1. Metabolic Enzyme/Protease Epigenetics Immunology/Inflammation Apoptosis Vitamin D Related/Nuclear Receptor Cell Cycle/DNA Damage
  2. PCSK9 Small Interfering RNA (siRNA) Pyroptosis PPAR NOD-like Receptor (NLR) Caspase Interleukin Related
  3. Inclisiran sodium

Inclisiran sodium  (Synonyms: ALN-PCSsc sodium)

Cat. No.: HY-132591A Purity: 99.08%
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Inclisiran sodium is a double-stranded small interfering RNA (siRNA) molecule. Inclisiran sodium inhibits the transcription of PCSK9. Inclisiran sodium inhibits Pyroptosis, activates PPARγ, and reduces NLRP3, cleaved caspase-1, IL-1β, and IL-18. Inclisiran sodium has anti-inflammatory, lipid-regulating and anti-atherosclerotic activities. Inclisiran sodium can be used in researches of hyperlipidemia and cardiovascular disease (CVD).

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

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Customer Review

Based on 7 publication(s) in Google Scholar

Other Forms of Inclisiran sodium:

Top Publications Citing Use of Products

    Inclisiran sodium purchased from MedChemExpress. Usage Cited in: Free Radic Biol Med. 2026 Mar 16:246:547-561.  [Abstract]

    Inclisiran sodium (5 mg/kg). Western blot and quantitative analysis of Aβ expression in the cortex of ApoE-/− mice.

    Inclisiran sodium purchased from MedChemExpress. Usage Cited in: Free Radic Biol Med. 2026 Mar 16:246:547-561.  [Abstract]

    Inclisiran sodium (5 mg/kg). Colocalization of Aβ in microvascular endothelial cells of ApoE −/− mouse brain (scale bar: 75 μm; DAPI (blue fluorescence) indicates cell nuclei, Aβ (green) and CD31 (red)).

    Inclisiran sodium purchased from MedChemExpress. Usage Cited in: Free Radic Biol Med. 2026 Mar 16:246:547-561.  [Abstract]

    Inclisiran sodium (5 mg/kg). Western blot and quantitative analysis of ACSL4 and GPX4 expression in the cortex of ApoE-/− mice.

    Inclisiran sodium purchased from MedChemExpress. Usage Cited in: Free Radic Biol Med. 2026 Mar 16:246:547-561.  [Abstract]

    Western blot and quantitative analyses of PCSK9 expression after ox-LDL (50 μg/mL) and Inclisiran (100 nmol/L) treatment in HCMEC/D3 cells.

    Inclisiran sodium purchased from MedChemExpress. Usage Cited in: Free Radic Biol Med. 2026 Mar 16:246:547-561.  [Abstract]

    Cell viability of HCMEC/D3 cells after treatment with ox-LDL (50 μg/mL) and Inclisiran (100 nmol/L) measured by CCK-8 assay.
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    Description

    Inclisiran sodium is a double-stranded small interfering RNA (siRNA) molecule. Inclisiran sodium inhibits the transcription of PCSK9. Inclisiran sodium inhibits Pyroptosis, activates PPARγ, and reduces NLRP3, cleaved caspase-1, IL-1β, and IL-18. Inclisiran sodium has anti-inflammatory, lipid-regulating and anti-atherosclerotic activities. Inclisiran sodium can be used in researches of hyperlipidemia and cardiovascular disease (CVD)[1][2][3].

    IC50 & Target[1][2][3]

    PPARγ

     

    NLRP3

     

    Caspase-1

     

    IL-1β

     

    In Vitro

    Inclisiran (50-200 nM; 48 h) sodium significantly inhibits cell death, cytotoxicity, and downregulates mRNA and protein expressions of pyroptosis-related factors in ox-LDL-induced HUVECs[2].
    Inclisiran (50-200 nM; 48 h) sodium inhibits ox-LDL-induced foam cell formation in Raw264.7 macrophages by activating the PPARγ pathway[3].

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

    Western Blot Analysis[2]

    Cell Line: Human umbilical vein endothelial cells (HUVECs) treated with 25 μg/mL ox-LDL
    Concentration: 50 nM, 100 nM, 200 nM
    Incubation Time: 48 h
    Result: Decreased the protein expression of NLRP3, ASC, cleaved caspase-1, GSDMD-N, IL-1β, and IL-18.

    Western Blot Analysis[3]

    Cell Line: Raw264.7 macrophages treated with ox-LDL
    Concentration: 50 nM, 100 nM, 200 nM
    Incubation Time: 48 h
    Result: Increased PPARγ, SR-B1, ApoE, ABCA1.
    Decreased SR-A, LOX-1, CD36.
    In Vivo

    Inclisiran (1-10 mg/kg; i.p.; 20 weeks) sodium inhibits the development of atherosclerosis and pyroptosis-related factor expression in high-fat diet-induced atherosclerotic ApoE-/- mice[2].

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

    Animal Model: Male ApoE-/- mice (8 weeks old, 17-20 g); high-fat diet (HFD)-induced atherosclerosis model[2]
    Dosage: 1, 5, 10 mg/kg (dissolved in PBS)
    Administration: Intraperitoneal injection; 20 weeks
    Result: Significantly reduced LDL-C, TC, TG, and increased HDL-C in plasma.
    Decreased aortic plaque area and lipid deposition.
    Decreased pyroptosis-related factors (NLRP3, ASC, GSDMD, IL-1β, IL-18).
    Molecular Weight

    16339.6 (free acid)

    Formula

    C529H707F12N176O316P43S6.xNa

    Appearance

    Solid

    Color

    White to light yellow

    SMILES

    [Inclisiran (sodium)]

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    -20°C, sealed storage, away from moisture

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

    Purity & Documentation

    Purity: 99.08%

    References
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    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    Product Name:
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    Cat. No.:
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