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Imipramine is considered an NE/5-HT reuptake inhibitor (NSRI), but has a higher affinity for SERT. How is this possible?
the demethylated metabolite is selective for NET
Which is non-TCA SNRI (selective for NE)?
B
Which is a common metabolic transformation for SSRIs?
dealkylation of a basic amine
if a patient takes imipramine, which other antidepressants will the patient test positive for in a drug test?
A
which is the most likely metabolite of desipramine?
A + D
which metabolite of citalopram likely has poor CNS penetration?
D
Which NSRI is least likely to cause QT prolongation?
C
the effect of an MAOI will diminish as soon as the drug is continued
false
Which metabolic event is very likely to occur with duloxetine?
n-dealkylation
which position on duloxetine is likely to undergo aromatic oxidation?
A
which position is most likely to undergo aromatic oxidation?
1
which is the most likely metabolite of clomipramine?
A
in the blood (pH = 7.4), SSRIs will most likely be ionized
true
SSRIs are best described as:
indirect agonists
Citalopram is formulated as the HBr salt. Which is the correct, formulated structure?
B
Which is an active metabolite of fluoxetine?
A
N-dealkylation is common for most SSRIs
true
Serotonin is the only important neurotransmitter in depression.
false
which is SERT selective?
A
which is NET selective?
C
which is not selective for SERT nor NET?
B