1674364-87-4
1674364-87-4 结构式
基本信息
中文别名
化合物 T15169 英文别名
DS-437DS-437 (DS437
DS-437 >=98% (HPLC)
Adenosine, 5'-S-[2-[[(ethylamino)carbonyl]amino]ethyl]-5'-thio-
DS-437价格(试剂级)
报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
2024/08/19 | HY-124131 | DS-437 DS-437 | 1674364-87-4 | 5mg | 800元 |
2024/08/19 | HY-124131 | DS-437 DS-437 | 1674364-87-4 | 10mM * 1mLin DMSO | 880元 |
2024/08/19 | HY-124131 | DS-437 DS-437 | 1674364-87-4 | 10mg | 1300元 |
常见问题列表
生物活性
DS-437 是双重蛋白精氨酸甲基转移酶 PRMT5/7 抑制剂,对两者的 IC50 均为 6 μM。 与其他 29 种人类蛋白质,DNA 和 RNA 甲基转移酶相比,DS-437 对 PRMT5 和 PRMT7 具有选择性。DS-437是 SAM 竞争性抑制剂。DS-437 还抑制 DNMT3A 和 DNMT3B,IC50 分别为 52 和 62 μM。DS-437 抑制 FOXP3 的甲基化。体外研究
DS-437 was able to inhibit methylation of an H4[1–24] peptide by the PRMT5–MEP50 complex under balanced conditions (cofactor and substrate concentrations set at their respective Km values) in a dose-dependent manner with an IC50 of 5.9 ± 1.4 μM.
DS-437 increased total CD8
+
and CD8
+
PD-1
+
T cells.
体内研究
DS-437 (10 mg/kg; i.p.; 5 times a week) has some beneficial effects on inhibiting tumor growth. The combination of DS-437 and the anti-p185 erbB2/neu antibody 4D5 had even more dramatic effects.
Animal Model: | Six to Ten weeks old female Balb/c mice (bearing CT26Her2 tumor cells) |
Dosage: | 10 mg/kg |
Administration: | i.p.; 5 times a week |
Result: | Had some beneficial effects on inhibiting tumor growth. |