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Raclopride Raclopride, also known as FLA 870, is a selective and potent dopamine D2/D3 receptor antagonist. It has high affinity (Kd = 1.2 nM) and high selectivity for D2 receptors in vitro and in vivo (IC50 = 32 nM). Uses: Antipsychotic agents. Synonyms: 3,5-Dichloro-N-[[(2S)-1-ethyl-2-pyrrolidinyl]methyl]-2-hydroxy-6-methoxybenzamide; (-)-Raclopride; FLA 870; FLA870; FLA-870; Benzamide, 3,5-dichloro-N-[[(2S)-1-ethyl-2-pyrrolidinyl]methyl]-2-hydroxy-6-methoxy-; Benzamide, 3,5-dichloro-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-6-methoxy-, (S)-; (S)-3,5-Dichloro-N-((1-ethylpyrrolidin-2-yl)methyl)-2-hydroxy-6-methoxybenzamide. Grades: ≥99% by HPLC. CAS No. 84225-95-6. Molecular formula: C15H20Cl2N2O3. Mole weight: 347.24. BOC Sciences 10
Raclopride Raclopride. Group: Biochemicals. Grades: Purified. CAS No. 84225-95-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. USBiological 5
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Raclopride Raclopride is a dopamine D 2 / D 3 receptor antagonist with potential antipsychotic effects. Raclopride binds to D 2 and D 3 receptor s with K i s of 1.8 nM and 3.5 nM, respectively [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 84225-95-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-103414. MedChemExpress MCE
(S)-(-)-Raclopride (Dopamine Receptor D2 Antagonist, (S)-Raclopride, Raclopride) D2-like dopamine receptor antagonist targeting D2R (pKi =8.0), D3R (pKi = 7.9), and 5-HT1A R (pKi=5.2). Used to explore D2 like receptor mediated effects in neuropathic pain, and in antagonism studies of DA receptors during heroin usage and cocaine. D2 Receptor selectivity in various preps shows IC50 values around 32nM. Group: Biochemicals. Grades: Highly Purified. CAS No. 84225-95-6. Pack Sizes: 10mg. Molecular Formula: C??H??Cl?N?O?. US Biological Life Sciences. USBiological 4
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