Name | 9-chloro-2-(furan-2-yl)-[1,2,4]triazolo[1,5-c]quinazolin-5-amine |
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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]. |
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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 |
Density | 1.72 g/cm3 |
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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 |
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RIDADR | NONH for all modes of transport |