Pecavaptan
Pecavaptan, a chemical probe, is an orally active and dual antagonist of V1a/V2 receptor (Ki=0.5 nM and 0.6 nM for human, respectively). Pecavaptan promotes an increase in urine production, which reduces the associated symptoms of water retention and edema.
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。
- CAS 番号: 1914998-56-3
- 分子式: C22H19Cl2F3N6O3
- 分子量:543.33
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
Vasopressin Receptor アイソフォーム固有の製品をすべて表示
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生物活性
|
human V1a Receptor 3.6 nM (IC50) |
canine V1a Receptor 4.4 nM (IC50) |
human V2 Receptor 1.7 nM (IC50) |
canine V2 Receptor 1.3 nM (IC50) |
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
化学情報
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CAS 番号 1914998-56-3
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分子量 543.33
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分子式 C22H19Cl2F3N6O3
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SMILES
O[C@H](C(F)(F)F)CN1C(C2=CC=C(Cl)C=C2)=NN(CC3=NN(C4=CC(Cl)=CC=C4)C([C@@H](O)C)=N3)C1=O
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別名
BAY 1753011
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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)