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CL 316243 disodium salt
murine-selective β3 adrenoceptor agonist

Catalog No.B6766
Size Price Stock Qty
10mg
$236.00
In stock
50mg
$997.00
In stock

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Sample solution is provided at 25 µL, 10mM.

Quality Control

Quality Control & MSDS

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Chemical structure

CL 316243 disodium salt

Protocol

In vitro experiment [1]:

Samples

LES smooth muscles

Preparation method

The solubility of this compound in sterile water is 100 mM. General tips for obtaining a higher concentration: Please warm the tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below - 20 °C for several months.

Reacting condition

0.01 ~ 300 μM

Applications

CL 316243 concentration-dependently decreased the basal tension of the LES smooth muscle, with an ECmax value of 1 × 10-4 M. At corresponding ECmax values, the smooth muscle relaxation induced by CL 316243 was significantly longer than that triggered by isoproterenol. The smooth muscle relaxation in the isoproterenol group began to recover within 5 mins but it cost 1 hr in the case of CL 316243.

Animal experiment [2]:

Animal models

Nonobese and nondiabetic Sprague-Dawley rats

Dosage form

1 mg/kg/day; s.c.; for 10 ~ 12 days

Applications

After 7 days of treatment, CL 316243 significantly increased food consumption, resting metabolic rates, as well as body core temperatures in rats. Besides, CL 316243 decreased the respiratory quotient by 14%. On day 11, an oral glucose load (2 g/kg) did not alter plasma glucose and insulin excursions. In addition, CL 316243 reduced abdominal and epididymal white fat pad weights, but doubled interscapular brown adipose tissue weight at the same time.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. Sarma DN, Banwait K, Basak A, DiMarino AJ, Rattan S. Inhibitory effect of beta3-adrenoceptor agonist in lower esophageal sphincter smooth muscle: in vitro studies. J Pharmacol Exp Ther. 2003 Jan;304(1):48-55.

[2]. de Souza CJ, Hirshman MF, Horton ES. CL-316,243, a beta3-specific adrenoceptor agonist, enhances insulin-stimulated glucose disposal in nonobese rats. Diabetes. 1997 Aug;46(8):1257-63.

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Chemical Properties

Cas No. 151126-84-0 SDF Download SDF
Chemical Name sodium 5-((S)-2-(((S)-2-(3-chlorophenyl)-2-hydroxyethyl)amino)propyl)benzo[d][1,3]dioxole-2,2-dicarboxylate
Canonical SMILES ClC1=CC([[email protected]@H](CN[[email protected]@H](C)CC2=CC=C3OC(C([O-])=O)(C([O-])=O)OC3=C2)O)=CC=C1.[Na+].[Na+]
Formula C20H18ClNNa2O7 M.Wt 465.8
Solubility Soluble to 100 mM in sterile water Storage Desiccate at -20°C
Physical Appearance Pale yellow solid Shipping Condition Evaluation sample solution : ship with blue ice.All other available size: ship with RT , or blue ice upon request
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.

Background

EC50: (3.0±0.3) X 10-8 M for β3 adrenoceptor [1].

Benzodioxole-containing phenethanolamine CL-316,243 is a murine-selective β3 adrenoceptor agonist which can correct obesity and elevated blood glucose in diabetic rodents, which offers an exciting possibility for the treatment of non-insulin-dependent diabetes as well as obesity without undesired β-mediated side effects [3]. β3 adrenoceptor is located mainly in adipose tissue and is involved in the regulation of lipolysis and thermogenesis.

In vitro: The compound was a potent stimulant of rat adipocyte lipolysis (β3 effect, EC50 = (3.0±0.3) X 10-8 M), had no effect on the rate of contraction of guinea pig atria (β1 effect, EC50 > 10-4 M), and had only a very limited ability to inhibit insulin-stimulated [14C] glucose incorporation into glycogen in isolated rat soleus muacle (β2 effect, IC50 = (3.0±1.0) X 10-5 M) [1].

In vivo: In rat, CL-316,243 treatment resulted in increased growth rates and significant changes in food consumption at the end of the 10-day treatment period. CL-316,243 treatment increased insulin responsiveness and sensitivity in non-insulin-resistant rodent species. The CL-316,243 induced increases in whole-body glucose disposal were due entirely to increases in adipose tissue glucose uptake, while muscle glucose uptake remained unaltered [2].

Clinical trial: So far, no clinical study has been conducted.

References:
[1] Bloom JD, Dutia MD, Johnson BD, Wissner A, Burns MG, Largis EE, Dolan JA, Claus TH.  Disodium (R,R)-5-[2-[[2-(3-chlorophenyl)-2-hydroxyethyl]-amino] propyl]-1,3-benzodioxole-2,2-dicar
-boxylate (CL 316,243).  A potent beta-adrenergic agonist virtually specific for beta 3 receptors. A promising antidiabetic and antiobesity agent. J Med Chem. 1992 Aug 7;35(16):3081-4.
[2] de Souza CJ, Hirshman MF, Horton ES.  CL-316,243, a beta3-specific adrenoceptor agonist, enhances insulin-stimulated glucose disposal in nonobese rats. Diabetes. 1997 Aug;46(8):1257-63.
[3] Kumar A, Shiloach J, Betenbaugh MJ, Gallagher EJ.  The beta-3 adrenergic agonist (CL-316,243) restores the expression of down-regulated fatty acid oxidation genes in type 2 diabetic mice. Nutr Metab (Lond). 2015 Mar 8;12:8.