ChemicalBook--->CAS DataBase List--->78095-19-9

78095-19-9

78095-19-9 Structure

78095-19-9 Structure
IdentificationBack Directory
[Name]

(R)-(+)-8-HYDROXY-DPAT HYDROBROMIDE
[CAS]

78095-19-9
[Synonyms]

Hydroxy-DPAT hydrobromide, (R)-(+)-8-
R(+)-8-HYDROXY-DPAT HYDROBROMIDE FULL 5- HT1A SEROTONIN
(R)-(+)-8-Hydroxy-2-(dipropylamino)tetralin hydrobromide
(R) (+) 8 Hydroxy DPAT hydrobromide,(R)(+)8HydroxyDPAT hydrobromide
(R)-(+)-2-Dipropylamino-8-hydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide, (R)-(+)-8-Hydroxy-2-(dipropylamino)tetralin hydrobromide
[Molecular Formula]

C16H25NO.BrH
[MDL Number]

MFCD00153810
[MOL File]

78095-19-9.mol
[Molecular Weight]

328.291
Chemical PropertiesBack Directory
[storage temp. ]

protect from light
[solubility ]

H2O: >10mg/mL at ±60°C (with sonication)
[form ]

solid
[color ]

white to off-white
[Optical Rotation]

[α]25/D +68.2°, c = 1 in methanol(lit.)
[Water Solubility ]

H2O: >10mg/mL at±60°C (with sonication)
[InChI]

1S/C16H25NO.BrH/c1-3-10-17(11-4-2)14-9-8-13-6-5-7-16(18)15(13)12-14;/h5-7,14,18H,3-4,8-12H2,1-2H3;1H/t14-;/m1./s1
[InChIKey]

BATPBOZTBNNDLN-PFEQFJNWSA-N
[SMILES]

Br.CCCN(CCC)[C@@H]1CCc2cccc(O)c2C1
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

22-26-36
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

(R)-(+)-8-Hydroxy-DPAT hydrobromide has been used as a 5-HT1A agonist:
  • in mice to test the activity of the serotonin receptor
  • to test its effect on zebrafish melanocyte migration and survival
  • to stimulate hippocampal neurons

[Biochem/physiol Actions]

(R)-(+)-8-Hydroxy-DPAT administration reduces aggressive behavior. It decreases food intake by modifying the sensitivity of 5-HT1A receptor during food deprivation.
[in vivo]

R(+)-8-OH-DPAT hydrobromide (0.05 mg/kg; s.c.) potentiates SUL (HY-B1059) (10 and 25 mg/kg)-induced dopamine (DA) release in the medial prefrontal cortex (mPFC)[1].

Animal Model:250-350 g, Male Sprague-Dawley albino rats[1]
Dosage:0.05 mg/kg
Administration:S.c.; 30 min before SUL
Result:Potentiated SUL (HY-B1059) (10 and 25 mg/kg)-induced dopamine (DA) release in the medial prefrontal cortex (mPFC).
[IC 50]

5-HT1A Receptor
[storage]

Store at -20°C
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