Desmethylimipramine
Brand names,
Desmethylimipramine
Analogs
Desmethylimipramine
Brand Names Mixture
Desmethylimipramine
Chemical_Formula
C18H22N2
Desmethylimipramine
RX_link
http://www.rxlist.com/cgi/generic2/desipram.htm
Desmethylimipramine
fda sheet
Desmethylimipramine
msds (material safety sheet)
Desmethylimipramine
Synthesis Reference
No information avaliable
Desmethylimipramine
Molecular Weight
266.381 g/mol
Desmethylimipramine
Melting Point
214-218 oC
Desmethylimipramine
H2O Solubility
No information avaliable
Desmethylimipramine
State
Solid
Desmethylimipramine
LogP
3.87
Desmethylimipramine
Dosage Forms
Tablet
Desmethylimipramine
Indication
For relief of symptoms in various depressive syndromes, especially endogenous depression.
Desmethylimipramine
Pharmacology
Desipramine, a tertiary amine tricyclic antidepressant, is structurally related to both the skeletal muscle relaxant cyclobenzaprine and the thioxanthene antipsychotics such as thiothixene. Desipramine is used to treat depression, pain of neuropathic origin, attention_deficit hyperactivity disorder, functional enuresis in children, panic and phobic disorder, and to manage some eating disorders. Desipramine inhibits the re-uptake of noradrenaline at the noradrenergic nerve endings and the re-uptake of serotonin (5-hydroxy tryptamine) at the serotoninergic nerve endings in the central nervous system. These two effects are considered to be the likely base of the antidepressant effect of Desipramine. The drug also has a strong anticholinergic effect and serves as an antagonist on a1 and H1 receptors.
Desmethylimipramine
Absorption
Desipramine hydrochloride is rapidly and almost completely absorbed from the gastrointestinal tract. 90.5% (range 73-92%) of desipramine binds to plasma proteins.
Desmethylimipramine
side effects and Toxicity
Male mice: LD50 = 290 mg/kg, female rats: LD50 = 320 mg/kg
Desmethylimipramine
Patient Information
No information avaliable
Desmethylimipramine
Organisms Affected
Humans and other mammals