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(±)-Salsolinol (hydrochloride)

Catalog No.GC13786

depolarize dopamineric neurons

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(±)-Salsolinol (hydrochloride) Chemical Structure

Cas No.: 79923-51-6

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100mg
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500mg
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Sample solution is provided at 25 µL, 10mM.

Description of (±)-Salsolinol (hydrochloride)

(±)-Salsolinol targets depolarize dopamineric neurons.

Dopaminergic neurons produce dopamine, a neurotransmitter with various roles in neurological functions. Progressive loss of dopaminergic neurons is considered as the cause of many motor symptoms associated with Parkinson’s disease.

In vitro: A previous study found that (±)-salsolinol could activate the μ-opioid receptor by the classical G protein-adenylate cyclase pathway. The agonist action of (±)-salsolinol was blocked by the μ-opioid antagonist. The EC50 for the purified stereoisomers (R)- salsolinol and (S)-salsolinol were 6 × 10-4 M and 9 × 10-6 M, respectively. It was found that (±)-salsolinol did not promote the recruitment of β-arrestin. Molecular docking studies showed that the interaction of (R)- and (S)-salsolinol with the μ-opioid receptor was similar to that predicted for the agonist morphine [1].

In vivo: Male Wistar rats were subjected to continuous i.p. dosing of salsolinol at 200 mg/kg for 2 or 4 weeks with either high-fat or normal diet. Results showed that salsolinol could reduce total body mass significantly with no differences in total food intake. In addition, the epididymal fat pad weight over final body mass ratio was lower in salsolinol treated rats with high fat diet. Moreover, the perimeter, e area, as well as short and long axis of the fad pad adipocytes decreased in salsolinol treated animals significantly [2].

Clinical trial: So far, no clinical study has been conducted.

References:
[1] Berríos-Cárcamo P, Quintanilla ME, Herrera-Marschitz M, Vasiliou V, Zapata-Torres G, Rivera-Meza M.  Racemic Salsolinol and its Enantiomers Act as Agonists of the μ-Opioid Receptor by Activating the Gi Protein-Adenylate Cyclase Pathway. Front Behav Neurosci. 2017 Jan 23;10:253. doi: 10.3389/fnbeh.2016.00253. eCollection 2016.
[2] Aleksandrovych V, Kurnik M, Biaas M, Bugajski A, Thor P, Gil K.  The effect of peripheral chronic salsolinol administration on fat pad adipocytes morphological parameters. Folia Med Cracov. 2016;56(1):81-95.

Chemical Properties of (±)-Salsolinol (hydrochloride)

Cas No. 79923-51-6 SDF
Chemical Name 1,2,3,4-tetrahydro-1-methyl-6,7-isoquinolinediol, monohydrochloride
Canonical SMILES CC1NCCC2=C1C=C(O)C(O)=C2.Cl
Formula C10H13NO2 • HCl M.Wt 215.7
Solubility Soluble in ethanol;Soluble in DMSO;Soluble in Water Storage Store at 4°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of (±)-Salsolinol (hydrochloride)

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1 mg 5 mg 10 mg
1 mM 4.6361 mL 23.1803 mL 46.3607 mL
5 mM 0.9272 mL 4.6361 mL 9.2721 mL
10 mM 0.4636 mL 2.318 mL 4.6361 mL
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Average Rating: 5 ★★★★★ (Based on Reviews and 32 reference(s) in Google Scholar.)

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