5'-deoxytoyocamycin has been researched along with 5-iodotubercidin in 3 studies
Studies (5'-deoxytoyocamycin) | Trials (5'-deoxytoyocamycin) | Recent Studies (post-2010) (5'-deoxytoyocamycin) | Studies (5-iodotubercidin) | Trials (5-iodotubercidin) | Recent Studies (post-2010) (5-iodotubercidin) |
---|---|---|---|---|---|
5 | 0 | 1 | 140 | 0 | 42 |
Protein | Taxonomy | 5'-deoxytoyocamycin (IC50) | 5-iodotubercidin (IC50) |
---|---|---|---|
Chain A, Mitogen-activated protein kinase 3 | Homo sapiens (human) | 0.9 | |
Mitogen-activated protein kinase 1 | Homo sapiens (human) | 1.2 | |
Adenosine kinase | Homo sapiens (human) | 0.1583 | |
Adenosine kinase | Mycobacterium tuberculosis H37Rv | 1.2 | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A | Homo sapiens (human) | 0.071 | |
Histone-lysine N-methyltransferase, H3 lysine-79 specific | Homo sapiens (human) | 7 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Browne, CE; DaRe, JM; Erion, MD; Kopcho, JJ; Schanzer, JM; Ugarkar, BG; Wiesner, JB | 1 |
Debnath, B; Jha, T; Srikanth, K | 1 |
Caballero, J; Fernández, M; González-Nilo, FD | 1 |
3 other study(ies) available for 5'-deoxytoyocamycin and 5-iodotubercidin
Article | Year |
---|---|
Adenosine kinase inhibitors. 1. Synthesis, enzyme inhibition, and antiseizure activity of 5-iodotubercidin analogues.
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.
Topics: Adenosine Kinase; Biodegradation, Environmental; Hydrophobic and Hydrophilic Interactions; Ligands; Pyrimidines; Pyrroles; Quantitative Structure-Activity Relationship | 2002 |
A CoMSIA study on the adenosine kinase inhibition of pyrrolo[2,3-d]pyrimidine nucleoside analogues.
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 |