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L755507

L755507
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Purity:99.88%
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L755507

Catalog No. T6872Cas No. 159182-43-1
L755507 is an effective, selective agonist of β3-AR(IC50=35 nM).
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Pack SizePriceAvailabilityQuantity
1 mg$45In Stock
5 mg$109In Stock
10 mg$176In Stock
25 mg$313In Stock
50 mg$468In Stock
100 mg$673In Stock
1 mL x 10 mM (in DMSO)$142In Stock
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Product Introduction

Bioactivity
Description
L755507 is an effective, selective agonist of β3-AR(IC50=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].
Chemical Properties
Molecular Weight584.73
FormulaC30H40N4O6S
Cas No.159182-43-1
Storage & Solubility Information
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 40 mg/mL (68.41 mM)
Ethanol: 58.5 mg/mL (100 mM)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM1.7102 mL8.5510 mL17.1019 mL85.5096 mL
5 mM0.3420 mL1.7102 mL3.4204 mL17.1019 mL
10 mM0.1710 mL0.8551 mL1.7102 mL8.5510 mL
20 mM0.0855 mL0.4275 mL0.8551 mL4.2755 mL
50 mM0.0342 mL0.1710 mL0.3420 mL1.7102 mL
Ethanol
1mg5mg10mg50mg
100 mM0.0171 mL0.0855 mL0.1710 mL0.8551 mL

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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