, specific antibiotic used to treat bacterial infections caused by Pseudomonas aeruginosa.Murepavadin (TFA) targets the LPS transporter portin D.
-
Cyclohexanecarboxyli...
环己烷甲酸是一种调味成分。
-
DZ2002
DZ2002 是一种口服有效的、可逆的、低细胞毒性的 III 型 SAHH 抑制剂 (Ki=17.9 nM),具有较好的免疫抑制活性。DZ2002 能通过逆转各种细胞类型的促纤维化表型来防止实验性皮肤纤维化的发展。DZ2002 可用于自身免疫性疾病,如狼疮综合征和系统性硬化症的研究。
021-51111890
购物车()
sales@molnova.cn

