5 fluorouridine

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.

5’(R)-C-Methyl-5-fluorouridine, a uridine analogue, potentially exhibits antiepileptic properties. Its analogues play a crucial role in researching anticonvulsant and anxiolytic effects and are essential in developing new antihypertensive agents [1].

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

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

2’-Deoxy-5-Fluorouridine 5’-phosphate triethyl ammonium salt is a valuable organic compound for life sciences research (catalog number TNU1203, CAS number 134-46-3).

3’-Deoxy-5’-O-(4,4’-Dimethoxytrityl)-3’-fluorouridine, with catalog number TNU1423 and CAS number 129015-60-7, is a valuable organic compound for life sciences research.

2'-Deoxy-2'-fluorouridine 5'-monophosphate triethyl ammonium, a purine nucleoside analog, demonstrates significant antitumor effects against indolent lymphoid malignancies by primarily inhibiting DNA synthesis and inducing apoptosis [1].

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

2'-Deoxy-5'-O-DMT-2'-fluorouridine, a nucleoside analogue derived from 5'-O-DMTr-5-FUDR, 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

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.

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.