Dazadrol

Antidepressant From Wikipedia, the free encyclopedia

Dazadrol is a synthetic antidepressant developed by Schering Corp in the late 1960s. It acts primarily as a noradrenaline reuptake inhibitor, increasing concentrations of noradrenaline in the synaptic cleft, which is believed to underlie its antidepressant effects.[1][2][3]

Other namesSch 12650
CAS Number
Quick facts Clinical data, Other names ...
Dazadrol
Clinical data
Other namesSch 12650
Identifiers
  • (4-chlorophenyl)-(4,5-dihydro-1H-imidazol-2-yl)-pyridin-2-ylmethanol
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.051.158 Edit this at Wikidata
Chemical and physical data
FormulaC15H14ClN3O
Molar mass287.75 g·mol−1
3D model (JSmol)
  • C1CN=C(N1)C(C2=CC=C(C=C2)Cl)(C3=CC=CC=N3)O
  • InChI=1S/C15H14ClN3O/c16-12-6-4-11(5-7-12)15(20,14-18-9-10-19-14)13-3-1-2-8-17-13/h1-8,20H,9-10H2,(H,18,19)
  • Key:DITYEPYMBCHKLF-UHFFFAOYSA-N
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Dazadrol is classified as a pyridinemethanol derivative and has been studied for its impact on neurological function and mood. In addition to its antidepressant activity, preclinical studies in rats have shown that it inhibits both basal and induced gastric acid secretion, indicating potential gastrointestinal effects.[1][3][4][2]

See also

References

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