Fenpentadiol
Source: Wikipedia, the free encyclopedia.
Chemical compound
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| Clinical data | |
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| Routes of administration | Oral |
| ATC code |
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| Legal status | |
| Legal status |
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| Identifiers | |
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ECHA InfoCard | 100.036.150  |
| Chemical and physical data | |
| Formula | C12H17ClO2 |
| Molar mass | 228.72 g·mol−1 |
Fenpentadiol (
tranquilizer and antidepressant that was formerly marketed in Europe.[1][2] It also has stimulant, sedative, and anxiolytic effects, with the latter two occurring only at higher doses.[3][4]
The following literature incidence of the fenpentadiol has been found and quoted:
In three articles the properties of a new psychotropic agent from the series of araliphatic alcohols — phenpentanediol (CXV) — were described (477-479). It is not easy to place this substance anywhere in the pharmacodynamic system of psychotropic agents: on the one hand it potentiates the barbiturate narcosis, on the other it increases motility and exploratory activity in mice and potentiates the effects of amphetamine.
— Farmaco. Edizione Scientifica. 1974. p. 90.
References
- ISBN 978-1-4757-2085-3.
- ISBN 0-911910-13-1.
- PMID 4396676.
- ISBN 0-12-040507-5.
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SNRIs Tooltip Serotonin–norepinephrine reuptake inhibitors | ||
NRIs Tooltip Norepinephrine reuptake inhibitors | ||
NDRIs Tooltip Norepinephrine–dopamine reuptake inhibitors | ||
NaSSAs Tooltip Noradrenergic and specific serotonergic antidepressants | ||
SARIs Tooltip Serotonin antagonist and reuptake inhibitors | ||
SMS Tooltip Serotonin modulator and stimulators | ||
| Others |
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TCAs Tooltip Tricyclic antidepressants |
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TeCAs Tooltip Tetracyclic antidepressants | ||
| Others | ||
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Miscellaneous | |
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III