Powder: -20°C for 3 years | In solvent: -80°C for 1 year
CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively.
パッケージサイズ | 在庫状況 | 単価(税別) | |||
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サンプルについてお問い合わせ | |||||
1 mg | 在庫あり | ¥ 9,000 | |||
5 mg | 在庫あり | ¥ 21,000 | |||
10 mg | 在庫あり | ¥ 30,500 | |||
25 mg | 在庫あり | ¥ 51,500 | |||
50 mg | 在庫あり | ¥ 76,500 | |||
100 mg | 在庫あり | ¥ 114,500 | |||
1 mL * 10 mM (in DMSO) | 在庫あり | ¥ 21,500 |
説明 | CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively. |
ターゲット&IC50 | A1 receptor:3.5 nM (ki), A2A receptor:4.2 nM (ki), p110γ:1.1 μM, A2B receptor:16 nM (ki), p110δ:8.47 μM, A3 receptor:51 nM (ki) |
In vitro | CGS 15943 inhibits the kinase activity of the class IB PI3K isoform p110γ (IC50: 1.1 μM). CGS 15943 shows slight inhibition on p110δ (IC50: 8.47 μM). 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. 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[3]. |
分子量 | 285.69 |
分子式 | C13H8ClN5O |
CAS No. | 104615-18-1 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 12.22 mg/mL (42.77 mM), Sonication is recommended.
You can also refer to dose conversion for different animals. 詳細
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CGS 15943 104615-18-1 GPCR/G Protein Neuroscience PI3K/Akt/mTOR signaling PI3K Adenosine Receptor Phosphoinositide 3-kinase P1 receptor CGS15943 inhibit CGS-15943 Inhibitor inhibitor