中文名 | 1,2,4,5-苯四胺四盐酸盐 |
英文名 | 1,2,4,5-tetraaminobenzene tetra hydrochloride |
别名 | 1,2,4,5-苯四胺 FAK自磷酸化抑制剂(Y15 1,2,4,5-苯四胺四盐酸盐 苯-1,2,4,5-四胺四盐酸盐 1,2,4,5-TETRAAMINOBENZENE 四盐酸盐 1,2,4,5-苯四胺 四盐酸盐,1,2,4,5-BENZENETETRAMINE TETRAHYDROCHLORIDE 1,2,4,5-苯四胺四盐酸盐,1,2,4,5-BENZENETETRAAMINE TETRAHYDROCHLORIDE 1,2,4,5-苯四胺四盐酸盐,1,2,4,5-BENZENETETRAAMINE TETRAHYDROCHLORIDE,1,2,4,5-苯四胺 四盐酸盐,1,2,4,5-BENZENETETRAMINE TETRAHYDROCHLORIDE |
英文别名 | benzene-1,2,4,5-tetramine 1,2,4,5-BenzenetetraminetetraHCl 1,2,4,5-BENZENETETRAMINE TETRAHYDROCHLORIDE 1,2,4,5-Benzenetetraamine tetrahydrochloride benzene-1,2,4,5-tetramine tetrahydrochloride 1,2,4,5-TETRAAMINOBENZENE TETRAHYDROCHLORIDE 1,2,4,5-benzenetetramine tetrahydro-chloride 1,2,4,5-tetraaminobenzene tetra hydrochloride (2,4,5-triaminophenyl)amine tetrahydrochloride benzene-1,2,4,5-tetrayltetraamine tetrahydrochloride 1,2,4,5-BENZENETETRAMINE TETRAHYDRO-CHLO RIDE, TECH. 1,2,4,5-Benzenetetramine tetrahydrochloride, 1,2,4,5-Tetraaminobenzene tetrahydrochloride |
CAS | 4506-66-5 |
EINECS | 224-822-6 |
化学式 | C6H11ClN4 |
分子量 | 174.63 |
InChI | InChI=1/C6H10N4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H,7-10H2 |
InChIKey | BZDGCIJWPWHAOF-UHFFFAOYSA-N |
密度 | 1.401g/cm3 |
熔点 | ≥300°C(lit.) |
沸点 | 400.9°C at 760 mmHg |
闪点 | 233.6°C |
蒸汽压 | 1.23E-06mmHg at 25°C |
溶解度 | H2O: 可溶物20mg/mL,澄清 |
折射率 | 1.827 |
存储条件 | room temp |
稳定性 | 从提供的购买之日起稳定2年。DMSO或蒸馏水中的溶液可以在-20 ° 下储存长达1个月。 |
外观 | 粉末 |
颜色 | , faint purple to dark brown |
BRN | 3701344 |
体外研究 | Y15 directly blocks autophosphorylation activity of FAK. Y15 inhibits Y397 phosphorylation of FAK starting at 0.1 μM in Panc-1 cells. At a dose of 100 μM, Y15 has the same or better inhibition as TAE226. Of note, total FAK is downregulated at higher doses of Y15. Y15 also blocks phosphorylation of the FAK downstream substrate, paxillin. Total paxillin is decreased at higher doses similar to FAK. Thus, Y15 inhibits FAK phosphorylation in a dose-dependent manner. MTS assay is completed using a range of Y15 doses on all cell lines (TT, K1, BCPAP, and TPC1, respectively).Y15 inhibited cell viability in a dose-dependent manner across all thyroid cell lines evaluated. IC 50 is 2.05, 5.74, 9.99, and 17.54 μM for TT, TPC1, BCPAP, and K1, respectively. |
体内研究 | Nude mice bearing Panc si-ctrl xenografts are treated with TAE226, a dual FAK and IGF-1R tyrosine kinase inhibitor, to provide a reference for the antitumor effect of dual inhibition of FAK and IGF-1R. Without drug treatment, Panc si5-IGF-1R xenografts grew slower than Panc si-ctrl xenografts (Panc si5-IGF-1R/PBS vs. Panc si-ctrl/PBS), suggesting moderate tumor suppression by inhibiting the IGF-1R pathway only. Further inhibition of FAK activity by Y15 treatment suppresses the growth of Panc si5-IGF-1R xenografts more drastically (Panc si5-IGF-1R/PBS vs. Panc si5-IGF-1R/Y15). A similar antitumor effect is seen in Panc si-ctrl xenografts treated with TAE226 (Panc si5-IGF-1R/Y15 vs. Panc si-ctrl/TAE226). Mice demonstrates normal grooming and eating habits throughout the experiment. |
危险品标志 | Xi - 刺激性物品 |
风险术语 | 36/37/38 - 刺激眼睛、呼吸系统和皮肤。 |
安全术语 | S26 - 不慎与眼睛接触后,请立即用大量清水冲洗并征求医生意见。 S36 - 穿戴适当的防护服。 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 10 |
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