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4-[2-(4-Fluoro-phenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-4H-pyridine-1-carboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122454-73-3

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122454-73-3 Usage

Category

Pyrrolo[1,2-a]imidazole derivatives

Contains

Pyridine ring, carboxylic acid functional group, ethyl ester moiety

Potential applications

Pharmaceutical research and drug development

Biological activities

Studied for kinase inhibition and potential anticancer properties

Specific properties and potential uses

Subject to further research and testing

Check Digit Verification of cas no

The CAS Registry Mumber 122454-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,5 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122454-73:
(8*1)+(7*2)+(6*2)+(5*4)+(4*5)+(3*4)+(2*7)+(1*3)=103
103 % 10 = 3
So 122454-73-3 is a valid CAS Registry Number.

122454-73-3Relevant academic research and scientific papers

Regulation of stress-induced cytokine production by pyridinylimidazoles inhibition of CSBP kinase

Gallagher, Timothy F.,Seibel, George L.,Kassis, Shouki,Laydon, Jeffrey T.,Blumenthal, Mary Jane,Lee, John C.,Lee, Dennis,Boehm, Jeffrey C.,Fier-Thompson, Susan M.,Abt, Jeffrey W.,Soreson, Margaret E.,Smietana, Juanita M.,Hall, Ralph F.,Garigipati, Ravi S.,Bender, Paul E.,Erhard, Karl F.,Krog, Arnold J.,Hofmann, Glenn A.,Sheldrake, Peter L.,McDonnell, Peter C.,Kumar, Sanjay,Young, Peter R.,Adams, Jerry L.

, p. 49 - 64 (2007/10/03)

Members of three classes of pyridinylimidazoles bind with varying affinities to CSBP (p38) kinase which is a member of a stress-induced signal transduction pathway. Based upon SAR and protein homology modeling, the pharmacophore and three potential modes of binding to the enzyme are presented. For a subset of pyridinylimidazoles, binding is shown to correlate with inhibition of CSBP kinase activity, whereas no significant inhibition of PKA, PKα and ERK kinase activity is observed.

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