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| Product | Description | |
|---|---|---|
| Raclopride | Raclopride. Group: Biochemicals. Grades: Purified. CAS No. 84225-95-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| 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. |  |
| Raclopride | Raclopride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3,5-Dichloro-N-[[(2S)-1-ethyl-2-pyrrolidinyl]methyl]-2-hydroxy-6-methoxybenzamide Hydrochloride. Product Category: Heterocyclic Organic Compound. CAS No. 98527-32-3. Molecular formula: C15H21Cl3N2O3. Mole weight: 383.7. Purity: 0.96. IUPACName: 3,5-dichloro-N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-6-methoxybenzamide;hydrochloride. Product ID: ACM98527323. Alfa Chemistry ISO 9001:2015 Certified. |  |
| (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. | Worldwide |
| S(?)-Raclopride (+)-tartrate salt | >97%, solid. Group: Fluorescence/luminescence spectroscopy. |  |
| 3,5-Dichloro-N-[[(2S)-1-ethylpyrrolidin-1-ium-2-yl]methyl]-2-hydroxy-6-methoxybenzamide;(2R,3R)-2,3,4-trihydroxy-4-oxobutanoate | 3,5-Dichloro-N-[[(2S)-1-ethylpyrrolidin-1-ium-2-yl]methyl]-2-hydroxy-6-methoxybenzamide;(2R,3R)-2,3,4-trihydroxy-4-oxobutanoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (S)-2-[(3,5-dichloro-6-methoxy-2-hydroxybenzamido)methyl]-1-ethylpyrrolidine L-tartrate; raclopride tartarate; raclopride tartrate; (S)-2-[(3,5-dichloro-6-methoxy-2-hydroxybenzamido)methyl]-1-ethylpyrrolidine L-tartrate; S(-)-RACLOPRIDE (+)-TARTRATE SALT. Product Category: Heterocyclic Organic Compound. CAS No. 98185-20-7. Molecular formula: C19H26Cl2N2O9. Mole weight: 497.324 g/mol. Purity: 0.96. IUPACName: 3,5-dichloro-N-[[(2S)-1-ethylpyrrolidin-1-ium-2-yl]methyl]-2-hydroxy-6-methoxybenzamide; (2R,3R)-2,3,4-trihydroxy-4-oxobutanoate. Product ID: ACM98185207. Alfa Chemistry ISO 9001:2015 Certified. | |
| Rac1 Inhibitor W56 | Rac1 Inhibitor W56 is a peptide comprising residues 45-60 of the guanine nucleotide exchange factor (GEF) recognition/activation site of Rac1. Synonyms: FLA 870; FLA-870; FLA870; Raclopride tartrate; MVDGKPVNLGLWDTAG. Grade: >97%. CAS No. 1095179-01-3. Molecular formula: C74H117N19O23S. Mole weight: 1671.93. |  |
| S-14506 hydrochloride | S-14506 hydrochloride is a potent 5-HT1A agonist, as well as 5-HT 2A/2C antagonist. S-14506 hydrochloride displays dopamine antagonist properties by blocking dopamine D2 receptors. S-14506 hydrochloride inhibits the in vivo binding of [3H]raclopride in striatum and olfactory bulbs. S-14506 hydrochloride has the potential for the research of anxiolytic agent [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 286369-38-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110024. | |
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