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].

2'-Deoxycytidine-13C9 (Deoxycytidine-13C9; Cytosine deoxyriboside-13C9; Deoxyribose cytidine-13C9) is the 13C-labeled version of 2'-Deoxycytidine. This deoxynucleoside has the capability to inhibit the biological activity of Brdu.

2'-Deoxycytidine-13C9,15N3 (Deoxycytidine-13C9,15N3; Cytosine deoxyriboside-13C9,15N3; Deoxyribose cytidine-13C9,15N3) is a 2'-Deoxycytidine labeled with isotopes 13C and 15N. This deoxynucleoside can inhibit the bioactivity of BrdU.

2'-Deoxycytidine-15N3 is a 15N-labeled form of 2'-deoxycytidine. This deoxynucleoside has the capability to inhibit the biological activity of BrdU.

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.