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742062-71-1

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742062-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 742062-71-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,2,0,6 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 742062-71:
(8*7)+(7*4)+(6*2)+(5*0)+(4*6)+(3*2)+(2*7)+(1*1)=141
141 % 10 = 1
So 742062-71-1 is a valid CAS Registry Number.

742062-71-1Relevant articles and documents

Identification of a novel 1,2 oxazine that can induce apoptosis by targeting NF-κB in hepatocellular carcinoma cells

Somu, Chaithanya,Mohan, Chakrabhavi Dhananjaya,Ambekar, Sachin,Dukanya,Rangappa, Shobith,Baburajeev,Sukhorukov, Alexey,Mishra, Srishti,Shanmugam, Muthu K,Chinnathambi, Arunachalam,Awad Alahmadi, Tahani,Alharbi, Sulaiman Ali,Basappa,Rangappa, Kanchugarakoppal S.

, (2020/03/03)

Constitutive activation of NF-κB is associated with proinflammatory diseases and suppression of the NF-κB signaling pathway has been considered as an effective therapeutic strategy in the treatment of various cancers including hepatocellular carcinoma (HCC). Herein, we report the synthesis of 1,2 oxazines and their anticancer potential. The antiproliferative studies presented 3-((4-(1H-benzo[d]imidazol-2-yl)piperidin-1-yl)methyl)-4-phenyl-4,4a,5,6,7,7a-hexahydrocyclopenta [e][1,2]oxazine(3i) as a lead cytotoxic agent against HCC cells. Flow cytometric analysis showed that 3i caused a substantial increase in the subG1 cell population. Annexin-V-FITC-PI staining showed a significant increase in the percentage of apoptotic cells on treatment with 3i. Transfection with p65 siRNA significantly reduced the 3i induced DNA fragmentation indicating that 3i may primarily mediate its proapoptotic effects by abrogating the NF-κB signaling. In addition, treatment of HCC cells with 3i decreased the DNA binding ability of NF-κB and NF-κB-dependent luciferase expression. Taken together, this report introduces 1,2-oxazine that potently targets the NF-κB signaling pathway in HCC cells.

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