deoxycytidine


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Related to deoxycytidine: deoxycytidine monophosphate, deoxythymidine

de·ox·y·cyt·i·dine

(dē-oks'ē-sī'ti-dēn),
2'-Deoxyribosylcytosine, one of the four major nucleosides of DNA (the others being deoxyadenosine, deoxyguanosine, and thymidine).

de·ox·y·cyt·i·dine

(dē-oks'ē-sī'ti-dēn)
One of the four major nucleosides of DNA (the others being deoxyadenosine, deoxyguanosine, and thymidine).
References in periodicals archive ?
DNA methylation that 5-Aza-2'- Inhibition of targets DNA deoxycytidine telomerase activity [103] methyltransferases and reactivation of c-Myc and p16 were observed.
Immunohistochemical and genetic evaluation of deoxycytidine kinase in pancreatic cancer: relationship to molecular mechanisms of gemcitabine resistance and survival.
Gemcitabine (GEM) is a deoxycytidine nucleoside analog that requires intracellular phosphorylation of the parent drug to yields the active di- and triphosphate metabolites.
Enhanced breadth of priming is achieved through the use of primers and probes containing 5-propynyl deoxycytidine and deoxyuridine nucleotides that offer increased affinity and base pairing selectivity (18,19).
A Summary of TNPACK Results Reference Test Problems (n) Schlick and (1) Rosenbrock's function (1,000) Fogelson [1992b] (2) Trigonometric function (1,000) (3) Potential energy function of deoxycytidine (87) (4) Energy function from models of platelet aggregation (640) Zou et al.
Methylated deoxycytidine: The HPLC analysis of the 5-methyldeoxycytidine (5mdC) content was done after hydrolysis of DNA with nucleases P1 and alkaline phosphatase as described elsewhere |8~.
Gemcitabine (GCB) is a deoxycytidine analogue that causes DNA damage, initiating cell death [18].
Wiberg, "Amber mutants of bacteriophage T4 defective in deoxycytidine diphosphatase and deoxycytidine triphosphatase on the role of 5-hydroxymethylcytosine in bacteriophage deoxyribonucleic acid," Journal of Biological Chemistry, vol.
Zeschnigk et al., "Impact of 5-aza-2'- deoxycytidine and epigallocatechin-3-gallate for induction of human regulatory T cells," Immunology, vol.
Hybridization ability and base pair geometry of modified deoxycytidine derivatives having a 4-N-carbamoyl group.
Emtricitabine (5-fluoro-1-(2R, 5S)-[2-(hydroxymethyl)-1,3oxathiolan-5-yl]cytosine) (Figure 1(a)) is a potent deoxycytidine nucleoside reverse transcriptase inhibitor for the treatment of human immunodeficiency virus (HIV) infection [1,2].