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1414286-80-8

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1414286-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1414286-80-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,4,2,8 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1414286-80:
(9*1)+(8*4)+(7*1)+(6*4)+(5*2)+(4*8)+(3*6)+(2*8)+(1*0)=148
148 % 10 = 8
So 1414286-80-8 is a valid CAS Registry Number.

1414286-80-8Downstream Products

1414286-80-8Relevant articles and documents

Selenium- and tellurium-containing redox modulators with distinct activity against macrophages: Possible implications for the treatment of inflammatory diseases

Doering, Mandy,Viswanathan, Uma M.,Burkholz, Torsten,Jacob, Claus,Diesel, Britta,Kiemer, Alexandra K.,Gruhlke, Martin C. H.,Slusarenko, Alan J.,Manikova, Dominika,Chovanec, Miroslav

, p. 10577 - 10585,9 (2012/12/12)

Various selenium- and tellurium-containing molecules are able to modulate the intracellular redox state of cells, an effect which may be used for the (selective) targeting of cancer cells, which are naturally under oxidative stress (OS). As macrophages also generate an environment rich in Reactive Oxygen Species (ROS) and nitric oxide (NO), they may represent an additional, prime target for such redox-modulating agents. A range of selenium and tellurium-containing quinones have therefore been synthesized and subsequently tested in macrophage culture. The tellurium agents were generally cytotoxic at very low concentrations, and their mode of action seemed to involve the upregulation of intracellular ROS levels. This redox-modulating effect was confirmed by simple yeast-based chemogenetic analysis in conjunction with in vitro redox assays and electrochemistry. Together, these studies point towards an intracellular build-up of superoxide radicals as the most likely cause of toxicity. In contrast, some of the selenium derivatives were less toxic and exerted a pronounced inhibitory effect on the formation of lipopolysaccharide- induced NO production. Whilst the Te-analogues therefore may enable the resolute, effective and fairly selective targeting of macrophages, the selenium agents could act less severely, but equally effectively by interfering with inflammatory signalling molecules.

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