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CL 316243 free acid exhibits an IC 50 of 0.6 μM and 1 μM for rat heart and rat soleus muscle, respectively. Additionally, it inhibits spontaneous contractions in isolated rat detrusor muscle strips in a concentration-dependent manner, with an average concentration for 50% maximal inhibition at 2.65 nM.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
10 mg | Inquiry | 10-14 weeks | |
50 mg | Inquiry | 10-14 weeks |
Description | CL 316243 free acid exhibits an IC 50 of 0.6 μM and 1 μM for rat heart and rat soleus muscle, respectively. Additionally, it inhibits spontaneous contractions in isolated rat detrusor muscle strips in a concentration-dependent manner, with an average concentration for 50% maximal inhibition at 2.65 nM. |
In vitro | CL 316243 free acid exhibits an IC 50 of 0.6 μM and 1 μM for rat heart and rat soleus muscle, respectively. Additionally, it inhibits spontaneous contractions in isolated rat detrusor muscle strips in a concentration-dependent manner, with an average concentration for 50% maximal inhibition at 2.65 nM. |
In vivo | Administering CL316243 free acid via subcutaneous injection (Subcutaneous Injectio;0.1 mg/kg/d;1 week) ignificantly increases the mRNA and protein expression levels of UCP1 in brown adipose tissue (BAT), independently of diet. In the study, male C57BL/6J mice were either fed a high-fat diet (HFD; 45%-kcal fat) or a control diet (ND; 10%-kcal fat) for 14 weeks. The dose of CL316243 was 0.1 mg/kg/day. This treatment was found to greatly enhance resistance against obesity in these mice. |
Molecular Weight | 421.83 |
Formula | C20H20ClNO7 |
Cas No. | 183720-02-7 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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