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21306-65-0

中文名称 S-[4-(苄氧基)苯基]-S-甲基-N-(对甲苯基磺酰基)-硫亚胺
英文名称 NPD-123
CAS 21306-65-0
分子式 C21H21NO3S2
分子量 399.53
MOL 文件 21306-65-0.mol
更新日期 2024/12/05 21:11:28
21306-65-0 结构式 21306-65-0 结构式

基本信息

中文别名
S-[4-(苄氧基)苯基]-S-甲基-N-(对甲苯基磺酰基)-硫亚胺
英文别名
TPh A
NPD-123
Triphenyl compound A
S-Methyl-S-(4-benzyloxy-phenyl)-N-(p-toluolsulfonyl)-sulfimid
S-[4-(Benzyloxy)phenyl]-S-methyl-N-(p-tolylsulfonyl)-sulfilimine
S-[p-(Benzyloxy)phenyl]-S-methyl-N-(p-tolylsulfonyl)-sulfilimine
N-{[4-(Benzyloxy)phenyl](methyl)-γ4-sulfanylidene}-4-methylbenzenesulfonamide
Benzenesulfonamide, 4-methyl-N-[methyl[4-(phenylmethoxy)phenyl]-λ4-sulfanylidene]-

物理化学性质

沸点587.6±60.0 °C(Predicted)
密度1.22±0.1 g/cm3(Predicted)
储存条件2-8°C
溶解度二甲基亚砜:>30mg/mL
形态白色粉末
颜色白色

安全数据

WGK Germany3
S-[4-(苄氧基)苯基]-S-甲基-N-(对甲苯基磺酰基)-硫亚胺价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2025/02/08HY-14454S-[4-(苄氧基)苯基]-S-甲基-N-(对甲苯基磺酰基)-硫亚胺
TPh A
21306-65-05mg1000元
2025/02/08HY-14454S-[4-(苄氧基)苯基]-S-甲基-N-(对甲苯基磺酰基)-硫亚胺
TPh A
21306-65-010 mM * 1 mLin DMSO1100元
2025/02/08HY-14454S-[4-(苄氧基)苯基]-S-甲基-N-(对甲苯基磺酰基)-硫亚胺
TPh A
21306-65-010mg1700元

常见问题列表

生物活性
TPh A (Triphenyl Compound A) 是核蛋白 pirin 的有效抑制剂,其 Ki 值为0.6 uM。TPh A 破坏 Bcl3-pirin 复合物的形成。TPh A 可作为相关的小分子工具调控细胞内的 Pirin。
体外研究

The Pirin is a nuclear protein with the nuclear factor I/CCAAT box transcription factor (NFI/CTF). Pirin proteins are highly conserved between mammals, plants, fungi, and prokaryotic organisms and are considered to belong to the cupin superfamily.TPh A (20 μM; 5 hours) reduces the amount of pirin-bound Bcl3 and inhibits the interaction between pirin and Bcl3 in HEK293T cells in a glutathione S-transferase (GST) pulldown assay (HEK293T cells are transfected with vectors that encoded bcl3-Myc and pirin-His6 for 43 h of transfection).TPh A (0-100 μM; 48 hours) does not exert any potent cytotoxic activity against many human cancer cell lines, it against MCF7, MDA-MB231, HeLa, DU145, HepG2, A549, HT1080, WM266-4, and SK-MEL-28 cells with IC 50 values >50 μM, and exhibits IC 50 values of 27 μM, 20 μM and 26 μM for PC3 HL60 and HT29 cells, respectively.TPhA (0-50 μM; 48 hours) inhibits cell migration in WM266-4 cells, SK-MEL-28 cell in a concentration-dependent manner.

Cell Viability Assay

Cell Line: MCF7, MDA-MB231, HeLa, DU145, HepG2, A549, HT1080, WM266-4, and SK-MEL-28 cells
Concentration: 0-100 μM
Incubation Time: 48 hours
Result: Did not exert any potent cytotoxic activity against many human cancer cell lines.
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