Drug intelligence / Profile preview

SKF-38393

Development stage
Discontinued
Lead developer
GSK
Modality
Small Molecules
Administration
Experimental (mainly Used In Research Via Various Injection Routes Including Intraperitoneal And Intravenous In Animal Studies)
01

Overview

SKF-38393 is a **synthetic small molecule** of the benzazepine chemical class that acts as a **selective partial agonist at dopamine D1-like receptors** (primarily the D1 and D5 subtypes). It is commonly used as a pharmacological tool in research to investigate dopaminergic mechanisms due to its receptor specificity. SKF-38393 exhibits **stimulant and anorectic (appetite-suppressing) effects**, and has been studied for its potential neuroprotective actions in models of Parkinson’s disease. It does not activate D2-like receptors, distinguishing it from many other dopaminergic agents. The compound and several of its derivatives were originally developed by GSK and are widely available for experimental use in neuroscience and pharmacology[1][3][5][7].

Other names
1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol5-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepineSKF-38393 hydrobromideSKF38393 hydrobromideSKF 38393 hydrobromideS(-)-SKF-38393 HCL(±)-SKF-38393 hydrochloride
02

Targets

SIGMAR1 (Sigma non-opioid intracellular receptor 1)DRD1 (Dopamine D1 Receptor)DRD5 (Dopamine D5 Receptor)INSR (Insulin receptor)

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