PSB-22269
PSB-22269 is a competitive GPR17 antagonist. PSB-22269 can be used in research on multiple sclerosis.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 分子式: C26H21NO6
- 分子量:443.45
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
製品説明
体外実験
PSB-22269 (30 min) inhibits GPR17-induced calcium mobilization in CHO-FITR-hGPR17 cells with pIC50 7.0[1].
PSB-22269 (0-1000 nM; 30 min) competitively inhibits GPR17-mediated calcium mobilization in 1321N1 astrocytoma cells with pIC50 6.90 and pKB 7.46[1].
PSB-22269 (20 min) inhibits GPR17 agonist-induced Gαi2 activation in HEK293 cells with pIC50 6.31[1].
PSB-22269 binds hGPR17 in the cell-free [3H]PSB-12150 binding assay using CHO-FITR cell membranes, with the reported overall IC50 range of 0.0089-0.13 µM[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
化学情報
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分子量 443.45
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分子式 C26H21NO6
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SMILES
COC1=CC(C(O)=O)=C(NC(C2=CC=C(C3=C(C4=CC=CC(OC)=C4)C=CC=C3)O2)=O)C=C1
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)