Weight | 280.415 g/mol |
---|---|
Formula | C19H24N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 4 |
imipramine (50-49-7)
Tofranil · Imipramine Hydrochloride · Janimine
Score:
#146 in Neuroscience
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#719 in Biology
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#777 in Chemistry
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- Cognitive-Behavioral Therapy, Imipramine, or Their Combination for Panic Disorder: A Randomized Controlled Trial (JAMA, 2000)
- A comparison of cognitive therapy, applied relaxation and imipramine in the treatment of panic disorder. (British Journal of Psychiatry, 1994)
- Tritiated imipramine binding sites are decreased in the frontal cortex of suicides (Science, 1982)
- Inhibition of Uptake of Tritiated-noradrenaline in the Intact Rat Brain by Imipramine and Structurally Related Compounds (Nature, 1964)
- Gender differences in treatment response to sertraline versus imipramine in chronic depression. (American Journal of Psychiatry, 2000)
- Drug Therapy in the Prevention of Recurrences in Unipolar and Bipolar Affective Disorders Report of the NIMH Collaborative Study Group Comparing Lithium Carbonate, Imipramine, and a Lithium Carbonate-Imipramine Combination (Archives of General Psychiatry, 1984)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Tofranil
- Imipramine Hydrochloride
- Janimine
- Imizin
- Pryleugan
- Imipramine Monohydrochloride
- Melipramine
- Imidobenzyle
- Norchlorimipramine
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SMILESCN(C)CCCN1C2=CC=CC=C2CCC3=CC=CC=C31
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InChIKeyBCGWQEUPMDMJNV-UHFFFAOYSA-N
- Pubchem - imipramine
- Wikipedia - imipramine
Imipramine, sold under the brand name Tofranil among others, is a tricyclic antidepressant (TCA) which is used mainly in the treatment of depression. It can also reduce symptoms of agitation and anxiety. The drug is also used to treat bedwetting.
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