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| Product | Description | |
|---|---|---|
| (-)-Quinpirole hydrochloride | (-)-Quinpirole hydrochloride is a selective dopamine D2 receptor agonist, with high affinity for the D2 and D3 dopamine receptor subtypes (Ki values are 4.8, ~24, ~30 and 1900 nM at D2, D3, D4 and D1 receptors respectively). Synonyms: (4aR-trans)-4,4a,5,6,7,8,8a,9-Octahydro-5-propyl-1H-pyrazolo[3,4-g]quinoline hydrochloride; (-)-Quinpirole hydrochloride; (-)Quinpirole hydrochloride; (-)-Quinpirole HCl; (-)Quinpirole HCl; (-) Quinpirole HCl; LY-171555; LY 171555; LY171555. Grades: ≥98% by HPLC. CAS No. 85798-08-9. Molecular formula: C13H21N3.HCl. Mole weight: 255.79. |  |
| (-)-Quinpirole Hydrochloride (Dopamine D2 Receptor Agonist, Quinpirole, Quinpirole, LY-171,555, LY 171555) | A potent, selective dopamine D2 receptor agonist with a Ki value of 4.8nM. Some D3(Ki = 24nM) and D4 (Ki = 30nM) receptor agonistic action has also been reported. In rat striatum studies in vitro, application of quinpriole inhibited single pulse dopamine overflow in a concentration-dependent manner (IC50 = 32.5nM). Group: Biochemicals. Grades: Highly Purified. CAS No. 85798-08-9. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| (?)-Quinpirole hydrochloride | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. |  |
| Amisulpride hydrochloride | Amisulpride hydrochloride could inhibit radioligand binding to native dopamine D2 receptor in membranes from the rat striatum with an IC50 value of 21nM. It has been revealed to displace [3H]raclopride binding in vivo with an ED50 value of 17.3±1.86mg/kg in the rat limbic system. It has been noted to inhibit quinpirole-induced [3H]thymidine with an IC50 value of 22±3nM. It is used to treat psychosis in schizophrenia and episodes of mania in bipolar disorder. It has been approved in February 2002 by FDA. Uses: Amisulpride hydrochloride is used to treat psychosis in schizophrenia and episodes of mania in bipolar disorder. Synonyms: DAN 2163 hydrochloride; DAN2163 hydrochloride; DAN-2163 hydrochloride; 4-amino-N-[(1-ethylpyrrolidin-2-yl)methyl]-5-ethylsulfonyl-2-methoxybenzamide;hydrochloride. Grades: >98%. CAS No. 81342-13-4. Molecular formula: C17H28N3O4SCl. Mole weight: 405.94. | |
| Quinelorane hydrochloride | Quinelorane hydrochloride, 2-aminopyridine analog of quinpirole, is a dopamine D2 and D3 receptor agonist (Ki= 5.7 and 3.4 nM respectively). Synonyms: (5aR,9aR)-5,5a,6,7,8,9,9a,10-Octahydro-6-propyl-pyrido[2,3-g]quinazolin-2-amine Dihydrochloride; (5aR-trans)-5,5a,6,7,8,9,9a,10-Octahydro-6-propyl-pyrido[2,3-g]quinazolin-2-amine Dihydrochloride; LY 163502; LY163502; LY-163502. Grades: ≥99% by HPLC. CAS No. 97548-97-5. Molecular formula: C14H22N4.2HCl. Mole weight: 319.27. | |
| Quinpirole hydrochloride | Quinpirole hydrochloride (LY 171555 hydrochloride) is a high-affinity agonist of dopamine D2/D3 receptor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY 171555 hydrochloride; (-)-LY 141865 hydrochloride. CAS No. 85798-08-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-B1752A. |  |
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