| Weight | 329.371 g/mol |
|---|---|
| Formula | C19H20FNO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
paroxetine (61869-08-7, 110429-35-1)
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- Paroxetine for the Prevention of Depression Induced by High-Dose Interferon Alfa (The New England Journal of Medicine, 2001)
- Active Tamoxifen Metabolite Plasma Concentrations After Coadministration of Tamoxifen and the Selective Serotonin Reuptake Inhibitor Paroxetine (Journal of the National Cancer Institute, 2003)
- Changes in Regional Brain Glucose Metabolism Measured With Positron Emission Tomography After Paroxetine Treatment of Major Depression (American Journal of Psychiatry, 2001)
- Efficacy of Paroxetine in the Treatment of Adolescent Major Depression: A Randomized, Controlled Trial (Journal of the American Academy of Child and Adolescent Psychiatry, 2001)
- Neurobehavioral effects of interferon- in cancer patients: Phenomenology and paroxetine responsiveness of symptom dimensions. (Neuropsychopharmacology, 2002)
- Regional brain metabolic changes in patients with major depression treated with either paroxetine or interpersonal therapy: preliminary findings. (Archives of General Psychiatry, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CNCC(C1C2=CC=C(C=C2)F)COC3=CC4=C(C=C3)OCO4
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InChIKeyAHOUBRCZNHFOSL-UHFFFAOYSA-N
- Pubchem - paroxetine
- Wikipedia - paroxetine
Paroxetine, also known by the trade names Paxil among others, is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. It is used to treat major depressive disorder, obsessive-compulsive disorder, social anxiety disorder, panic disorder, posttraumatic stress disorder, generalized anxiety disorder and premenstrual dysphoric disorder. It has also been used in the treatment of hot flashes and night sweats associated with menopause.
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