DFP00173
CAS No. 672286-03-2
DFP00173 ( —— )
产品货号. M26152 CAS No. 672286-03-2
DFP00173 是一种有效的选择性水通道蛋白 3 (AQP3) 抑制剂。 DFP00173 抑制小鼠和人类 AQP3,IC50 约为 0.1-0.4 μM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥779 | 有现货 |
|
| 10MG | ¥1245 | 有现货 |
|
| 25MG | ¥1841 | 有现货 |
|
| 50MG | ¥3125 | 有现货 |
|
| 100MG | ¥4302 | 有现货 |
|
| 200MG | ¥5994 | 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 | ¥857 | 有现货 |
|
生物学信息
-
产品名称DFP00173
-
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DFP00173 是一种有效的选择性水通道蛋白 3 (AQP3) 抑制剂。 DFP00173 抑制小鼠和人类 AQP3,IC50 约为 0.1-0.4 μM。
-
产品描述DFP00173 is a potent and selective aquaporin 3 (AQP3) inhibitor. DFP00173 inhibits mouse and human AQP3 with IC50 of ~0.1-0.4 μM. Compared with the homologous AQP subtypes AQP7 and AQP9, DFP00173 is selective for AQP3.(In Vitro):DFP00173 inhibits the glycerol permeability of human red blood cells with IC50 of ~0.2 μM.
-
体外实验DFP00173 inhibits the glycerol permeability of human erythrocytes with an IC50 of ~0.2 μM.
-
体内实验——
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number672286-03-2
-
分子量332.16
-
分子式C11H7Cl2N3O3S
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : ≥ 100 mg/mL (301.06 mM)
-
SMILES[O-][N+](=O)c1cc(NC(=O)Nc2c(Cl)cccc2Cl)cs1
-
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.S Moein Moghimi, et al. Allergic Reactions and Anaphylaxis to LNP-Based COVID-19 Vaccines. Mol Ther. 2021 Mar 3;29(3):898-900.
产品手册
关联产品
-
ATP dimagnesium
ATP (Adenosine 5'-triphosphate) dimagnesium 是体内能量储存和代谢的重要物质,为代谢提供能量,同时在细胞中作为辅酶发挥作用。ATP dimagnesium 是免疫和炎症中重要的内源性信号分子。
-
Ganoderenic acid E
Ganoderenic acid E is a natural product.
-
ELA-32 (human)
Potent, high affinity apelin receptor agonist (IC50 = 0.27 nM; Kd = 0.51 nM). Exhibits no binding GPR15 and GPR25. Activates the PI3K/AKT pathway and promotes self-renewal of hESCs via cell-cycle progression and protein translation. Also potentiates the TGFβ pathway, priming hESCs toward the endoderm lineage. Stimulates angiogenesis in HUVEC cells. Relaxes mouse aortic vessels. Functions as an anorexigenic hormone through activation of the AVP and CRH neurons in the PVN.
021-51111890
购物车()
sales@molnova.cn

