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TAS1553
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
TAS1553图片
CAS NO:2166023-31-8
包装与价格:
包装价格(元)
1 mg电议
2 mg电议
5 mg电议
10 mg电议
25 mg电议
50 mg电议
100 mg电议

产品介绍
TAS1553 是一种有效的具有口服活性的蛋白-蛋白相互作用 (PPI) 抑制剂,其IC50值为 0.0396 μM。TAS1553 抑制 DNA 复制并减少细胞内 dATP 池。TAS1553 诱导细胞Apoptosis" style="display: inline; color: #c13a36">凋亡 (Apoptosis),可用于癌症研究。

产品描述

TAS1553 is a potent, orally active protein–protein interaction (PPI) inhibitor with an IC 50 values of 0.0396 μM. TAS1553 inhibits DNA replication and reduces intracellular dATP pool. TAS1553 induces apoptosis and can be used for cancer research [1].

体外活性

TAS1553 (0.001-1 μM) dose-dependently inhibits the enzymatic activity of RNR [1]. TAS1553 (3 d) has anti-proliferative activity against both solid and hematological human cancer cell lines and the GI 50 values ranged from 0.228 to 4.15 μM [1]. TAS1553 (1-10 μM; 0-2 h; HCC38 and MV-4-11 cells) reduces intracellular dATP pool in a dose- and time-dependent manner, which is a critical metabolite for DNA replication [1]. TAS1553 (0-10 μM; 0-24 h; HCC38 and MV-4-11 cells) induces the replication stress and apoptosis in a dose- and time-dependent manner [1]. Western Blot Analysis [1] Cell Line: HCC38 and MV-4-11 cells Concentration: 0, 0.1, 0.3, 1, 3 and 10 μM Incubation Time: 0, 1, 2, 4, 8 and 24 hours Result: Increased the expression of Ser345, Ser4, Ser8 and Thr21 phosphorylation. Increaed the levels cleaved PARP and cleaved caspase-3.

体内活性

TAS1553 (25-200 mg/kg; p.o.; for 24 h; female F344/NJcl-rnu/rnu rats and BALB/cAJcl-nu/nu mice) shows RNR inhibitory effect in vivo [1]. TAS1553 (50-200 mg/kg; p.o.; daily, for 15 d; female F344/NJcl-rnu/rnu rats and BALB/cAJcl-nu/nu mice) has antitumor activity in vivo [1]. Animal Model: Female F344/NJcl-rnu/rnu rats and BALB/cAJcl-nu/nu mice [1] Dosage: 25, 50, 100 and 200 mg/kg Administration: Oral administration; for 24hours Result: Reduces intracellular dATP pool and induces the replication stress and apoptosis. Animal Model: Female F344/NJcl-rnu/rnu rats and BALB/cAJcl-nu/nu mice [1] Dosage: 50, 100 and 200 mg/kg Administration: Oral administration; daily, for 15 days Result: Inhibited tumor growth in the treated group/control group (T/C) were 52.0 (50 mg/kg), 45.0 (100 mg/kg) and 29.4% (200 mg/kg), respectively.

Cas No.

2166023-31-8

分子式

C20H20ClFN4O5S

分子量

482.91

别名

TAS1553

储存和溶解度

DMSO:90mg/mL (186.4mM),Need ultrasonic
Powder: -20°C for 3 years
In solvent: -80°C for 2 years