1-((1,2,3,4)-2-fluoro-3-hydroxy-4-( hydroxymethyl)cyclopentyl)- 5- iodo- 2,4(1H,3H)- pyrimidinedione

Subscribe to Selected New Research on 1-((1,2,3,4)-2-fluoro-3-hydroxy-4-( hydroxymethyl)cyclopentyl)-5-iodo-2,4(1H,3H)-pyrimidinedione

4 relevant articles (1 outcomes, 0 trials/studies) found for this Bio-Agent

Description: RN and structure given in first source

Also Known As:

C-FIAU

Relationship Network

Bio-Agent Context: Research Results

Heterocyclic Compounds: 23

1-Ring Heterocyclic Compounds

Pyrimidines: 269

Pyrimidine Nucleosides: 38

1-((1,2,3,4)-2-fluoro-3-hydroxy-4-( hydroxymethyl)cyclopentyl)-5-iodo-2,4(1H,3H)-pyrimidinedione: 4

Nucleic Acids, Nucleotides, and Nucleosides: 1

Nucleosides: 591

Pyrimidine Nucleosides: 38

1-((1,2,3,4)-2-fluoro-3-hydroxy-4-( hydroxymethyl)cyclopentyl)-5-iodo-2,4(1H,3H)-pyrimidinedione: 4

Related Diseases

1.	Infection 08/29/2000 - "The intracellular uptake of [(14)C]FIAU increased with increasing multiplicity of infection and with time after infection" 11/01/2003 - "After infection of C6 cells with AdCMV- HSV1-tk (1.5x10(8) pfu), [(18)F]FHBG and [(3)H]PCV accumulation was significantly greater than that of [(14)C]FIAU ( P<0.01)" Get all the results and reference details, order at left...
2.	Neoplasms (Cancer) 07/06/2001 - "The [(14)C]FIAU radioactivity and bacterial count data strongly support a Salmonella(TK)-dependent [(14)C]FIAU accumulation of at least 30-fold higher in tumor tissue compared to muscle tissue" 03/01/2007 - "EXPERIMENTAL DESIGN: Immunoblot, luciferase reporter assay, and in vitro assay with [(14)C]FIAU were used to show the effects of bortezomib on the induction of lytic gene expression of EBV-associated tumor cells" Get all the results and reference details, order at left...
2 Diseases and 4 more articles analyzed in the Research Interface, order at left...

Related Drugs and Biologics

1.	9- (4- ((18)F)fluoro- 3- hydroxymethylbutyl)guanine
2.	Luciferases
3.	bortezomib (Velcade)
3 Drugs and Important Bio-Agents and 2 more articles analyzed in the Research Interface, order at left...

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