Leonurine

CAS No. 24697-74-3

Leonurine( SCM-198 )

Catalog No. M13719 CAS No. 24697-74-3

Leonurine (SCM-198) is a natural alkaloid that exhibits cardio-and neuronal-protective effects both in vitro and in vivo.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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2MG 49 In Stock
5MG 63 In Stock
10MG 97 In Stock
25MG 209 In Stock
50MG 367 In Stock
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Biological Information

  • Product Name
    Leonurine
  • Note
    Research use only, not for human use.
  • Brief Description
    Leonurine (SCM-198) is a natural alkaloid that exhibits cardio-and neuronal-protective effects both in vitro and in vivo.
  • Description
    Leonurine (SCM-198) is a natural alkaloid that exhibits cardio-and neuronal-protective effects both in vitro and in vivo, occupies the caspase recruitment site of Apaf-1, blocks its interaction with procaspase-9; attenuates doxorubicin-induced apoptosis in H9c2 cardiac muscle cells, protects middle cerebral artery occluded rats through antioxidant effect and regulation of mitochondrial function, attenuates myocardial fibrotic response via inhibition of NADPH oxidase 4 (Nox4).
  • 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. 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. 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.
  • 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. 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. Leonurine (20?mg/kg, p.o.) ameliorates osteoarthritis development in mouse DMM model.
  • Synonyms
    SCM-198
  • Pathway
    Apoptosis
  • Target
    Apaf-1
  • Recptor
    Apaf-1
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    24697-74-3
  • Formula Weight
    311.338
  • Molecular Formula
    C14H21N3O5
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 6 mg/mL 19.27 mM
  • SMILES
    O=C(OCCCCNC(N)=N)C1=CC(OC)=C(O)C(OC)=C1
  • Chemical Name
    Benzoic acid, 4-hydroxy-3,5-dimethoxy-, ester with (4-hydroxybutyl)guanidine (8CI)

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Loh KP, et al. Stroke. 2010 Nov;41(11):2661-8. 2. Xin H, et al. Eur J Pharmacol. 2009 Jun 10;612(1-3):75-9. 3. Liu XH, et al. Free Radic Biol Med. 2013 Jan;54:93-104. 4. Wang Y, et al. Sci Rep. 2016 Jul 22;6:29820.
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  • Leonurine

    Leonurine (SCM-198) is a natural alkaloid that exhibits cardio-and neuronal-protective effects both in vitro and in vivo.