Desipramine
Brand names,
Desipramine
Analogs
Desipramine
Brand Names Mixture
Desipramine
Chemical_Formula
C18H22N2
Desipramine
RX_link
http://www.rxlist.com/cgi/generic2/desipram.htm
Desipramine
fda sheet
Desipramine
msds (material safety sheet)
Desipramine
Synthesis Reference
No information avaliable
Desipramine
Molecular Weight
266.381 g/mol
Desipramine
Melting Point
214-218 oC
Desipramine
H2O Solubility
No information avaliable
Desipramine
State
Solid
Desipramine
LogP
3.87
Desipramine
Dosage Forms
Tablet
Desipramine
Indication
For relief of symptoms in various depressive syndromes, especially endogenous depression.
Desipramine
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.
Desipramine
Absorption
Desipramine hydrochloride is rapidly and almost completely absorbed from the gastrointestinal tract. 90.5% (range 73-92%) of desipramine binds to plasma proteins.
Desipramine
side effects and Toxicity
Male mice: LD50 = 290 mg/kg, female rats: LD50 = 320 mg/kg
Desipramine
Patient Information
No information avaliable
Desipramine
Organisms Affected
Humans and other mammals