luridine

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.

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.

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.

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.

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.

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].

N3-(2S)-[2-(tert-Butoxycarbonyl)amino-3-(tert-butoxy carbonyl)]propyluridine, a uridine analog, exhibits potential for antiepileptic effects and holds promise for research into anticonvulsant and anxiolytic activities, as well as the development of novel antihypertensive agents [1].

2'-Deoxy-2'-fluoro-N3-[3-(tert-butoxycarbonyl)amino]propyluridine, a purine nucleoside analog, exhibits broad antitumor activity, especially against indolent lymphoid malignancies, through mechanisms such as DNA synthesis inhibition and apoptosis induction, among others [1].

Fialuridine (DRG-0098) is a DNA-directed DNA polymerase inhibitor potentially for the treatment of HBV infection with potent activity against hepatitis B virus in vitro and in vivo.

Doxifluridine (Standard) is a reference standard for research and analysis in studies involving Doxifluridine. 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.

5-Taurinomethyluridine, Trifluoroacetate Salt (Standard) is a reference standard of 5-Taurinomethyluridine, Trifluoroacetate Salt intended for quantitative analysis, quality control, and related biochemical research applications.

5-Taurinomethyluridine, Trifluoroacetic Salt-[13C2,D2] (Standard) is a reference standard of 5-Taurinomethyluridine, Trifluoroacetic Salt-[13C2,D2] intended for quantitative analysis, quality control, and related biochemical research applications.

Trifluridine-[13C, 15N2] (Standard) is a reference standard of Trifluridine-[13C, 15N2] intended for quantitative analysis, quality control, and related biochemical research applications.

5-Methyluridine 5′-triphosphate (5-Methyl-UTP) is a UTP analog. It enhances the incorporation of [3H]-GMP more effectively than UTP during RNA polymerase I reactions.

2′-O-Methyluridine is a natural product that found in RNA such as rRNA, snRNA, snoRNA and tRNA in Archaea, Bacteria, and Eukaryota.

3'-Deoxy-3'-alpha-C-methyluridine is a Nucleoside; Used for nucleoside and nucleic acid modifications.