2’-Azido-2’-deoxycytidine is a purine nucleoside analogue that exhibits significant anticancer properties by inhibiting DNA synthesis and inducing apoptosis, particularly in indolent lymphoid malignancies. This compound serves as a versatile click chemistry reagent, containing an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) with alkyne, DBCO, or BCN-containing molecules. Additionally, 2’-Azido-2’-deoxycytidine requires dual phosphorylation to function as an inhibitor of ribonucleotide reductase, positioning it as a valuable tool in cancer research and therapeutic development.
2’-Azido-2’-deoxycytidine is a purine nucleoside analogue that exhibits significant anticancer properties by inhibiting DNA synthesis and inducing apoptosis, particularly in indolent lymphoid malignancies. This compound serves as a versatile click chemistry reagent, containing an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) with alkyne, DBCO, or BCN-containing molecules. Additionally, 2’-Azido-2’-deoxycytidine requires dual phosphorylation to function as an inhibitor of ribonucleotide reductase, positioning it as a valuable tool in cancer research and therapeutic development.
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