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1-(2-hydroxyethyl)-3,7,9-trimethylxanthinium iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1220124-84-4

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1220124-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1220124-84-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,0,1,2 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1220124-84:
(9*1)+(8*2)+(7*2)+(6*0)+(5*1)+(4*2)+(3*4)+(2*8)+(1*4)=84
84 % 10 = 4
So 1220124-84-4 is a valid CAS Registry Number.

1220124-84-4Downstream Products

1220124-84-4Relevant academic research and scientific papers

A theobromine derived silver N-heterocyclic carbene: Synthesis, characterization, and antimicrobial efficacy studies on cystic fibrosis relevant pathogens

Panzner, Matthew J.,Hindi, Khadijah M.,Wright, Brian D.,Taylor, Jane B.,Han, Daniel S.,Youngs, Wiley J.,Cannon, Carolyn L.

, p. 7308 - 7313 (2009)

The increasing incidence of multidrug-resistant (MDR) pulmonary infections in the cystic fibrosis (CF) population has prompted the investigation of innovative silver based therapeutics. The functionalization of the naturally occurring xanthine theobromine

Synthesis and anticancer activity of silver(I)-N-heterocyclic carbene complexes derived from the natural xanthine products caffeine, theophylline and theobromine

Mohamed, Heba A.,Lake, Benjamin R. M.,Laing, Thomas,Phillips, Roger M.,Willans, Charlotte E.

, p. 7563 - 7569 (2015/04/27)

A new library of silver(I)-N-heterocyclic carbene complexes prepared from the natural products caffeine, theophylline and theobromine is reported. The complexes have been fully characterised using a combination of NMR spectroscopy, mass spectrometry, elemental analysis and X-ray diffraction analysis. Furthermore, the hydrophobicity of the complexes has been measured. The silver(I)-N-heterocyclic carbenes have been evaluated for their antiproliferative properties against a range of cancer cell lines of different histological types, and compared to cisplatin. The data shows different profiles of response when compared to cisplatin in the same panel of cells, indicating a different mechanism of action. Furthermore, it appears that the steric effect of the ligand and the hydrophobicity of the complex both play a role in the chemosensitivity of these compounds, with greater steric bulk and greater hydrophilicity delivering higher cytotoxicity.

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