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  • DC Chemicals Limited
  • China
  • Product Name: CGS-15943
  • Price: ¥550.0/100mg ¥900.0/250mg ¥1900.0/1g
  • Purity: 98.0%
  • Stocking Period: 1 Day
  • Contact: Tony Cao

104615-18-1

104615-18-1 structure
104615-18-1 structure
  • Name: CGS 15943
  • Chemical Name: 9-chloro-2-(furan-2-yl)-[1,2,4]triazolo[1,5-c]quinazolin-5-amine
  • CAS Number: 104615-18-1
  • Molecular Formula: C13H8ClN5O
  • Molecular Weight: 285.68900
  • Catalog: Signaling Pathways GPCR/G Protein Adenosine Receptor
  • Create Date: 2017-03-06 20:34:57
  • Modify Date: 2024-01-09 13:13:47
  • CGS 15943 is an adenosine A2 receptor antagonist and reduces stroke injury in the Mongolian gerbil[1]. CGS 15943 is a selectively p110γ inhibitor with an IC50 of 1.1 μM, shows inhibitory effect on p110δ (IC50=8.47 μM), has an anti-carcinogenic effect on HCC and PDAC cells[2].

Name 9-chloro-2-(furan-2-yl)-[1,2,4]triazolo[1,5-c]quinazolin-5-amine
Synonyms MFCD01529897
Description CGS 15943 is an adenosine A2 receptor antagonist and reduces stroke injury in the Mongolian gerbil[1]. CGS 15943 is a selectively p110γ inhibitor with an IC50 of 1.1 μM, shows inhibitory effect on p110δ (IC50=8.47 μM), has an anti-carcinogenic effect on HCC and PDAC cells[2].
Related Catalog
Target

p110γ:1.1 μM (IC50)

p110δ:8.47 μM (IC50)

adenosine A2 receptor

In Vitro CGS 15943 (0-20 μM; 72 hours) inhibits growth of HLF and SK-Hep-1 cells, as well as HepG2 and PLC-PRF-5 cells[2]. CGS 15943 (0-20 μM; 24 hours) reduces the phosphorylation of Akt at its residues Ser473 and Thr308 in HLF and Sk-Hep-1 cells[2]. Cell Viability Assay[2] Cell Line: HLF, SK-Hep-1, HepG2 and PLC-PRF-5 cells Concentration: 0 μM; 1 μM; 5 μM; 10 μM; 20 μM Incubation Time: 24 hours Result: Inhibited growth of four distinct HCC cell lines. Western Blot Analysis[2] Cell Line: HLF and Sk-Hep-1 cells Concentration: 0 μM; 1 μM; 5 μM; 10 μM; 20 μM Incubation Time: 24 hours Result: Inhibited the PI3K/Akt pathway in HLF and Sk-Hep-1 cells
References

[1]. Gao Y, et al. CGS 15943, an adenosine A2 receptor antagonist, reduces cerebral ischemic injury in the Mongolian gerbil. Life Sci. 1994;55(3):PL61-5.

[2]. Edling CE, et al. Caffeine and the analog CGS 15943 inhibit cancer cell growth by targeting the phosphoinositide 3-kinase/Akt pathway. Cancer Biol Ther. 2014 May;15(5):524-32.

Density 1.72 g/cm3
Boiling Point 566.6ºC at 760 mmHg
Melting Point 278-279 °C
Molecular Formula C13H8ClN5O
Molecular Weight 285.68900
Flash Point 296.5ºC
Exact Mass 285.04200
PSA 82.24000
LogP 3.35430
Vapour Pressure 7.4E-13mmHg at 25°C
Index of Refraction 1.84
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport