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N4-benzoyl-2'-deoxycytidine-5'-tosylate is a complex organic compound with the molecular formula C22H22N3O7S. It is a derivative of deoxycytidine, a nucleoside that is a component of DNA. The compound is characterized by the presence of a benzoyl group attached to the nitrogen atom at position 4 of the cytidine base, and a tosyl group (tosylate) attached to the 5' carbon of the deoxyribose sugar. This chemical modification can affect the compound's reactivity and its interactions with enzymes or other molecules, potentially making it useful in medicinal chemistry for the development of new drugs or as a research tool to study DNA metabolism and replication.

5174-26-5

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5174-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5174-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5174-26:
(6*5)+(5*1)+(4*7)+(3*4)+(2*2)+(1*6)=85
85 % 10 = 5
So 5174-26-5 is a valid CAS Registry Number.

5174-26-5Downstream Products

5174-26-5Relevant academic research and scientific papers

α,β-Difluoromethylene deoxynucleoside 5′-triphosphates: A convenient synthesis of useful probes for DNA polymerase β structure and function

Upton, Thomas G.,Kashemirov, Boris A.,McKenna, Charles E.,Goodman, Myron F.,Prakash, G. K. Surya,Kultyshev, Roman,Batra, Vinod K.,Shock, David D.,Pedersen, Lars C.,Beard, William A.,Wilson, Samuel H.

, p. 1883 - 1886 (2009)

αβ-Difluoromethylene deoxynucleoside 5′-triphosphates (dNTPs, N = A or C) are advantageously obtained via phosphorylation of corresponding dNDP analogues using catalytic ATP, PEP, nucleoside diphosphate kinase, and pyruvate kinase. DNA pol β Kdd values for the α, β-CF2 and unmodified dNTPs, α, β-NH dUTP, and the α, β-CH2 analogues of dATP and dGTP are discussed in relation to the conformations of α, β-CF2 dTTP versus α, β-NH dUTP bound into the enzyme active site.2009 American Chemical Society.

Pyrimidine-purine and pyrimidine heterodinucleosides synthesis containing a triazole linkage

Lucas,Elchinger,Faugeras,Zerrouki

experimental part, p. 168 - 177 (2011/08/02)

This article describes a synthetic route to generate two purine-pyrimidine and pyrimidine heterodinucleosides. Both microwave activated regioselective alkylation using hydride and copper-catalyzed-azide-alkyne-cycloaddition (CuAAC) were used in order to perform the synthesis.

DNG cytidine: Synthesis and binding properties of octameric guanidinium-linked deoxycytidine oligomer

Szabo, Istvan E.,Bruice, Thomas C.

, p. 4233 - 4244 (2007/10/03)

The synthesis of guanidinium-linked cytidyl oligomer (DNG-C8), a cationic DNA analog, and the corresponding cytidine monomers is described. The DNG monomer synthesis was streamlined to produce a shorter route to the final monomer than previously reported for thymidine and subsequent solid-phase synthesis produced an octameric cytidyl DNG strand. Because octameric deoxyguanosine would be used as the complementary strand in our studies, it was necessary to investigate guanosine self-association. Singular value decomposition was used to mathematically deconvolve the spectral data and confirm the presence of transitions due to DNA-G8 self-association. Job plots show the binding stoichiometry of DNG-C8 with DNA-G 8 to be 1:1. Thermal denaturation studies of the DNG-C 8·DNA-G8 duplex established a T m≥90°C and a ΔG°=-13.3kcalmol-1, indicating the DNG-C8·DNA-G8 duplex is over 1000 times more stable than that of DNA-C8·DNA-G8.

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