2'deoxycytidine

5-O-TBDMS-N4-Benzoyl-2-deoxycytidine is a modified nucleoside used in the synthesis of deoxyribonucleic acid (DNA) or nucleic acid.

5'-O-(Tert-butyldimethylsilyl)-5-iodo-2'-deoxycytidine is a useful organic compound for research related to life sciences. The catalog number is T67323 and the CAS number is 666848-11-9.

Sp-2'-Deoxycytidine-5'-O-(1-thiotriphosphate) (Sp-dCTP-α-S), an isomer of the sulfur-containing nucleotide derivative dCTP-α-S, functions as an inhibitor of the deoxynucleoside triphosphate triphosphohydrolase SAMHD1, with an inhibition constant (Ki) of 6.3 µM.

5'-O-(4,4'-Dimethoxytrityl)-2'-deoxycytidine is a Nucleoside Derivative - Protected nucleoside with NH2/OH open.

N4-Bz-3'-O-DMTr-2'-deoxycytidine 5'-O-CE-phosphoramidite is a Nucleoside Phosphoramidite.

Nucleoside Derivatives - Halo-nucleosides, 2'-Modified nucleosides

Nucleoside Derivatives - Amino-nucleosides, 2'-Modified nucleosides

2',5-Difluoro-2'-deoxycytidine has potent anti-HCV activity and toxicity to rRNA.

4'-Ethynyl-2'-deoxycytidine is an anticancer nucleoside used in research on acute lymphoblastic leukemia and diffuse large B-cell lymphoma.

N4-Acetyl-5'-O-(4,4'-dimethoxytrityl)-5-methyl-2'-deoxycytidine, a purine nucleoside analog, exhibits broad antitumor activity against indolent lymphoid malignancies by inhibiting DNA synthesis and inducing apoptosis [1].

5'-Ethynyl-2'-deoxycytidine (EdC) functions as a nucleoside analog effectively inhibiting the replication of herpes simplex virus-1 (HSV-1) KOS strain with an ID50 of 0.2 μg/mL. Additionally, it decreases virus-induced cytopathogenic effects in PRK cells for HSV-1, HSV-2, and vaccinia virus strains, demonstrating MIC values between 0.2 to 5 μg/mL. EdC acts as a thymidylate synthetase inhibitor, selectively impacting the DNA incorporation rates of [1',2'-3H]deoxyuridine compared to [CH3-3H]deoxythymidine in PRK cells with ID50s of 3 and 120 μg/mL, respectively. It further inhibits thymidine synthetase and curtails L1210 cell proliferation, a process reversible by deoxythymidine (ID50s are 4.4 and 1,000 μg/mL, respectively). Also, EdC is utilized in monitoring DNA synthesis and cellular replication through click chemistry conjugation, linking its ethynyl group with the azido group of various fluorochromes.

5-Aza-4'-thio-2'-deoxycytidine (5-Aza-T-dCyd), a sulfur-containing deoxy-cytidine analog, serves as an orally active inhibitor of DNA methyltransferase I (DNMT1). It exhibits potential antitumor effects and DNA hypomethylating properties [1].

N4-Ethyl-2'-deoxycytidine is a Nucleoside Derivative - N-Methylated alkylated nucleoside.

2'-Deoxycytidine (Deoxycytidine) hydrate is a component of nucleic acids.

5-Carboxy-2′-deoxycytidine is a metabolite of Trifluridine.

Nucleoside Derivatives - Fluoro-modified nucleosides; 2'-Modified nucleosides; Nucleoside Phosphoramidites

Nucleoside Derivatives –Other modified nucleosides

Nucleoside Derivatives –Protectednucleosidesw/NH2/OH open

N4-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxycytidine (5'-O-DMT-N4-Bz-dC) is a chemical compound used in the synthesis of oligodeoxynucleotides with a 3'-S-phosphorothiolate (3'-PS) linkage, valuable for investigating enzyme-catalyzed cleavage mechanisms in DNA.

N4-Acetyl-5'-O-(4,4'-dimethoxytrityl)-5-methyl-2'-deoxy   cytidine is a useful organic compound for research related to life sciences and the catalog number is TNU1519.

Decitabine (Deoxycytidine) is a deoxycytidine analog, a DNA methyltransferase inhibitor with oral activity. Decitabine has antitumor activity and antimetabolic activity. Decitabine induces cell cycle arrest and apoptosis.

2'-Deoxycytidine hydrochloride is the hydrochloride form of 2'-Deoxycytidine, an important deoxyribonucleoside analog commonly used in DNA synthesis and potentially anticancer, and its derivative Gemcitabine has been developed as an anticancer drug.2'-Deoxycytidine 2'-Deoxycytidine hydrochloride protects mice from the lethal toxicity of cytosine arabinoside(araC).

2'-Deoxycytidine-5'-monophosphoric acid (2'-Deoxycytidine 5'-monophosphate) is a substrate of uridine monophosphate (UMP)/cytidine monophosphate (CMP) kinase (EC 2.7.4.4) that forms dCDP, which, upon phosphorylation to dCTP, supports DNA biosynthesis.

2'-Deoxycytidine is one of the major nucleosides of DNA consisting of cytosine and deoxyribose and inhibits the biological effects of bromodeoxyuridine (Brdu). The nucleoside consists only of a pentose sugar attached to a purine or pyrimidine base and has no phosphate group. When N1 is attached to C1 of deoxyribose, deoxyribosides and nucleotides are formed from cytosine and deoxyribose; deoxycytidine monophosphate (dCMP), deoxycytidine diphosphate (dCDP), and deoxycytidine triphosphate (dCTP). cTP is the source of cytosine in RNA (ribonucleic acid) and deoxycytidine triphosphate (dCTP) is the source of deoxycytidine in DNA (deoxyribonucleic acid). Itaconic acid is a polymer.