Page last updated: 2024-10-15
nk314
Description
NK314: a benzo[c]phenanthridine that inhibits topoisomerase IIalpha and G2 cell cycle arrest; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
---|---|
PubMed CID | 156596431 |
MeSH ID | M0512543 |
Synonyms (8)
Synonym |
---|
nk314 |
208237-49-4 |
1h-(1,3)benzodioxolo(5,6-c)pyrrolo(1,2-f)phenanthridinium, 2,3-dihydro-4-hydroxy-5-methoxy-, chloride (1:1) |
1-hydroxy-2-methoxy-11a,13,14,15-tetrahydro-6ah-(1,3)dioxolo(4',5':4,5)benzo(1,2-c)pyrrolo(1,2-f)phenanthridin-12-ium chloride |
nk-314 |
bh68fxm7x8 , |
1h-(1,3)benzodioxolo(5,6-c)pyrrolo(1,2-f)phenanthridinium, 2,3-dihydro-4-hydroxy-5-methoxy-, chloride |
unii-bh68fxm7x8 |
Research Excerpts
Overview
NK314 is a novel synthetic benzo[c]phenanthridine alkaloid. It has recently entered clinical trials as an antitumor compound.
Excerpt | Reference |
---|---|
"NK314 is a novel synthetic benzo[c]phenanthridine alkaloid that has recently entered clinical trials as an antitumor compound, based on impressive activities in preclinical models. " | ( Inhibition of topoisomerase IIalpha and G2 cell cycle arrest by NK314, a novel benzo[c]phenanthridine currently in clinical trials. Guo, L; Liu, X; Nishikawa, K; Plunkett, W, 2007) |
"NK314 is a novel synthetic benzo[c]phenanthridine alkaloid that shows strong antitumor activity. " | ( NK314, a novel topoisomerase II inhibitor, induces rapid DNA double-strand breaks and exhibits superior antitumor effects against tumors resistant to other topoisomerase II inhibitors. Kagaya, S; Miyazaki, O; Nishikawa, K; Okamoto, K; Onda, T; Seno, C; Toyoda, E, 2008) |
Compound-Compound Interactions
Excerpt | Reference |
---|---|
"Topoisomerase II (Topo2) inhibitors in combination with cisplatin represent a common treatment modality used for glioma patients." | ( Comparison of the effect of three different topoisomerase II inhibitors combined with cisplatin in human glioblastoma cells sensitized with double strand break repair inhibitors. Galita, G; Kopa, P; Macieja, A; Majsterek, I; Pastwa, E; Poplawski, T, 2019) |
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
Research
Studies (7)
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 3 (42.86) | 24.3611 |
2020's | 1 (14.29) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 7 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |