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123039-93-0

123039-93-0 Structure

123039-93-0 Structure
IdentificationBack Directory
[Name]

DIHYDREXIDINE HYDROCHLORIDE
[Synonyms]

DAR-0100
DihydrexidineHCl
Dihydrexidine hydroc
DIHYDROXIDINE HYDROCHLORIDE
DIHYDREXIDINE HYDROCHLORIDE
Benzo[a]phenanthridine-10,11-diol, 5,6,6a,7,8,12b-hexahydro-, (6aR,12bS)-rel-
(+/-)-TRANS-10,11-DIHYDROXY-5,6,6A,7,8,12B-HEXAHYDROBENZO[A]PHENANTHRIDINE HYDROCHLORIDE
[MDL Number]

MFCD01860859
[MOL File]

123039-93-0.mol
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

Soluble in DMSO
Hazard InformationBack Directory
[Biological Activity]

A potent, full efficacy dopamine D 1 agonist which shows no agonist activity at peripheral D 2 receptors or adrenoceptors at doses which cause maximal stimulation of D 1 sites. The compound appears to be fully bioavailable in brain and exhibits profound antiparkinsonism effects in vivo .
[in vivo]

Dihydrexidine has poor oral bioavailability and a relatively short half-life of 1 to 2 h[3].
Dihydrexidine (3 mg/kg; i.p.) produces prominent dopamine D1 receptor agonist effects in vivo[4].

Animal Model:Adult male Sprague–Dawley rats (275-300 g)[4]
Dosage:Adult male Sprague–Dawley rats (275-300 g)[4]
Administration:Intraperitoneal injection
Result:Produces prominent dopamine D1 receptor agonist effects in vivo
[IC 50]

D1 Receptor: 10 nM (IC50)
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