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N-(4-((4-carboxyphenyl)(4-(dimethylamino)phenyl)methylene)cyclohexa-2,5-dien-1-ylidene)-N-methylmethanaminium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42297-54-1

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42297-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42297-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,9 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42297-54:
(7*4)+(6*2)+(5*2)+(4*9)+(3*7)+(2*5)+(1*4)=121
121 % 10 = 1
So 42297-54-1 is a valid CAS Registry Number.

42297-54-1Downstream Products

42297-54-1Relevant academic research and scientific papers

Searching for the Optimal Fluorophore to Label Antimicrobial Peptides

Zhao, Can,Fernandez, Antonio,Avlonitis, Nicolaos,Vande Velde, Greetje,Bradley, Mark,Read, Nick D.,Vendrell, Marc

, p. 689 - 696 (2016)

With the advent of antimicrobial resistance, there is an urgent need for new strategies to treat infectious diseases. Antimicrobial peptides are considered as promising candidates, and therefore there is a need to understand their mechanism of action in order to exploit their therapeutic potential. To this end, fluorescent analogs are powerful tools to analyze their behavior and subcellular localization in cells and in vivo. However, the conjugation of fluorophores to antimicrobial peptides, especially in short sequences, can impair their biological activity, making the selection of the fluorescent label an essential step in these studies. In the present work, we have systematically modified a model antifungal hexapeptide with a collection of fluorophores covering broad physicochemical and spectral properties. The resulting conjugates have been examined in two different fungal species, in terms of their activity and intracellular localization. The biological results confirm the influence of the different fluorescent moieties on the subcellular localization of antimicrobial sequences, and provides an insight on the optimal fluorophores to be used in the preparation of fluorescent peptides for different bioimaging assays.

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