Fenpentadiol

Fenpentadiol
Clinical data
Routes of
administration
Oral
ATC code none
Legal status
Legal status
  • ℞ (Prescription only)
Identifiers
CAS Number 15687-18-0
PubChem (CID) 85896
ChemSpider 77482
UNII BLO7300903 YesY
ChEMBL CHEMBL2106273
Chemical and physical data
Formula C12H17ClO2
Molar mass 228.72 g/mol

Fenpentadiol (INN) (brand names Tredum, Trefenum; developmental code name Rd-292), also known as phenpentanediol, is a drug described as a 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

  1. ↑ J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 258–. ISBN 978-1-4757-2085-3.
  2. ↑ O'Neil, Maryadele J. (2001). The Merck index: an encyclopedia of chemicals, drugs, and biologicals. Rahway, NJ: Merck Research Laboratories. ISBN 0-911910-13-1.
  3. ↑ Ginet J, Levy JC, Rolland D (January 1971). "[Psychotropic activity under the influence of fenpentadiol]". Arzneimittel-Forschung (in German). 21 (1): 1–8. PMID 4396676.
  4. ↑ Heinzelman, Richard Voorhees (1972). Cornelius K. Cain, ed. Academic Press. p. 316. ISBN 0-12-040507-5 https://books.google.com/books?id=52joNWUvZakC&lpg=PA11&as_brr=3&pg=PA11#v=onepage. Missing or empty |title= (help)


This article is issued from Wikipedia - version of the 10/1/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.