Benactyzine

Chemical compound From Wikipedia, the free encyclopedia

Benactyzine is an anticholinergic drug that was used in the treatment of clinical depression and anxiety disorders before it was pulled from the U.S. market by the FDA due to serious side effects.[2]

ATC code
  • none
Legal status
  • BR: Class C1 (Other controlled substances)[1]
  • In general: ℞ (Prescription only)
Quick facts Clinical data, AHFS/Drugs.com ...
Benactyzine
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • BR: Class C1 (Other controlled substances)[1]
  • In general: ℞ (Prescription only)
Identifiers
  • 2-(diethylamino)ethyl hydroxy(diphenyl)acetate
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.005.568 Edit this at Wikidata
Chemical and physical data
FormulaC20H25NO3
Molar mass327.424 g·mol−1
3D model (JSmol)
  • O=C(OCCN(CC)CC)C(O)(c1ccccc1)c2ccccc2
  • InChI=1S/C20H25NO3/c1-3-21(4-2)15-16-24-19(22)20(23,17-11-7-5-8-12-17)18-13-9-6-10-14-18/h5-14,23H,3-4,15-16H2,1-2H3 checkY
  • Key:IVQOFBKHQCTVQV-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)
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Its use for these indications was limited by side effects such as dry mouth and nausea, and at high doses it can cause more severe symptoms such as deliriant and hallucinogenic effects.[2] "Large doses of benactyzine in normal subjects may produce a state resembling the action of mescaline or LSD."[3]

Brand names have included: Suavitil, Phebex, Phobex, Cedad, Cevanol, Deprol, Lucidil, Morcain, Nutinal, Parasan. While there was some tentative evidence of effectiveness when combined with meprobamate, with the medication no longer available it is not clinically important.[4]

History

Benactyzine was brought to market in the US in 1957 by Merck under the tradename, Suavitil.[5]

See also

References

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