To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
Languages
Recent
Show all languages
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

From Wikipedia, the free encyclopedia

Diberal[1]
Names
IUPAC name
5-ethyl-5-(4-methylpentan-2-yl)-1,3-diazinane-2,4,6-trione
Other names
  • DMBB
  • 5-Ethyl-5-(1,3-dimethylbutyl)barbituric acid
  • 5-(1,3-Dimethylbutyl)-5-ethylbarbituric acid
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C12H20N2O3/c1-5-12(8(4)6-7(2)3)9(15)13-11(17)14-10(12)16/h7-8H,5-6H2,1-4H3,(H2,13,14,15,16,17)
    Key: KXHLANWWTKSOMW-UHFFFAOYSA-N
  • CCC1(C(=O)NC(=O)NC1=O)C(C)CC(C)C
Properties
C12H20N2O3
Molar mass 240.303 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Diberal, also known as 5-(1,3-Dimethylbutyl)-5-ethylbarbituric acid or DMBB, is an atypical barbiturate. This compound can be either convulsant or anticonvulsant depending on which enantiomer is used.

Pharmacology

Diberal, unlike most barbiturates, can have convulsant actions. This is uncommon, as barbiturates typically enhance the function of GABA as allorestic modulators and agonists (at higher doses),[2] therefore having anticonvulsant properties. Depending on which isomer is used, it can have either convulsant or anticonvulsant actions.

The different pharmacological profile between isomers is thought to be due to the differences in the formation of hydrogen bonds at the binding sites.[3]

(+)-Isomer

(+)-DMBB is the atypical enantiomer of diberal. It is atypical in the means that it has convulsant action, unlike most barbiturate drugs.[4]

(−)-Isomer

Unlike (+)-DMBB, the (−)-isomer is similar to most barbiturates by having anticonvulsant action. It has been found that administration of (−)-DMBB reverses the convulsant actions of (+)-DMBB.[3] (−)-DMBB is slightly more potent than pentobarbital in its depressant properties.[5]

References

  1. ^ "Diberal".
  2. ^ Suddock, J. T.; Kent, K. J.; Cain, M. D. (2024). "Barbiturate Toxicity". StatPearls. PMID 29763050.
  3. ^ a b "Mechanism of Action of Barbiturates" (PDF).
  4. ^ Desai, Rooma; Savechenkov, Pavel Y.; Zolkowska, Dorota; Ge, Ri Le; Rogawski, Michael A.; Bruzik, Karol S.; Forman, Stuart A.; Raines, Douglas E.; Miller, Keith W. (2015). "Contrasting actions of a convulsant barbiturate and its anticonvulsant enantiomer on the α1β3γ2L GABAA receptor account for their in vivo effects". The Journal of Physiology. 593 (22): 4943–4961. doi:10.1113/JP270971. PMC 4650410. PMID 26378885.
  5. ^ Downes, Hall; Perry, Roger S.; Ostlund, Richard E.; Karler, Ralph (December 1970). "A Study of the Excitatory Effects of Barbiturates". Journal of Pharmacology and Experimental Therapeutics. 175 (3): 692–699. PMID 5489924.
This page was last edited on 3 February 2024, at 14:47
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.