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(-)-Quinpirole hydrochloride

CAS No.
85798-08-9
Chemical Name:
(-)-Quinpirole hydrochloride
Synonyms
LY-171,555;(-)-LY 171555;()-Quinpirole;(4ar-trans)-lorid;(-)-Quinpirole HCl;(?)-Quinpirole hydrochloride;(-)-Quinpirole hydrochloride;(-)-quinpirole monohydrochloride;(-)-QUINPIROLE HYDROCHLORIDE (LY-171555) SELECTIVE D2 DOPAMINE;4-g)quinolone,4,4a,5,6,7,8,8a,9-octahydro-5-propyl-1h-pyrazolo(monohydroch
CBNumber:
CB4687090
Molecular Formula:
C13H22ClN3
Molecular Weight:
255.79
MDL Number:
MFCD00069336
MOL File:
85798-08-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:52:56

(-)-Quinpirole hydrochloride Properties

storage temp. -20°C
solubility 0.1 M HCl: soluble23mg/mL
form solid
color white
optical activity [α]25/D 124.5°, c = 0.4 in H2O(lit.)
Water Solubility water: 7.3mg/mL
Stability Hygroscopic
InChI 1S/C13H21N3.ClH/c1-2-5-16-6-3-4-10-7-12-11(8-13(10)16)9-14-15-12;/h9-10,13H,2-8H2,1H3,(H,14,15);1H/t10-,13-;/m1./s1
InChIKey HJHVRVJTYPKTHX-HTMVYDOJSA-N
SMILES Cl.[H][C@]12CCCN(CCC)[C@]1([H])Cc3c[nH]nc3C2
FDA UNII T6I2W5V2K1
UNSPSC Code 12352200
NACRES NA.77

SAFETY

Risk and Safety Statements

PPE Eyeshields, Gloves, type N95 (US)
WGK Germany  3
RTECS  UR0809270
Storage Class 11 - Combustible Solids

(-)-Quinpirole hydrochloride price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Q102 (?)-Quinpirole hydrochloride ≥98% (HPLC), solid 85798-08-9 10mg $174 2026-04-30 Buy
Sigma-Aldrich Q102 (?)-Quinpirole hydrochloride ≥98% (HPLC), solid 85798-08-9 25mg $481 2026-04-30 Buy
Sigma-Aldrich 5.05982 (-)-Quinpirole Hydrochloride - CAS 85798-08-9 - Calbiochem 85798-08-9 10mg $184 2022-05-15 Buy
TRC TRC-Q796713-5MG (-)-Quinpirole Hydrochloride 85798-08-9 5mg $320 2026-06-03 Buy
Usbiological 217725 (-)-Quinpirole hydrochloride 85798-08-9 10mg $529 2026-06-03 Buy
Product number Packaging Price Buy
Q102 10mg $174 Buy
Q102 25mg $481 Buy
5.05982 10mg $184 Buy
TRC-Q796713-5MG 5mg $320 Buy
217725 10mg $529 Buy

(-)-Quinpirole hydrochloride Chemical Properties, Uses, Production

Uses

Antihypertensive.

Uses

(-)-Quinpirole hydrochloride has been used as a selective D2 dopamine (DA) receptor agonist in various experiments.

Biological Activity

(-)-quinpirole hydrochloride is an agonist of dopamine d2-like receptor [1].dopamine d2-like receptor reduces neuron’s excitability after activation by dopamine, making it an important drug target in schizophrenia and parkinson’s disease, but its ligands also cause cognitive inflexibility such as poor reversal learning [1, 2].in spiny neurons, (-)-quinpirole hydrochloride (5 ~ 10 μm) markedly reduced evoked firing in area x and lobus parolfactorius (lpo). unlike the enhancement of excitability by dopamine d1 receptor activation, the reduction in evoked firing by (-)-quinpirole hydrochloride was not voltage-dependent. this effect was antagonized by the dopamine d2-like receptor antagonist sulpiride (10 μm), which suggested that the effect of (-)-quinpirole hydrochloride was specific to dopamine d2-like receptor [2].in rats, (-)-quinpirole hydrochloride (0.01, 0.025, 0.1, 0.25, and 0.5 mg/kg) impaired both visual reversal learning task and spatial probabilistic reversal learning (prl) task in a dose-dependent manner. in analysis of the probe trials on the visual task, (-)-quinpirole hydrochloride at 0.25 mg/kg induced a complete blockade of learning from negative feedback, whilst learning from positive feedback was intact. estimated parameters from the model that best described the prl choice data revealed a steep and selective decrease in learning rate from losses [1].[1]. alsiö j, phillips b u, sala-bayo j, et al. dopamine d2-like receptor stimulation blocks negative feedback in visual and spatial reversal learning in the rat: behavioural and computational evidence. psychopharmacology (berl), 2019, 236(8): 2307-2323.[2]. ding l, perkel d j. dopamine modulates excitability of spiny neurons in the avian basal ganglia. the journal of neuroscience, 2002, 22(12): 5210-5218.

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.

in vivo

DA content is left brain biased across groups, and although this asymmetry appears greater in saline controls than all drug-treated groups, there is not a significant interaction between Side and Group. When each side is considered separately it can be seen that in the left brain structure, DA levels progressively decrease with chronic quinpirole treatment, with the QQ rats differing significantly from saline controls. In contrast, right cortical DA levels are only altered significantly (increased) by acute Quinpirole. It can be found that DOPAC levels are also left brain biased across groups. However, no significant Group or interaction effects are found. Rats receiving acute Quinpirole show a selective increase in DA content and decrease in turnover ratio, relative to either saline controls or the QS group. Sensitized (QQ) rats however, have elevated DOPAC levels in comparison to the acute quinpirole group. In striatum as well, all three measures of DA function differed significantly across groups (DA, F3,33=6.27, P=0.0020; DOPAC, F3,33=7.98, P=0.0004; turnover ratio, F3,33=16.85, P<0.0001). In the acute quinpirole rats, both DOPAC and turnover ratio are significantly reduced relative to all other groups. In QQ rats, DOPAC levels are significantly greater than all other groups, while for turnover ratio, both chronic quinpirole groups were increased compared to both chronic saline groups[1].

storage

Desiccate at -20°C

(-)-Quinpirole hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

(-)-Quinpirole hydrochloride Suppliers

Global Suppliers ( 59)
Supplier Tel Email Country ProdList Advantage
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51389 80
EMMX Biotechnology LLC 888-539-0666 info@emmx.com United States 8435 60
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9799 58
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60
BOC Sciences 16314854226; +8616314854226 inquiry@bocsci.com United States 19852 58
TargetMol Chemicals Inc. +1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32431 58
InvivoChem +1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6378 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11123 58
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8137 58

View Latest Price from (-)-Quinpirole hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Quinpirole Hydrochloride pictures 2026-07-15 Quinpirole Hydrochloride
85798-08-9
$99.00 98.00% 10g TargetMol Chemicals Inc.
Quinpirole Hydrochloride pictures 2026-07-15 Quinpirole Hydrochloride
85798-08-9
$99.00 98.00% 10g TargetMol Chemicals Inc.
(4AR-TRANS)-4,4A,5,6,7,8,8A,9-OCTAHYDRO-5-PROPYL-1H-PYRAZOLO[3,4-G]QUINOLINE HYDROCHLORIDE TRANS-(-)-4AR-4,4A,5,6,7,8,8A,9-OCTAHYDRO-5-PROPYL-1H-PYRAZOLO[3,4-G] QUINOLINE HYDROCHLORIDE (4ar-trans)-lorid 4-g)quinolone,4,4a,5,6,7,8,8a,9-octahydro-5-propyl-1h-pyrazolo(monohydroch (-)-QUINPIROLE HYDROCHLORIDE (LY-171555) SELECTIVE D2 DOPAMINE (-)-quinpirole monohydrochloride trans-(–)-(4aR)-4,4a,5,6,7,8,8a,9-Octahydro-5-propyl-1H-pyrazolo[3,4-g]quinoline monohydrochloride LY-171,555 (4aR,8aR)-5-propyl-1,4,4a,6,7,8,8a,9-octahydropyrazolo[3,4-g]quinoline:hydrochloride ()-Quinpirole (-)-LY 171555 (-)-Quinpirole HCl 1H-Pyrazolo[3,4-g]quinoline,4,4a,5,6,7,8,8a,9-octahydro-5-propyl-, hydrochloride (1:1), (4aR,8aR)- (4AR,8aR)-5-propyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrazolo[3,4-g]quinoline hydrochloride (?)-Quinpirole hydrochloride (-)-Quinpirole hydrochloride 85798-08-9