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[CAS NO. 24735-18-0]??Leonurine hydrochloride

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PRODUCTS SPECIFICATIONS [24735-18-0]

Catalog
HY-N0741A
Brand
MCE
CAS
24735-18-0

DESCRIPTION [24735-18-0]

Overview

MDL-
Molecular Weight347.79
Molecular FormulaC14H22ClN3O5
SMILESO=C(OCCCCNC(N)=N)C1=CC(OC)=C(O)C(OC)=C1.[H]Cl

For research use only. We do not sell to patients.


Summary

Leonurine hydrochloride is an alkaloid isolated from Leonurus artemisia , with anti-oxidative and anti-inflammatory.


In Vitro

Leonurine (0, 5, 10, 20, 40, 80 μM) causes diminution in lipid accumulation, cellular cholesterol content, including total cholesterol (TC), free cholesterol (FC) and cholesteryl ester (CE), and increase in apoA-I- or HDL-mediated cholesterol efflux after treatment for 24 h. Leonurine also significantly and dose-dependently increases the expressions of ABCA1 and ABCG1 at the mRNA and protein levels in human THP-1 macrophages, and such effect is involved in PPARγ [1] . Leonurine hydrochloride (LH) shows protective effect on cell viability of HepG2 and HL-7702 cells incubated with palmitic acid (PA) of free fatty acid (FFA) for 24?h. Leonurine hydrochloride (125, 250, 500?μM) improves cellular lipid accumulation in HepG2 and HL-7702 cells via activating AMPK/SREBP1 pathway [2] . Leonurine (5, 10, 20?μM) inhibits the expression of iNOS, COX-2, PGE2, NO, TNF-α, and IL-6 in IL-1β-induced human chondrocytes, suppresses ECM degradation in human OA chondrocytes, and blocks IL-1β-induced PI3K and Akt phosphorylation in a dose-dependent manner [3] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


In Vivo

Leonurine (10 mg/kg/d, p.o.) significantly increases the expressions of PPARγ, LXRα, ABCA1 and ABCG1, and decreases both TG and TC levels in serum of mice [1] . Leonurine hydrochloride (50, 100, 200 mg/kg) improves intracellular lipid accumulation via activating AMPK/SREBP1 pathway, enhances biochemical parameters, reduces hepatic lipoperoxide and increases antioxidant levels in mice [2] . Leonurine (20?mg/kg, p.o.) ameliorates osteoarthritis development in mouse DMM model [3] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


Appearance

Solid



Shipping

Room temperature in continental US; may vary elsewhere.


Storage

4°C, sealed storage, away from moisture

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)


Solvent & Solubility

In Vitro:

DMSO : ≥ 31 mg/mL ( 89.13 mM )

H 2 O : 5 mg/mL ( 14.38 mM ; Need ultrasonic)

* "≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.8753 mL 14.3765 mL 28.7530 mL
5 mM 0.5751 mL 2.8753 mL 5.7506 mL
10 mM 0.2875 mL 1.4376 mL 2.8753 mL
* Please refer to the solubility information to select the appropriate solvent.


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