CAS NO: | 862281-92-3 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | PF-00446687 is a potent, selectivemelanocortin-4 receptor(MC4R) agonist withEC50of 12 ± 1 nM[1]. Pf-446687 is brain penetrant[2]. | ||||||||||||||||
IC50& Target | EC50: 12 ± 1 nM (MC4R)[1] | ||||||||||||||||
体外研究 (In Vitro) | PF-00446687 binds MC4 receptor with a Kiof 27±4 nM. PF-00446687 has a relatively weak activity at the MC1, MC3, and MC5 receptors with EC50s of 1.02±0.30 μM, 1.16±0.35 μM, and 1.98±0.20 μM, respectively. The broad off-target profiles of PF-00446687 are assessed in the CEREP Bioprint wide ligand screening panel, with the most potent binding activities being at the σ receptor (Ki=330 nM), the sodium ion channel (Ki=690 nM), and the muscarinic M2 receptor (Ki=730 nM)[1]. | ||||||||||||||||
体内研究 (In Vivo) | Pf-446687 is highly selective for MC4R and is both brain penetrant and stable in vivo. Peripheral administration of the brain penetrant MC3/4R receptor peptide agonist, Melanotan II (MTII), and the highly selective, small molecule MC4R agonist, Pf-446687, enhances partner preference formation in the prairie vole, but not in the non-monogamous meadow vole[2]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 470.59 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C28H36F2N2O2 | ||||||||||||||||
CAS 号 | 862281-92-3 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 62.5 mg/mL(132.81 mM;Need ultrasonic) 配制储备液
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