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名称
Ethynylcytidine, DNA 定向 RNA 聚合酶 III 亚基 RPC1 抑制剂
别名
乙炔胞苷
英文名称
Ethynylcytidine
货号
E656653-1ml
包装规格
1ml
浓度
10mM in DMSO
储存温度
-80℃储存
运输条件
超低温冰袋运输
产品介绍
Ethynylcytidine (ECyD), a nucleoside analog and a potent inhibitor of RNA synthesis , inhibits RNA polymerases I, II and II. Ethynylcytidine has robust antitumor activity in a wide range of models of cancer In Vitro The IC 50 values of Ethynylcytidine in the five human tumors with 4, 24 and 72 h exposure range from 0.114 to 1.032 μM, 0.015 to 0.067 μM, and 0.008 to 0.058 μM, respectively. These results suggest that the cytotoxicity of Ethynylcytidine tends to become stronger as the exposure time becomes longer. The differences in IC 50 values between the 24 and 72 h exposure times are not large, and Ethynylcytidine appeares to show sufficiently potent cytotoxicity at the 24 h exposure time in all 5 human tumors. Even at the 4 h exposure time, Ethynylcytidine clearly shows potent cytotoxicity with IC 50 values at submicromolar concentrations in 4 of the 5 human tumors. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo In both OCUM-2MD3 and LX-1 xenografts, tumor regression is noted and a very potent antitumor effect with an tumor growth inhibition rate (IR) on day 15 of approximately 90% or even higher is observed at the minimum toxic doses of Ethynylcytidine (TAS-106) on all three administration schedules. In particular, administration of Ethynylcytidine at 6 mg/kg once weekly exhibits a marked tumor shrinking effect with an IR of 98% against the LX-1 tumor. While Ethynylcytidine treatment on an either 3 or 5 times weekly schedule has a potent antitumor effect with an IR of approximately 85%, the IR of Ethynylcytidine once weekly is less than 60% and its antitumor effect is rather weak . MCE has not independently confirmed the accuracy of these methods. They are for reference only. IC50& Target:nucleoside antimetabolite
生化机理
乙炔胞苷(ECyD)是一种核苷类似物,也是一种有效的 RNA 合成抑制剂,可抑制 RNA 聚合酶 I、II 和 II。乙炔胞苷在多种癌症模型中具有强大的抗肿瘤活性。
CAS号
180300-43-0(DMSO)
分子式
C11H13N3O5
分子量
267.24 g/mol
Smiles
C#CC1(C(OC(C1O)N2C=CC(=NC2=O)N)CO)O
Reaxy-Rn
30263185
作用类型
抑制剂
作用机制
DNA 定向 RNA 聚合酶 III 亚基 RPC1 抑制剂
Safety
「No Dangerous Attributes」
Related
「No upstream and downstream information yet」
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「No technical documents」
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Research chemical 1ml

Research chemical 1ml; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 1ml.

item number:E656653-1ml
Product model:1ml
level: 1ml
Lead Time:30days
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