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1 Side effects. 2 Society and culture. 3 See also. ... Ethylmorphine (also known as codethyline, dionine, and ethyl morphine) is an opioid analgesic and antitussive ...
Emoxypine (2-ethyl-6-methyl-3-hydroxypyridine), also known as Mexidol or Mexifin, a succinate salt, is chemical compound which is claimed by its manufacturer, the Russian company Pharmasoft Pharmaceuticals, to have antioxidant and actoprotector properties, [2] [3] but these purported properties of emoxypine have not been proven. [4]
Eutylone (also known as β-keto-1,3-benzodioxolyl-N-ethylbutanamine, bk-EBDB, and N-ethylbutylone) is a stimulant and empathogenic drug of the phenethylamine, amphetamine, phenylisobutylamine, and cathinone families which was developed in the 1960s, [3] [4] which is classified as a designer drug. [5]
Butabarbital (brand name Butisol) is a prescription barbiturate sleep aid and anxiety medication.Butabarbital has a particularly fast onset of effects and short duration of action compared to other barbiturates, which makes it useful for certain applications such as treating severe insomnia, relieving general anxiety and relieving anxiety before surgical procedures; however it is also ...
In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula −C 4 H 9, derived from either of the two isomers (n-butane and isobutane) of butane.
It has primarily anxiolytic and anticonvulsant effects in animal tests, but with no sedative effects even at 50 times the effective anxiolytic dose. [ 2 ] [ 3 ] In human trials on healthy volunteers, TPA-023 was comparable to lorazepam , but lacked negative effects on cognition, memory, alertness or coordination seen with the latter drug. [ 4 ]
Ethyl butylacetylaminopropionate is an insect repellent whose trade name is IR3535 and was developed and commercialized by Merck KGaA (Germany). It is a colorless and odorless oil with a good skin feel in final products, and it is biodegradable. [1] [2] [3]
It has a modest affinity to the 5-HT [1A, 1E, 2B, 7] receptors, and little to no affinity at the 5-HT [2A, 2C, 3, 4, 5A, 6] receptors. Eletriptan has no significant affinity or pharmacological activity at adrenergic α 1, α 2, or β; dopaminergic D 1 or D 2; muscarinic; or opioid receptors. Eletriptan could be efficiently co-administered with ...