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1315482-48-4

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1315482-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1315482-48-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,4,8 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1315482-48:
(9*1)+(8*3)+(7*1)+(6*5)+(5*4)+(4*8)+(3*2)+(2*4)+(1*8)=144
144 % 10 = 4
So 1315482-48-4 is a valid CAS Registry Number.

1315482-48-4Downstream Products

1315482-48-4Relevant articles and documents

Systematic study of protein detection mechanism of self-assembling 19F NMR/MRI nanoprobes toward rational design and improved sensitivity

Takaoka, Yousuke,Kiminami, Keishi,Mizusawa, Keigo,Matsuo, Kazuya,Narazaki, Michiko,Matsuda, Tetsuya,Hamachi, Itaru

, p. 11725 - 11731 (2011/09/16)

19F NMR/MRI probe is expected to be a powerful tool for selective sensing of biologically active agents owing to its high sensitivity and no background signals in live bodies. We have recently reported a unique supramolecular strategy for specific protein detection using a protein ligand-tethered self-assembling 19F probe. This method is based on a recognition-driven disassembly of the nanoprobes, which induced a clear turn-on signal of 19F NMR/MRI. In the present study, we conducted a systematic investigation of the relationship between structure and properties of the probe to elucidate the mechanism of this turn-on 19F NMR sensing in detail. Newly synthesized 19F probes showed three distinct behaviors in response to the target protein: off/on, always-on, and always-off modes. We clearly demonstrated that these differences in protein response could be explained by differences in the stability of the probe aggregates and that "moderate stability" of the aggregates produced an ideal turn-on response in protein detection. We also successfully controlled the aggregate stability by changing the hydrophobicity/hydrophilicity balance of the probes. The detailed understanding of the detection mechanism allowed us to rationally design a turn-on 19F NMR probe with improved sensitivity, giving a higher image intensity for the target protein in 19F MRI.

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