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...eational drug use|recreational use]] as a [[dissociative]] [[anesthetic]]. It is also used as an [[Oxidizing agent|oxidizer]] in [[rocket]]ry and in [[Au ...greenhouse gas]] and [[air pollutant]]. Considered over a 100 year period, it has 298 times more impact per unit weight than [[carbon dioxide]].<ref>2007

...SH)|publisher= National Library of Medicine|accessdate= 2006-03-10}}</ref> It possesses [[anxiolytic]], [[anticonvulsant]], [[hypnotic]], [[sedative]], [ ...most frequently prescribed medications in the world for the past 40 years. It was first synthesized by Dr. [[Leo Sternbach]].<ref>{{cite journal | author

...ally a [[gamma-Aminobutyric acid|GABA]] [[Analogue (chemistry)|analogue]]. It was originally developed for the treatment of [[epilepsy]], and currently, ...thought to involve [[voltage-gated]] [[N-type calcium]] [[ion channels]]. It is thought to bind to the α2δ subunit ([[CACNA2D1|1]] and [[CACNA2D2|2]])

...depth of anesthesia with hexobarbital which makes it quite dangerous, and it has now been replaced by safer drugs in human medicine, usually [[thiopenta ...uthor = Korkmaz S, Ljungblad E, Wahlström G | title = Interaction between flumazenil and the anesthetic effects of hexobarbital in the rat. | journal = Brain Re