Compounds > 5-chlorotubercidin
Page last updated: 2024-08-26

5-chlorotubercidin and bromotubercidin

5-chlorotubercidin has been researched along with bromotubercidin in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19903 (42.86)18.7374
1990's0 (0.00)18.2507
2000's4 (57.14)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Drach, JC; Nassiri, MR; Pudlo, JS; Saxena, NK; Townsend, LB; Turk, SR1
Balzarini, J; Bergstrom, DE; Brattesani, AJ; De Clercq, E; Ogawa, MK; Reddy, PA; Schweickert, MJ1
Browne, CE; DaRe, JM; Erion, MD; Kopcho, JJ; Schanzer, JM; Ugarkar, BG; Wiesner, JB1
Debnath, B; Jha, T; Srikanth, K1
González, MP; Moldes del Carmen Terán, M1
Caballero, J; Fernández, M; González-Nilo, FD1
Bergstrom, DE; Brattesani, AJ1

Other Studies

7 other study(ies) available for 5-chlorotubercidin and bromotubercidin

ArticleYear
Synthesis and antiviral activity of certain 4- and 4,5-disubstituted 7-[(2-hydroxyethoxy)methyl]pyrrolo[2,3-d]pyrimidines.
    Journal of medicinal chemistry, 1988, Volume: 31, Issue:11

    Topics: Acyclovir; Aminoglycosides; Anti-Bacterial Agents; Cell Survival; Chemical Phenomena; Chemistry; Cytomegalovirus; Humans; Tubercidin

1988
Antiviral activity of C-5 substituted tubercidin analogues.
    Journal of medicinal chemistry, 1984, Volume: 27, Issue:3

    Topics: Animals; Antibiotics, Antineoplastic; Antiviral Agents; Chlorocebus aethiops; DNA Viruses; HeLa Cells; Humans; Mice; Pyrimidine Nucleosides; Rabbits; Ribonucleosides; RNA Viruses; Toyocamycin; Tubercidin

1984
Adenosine kinase inhibitors. 1. Synthesis, enzyme inhibition, and antiseizure activity of 5-iodotubercidin analogues.
    Journal of medicinal chemistry, 2000, Jul-27, Volume: 43, Issue:15

    Topics: Adenosine Kinase; Animals; Anticonvulsants; Electroshock; Enzyme Inhibitors; Humans; Male; Rats; Recombinant Proteins; Seizures; Structure-Activity Relationship; Tubercidin

2000
QSAR study on adenosine kinase inhibition of pyrrolo[2,3-d]pyrimidine nucleoside analogues using the hansch approach.
    Bioorganic & medicinal chemistry letters, 2002, Mar-25, Volume: 12, Issue:6

    Topics: Adenosine Kinase; Biodegradation, Environmental; Hydrophobic and Hydrophilic Interactions; Ligands; Pyrimidines; Pyrroles; Quantitative Structure-Activity Relationship

2002
A TOPS-MODE approach to predict adenosine kinase inhibition.
    Bioorganic & medicinal chemistry letters, 2004, Jun-21, Volume: 14, Issue:12

    Topics: Adenosine Kinase; Enzyme Inhibitors; Models, Molecular; Predictive Value of Tests; Quantitative Structure-Activity Relationship

2004
A CoMSIA study on the adenosine kinase inhibition of pyrrolo[2,3-d]pyrimidine nucleoside analogues.
    Bioorganic & medicinal chemistry, 2008, May-01, Volume: 16, Issue:9

    Topics: Adenosine Kinase; Computer Simulation; Databases, Factual; Enzyme Inhibitors; Models, Chemical; Models, Molecular; Molecular Structure; Nucleosides; Pyrimidines; Pyrroles; Quantitative Structure-Activity Relationship; Reproducibility of Results; Stereoisomerism

2008
Halogenation of tubercidin by N-halosuccinimides. A direct route to 5-bromotubercidin, a reversible inhibitor of RNA synthesis in eukaryotic cells.
    Nucleic acids research, 1980, Dec-20, Volume: 8, Issue:24

    Topics: Bromosuccinimide; Chemical Phenomena; Chemistry; Magnetic Resonance Spectroscopy; Ribonucleosides; RNA; Spectrophotometry, Ultraviolet; Succinimides; Tubercidin

1980