5’(R)-C-Methyl-5-fluorouridine, a uridine analogue, possesses potential antiepileptic properties. Its analogues are instrumental in investigating anticonvulsant and anxiolytic effects and are pivotal in crafting novel antihypertensive agents [1].

5-Fluorouridine 5'-O-β-D-galactopyranoside, also known as 5'-O-β-D-galactosyl-5-fluorouridine, is a prodrug of 5-Fluorouridine. 5-Fluorouridine 5'-O-β-D-galactopyranoside can be enzymatically converted by β-D-galactosidase into 5-Fluorouridine, which is a highly effective antineoplastic agent.

5-Iodo-3'-deoxy-3'-fluorouridine is a Nucleoside, fluoro-modified nucleoside, halo-nucleoside.

2’-Deoxy-2’-fluorouridine 5’-monophosphate triethyl ammonium, a purine nucleoside analog, exhibits extensive antitumor effects against indolent lymphoid malignancies. Its anticancer mechanisms primarily involve the inhibition of DNA synthesis and the induction of apoptosis [1].

2’-Deoxy-5-Fluorouridine 5’-phosphate triethyl ammonium salt is a useful organic compound for research related to life sciences. The catalog number is TNU1203 and the CAS number is 134-46-3.

3’-Deoxy-5’-O-(4,4’-dimethoxytrityl)-3’-fluorouridine is a useful organic compound for research related to life sciences. The catalog number is TNU1423 and the CAS number is 129015-60-7.

3'-Deoxy-3'-fluoro-5-fluorouridine is a Nucleoside Derivative - Fluoro-modified nucleoside, 5-modified pyrimidine nucleoside, 3'-Modified nucleoside.

5-fluorouridine is also known as FUrd, 5-Fluorouracil 1-beta-D-ribofuranoside, 5-Fur, or 5-Fluoro-uridine. 5-fluorouridine is a solid. This compound belongs to the pyrimidine nucleosides and analogues. These are compounds comprising a pyrimidine base attached to a sugar. 5-fluorouridine is known to target uridine phosphorylase. FUrd is often used in chemical and biochemical comparison studies with fluorouracil and thymine analogs.

2'-Deoxy-5'-O-DMT-2'-fluorouridine is a nucleoside analogue compound derived from 5'-O-DMTr-5-FUDR. This compound exhibits strong anti-yellow fever (YFV) activity.

2'-O-Acetyl-5'-O-(p-toluoyl)-3'-deoxy-3'-fluoro-5-fluorouridine is a Nucleoside Derivative - Fluoro-modified nucleoside, 5-modified pyrimidine nucleoside, 3'-Modified nucleoside.

3'-Deoxy-3'-a-C-methyl-5-fluorouridine is a Nucleoside Derivative - 3'-Modified nucleoside, 5-Modified pyrimidine nucleoside, Fluoro-modified nucleoside.

3'-Deoxy-5'-O-(4,4'-dimethoxytrityl)-3'-fluorouridine-2'-CED-phosphoramidite is a Nucleoside Phosphoramidite.

Nucleoside Phosphates;

Nucleoside Derivatives –Fluoro-modified nucleosides; 5’-Modified nucleosides, 2’-Modified nucleosides

Nucleoside Derivatives - 3’-Deoxy nucleosides, 5-Modified pyrimidine nucleosides, Fluoro-modified nucleosides

Nucleoside Derivatives - Azido-nucleosides, 5’-Modified nucleosides, 2’-Modified nucleosides, Fluoro-modified nucleosides

Nucleoside Derivatives - Amino-nucleosides, 3’-Modified nucleosides, Fluoro-modified nucleosides, 5-Modified pyrimidine nucleosides

Nucleoside Derivatives - Azido-nucleosides, 3’-Modified nucleosides, 5-Modified pyrimidine nucleosides; Fluoro-modified nucleosides

Nucleoside Derivatives - 3’-Modified nucleosides, Fluoro-modified nucleosides, 5-Modified pyrimidine nucleosides

Nucleoside Derivatives - 5’-Modified nucleosides, 5-Modified pyrimidine nucleosides, Fluoro-modified nucleosides

Halo-nucleoside; Fluoro-modified nucleoside

Nucleoside Derivatives - Halo-nucleoside; 5-modified nucleosides; 2’-Modified nucleosides; Fluoro-modified nucleosides

Capecitabine-d11 is a deuterated compound of Capecitabine. Capecitabine has a CAS number of 154361-50-9. Capecitabine is a fluoropyrimidine carbamate belonging to the class of antineoplastic agents called antimetabolites. As a prodrug, capecitabine is selectively activated by tumor cells to its cytotoxic moiety, 5-fluorouracil (5-FU); subsequently, 5-FU is metabolized to two active metabolites, 5-fluoro-2-deoxyuridine monophosphate (FdUMP) and 5-fluorouridine triphosphate (FUTP) by both tumor cells and normal cells. FdUMP inhibits DNA synthesis and cell division by reducing normal thymidine production, while FUTP inhibits RNA and protein synthesis by competing with uridine triphosphate for incorporation into the RNA strand.

Potassium oxonate (Potassium azaorotate) is a uricase inhibitor that prevents metabolism and excretion of uric acid and induces embryotoxicity and nephrotoxicity in rats.

Capecitabine (Capecitibine) is a fluoropyrimidine carbamate belonging to the class of antineoplastic agents called antimetabolites. As a prodrug, capecitabine is selectively activated by tumor cells to its cytotoxic moiety, 5-fluorouracil (5-FU); subsequently, 5-FU is metabolized to two active metabolites, 5-fluoro-2-deoxyuridine monophosphate (FdUMP) and 5-fluorouridine triphosphate (FUTP) by both tumor cells and normal cells. FdUMP inhibits DNA synthesis and cell division by reducing normal thymidine production, while FUTP inhibits RNA and protein synthesis by competing with uridine triphosphate for incorporation into the RNA strand.