DMA trihydrochloride; 纯度: 98.01%
DMA trihydrochloride 是一种荧光化合物 (λex=340 nm, λem=478 nm)。
DMA trihydrochloride Chemical Structure
CAS No. : 2095832-33-8
| 规格 | 价格 | 是否有货 | 数量 |
|---|---|---|---|
| Free Sample (0.1-0.5 mg) | ; | Apply now | ; |
| 10;mM;*;1 mL in Water | ￥763 | In-stock | |
| 5 mg | ￥600 | In-stock | |
| 10 mg | ￥900 | In-stock | |
| 25 mg | ￥2000 | In-stock | |
| 50 mg | ￥3600 | In-stock | |
| 100 mg | ￥6600 | In-stock | |
| 200 mg | ; | 询价 | ; |
| 500 mg | ; | 询价 | ; |
* Please select Quantity before adding items.
DMA trihydrochloride 相关产品
bull;相关化合物库:
- Bioactive Compound Library Plus
- Anti-Cancer Compound Library
| 生物活性 |
DMA trihydrochloride is a fluorescent compound (λex=340 nm, λem=478 nm). |
IC50 Target |
IC50: 3.4 μM (HeLa cell), 5.3 μM (MCF7 cell)[1] |
||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 体外研究 (In Vitro) |
The newly synthesized bisbenzimidazole derivatives DMA (6c) is evaluated for their cytotoxicity against human tumor cell lines, which are cervix carcinoma cell line (HeLa), breast carcinoma cell line (MCF7) and brain glioma cell line (U87) in comparison to Hoechst. In case of MCF7, the IC50 is observed at 5.3 μM for DMA. The IC50 determined in the case of HeLa is 3.4 μM for DMA[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
||||||||||||||||
| Clinical Trial |
|
||||||||||||||||
| 分子量 |
577.93 |
||||||||||||||||
| Formula |
C27H31Cl3N6O2 |
||||||||||||||||
| CAS 号 |
2095832-33-8 |
||||||||||||||||
| 运输条件 |
Room temperature in continental US; may vary elsewhere. |
||||||||||||||||
| 储存方式 |
4deg;C, sealed storage, away from moisture and light *In solvent : -80deg;C, 6 months; -20deg;C, 1 month (sealed storage, away from moisture and light) |
||||||||||||||||
| 溶解性数据 |
In Vitro:;
H2O : 15.9 mg/mL (27.51 mM; Need ultrasonic and warming) 配制储备液
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。 |
||||||||||||||||
| 参考文献 |
|
| Cell Assay |
Various human tumor cells (U87, HeLa and MCF7) are maintained as monolayer at 37°C in 5% CO2 using DMEM medium. Approximately 3000-8000 cells/well are seeded in 96-well plates containing 200 μL of medium and incubated for 24 h. The culture medium is replaced by fresh medium containing 1, 10, 50, 100 μM of DMA (6c) and incubated for 24, 48 and 72 h. The cell viability is determined by the MTT assay. The light absorbance is measured using a microplate reader[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
|---|---|
| 参考文献 |
|
