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  • DC Chemicals Limited
  • China
  • Product Name: BNS-22
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

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: 2024-01-10 22:28:13
  • 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