Page last updated: 2024-10-15

tetrazanbigen

Description

tetrazanbigen: a synthetic azagonane with significant antitumor effects on common solid tumors; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID124203923
CHEMBL ID4781829
MeSH IDM0550880

Synonyms (5)

Synonym
tetrazanbigen, >=98% (hplc)
tnbg
CHEMBL4781829
tetrazanbigen
AKOS040754174

Research Excerpts

Overview

Tetrazanbigen (TNBG) is a newly synthesized compound with an isoquinoline moiety. Its antitumour effects were evaluated in in-vitro and in- vivo models.

ExcerptReference
"Tetrazanbigen (TNBG) is a newly synthesized compound with an isoquinoline moiety, and its antitumour effects were evaluated in in-vitro and in-vivo models."( Antitumour effects of tetrazanbigen against human hepatocellular carcinoma QGY-7701 through inducing lipid accumulation in vitro and in vivo.
Chen, X; Lan, Z; Li, L; Li, W; Xia, Z; Yang, X; Yu, Y; Yuan, Y; Zhang, X; Zheng, X, 2015
)
"Tetrazanbigen (TNBG) is a novel synthetic antitumor drug with significant antitumor effects on common solid tumors in vitro and in vivo. "( Effects of tetrazanbigen on the protein expression in human hepatocellular carcinoma cell line QGY-7701.
Gu, R; Huang, K; Li, L; Li, W; Liu, H; Yang, X; Yu, Y; Yuan, Y, 2009
)
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID1707994Inhibition of colony formation in human A549 cells at 3 uM incubated for 3 days followed by drug-free medium replacement for every 3 days for 12 days by crystal violet staining based assay
AID1707992Thermodynamic solubility in pH 7.4 phosphate buffer incubated for 6 hrs followed by further incubation for 18 hrs with shaking by UV-HPLC analysis
AID1707991Antiproliferative activity against human QSG7701 cells assessed as reduction in cell viability incubated for 72 hrs by CCK8 assay
AID1708062Induction of apoptosis in human A549 cells at 2 uM incubated for 48 hrs by FITC Annexin V/propidium iodide staining based flow cytometry
AID1707989Antiproliferative activity against human LoVo cells assessed as reduction in cell viability incubated for 72 hrs by CCK8 assay
AID1707990Antiproliferative activity against human A549 cells assessed as reduction in cell viability incubated for 72 hrs by CCK8 assay
AID1707988Antiproliferative activity against human HepG2 cells assessed as reduction in cell viability incubated for 72 hrs by CCK8 assay
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's3 (60.00)24.3611
2020's1 (20.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]