Activity and electrochemical properties: iron complexes of the anticancer drug triapine and its analogs.
Antineoplastic Agents
/ chemistry
Cell Line, Tumor
Cell Proliferation
/ drug effects
Coordination Complexes
/ chemistry
Electrochemistry
/ methods
Enzyme Inhibitors
/ chemistry
Humans
Iron
/ chemistry
Molecular Structure
Oxidation-Reduction
/ drug effects
Pyridines
/ chemistry
Ribonucleotide Reductases
/ antagonists & inhibitors
Thiosemicarbazones
/ chemistry
Tyrosine
/ chemistry
Anticancer drug
Electrochemistry
Ligand binding
Redox chemistry
Thiosemicarbazone metal complexes
Journal
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
ISSN: 1432-1327
Titre abrégé: J Biol Inorg Chem
Pays: Germany
ID NLM: 9616326
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
18
04
2019
accepted:
03
06
2019
pubmed:
30
6
2019
medline:
14
7
2020
entrez:
29
6
2019
Statut:
ppublish
Résumé
Triapine (3-AP), is an iron-binding ligand and anticancer drug that is an inhibitor of human ribonucleotide reductase (RNR). Inhibition of RNR by 3-AP results in the depletion of dNTP precursors of DNA, thereby selectively starving fast-replicating cancer cells of nucleotides for survival. The redox-active form of 3-AP directly responsible for inhibition of RNR is the Fe(II)(3-AP)
Identifiants
pubmed: 31250199
doi: 10.1007/s00775-019-01675-0
pii: 10.1007/s00775-019-01675-0
pmc: PMC7849610
mid: NIHMS1663341
doi:
Substances chimiques
Antineoplastic Agents
0
Coordination Complexes
0
Enzyme Inhibitors
0
Pyridines
0
Thiosemicarbazones
0
3-aminopyridine-2-carboxaldehyde thiosemicarbazone
143621-35-6
Tyrosine
42HK56048U
Iron
E1UOL152H7
Ribonucleotide Reductases
EC 1.17.4.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
621-632Subventions
Organisme : NCI NIH HHS
ID : P50 CA211015
Pays : United States
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