2'-Deoxyguanosine-5'-triphosphate (Pubchem)
dNTP Pool
Pool identifier POOL001628
Members of this Pool
Members of control pools
POOL001664
Last modified: 10/Sep/2021
Results
Publication
Petrelli R, Meli M, Vita P, Torquati I, Ferro A, Vodnala M, D'Alessandro N, Tolomeo M, Del Bello F, Kusumanchi P, Franchetti P, Grifantini M, Jayaram HN, Hofer A, Cappellacci L: From the covalent linkage of drugs to novel inhibitors of ribonucleotide reductase: synthesis and biological evaluation of valproic esters of 3'-C-methyladenosine., Bioorg Med Chem Lett, 2014

PubMed
Value 48
Dimension %
Error (standard deviation) 5
Relative compared to control
Data presentation in publication diagram
Source
Source organism human (Homo sapiens)
Taxonomy 9606
Sample source cell line
CLO Cell line name HL-60 cell (CLO:0003775)
Cell line/type as in publication HL-60 acute promyelocytic cell line
Compartment whole cell
Experiment Details
Measurement type HPLC-UV
Extraction method acid extraction
Remarks to measurement type Hofer 1998.
Growth conditions 0.3 mM A167 treatment
Treatment
Drug/stress type drug
Applied drug 5'-O-valproyl-3'-C-methyladenosine (A167)
Treatment details/effects Ribonucleotide reductase (RNR) inhibitor
Genes and Proteins
No genes or proteins manipulated.