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1-(4-bromophenyl)-2-(5-(2-chloropyridin-4-yl)-1,3,4-oxadiazol-2-ylthio)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1380395-65-2

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1380395-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380395-65-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,3,9 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1380395-65:
(9*1)+(8*3)+(7*8)+(6*0)+(5*3)+(4*9)+(3*5)+(2*6)+(1*5)=172
172 % 10 = 2
So 1380395-65-2 is a valid CAS Registry Number.

1380395-65-2Downstream Products

1380395-65-2Relevant academic research and scientific papers

Containing 2 - mercapto acetophenone 1, 3, 4 - oxadiazole derivative and its preparation and anti-tumor activity

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Paragraph 0043; 0044; 0045; 0055; 0056; 0057, (2017/08/25)

The invention relates to a 2-mercaptoacetophenone-containing 1, 3, 4-oxadiazole derivative, which is characterized by having a general formula as the following. In the formula, R1 represents the following, and R2 represents -H -Br. The 2-mercaptoacetophen

Synthesis, biological evaluation and molecular docking studies of novel 2-(1,3,4-oxadiazol-2-ylthio)-1-phenylethanone derivatives

Zhang, Li-Rong,Liu, Zhi-Jun,Zhang, Hui,Sun, Jian,Luo, Yin,Zhao, Ting-Ting,Gong, Hai-Bin,Zhu, Hai-Liang

, p. 3615 - 3621 (2012/07/27)

In present study, a series of new 2-(1,3,4-oxadiazol-2-ylthio)-1- phenylethanone derivatives (6a-6x) as potential focal adhesion kinase (FAK) inhibitors were synthesized. The bioassay assays demonstrated that compound 6i showed the most potent activity, which inhibited the growth of MCF-7 and A431 cell lines with IC50 values of 140 ± 10 nM and 10 ± 1 nM, respectively. Compound 6i also exhibited significant FAK inhibitory activity (IC50 = 20 ± 1 nM). Docking simulation was performed to position compound 6i into the active site of FAK to determine the probable binding model.

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