VU6015241
VU6015241 is a selective, blood-brain barrier-permeable M4 mAChR Antagonist with a Ki value of 43.3 nM. VU6015241 is used for the research of dystonia and related movement disorders.
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: 2264025-00-3
- 分子式: C26H35N5O2
- 分子量:449.59
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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
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mAChR4 43.3 nM (Ki) |
VU6015241 potently inhibits acetylcholine-stimulated calcium mobilization in hM4/Gqi5-CHO cells with an IC50 of 71 nM[1].
VU6015241 inhibits acetylcholine-stimulated calcium mobilization in rM4-CHO cells with an IC50 of 44 nM[1].
VU6015241 is highly selective for human and rat M4 receptors, with IC50 values >10,000 nM at hM1, hM2, rM1, rM2, rM3, and rM5 receptors expressed in CHO cells[1].
VU6015241 has a predicted low rat hepatic clearance of 6.2 mL/min/kg[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| Species | Dose | Route | CLplasma | Vss | T1/2 (Elimination) | MRT | AUC0-last | AUC0-∞ |
|---|---|---|---|---|---|---|---|---|
| Rat[1] | 3 mg/kg | i.v. | 257 mL/min/kg | 147 L/kg | 8.6 h | 9.33 h | 181 ng·h/mL | 202 ng·h/mL |
VU6015241 (30 mg/kg; i.p.; single dose) administered intraperitoneally at 30 mg/kg to mice results in moderate brain exposure with a Kp of 0.38, which is higher than the brain exposure observed in rats at the same dose and route[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
化学情報
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CAS 番号 2264025-00-3
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分子量 449.59
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分子式 C26H35N5O2
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SMILES
CC(NC(C=C1)=CC=C1C(N=N2)=CC=C2NC[C@H]3C4(CCN(CC4)CC5CCOCC5)C3)=O
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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)