4-(苯并[D]噻唑-2-基)-2-甲氧基苯酚
4-(苯并[D]噻唑-2-基)-2-甲氧基苯酚
4-(苯并[D]噻唑-2-基)-2-甲氧基苯酚 性质
| 储存条件 | 2-8°C |
|---|---|
| 溶解度 | DMF:30mg/mL; DMSO:30mg/mL; DMSO:PBS (pH 7.2) (1:9):0.1 mg/ml;乙醇:1mg/mL |
| 形态 | 结晶固体 |
| 颜色 | 浅黄至黄色 |
4-(苯并[D]噻唑-2-基)-2-甲氧基苯酚 用途与合成方法
YL-109 (0.001-10 μM; 96 h or 24 h) inhibits cell proliferation, motility, and invasiveness in breast cancer cells.
YL-109 (1 μM) increases both CHIP mRNA and protein levels in MDA-MB-231 cells.
Cell Proliferation Assay
| Cell Line: | MCF-7 and MDA-MB-231 cells |
| Concentration: | 0.001, 0.01, 0.1, 1, 10 μM |
| Incubation Time: | 96 hours |
| Result: | Strongly inhibited cell proliferation of MCF-7 and MDA-MB-231 cells in a dose-dependent manner (IC 50 =85.8 nM and 4.02 μM, respectively). |
YL-109 (15 mg/kg; s.c. for every 2 d) inhibits both tumor growth and cancer metastasis of breast cancer cells in vivo.
| Animal Model: | BALB/cAjcl-nu/nu female mice (4-5 weeks) inoculated with MCF-7 or MDA-MB-231 cells |
| Dosage: | 15 mg/kg |
| Administration: | S.c. every 2 days for 63 days |
| Result: | Suppressed tumor growth in mice injected with MCF-7 and MDA-MB-231 cells. |
121-33-5
137-07-5
36341-25-0
以香兰素和2-氨基苯硫酚为原料合成2-(4-羟基-3-甲氧基苯基)苯并噻唑的一般步骤:在催化反应中,将香兰素(3mmol)、2-氨基苯硫酚(3mmol)和CdS纳米球(5mg)的混合物置于100mL双壁石英烧瓶中,该烧瓶配备有水入口和出口以维持反应温度在室温。反应在甲醇(20mL)中进行,并在搅拌条件下将反应混合物暴露于可见光下照射指定时间(参见表3)。反应进程通过薄层色谱(TLC)和气相色谱(GC)监测。反应完成后,通过旋转蒸发去除甲醇,将残余物溶解于二氯甲烷中。通过离心分离催化剂与反应混合物。随后,蒸发二氯甲烷至干,产物通过硅胶G60柱色谱法进行纯化。
参考文献:
[1] Chemistry Letters, 2004, vol. 33, # 3, p. 274 - 275
[2] Tetrahedron Letters, 2013, vol. 54, # 9, p. 1090 - 1096
[3] Heterocycles, 2007, vol. 71, # 8, p. 1837 - 1842
[4] Research on Chemical Intermediates, 2015, vol. 41, # 10, p. 7509 - 7516
[5] Journal of Heterocyclic Chemistry, 2009, vol. 46, # 1, p. 91 - 95
4-(苯并[D]噻唑-2-基)-2-甲氧基苯酚 价格(试剂级)
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2025-12-22 | HY-18619 | 4-(苯并[D]噻唑-2-基)-2-甲氧基苯酚 | 36341-25-0 | 5mg | 550 |
| 2025-12-22 | HY-18619 | 4-(苯并[D]噻唑-2-基)-2-甲氧基苯酚 | 36341-25-0 | 10mM * 1mLin DMSO | 600 |