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1-(2-Nitro)-phenylethylphosphat, Triethylammonium-Salz is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131376-71-1

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131376-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131376-71-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,7 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131376-71:
(8*1)+(7*3)+(6*1)+(5*3)+(4*7)+(3*6)+(2*7)+(1*1)=111
111 % 10 = 1
So 131376-71-1 is a valid CAS Registry Number.

131376-71-1Upstream product

131376-71-1Downstream Products

131376-71-1Relevant academic research and scientific papers

Rapid photolytic release of adenosine 5'-triphosphate from a protected analogue: Utilization by the Na:K pump of human red blood cell ghosts

Kaplan,Forbush III,Hoffman

, p. 1929 - 1935,1930, 1932 (1978)

2-Nitrobenzyl phosphate and 1-(2-nitro)phenylethyl phosphate have been synthesized and demonstrated to be suitable as photolabile sources of inorganic phosphate. The same protecting groups were attached to the terminal phosphate of adenosine 5'-triphosphate. These 'caged ATP' compounds released adenosine 5'-triphosphate on illumination at 340 nm in aqueous solution and P3-1-(2-nitro)phenylethyl-ATP gave about a 70% yield in under 30 s. The unphotolyzed caged ATP was neither a substrate nor inhibitor of purified renal Na,K-ATPase (EC 3.6.1.3). Following photolysis in the presence of the enzyme, the liberated ATP was hydrolyzed but at an inhibited rate. The photo-dependent inhibition could be eliminated by prior addition of glutathione or bisulfite to the irradiated solution. Caged ATP was incorporated into resealed human erythrocyte ghosts prepared from red blood cells depleted of internal energy stores. While the Na:K pump was unable to use incorporated caged ATP as a substrate, the ATP liberated by photolysis activated the pump as evidenced by measurements of K-dependent, ouabain-sensitive Na efflux. Thus the caged ATP can be used as a stable source of ATP unmetabolizable by intracellular ATPases until the ATP is released following photolytic irradiation.

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