Powder: -20°C for 3 years | In solvent: -80°C for 1 year
L755507 is an effective, selective agonist of β3-AR(IC50=35 nM).
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 | ¥ 10,500 | |||
5 mg | 在庫あり | ¥ 25,000 | |||
10 mg | 在庫あり | ¥ 40,500 | |||
25 mg | 在庫あり | ¥ 72,000 | |||
50 mg | 在庫あり | ¥ 107,500 | |||
100 mg | 在庫あり | ¥ 154,500 | |||
1 mL * 10 mM (in DMSO) | 在庫あり | ¥ 32,500 |
説明 | L755507 is an effective, selective agonist of β3-AR(IC50=35 nM). |
ターゲット&IC50 | β3-adrenoceptor:35 nM |
In vitro | L-755,507 displays an excellent activity profile as an extremely potent human β3 adrenergic receptor agonist (β3 EC50 0.43 nM), with >440-fold selectivity over β1 and β2 binding[1]. L755507 causes a robust concentration-dependent increase in cAMP accumulation in CHO-K1 cells expressing human β3-adrenoceptors(pEC50 values of 12.3)[4]. In a recent study employing a high-throughput screen to identify chemicals capable of modulating HR-mediated genome editing, L-755507 is identified that could enhance HR repair by up to ninefold[3]. |
In vivo | Acute exposure of rhesus monkeys to L-755,507 elicits lipolysis and metabolic rate elevation, and that chronic exposure increases uncoupling protein 1 expression in rhesus brown adipose tissue[2]. |
分子量 | 584.73 |
分子式 | C30H40N4O6S |
CAS No. | 159182-43-1 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 58.5 mg/mL (100 mM)
Ethanol: 58.5 mg/mL (100 mM)
You can also refer to dose conversion for different animals. 詳細
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L755507 159182-43-1 DNA Damage/DNA Repair GPCR/G Protein Neuroscience CRISPR/Cas9 Adrenergic Receptor HDR β3-AR inhibit Beta Receptor Inhibitor L-755507 L 755507 inhibitor