| Weight | 271.36 g/mol |
|---|---|
| Formula | C17H21NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 7 |
Nisoxetine
3-(o-methoxyphenoxy)-N-methyl-3-phenylpropylamine · LY 135252 · N-methyl-gamma-(2-methylphenoxy)phenylpropanolamine
53179-07-0, 57754-86-6, 57226-61-6
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- dl-N-methyl-3-(O-methoxyphenoxy)-3-phenylpropylamine hydrochloride, Lilly 94939, a potent inhibitor for uptake of norepinephrine into rat brain synaptosomes and heart (Life Sciences, 1975)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-(o-methoxyphenoxy)-N-methyl-3-phenylpropylamine
- LY 135252
- N-methyl-gamma-(2-methylphenoxy)phenylpropanolamine
- DL-N-methyl-3-(o-methoxyphenoxy)-N-methyl-3-phenylpropylamine
- 3-(2-methoxyphenoxy)-N-methyl-3-phenylpropylamine
- LY-135252
- Lilly 94939
- Lilly 135252
- nisoxetine hydrochloride
- LY 94939
- nisoxetine hydrochloride, (+-)-isomer
- nisoxetine, (+-)-isomer
-
SMILESCNCCC(C1=CC=CC=C1)OC2=CC=CC=C2OC
-
InChIKeyITJNARMNRKSWTA-UHFFFAOYSA-N
- Pubchem - Nisoxetine
- Wikipedia - nisoxetine
Nisoxetine, originally synthesized in the Lilly research laboratories during the early 1970s, is a potent and selective inhibitor for the reuptake of norepinephrine (noradrenaline) into synapses. It currently has no clinical applications in humans, although it was originally researched as an antidepressant. Nisoxetine is now widely used in scientific research as a standard selective norepinephrine reuptake inhibitor.
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