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947016-30-0

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947016-30-0 Usage

Chemical class

Indole alkaloids

Derivative of

Tryptophan (an amino acid)

Natural occurrence

Fermented products (wine, beer, bread), produced by certain bacteria and fungi

Potential effects

Mood and sleep, signaling molecule in microbial communities

Known for

Pleasant aroma, contributes to flavor profile of fermented products

Potential use in therapy

Anti-inflammatory, anti-cancer

Check Digit Verification of cas no

The CAS Registry Mumber 947016-30-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,0,1 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 947016-30:
(8*9)+(7*4)+(6*7)+(5*0)+(4*1)+(3*6)+(2*3)+(1*0)=170
170 % 10 = 0
So 947016-30-0 is a valid CAS Registry Number.

947016-30-0Relevant articles and documents

Rational Design of Fluorescent Bioimaging Probes by Controlling the Aggregation Behavior of Squaraines: A Special Effect of Ionic Liquid Pendants

Wang, Wenhai,Fu, Afu,Lan, Jingbo,Gao, Ge,You, Jingsong,Chen, Lijuan

, p. 5129 - 5137 (2010)

We herein present an effective strategy to create water-soluble fluorescent bioimaging dyes by introducing the imidazolium-based ionic liquid (IL) pendants into a fluorescent skeleton. A new type of water-soluble imidazolium-anchored squaraine dye was synthesized accordingly. The relationship between the aggregate of squaraines and their fluorescent cell imaging application was elucidated in detail. Firstly, the aggregation behavior of squaraines in water solutions could be suppressed by varying the alkyl chain attached to the imidazolium unit. Secondly, the capability of cellular uptake and staining of dyes was also dramatically enhanced upon increasing the length of the paraffinic chain. These squaraine dyes displayed an excellent photostability that could permit real-time fluorescence bioimaging experiments to be monitored over a long time period with constant sample irradiation. Additionally, we designed for the first time an FeII-ion probe on the basis of an attack of the hydroxyl radical to the four-membered ring of squaraine. The results demonstrated that the imidazolium-anchored squaraines could perform naked-eye detection of the Fe2+ ion over a wide range of other interfering metals in aqueous media. More surprisingly, this process showed a fluorescence turn-off and -on response through the regeneration of squaraines in cells.

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