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501417-22-7

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501417-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501417-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,4,1 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 501417-22:
(8*5)+(7*0)+(6*1)+(5*4)+(4*1)+(3*7)+(2*2)+(1*2)=97
97 % 10 = 7
So 501417-22-7 is a valid CAS Registry Number.

501417-22-7Downstream Products

501417-22-7Relevant academic research and scientific papers

5-Iodo-2-arylalkylthio-6-aryl pyrimidin-4(3H)-ones as non-nucleoside anti-HBV agents

Zhang, Yu,Sun, Xuefeng,Fan, Ningning,Zhao, Jianxiong,Tu, Jing,Chen, Xiangmei,Liu, Junyi,Wang, Xiaowei

, p. 1438 - 1443 (2015)

A series of 5-iodo-2-arylalkylthio-6-aryl pyrimidin-4(3H)-ones, which can be considered as S-DABO derivatives, have been synthesized and their antiviral effect on extracellular HBV DNA was evaluated using the HepAD38 cell system. Compounds 6d1 and 6e3 exhibited more potent anti-HBV activity than lamivudine with EC50 values of 0.376 μM and 0.469 μM, respectively. In addition, inhibition of intracellular HBV DNA, pgRNA, HBeAg and HBsAg of compounds 6d1 and 6e3 was examined to initially infer the action mechanism. RT-PCR analysis of pgRNA demonstrated that these new S-DABO analogues could not interfere with HBV transcription. TRFIA analysis revealed that compounds 6d1 and 6e3 effectively reduced the secretion of HBeAg. These results demonstrated that 5-iodo-2-arylalkylthio-6-aryl pyrimidin-4(3H)-ones possess anti-HBV abilities and could be used as potential agents against HBV infection with an additional merit of low cytotoxicity.

2-Arylthio-5-iodo pyrimidine derivatives as non-nucleoside HBV polymerase inhibitors

Wang, Jie,Zhang, Liang,Zhao, Jianxiong,Zhang, Yu,Liu, Qingchuan,Tian, Chao,Zhang, Zhili,Liu, Junyi,Wang, Xiaowei

, p. 1573 - 1578 (2018/02/21)

In this study, a series of 2-arylthio-5-iodo pyrimidine derivatives, as non-nucleoside hepatitis B virus inhibitors, were evaluated and firstly reported as potential anti-HBV agents. To probe the mechanism of active agents, DHBV polymerase was isolated and a non-radioisotopic assay was established for measuring HBV polymerase. The biological results demonstrated that 2-arylthio-5-iodo pyrimidine derivatives targeted HBV polymerase. In addition, pharmacophore models were constructed for future optimization of lead compounds. Further study will be performed for the development of non-nucleoside anti-HBV agents.

Preparation method of 2,5,6 substituted pyrimidone derivative and application thereof in serving as anti-hepatitis virus drugs

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Paragraph 0039; 0040; 0041; 0042, (2017/07/22)

The invention discloses a novel 2,5,6 substituted pyrimidone derivative which is a compound as shown in a formula (I). The novel 2,5,6 substituted pyrimidone derivative has good anti-HBV virus activity, and details of the definitions of all radical groups are shown in the description. The invention further discloses a preparation method of the derivative, a pharmaceutical composition containing the derivative and application of the 2,5,6 substituted pyrimidone derivative and the pharmaceutical composition containing the 2,5,6 substituted pyrimidone derivative in serving as anti-HBV drugs. Please see the formula I in the description.

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