Pentobarbital sodium salt

Enhances GABAergic activity CAS# 57-33-0

Pentobarbital sodium salt

Catalog No. BCC6231----Order now to get a substantial discount!

Product Name & Size Price Stock
Pentobarbital sodium salt:50mg $58.00 In stock
Pentobarbital sodium salt:100mg $99.00 In stock
Pentobarbital sodium salt:250mg $232.00 In stock
Pentobarbital sodium salt:500mg $406.00 In stock
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Chemical structure

Pentobarbital sodium salt

3D structure

Chemical Properties of Pentobarbital sodium salt

Cas No. 57-33-0 SDF Download SDF
PubChem ID 23676152 Appearance Powder
Formula C11H17N2NaO3 M.Wt 248.25
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble to 100 mM in water
Chemical Name 5-Ethyl-5-(1-methylbutyl)-2,4,6(1H,3H,5H)-pyrimidinetrione sodium salt
SMILES CCCC(C)C1(C(=O)NC(=NC1=O)[O-])CC.[Na+]
Standard InChIKey QGMRQYFBGABWDR-UHFFFAOYSA-M
Standard InChI InChI=1S/C11H18N2O3.Na/c1-4-6-7(3)11(5-2)8(14)12-10(16)13-9(11)15;/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16);/q;+1/p-1
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.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Biological Activity of Pentobarbital sodium salt

DescriptionEnhances GABAergic activity. Short-acting barbiturate; long-acting barbiturate also available.

Pentobarbital sodium salt Dilution Calculator

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Pentobarbital sodium salt Molarity Calculator

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Preparing Stock Solutions of Pentobarbital sodium salt

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.0282 mL 20.141 mL 40.282 mL 80.5639 mL 100.7049 mL
5 mM 0.8056 mL 4.0282 mL 8.0564 mL 16.1128 mL 20.141 mL
10 mM 0.4028 mL 2.0141 mL 4.0282 mL 8.0564 mL 10.0705 mL
50 mM 0.0806 mL 0.4028 mL 0.8056 mL 1.6113 mL 2.0141 mL
100 mM 0.0403 mL 0.2014 mL 0.4028 mL 0.8056 mL 1.007 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Pentobarbital sodium salt

Modulation of GABA(A) receptor channel gating by pentobarbital.[Pubmed:11744750]

J Physiol. 2001 Dec 15;537(Pt 3):715-33.

1. We have studied the kinetic properties of channel gating of recombinant alpha 1 beta 2 gamma 2L GABA(A) receptors transiently expressed in human embryonic kidney 293 cells, using the cell-attached, single-channel patch-clamp technique. The receptors were activated by GABA, beta-alanine or piperidine-4-sulfonic acid (P4S), and the effects of pentobarbital (PB) on single-channel activity were examined. 2. At relatively high concentrations of agonist, single-channel activity occurred in well-defined clusters. In global terms, PB increased the mean open time for events in clusters, without changing the mean closed time. The addition of PB shifted the curve relating the probability of being open in a cluster (P(o)) to lower agonist concentrations, and that shift could be accounted for by the changes in mean open time. 3. The intracluster closed-time histograms contained four components. The durations and relative frequencies of these closed-dwell components were not affected by the presence of 40 microM PB, at any agonist concentration. The duration of one component was dependent upon the concentration of agonist used to activate the receptor. Accordingly, the inverse of the mean duration of this component will be called the effective opening rate. 4. The channel-opening rate constant (beta) was determined from the value of the effective opening rate at a saturating agonist concentration. beta was about 1900 s(-1) when the receptors were activated by GABA, 1500 s(-1) when activated by beta-alanine, and too low to be determined when P4S was administered. In the presence of 40 microM PB, beta was about 1500 s(-1) when the receptors were activated by GABA, 1400 s(-1) when activated by beta-alanine, and 50 s(-1) when activated by P4S. Hence, the potentiating effect of PB is not mediated by a change in beta. The concentration of agonist producing a half-maximal effective opening rate also remained unaffected in the presence of PB, indicating that receptor affinity for agonists is not influenced by PB. 5. The distributions of the intracluster open durations elicited by GABA could be described by the sum of three exponentials, with mean durations of about 0.4, 2.4 and 6.3 ms. The duration and relative frequency of the components did not change with GABA concentration (20 microM to 1 mM). In the presence of 40 microM PB, however, the mean duration of the longest of the open times increased (mean durations of about 0.4, 2.0 and 13 ms). The intracluster open durations elicited by beta-alanine could be described by the sum of two exponential components (1.1 and 3.5 ms). However, in the presence of 40 microM PB the open-time distribution contained three exponential components (0.2, 2 and 10 ms). Finally, openings elicited by P4S exhibited two components (0.3 and 0.9 ms). In the presence of 40 microM PB, three components could be distinguished (0.5, 2.5 and 13 ms). 6. These observations indicate that the potentiating effect of PB on GABA type A (GABA(A)) receptors reflects effects on the open state(s) of the receptors. In the case of receptors activated by GABA, the observations are consistent with the idea that the action is the result of PB stabilizing one of the open states. The actions on receptors activated by P4S or beta-alanine are also broadly consistent with this idea. However, the changes in open-time distributions caused by PB appear to be more complex. Possible explanations of the effects of PB on gating by different agonists are considered.

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