(-)-QUINPIROLE HYDROCHLORIDE
- CAS No.
- 85798-08-9
- Chemical Name:
- (-)-QUINPIROLE HYDROCHLORIDE
- Synonyms
- LY-171,555;()-Quinpirole;(-)-LY 171555;(4ar-trans)-lorid;(-)-QUINPIROLE HCL;(-)-Quinpirole HCl;(-)-QUINPIROLE HYDROCHLORIDE;(-)-QUINPIROLE HYDROCHLORIDE;(-)-quinpirole monohydrochloride;(-)-QUINPIROLE HYDROCHLORIDE (LY-171555) SELECTIVE D2 DOPAMINE
- CBNumber:
- CB4687090
- Molecular Formula:
- C13H22ClN3
- Molecular Weight:
- 255.79
- MOL File:
- 85798-08-9.mol
- MSDS File:
- SDS
- Modify Date:
- 2023/6/30 15:45:59
(-)-QUINPIROLE HYDROCHLORIDE price More Price(4)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich(India) | Q102 | (−)-Quinpirole hydrochloride ≥98% (HPLC), solid | 85798-08-9 | 10MG | ₹18803.03 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | Q102 | (−)-Quinpirole hydrochloride ≥98% (HPLC), solid | 85798-08-9 | 25MG | ₹42206.68 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | Q102 | (−)-Quinpirole hydrochloride ≥98% (HPLC), solid | 85798-08-9 | 100MG | ₹141309.55 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | 5.05982 | (-)-Quinpirole Hydrochloride - CAS 85798-08-9 - Calbiochem | 85798-08-9 | 10MG | ₹16930 | 2022-06-14 | Buy |
(-)-QUINPIROLE HYDROCHLORIDE Chemical Properties,Uses,Production
Uses
(-)-Quinpirole hydrochloride has been used as a selective D2 dopamine (DA) receptor agonist in various experiments.
Biochem/physiol Actions
Quinpirole is a dopamine agonist with high affinity for the D2 and D3 dopamine receptor subtypes. Specific [3H]quinpirole binding in rat brain was saturable, and dependent on temperature, membrane concentration, sodium concentration and guanine nucleotides. The putative D2 dopamine receptor agonist quinpirole (LY 171,555) is the most widely used D2 agonist in in vivo and in vitro studies. Quinpirole hydrochloride is an active enantiomer of (±)-quinpirole.Saturation analysis revealed high affinity binding characteristics (KD = 2.3 +/- 0.3 nM) which were confirmed by association-dissociation kinetics. The regional distribution of [3H]quinpirole binding sites roughly paralleled the distribution of [3H]spiperone binding sites, with greatest densities present in the striatum, nucleus accumbens and olfactory tubercles. A variety of drugs, most notably monoamine oxidase inhibitors (MAOls), inhibit the binding of [3H]quinpirole, but not [3H]spiperone or [3H](-)N-n-Propylnorapomorphine, in rat striatal membranes by a mechanism that does not appear to involve the enzymatic activity of MAO. Clinically antidepressant MAOIs exhibited selectivity between sites labeled by [3H]quinpirole and [3H]spiperone as did a number of structurally related propargylamines and N-acylethylenediamine derivatives and other drugs such as debrisoquin and phenylbiguanide. The MAOIs clorgyline and Ro 41-1049 were the most potent. MAOIs interact with a novel binding site that is labeled by [3H]quinpirole or that modulates [3H]quinpirole binding. This site may be associated with D2-like dopamine receptors.
(-)-QUINPIROLE HYDROCHLORIDE Preparation Products And Raw materials
Raw materials
Preparation Products
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