Eterobarb
Eterobarb is a barbiturate derivative that has been used in the past as a sedative and hypnotic agent. It is known for its ability to depress the central nervous system, leading to effects such as sedation, anxiolysis, and hypnosis.
Chemical Structure and Properties[edit | edit source]
Eterobarb belongs to the class of barbiturates, which are derivatives of barbituric acid. The chemical structure of Eterobarb includes a pyrimidine ring fused with a urea moiety, characteristic of barbiturates. This structure allows it to interact with the gamma-aminobutyric acid (GABA) receptors in the brain, enhancing the inhibitory effects of GABA and leading to its sedative properties.
Pharmacology[edit | edit source]
Eterobarb acts primarily by binding to the GABA_A receptors in the central nervous system. This binding increases the duration of the chloride ion channel opening, leading to hyperpolarization of the neuron and a decrease in neuronal excitability. The result is a calming effect on the brain, which can induce sleep and reduce anxiety.
Medical Uses[edit | edit source]
Eterobarb was historically used for its sedative and hypnotic properties. It was prescribed for the treatment of insomnia, anxiety disorders, and as a pre-anesthetic agent. However, due to the development of safer and more effective medications, its use has significantly declined.
Side Effects and Risks[edit | edit source]
The use of Eterobarb, like other barbiturates, is associated with several side effects. These can include drowsiness, dizziness, nausea, and headache. More severe risks involve respiratory depression, dependence, and withdrawal symptoms. Overdose of Eterobarb can be fatal, leading to coma and death.
Regulation and Legal Status[edit | edit source]
Due to its potential for abuse and dependence, Eterobarb is classified as a controlled substance in many countries. Its medical use is highly restricted, and it is generally only available through special prescription.
See Also[edit | edit source]
References[edit | edit source]
External Links[edit | edit source]
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Contributors: Prab R. Tumpati, MD