Top Suppliers:I want be here


1151668-24-4

1151668-24-4 structure
1151668-24-4 structure
  • Name: BNS-22
  • Chemical Name: 8-(3,4-Dihydro-1(2H)-quinolinylcarbonyl)-5,7-dimethoxy-4-propyl-2H-chromen-2-one
  • CAS Number: 1151668-24-4
  • Molecular Formula: C24H25NO5
  • Molecular Weight: 407.459
  • Catalog: Signaling Pathways Cell Cycle/DNA Damage Topoisomerase
  • Create Date: 2018-07-06 07:48:48
  • Modify Date: 2025-08-24 21:55:09
  • BNS-22 is a DNA topoisomerase II (TOP2) catalytic inhibitor with the IC50 values of 2.8 μM and 0.42 μM for human TOP2α and TOP2β, respectively. BNS-22 induces abnormal division and has anti-proliferative activity[1].

Name 8-(3,4-Dihydro-1(2H)-quinolinylcarbonyl)-5,7-dimethoxy-4-propyl-2H-chromen-2-one
Synonyms MFCD22628799
2H-1-Benzopyran-2-one, 8-[(3,4-dihydro-1(2H)-quinolinyl)carbonyl]-5,7-dimethoxy-4-propyl-
8-(3,4-Dihydro-1(2H)-quinolinylcarbonyl)-5,7-dimethoxy-4-propyl-2H-chromen-2-one
Description BNS-22 is a DNA topoisomerase II (TOP2) catalytic inhibitor with the IC50 values of 2.8 μM and 0.42 μM for human TOP2α and TOP2β, respectively. BNS-22 induces abnormal division and has anti-proliferative activity[1].
Related Catalog
Target

topoisomerase II alpha:2.8 μM (IC50, in human)

topoisomerase II beta:0.42 μM (IC50, in human)

In Vitro BNS-22 (0-30 μM, 24-48 h) can inhibit cell growth and influence on cell cycle progression of the human cervical epidermoid carcinoma cell line HeLa in a dose-dependent manner[1]. BNS-22 (0-30 μM, 0-6 h) does not induce DNA damage and has an antagonistic effect on TOP2 toxin-mediated DNA damage[1]. Cell Proliferation Assay[1] Cell Line: HeLa cell lines Concentration: 0-30 μM Incubation Time: 24 h, 48 h Result: Inhibited cell growth with the IC50 value of 4.9 μM after 24 hours and 1.0 μM after 48 hours. Cell Cycle Analysis[1] Cell Line: HeLa cell lines Concentration: 0-30 μM Incubation Time: 24 h Result: Increased number of cells in G2/M phase. Disrupted mitotic spindle formation and induced polyploid cell formation at 3 μM. Western Blot Analysis[1] Cell Line: HeLa cell lines Concentration: 0-30 μM Incubation Time: 0, 30 min, 1 h, 2 h, 4 h, 6 h Result: Decreased etoposide-induced γ-H2AX expression and decreased total cellular TOP2β levels, but not TOP2α levels.
References

[1]. Makoto Kawatani, et al. Identification of a small-molecule inhibitor of DNA topoisomerase II by proteomic profiling. Chem Biol. 2011 Jun 24;18(6):743-51.

Density 1.2±0.1 g/cm3
Boiling Point 622.7±55.0 °C at 760 mmHg
Molecular Formula C24H25NO5
Molecular Weight 407.459
Flash Point 330.4±31.5 °C
Exact Mass 407.173279
LogP 4.10
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.593
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
RIDADR NONH for all modes of transport
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.