l-uridine

L-Uridine is the enantiomer of D-uridine, a nucleoside that acts as a phosphate acceptor for nucleoside phosphotransferase, in the normal RNA component of a normal RNA isolated from Polyporaceae fungus Poria cocos (Schw.) L-Uridine has potential antiviral activity.

3'-Azido-3'-deoxy-beta-L-uridine is a nucleoside derivative.

2'-Deoxy-2'-fluoro-l-uridine is a nucleoside analogue and an L-nucleoside with potential antiviral activity. It interferes with viral nucleic acid synthesis for antiviral research.

3'-Azido-3'-deoxy-5-methyl-beta-L-uridine is a Nucleoside Derivative - L-nucleoside, Azido-nucleoside.

3'-Azido-3'-deoxy-5-fluoro-beta-L-uridine is a Nucleoside Derivative - L-nucleoside, Azido-nucleoside, Fluoro-modified nucleoside, 5-Modified pyrimidine nucleoside.

5-Naphthyl-beta-methylaminocarbony-2'-O-methyl-uridine is a 5 modified pyrimidine nucleoside; 2'-O-Methyl nucleoside.

Trifluridine (NSC-75520) is a fluorinated thymidine analog with potential antineoplastic activity. Trifluridine is incorporated into DNA and inhibits thymidylate synthase, resulting in inhibition of DNA synthesis, inhibition of protein synthesis, and apoptosis. This agent also exhibits antiviral activity.

Doxifluridine (AMC 0101) is a fluoropyrimidine derivative and oral prodrug of the antineoplastic agent 5-fluorouracil (5-FU) with antitumor activity. Doxifluridine, designed to circumvent the rapid degradation of 5-FU by dihydropyrimidine dehydrogenase in the gut wall, is converted into 5-FU in the presence of pyrimidine nucleoside phosphorylase. 5-FU interferes with DNA synthesis and subsequent cell division by reducing normal thymidine production and interferes with RNA transcription by competing with uridine triphosphate for incorporation into the RNA strand.

PSI-6206 (RO 2433) (RO2433) is a selective HCV RNA polymerase inhibitor.

Uridine triacetate (RG 2133 triacetate) (Tri-O-acetyl uridine), an orally active prodrug of uridine, is efficiently absorbed in the gut and swiftly deacetylated in the circulation to release free uridine. It is utilized in the research of 5-fluorouracil (5-FU) and capecitabine toxicity, particularly targeting early-onset cardiac or central nervous system (CNS) complications.

5-Methyluridine (Thymine riboside) is an endogenous methylated nucleoside found in human fluids; methylated purine bases are present in higher amounts in tumor-bearing patients compared to healthy controls.DNA hypermethylation is a common finding in malignant cells and has been explored as a therapeutic target for hypomethylating agents.

2'-O-Methyl-5-iodouridine (5-Iodo-2'-O-methyluridine) is a purine nucleoside analog that targets malignant tumors of the inert lymphatic system and possesses a broad spectrum of antitumor activity. The anticancer mechanism of 2'-O-Methyl-5-iodouridine is dependent on the inhibition of DNA synthesis and induction of apoptosis.

5-Bromo-2',3',5'-tri-O-acetyluridine is a purine nucleoside analog that is being explored to improve Alzheimer's and Parkinson's diseases.

2'-Fluorothymidine (2'-Deoxy-2'-fluoro-5-Methyluridine) belongs to the thymidine (TdR) and methyluridine isozymes and is a highly selective substrate for thymidine kinase type 2 (TK2).hCYP3A4 Fluorogenic substrate 2 is a chelator of thymidine and methyluridine.

3-Methyluridine is a modified nucleoside of cellular RNA.

Raluridine is a RNA-directed DNA polymerase inhibitor potentially for the treatment of HIV infection. 935U83 inhibited virus growth with an average 50% inhibitory concentration (IC50: 1.8 microM) corresponding IC50s were 0.10 microM for FLT (3'-deoxy-3'-f

5-Methyluridine5'-monophosphate [Ribothymidylic acid] is a derivative of 5-Methyluridine.

Fosfluridine tidoxil, a thymidylate synthase inhibitor, is used potentially for the treatment of colorectal cancer, and breast cancer.

Trifluridine/tipiracil hydrochloride mixture (TAS-102) is a novel oral combination drug containing trifluridine (TFT) and tipiracil hydrochloride (TTP) in a 2:1 molar ratio.

5-Ethynyluridine is a clickable form of uridine.1It is incorporated into cellular RNA, but not DNA, and has been used to detect transcriptionin vitroandin vivo. 1.Jao, C.Y., and Salic, A.Exploring RNA transcription and turnover in vivo by using click chemistryProc. Natl. Acad. Sci. USA105(41)15779-15784(2008)

L-5-Methyluridine, an L-configuration of 5-Methyluridine, is an endogenous methylated nucleoside present in human fluids.

2'-Deoxy-2'-fluoro-N3-[(pyrid-2-yl)methyl]uridine, a uridine analogue, demonstrates potential antiepileptic properties and its analogues are studied for anticonvulsant and anxiolytic effects, as well as for creating new antihypertensive agents [1].

3'-O-(4,4'-Dimethoxy trityl)-2'-O-(2-methoxyethyl)-5-methyluridine, a purine nucleoside analog, exhibits extensive antitumor properties against indolent lymphoid malignancies through mechanisms such as DNA synthesis inhibition and apoptosis induction among others [1].

2'-O-Methyl-5-methyluridine 5'-triphosphate (triethylammonium), a thymidine analog, exhibits insertional activity in replicated DNA, enabling its application in labeling cells and monitoring DNA synthesis [1].