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10-(2-<2-(2-azidoethoxy)ethoxy>ethoxy)decanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

239115-55-0

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239115-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 239115-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,9,1,1 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 239115-55:
(8*2)+(7*3)+(6*9)+(5*1)+(4*1)+(3*5)+(2*5)+(1*5)=130
130 % 10 = 0
So 239115-55-0 is a valid CAS Registry Number.

239115-55-0Downstream Products

239115-55-0Relevant academic research and scientific papers

Design and synthesis of a biotinylated chemical probe for detecting the molecular targets of an inhibitor of the production of the Pseudomonas aeruginosa virulence factor pyocyanin

Baker, Ysobel R.,Galloway, Warren R.J.D.,Hodgkinson, James T.,Spring, David R.

, p. 11783 - 11796 (2013)

Pseudomonas aeruginosa is a human pathogen associated with a variety of life-threatening nosocomial infections. This organism produces a range of virulence factors which actively cause damage to host tissues. One such virulence factor is pyocyanin, known to play a crucial role in the pathogenesis of P. aeruginosa infections. Previous studies had identified a novel compound capable of strongly inhibiting the production of pyocyanin. It was postulated that this inhibition results from modulation of an intercellular communication system termed quorum sensing, via direct binding of the compound with the LasR protein receptor. This raised the possibility that the compound could be an antagonist of quorum sensing in P. aeruginosa, which could have important implications as this intercellular signaling mechanism is known to regulate many additional facets of P. aeruginosa pathogenicity. However, there was no direct evidence for the binding of the active compound to LasR (or any other targets). Herein we describe the design and synthesis of a biotin-tagged version of the active compound. This could potentially be used as an affinity-based chemical probe to ascertain, in a direct fashion, the active compound's macromolecular biological targets, and thus better delineate the mechanism by which it reduces the level of pyocyanin production.

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