相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 保质期:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 英文名:
Dehydrocorydaline Chloride
- 库存:
现询
- 供应商:
北京索莱宝科技有限公司
- CAS号:
10605-03-5
- 规格:
50mg/25mg/10mg/5mg/1mg
| 规格: | 50mg | 产品价格: | ¥4953.0 |
|---|---|---|---|
| 规格: | 25mg | 产品价格: | ¥3465.0 |
| 规格: | 10mg | 产品价格: | ¥1990.0 |
| 规格: | 5mg | 产品价格: | ¥1390.0 |
| 规格: | 1mg | 产品价格: | ¥523.0 |
| 基本信息 | |
| CAS | No.10605-03-5 |
| 中文名称 | 盐酸脱氢紫堇碱 |
| 英文名称 | Dehydrocorydaline Chloride |
| 别名 | 盐酸脱氢紫堇碱;dehydrocorydalinechloride;ddehydrocorydalinechloride;Dansyl-D-Phe; |
| 分子式 | C22H24ClNO4 |
| 分子量 | 401.88 |
| 溶解性 | Soluble in DMSO |
| 纯度 | ≥98% |
| 外观(性状) | Light yellow to yellow Solid |
| 储存条件 | Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year |
| MDL | MFCD01937870 |
| SMILES | CC1=C2C=CC(=C(C2=C[N+]3=C1C4=CC(=C(C=C4CC3)OC)OC)OC)OC.[Cl-] |
| 靶点 | AChE |
| 通路 | Neuronal Signaling |
| 背景说明 | Dehydrocorydaline Chloride是一种 AChE 抑制剂。 |
| 生物活性 | Dehydrocorydaline chloride (13-Methylpalmatine chloride) is an alkaloid that regulates protein expression of Bax, Bcl-2; activates caspase-7, caspase-8, and inactivates PARP. Dehydrocorydaline chloride elevates p38 MAPK activation. Anti-inflammatory and anti-cancer activities[1-2]. |
| In Vitro | Dehydrocorydaline significantly inhibits MCF-7 cell proliferation in a dose- dependent manner, which can be reversed by a caspase-8 inhibitor, Z-IETD-FMK. Dehydrocorydaline increases DNA fragments without affecting ΔΨm. Western blotting assay shows that dehydrocorydaline dose-dependently increases Bax protein expression and decreases Bcl-2 protein expression. Furthermore, dehydrocorydaline induces activation of caspase-7,-8 and the cleavage of PARP without affecting caspase-9. These results show that dehydrocorydaline inhibits MCF-7 cell proliferation by inducing apoptosis mediated by regulating Bax/Bcl-2, activating caspases as well as cleaving PARP[1].Treatment of C2C12 myoblasts with 500 nM Dehydrocorydaline increases the expression levels of muscle-specific proteins, including MyoD, myogenin and myosin heavy chain. Treatment with Dehydrocorydaline elevates p38 MAPK activation and the interaction of MyoD with an E protein. Furthermore, defects in differentiation-induced p38 MAPK activation and myoblast differentiation induced by depletion of the promyogenic receptor protein Cdo in C2C12 myoblasts are restored by Dehydrocorydaline treatment[2]. |
| 细胞实验 | Briefly, MCF-7 cells (1×104 cells/well) are seeded in 96-well plates and treated with different concentrations of dehydrocorydaline (0-200 μM) for 24 h. The cell viability is determined. To explore the role of caspase-8 in dehydrocorydaline induced cytotoxicity, a caspase-8 inhibitor Z-IETD-FMK (10 μM) is co-incubated with 200 μM dehydrocorydaline.[1] |
| 数据来源文献 | [1]. Xu Z, et al. Dehydrocorydaline inhibits breast cancer cells proliferation by inducing apoptosis in MCF-7 cells. Am J Chin Med. 2012;40(1):177-85. [2]. Yoo M, et al. Dehydrocorydaline promotes myogenic differentiation via p38 MAPK activation. Mol Med Rep. 2016 Oct;14(4):3029-36. |
| 单位 | 瓶 |
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Sci Signal 封面文章:赵振东 / 王健伟等揭示转录因子 ID2 抑制抗病毒天然免疫机制
-induced activation of IRF3 的研究论文,并被选为当期期刊封面。 宿主细胞通过模式识别受体(PRR)识别病原体核酸、蛋白等分子模式(PMP),激活下游信号通路,通过分子级联反应诱导 I 型干扰素(IFN-I)和 III 型干扰素(IFN-III)的产生,发挥抗病毒作用。其中,TBK1/IKKε-IRF3 信号转导在病毒诱导的天然免疫应答中发挥至关重要的作用。 ID2 是一种转录调节分子,属于 ID 蛋白家族成员,主要发挥基因的转录调控作用。ID2 在多种细胞,尤其是免疫细胞的发育
测定 144-62-7 20mg SAC2020 N-乙酰神经氨酸 含量测定 131-48-6 20mg SAC2021 原儿茶酸 含量测定 99-50-3 20mg 注:除此之外还有更多可溯源 含量标准品, 欢迎登录索莱宝商城及微官网
); 固件包括符合0SI七层协议的LonTalk协议,I/0驱动程序和事件驱动多任务调度程序; 服务引脚用于远程识别和诊断; 48位内部Neuron ID用于唯一识别Neuron芯片; 在两大系列中,3120芯片内部包含E2PROM、RAM和ROM存储器,而3150芯片内部无ROM,但拥有访问外部存储器的接口,可根据实际情况灵活配置存储器。 (2)收发器 提供神经芯片与Lonworks网络的物理
技术资料暂无技术资料 索取技术资料











