| Identification | Back Directory | [Name]
S(-)RACLOPRIDE L-TARTRATE >97% SELECTIVE D2 DOPAMINE | [CAS]
98185-20-7 | [Synonyms]
Raclopride tartrate
s(-)-raclopride (+)-tartrate salt
S(-)RACLOPRIDE L-TARTRATE >97% SELECTIVE D2 DOPAMINE
3,5-dichloro-n-(1-ethylpyrrolidin-2-ylmethyl)-2-hydroxy-6-methoxybenzamide tartrate salt
(S)-(-)-3,5-dichloro-N-<(1-ethyl-2-pyrrolidinyl)methyl>-6-methoxysalicylamide L-(+)-tartrate | [Molecular Formula]
C19H26Cl2N2O9 | [MDL Number]
MFCD00274072 | [MOL File]
98185-20-7.mol | [Molecular Weight]
497.32 |
| Chemical Properties | Back Directory | [solubility ]
H2O: soluble89mg/mL | [form ]
solid | [color ]
white | [Water Solubility ]
H2O: 89mg/mL | [InChIKey]
QULBVRZTKPQGCR-NDAAPVSOSA-N | [SMILES]
O[C@H]([C@@H](O)C(O)=O)C(O)=O.CCN1CCC[C@H]1CNC(=O)c2c(O)c(Cl)cc(Cl)c2OC |
| Hazard Information | Back Directory | [Uses]
S(-)-Raclopride (+)-tartrate salt is a D2DR inhibitor; D1 and D2 dopamine receptor antagonists. | [Biochem/physiol Actions]
Selective D2 dopamine receptor antagonist. | [in vivo]
Raclopride tartrate (0.1, 0.3, or 0.6 mg/kg; IP; 30 min; albino male mice of the OF1 strain) significantly reduces time allocated to attack behavior[2]. | [IC 50]
D2 Receptor: 1.8 nM (Ki); D3 Receptor: 3.5 nM (Ki); D4 Receptor: 2400 nM (Ki); D1 Receptor: 18000 nM (Ki) |
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