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2,5-Cyclohexadiene-1,4-dione, 2-(10-hydroxydecyl)-3,5,6-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80479-71-6

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80479-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80479-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,7 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80479-71:
(7*8)+(6*0)+(5*4)+(4*7)+(3*9)+(2*7)+(1*1)=146
146 % 10 = 6
So 80479-71-6 is a valid CAS Registry Number.

80479-71-6Downstream Products

80479-71-6Relevant academic research and scientific papers

BENZOQUINONE DERIVATIVES AS MODULATORS OF MITCHONDRIAL FUNCTION

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Page/Page column 37, (2012/03/10)

The present invention relates to benzoquinone derivatives which are efficient as modulators of mitochondrial function and as such are useful for the treatment of pathological conditions where mitochondrial function is impaired.

Synthesis and characterization of mitoQ and idebenone analogues as mediators of oxygen consumption in mitochondria

Duveau, Damien Y.,Arce, Pablo M.,Schoenfeld, Robert A.,Raghav, Nidhi,Cortopassi, Gino A.,Hecht, Sidney M.

experimental part, p. 6429 - 6441 (2010/10/03)

Analogues of mitoQ and idebenone were synthesized to define the structural elements that support oxygen consumption in the mitochondrial respiratory chain. Eight analogues were prepared and fully characterized, then evaluated for their ability to support oxygen consumption in the mitochondrial respiratory chain. While oxygen consumption was strongly inhibited by mitoQ analogues 2-4 in a chain length-dependent manner, modification of idebenone by replacement of the quinone methoxy groups by methyl groups (analogues 6-8) reduced, but did not eliminate, oxygen consumption. Idebenone analogues 6-8 also displayed significant cytoprotective properties toward cultured mammalian cells in which glutathione had been depleted by treatment with diethyl maleate.

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