749234-11-5
基本信息
4,5,6,7-四溴-N,N-二甲基-1H-苯并[D]咪唑-2-胺
DMAT(CK2 Inhibitor)
CASEIN KINASE II INHIBITOR
CK2 INHIBITOR
2-Dimethylamino-4,5,6,7-tetrabromobenzimidazole
4,5,6,7-tetrabromo-N,N-dimethyl-1H-benzimidazol-2-amine
1H-Benzimidazol-2-amine, 4,5,6,7-tetrabromo-N,N-dimethyl-
4,5,6,7-tetrabroMo-N,N-diMethyl-1H-benzo[d]iMidazol-2-aMine
物理化学性质
| 熔点 | >330℃ (Decomposition) |
| 沸点 | 497.7±55.0 °C(Predicted) |
| 密度 | 2.410±0.06 g/cm3(Predicted) |
| 储存条件 | -20°C储存 |
| 溶解度 | ≥23.85 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O |
| 酸度系数(pKa) | 4.55±0.30(Predicted) |
| 形态 | 固体 |
| 颜色 | White to off-white |
| InChI | 1S/C9H7Br4N3/c1-16(2)9-14-7-5(12)3(10)4(11)6(13)8(7)15-9/h1-2H3,(H,14,15) |
| InChIKey | SLPJGDQJLTYWCI-UHFFFAOYSA-N |
| SMILES | CN(C)c1nc2c(Br)c(Br)c(Br)c(Br)c2[nH]1 |
安全数据
| 危险性符号(GHS) |  GHS07 |
| 警示词 | 警告 |
| 危险性描述 | H315-H319-H335 |
| 防范说明 | P261-P264-P271-P280-P302+P352-P305+P351+P338 |
| WGK Germany | WGK 3 |
| 存储类别 | 11 - Combustible Solids |
| 危险性类别 | Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
2-二甲基氨基-4,5,6,7-四溴苯并咪唑价格(试剂级)
| 报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
| 2026/09/15 | HY-15535 | 2-二甲基氨基-4,5,6,7-四溴苯并咪唑 DMAT | 749234-11-5 | 5 mg | 465元 |
| 2026/09/15 | HY-15535 | 2-二甲基氨基-4,5,6,7-四溴苯并咪唑 DMAT | 749234-11-5 | 10 mM * 1 mL in DMSO | 488元 |
| 2026/09/15 | HY-15535 | 2-二甲基氨基-4,5,6,7-四溴苯并咪唑 DMAT | 749234-11-5 | 10 mg | 744元 |
常见问题列表
|
CK2 0.13 μM (IC 50 , Human CK2) |
PIM1 0.148 μM (IC 50 ) |
PIM2 1.6 μM (IC 50 ) |
PIM3 0.097 μM (IC 50 ) |
HIPK2 0.37 μM (IC 50 ) |
HIPK3 0.59 μM (IC 50 ) |
DYRK1a 0.41 μM (IC 50 ) |
DYRK2 0.35 μM (IC 50 ) |
DYRK3 1.7 μM (IC 50 ) |
PKD1 0.18 μM (IC 50 ) |
CDK2 0.64 μM (IC 50 ) |
DMAT (1 μM-2.5 μM) DMAT is more efficient in killing antiestrogen resistant cells than parental antiestrogen sensitive MCF-7 cells. DMAT-induced cell death of antiestrogen resistant cells is mediated by caspases. DMAT inhibits CK2 activity but the inhibition is similar in the three cell lines, MCF-7, TAMR-1 and 182R-6. DMAT has effects on H295R cell proliferation at concentrations of 10 -4 and 10 -5 mol/Las compared with the control. DMAT (100 μM) significantly increases apoptosis of H295R cells. DMAT (1 nM-1 μM) significantly decreases aldosterone release into supernatants of 72-h H295R cell cultures as compared with the control. DMAT also inhibits PIM1 by a mechanism which is competitive with respect to ATP, and it is a powerful inhibitor of kinases other than CK2.
DMAT application in vivo reduces tumor growth in a xenotransplant model by interference with tumor cell proliferation. Biochemical parameters and histology following DMAT administration revealed no alterations in liver tissue.