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Nicotinamide Hydrochloride  (Synonyms: Niacinamide Hydrochloride; Nicotinic acid amide Hydrochloride)

Cat. No.: HY-B0150A
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Nicotinamide Hydrochloride is a form of vitamin B3 or niacin. Nicotinamide Hydrochloride inhibits SIRT2 activity (IC50: 2 μM). Nicotinamide Hydrochloride also inhibits SIRT1. Nicotinamide Hydrochloride increases cellular NAD+, ATP, ROS levels. Nicotinamide Hydrochloride inhibits tumor growth and improves survival. Nicotinamide Hydrochloride also has anti-HBV activity.

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

Nicotinamide Hydrochloride Chemical Structure

Nicotinamide Hydrochloride Chemical Structure

CAS No. : 25334-23-0

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Other In-stock Forms of Nicotinamide Hydrochloride:

Other Forms of Nicotinamide Hydrochloride:

Top Publications Citing Use of Products

58 Publications Citing Use of MCE Nicotinamide Hydrochloride

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    Nicotinamide Hydrochloride purchased from MedChemExpress. Usage Cited in: Pharmacol Res. 2024 Dec 31:107573.  [Abstract]

    Nicotinamide (NAM) (10 μM) enhanced ISO (10 μM)-induced YAP acetylation in neonatal rat cardiomyocytes (NRCMs).

    Nicotinamide Hydrochloride purchased from MedChemExpress. Usage Cited in: Oncoimmunology. 2025 Dec;14(1):2460281.  [Abstract]

    Nicotinamide (NAM) (6 h) promotes CPT2 acetylation in SK-N-AS cells.

    Nicotinamide Hydrochloride purchased from MedChemExpress. Usage Cited in: Apoptosis. 2024 Dec 25.  [Abstract]

    Nicotinamide (NAM) (20 mM; pretreatment for 24 hours before LPS exposure in MLE-12 cells) increases GPX4 acetylation levels in MLE-12 cells.

    Nicotinamide Hydrochloride purchased from MedChemExpress. Usage Cited in: Cell Death Differ. 2023 Oct 12.  [Abstract]

    Nicotinamide (NAM) (10 mM, 4 h)​​ enhances RACK1 acetylation levels in OVCAR3 and SKOV3 cells in combination with Trichostatin A (TSA) (HY-15144) (0.2 μM, 4 h).

    Nicotinamide Hydrochloride purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2022 May 17;8(1):265.  [Abstract]

    Nicotinamide (NAM) (6-8 h) upregulates stathmin1 acetylation in 293T cells transfected with stathmin1-Flag plasmids.

    Nicotinamide Hydrochloride purchased from MedChemExpress. Usage Cited in: Nat Commun. 2021 Jul 9;12(1):4227.  [Abstract]

    Nicotinamide (80 μM; 4-8 h) markedly increases GLDC K514 acetylation in U251 and U87 cells.

    Nicotinamide Hydrochloride purchased from MedChemExpress. Usage Cited in: Hum Reprod. 2020 Mar 27;35(3):494-503.  [Abstract]

    Nicotinamide (NAM) (40 mM; 1 h) increases the global level of lysine 2-hydroxyisobutyrylation along the human sperm tail.

    Nicotinamide Hydrochloride purchased from MedChemExpress. Usage Cited in: Hum Reprod. 2019 Jul 8;34(7):1186-1194.  [Abstract]

    Nicotinamide (NAM) (20-40 mM; 1 h) increases global levels of Kac (lysine acetylation) and Kglu (lysine glutarylation) in human sperm.

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    Description

    Nicotinamide Hydrochloride is a form of vitamin B3 or niacin. Nicotinamide Hydrochloride inhibits SIRT2 activity (IC50: 2 μM). Nicotinamide Hydrochloride also inhibits SIRT1. Nicotinamide Hydrochloride increases cellular NAD+, ATP, ROS levels. Nicotinamide Hydrochloride inhibits tumor growth and improves survival. Nicotinamide Hydrochloride also has anti-HBV activity[1][2][3][4].

    IC50 & Target[1][2]

    Human Endogenous Metabolite

     

    SIRT2

    2 μM (EC50)

    SIRT1

    50-180 μM (IC50)

    In Vitro

    Nicotinamide Hydrochloride (0-50 mM, 24/48 h ) reduces cell number in a time-dependent and dose-dependent manner in A375 and SK-MEL-28 cells[1].
    Nicotinamide Hydrochloride (10-50 mM, 24 h ) makes A375 cells undergo accumulation in G1 phase, reduction in S phase, and increase inthe sub-G1 (apoptosis) phase[1].
    Nicotinamide Hydrochloride (1-50 mM, 6 h ) increases NAD+, ATP and ROS levels in A375 and SK-MEL-28 cells[1].
    Nicotinamide Hydrochloride (0.01-20 mM, 1 h) inhibits purified SIRT2 enzymatic activity in vitro with an EC50 of 2 μM[1].
    Nicotinamide Hydrochloride (0-64 mM) inhibits HBV replication in HepAD38 and HepG2.2.15 cells[3].
    Nicotinamide Hydrochloride (10 mM, on day 13) promotes pancreatic cell differentiation from human embryonic stem cells (hESCs) through CK1 and ROCK inhibition[4].

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

    Cell Viability Assay[1]

    Cell Line: A375, SK-MEL-28, mouse B16-F10 cell
    Concentration: 0, 1, 20, 50 mM
    Incubation Time: 24 h, 48 h
    Result: Reduced cell number in a dose-dependent manner with a strong inhibitory effect at 20mM and an almost complete effect at 50 mM.

    Cell Cycle Analysis[1]

    Cell Line: A375, SK-MEL-28
    Concentration: 10, 20, 50 mM
    Incubation Time: 24 h
    Result: Arrested A375 cells in G1 phase.
    In Vivo

    Nicotinamide Hydrochloride (Intraperitoneal injection, 1500 and 1800 mg/Kg, 5 days per week) inhibits tumor growth in murine metastatic melanoma model[1].
    Nicotinamide Hydrochloride (Intraperitoneal injection, 1800 mg/Kg, once a day, murine metastatic melanoma model) affects IFN-γ (a key mediator of cell-mediated anti-tumor immunity), increases the plasma levels of Eotaxin and IL-5, reduces the plasma levels of IL-3, IL-12, RANTES and IL-10[1].
    Nicotinamide Hydrochloride (vein injection, 0-200 mg/kg, 5 days) inhibits HBV replication in HBV-transgenic mice[3].

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

    Animal Model: C57BL/6 mice (subcutaneous injected with B16-F10 cells)[1]
    Dosage: 1000, 1500, 1800 mg/Kg.
    Administration: Intraperitoneal injection, 5 days per week (followed by 2-day rest) or once a day.
    Result: Inhibited tumor growth at 1500 and 1800 mg/Kg, and had no effect on the body weight.
    Increased the frequency of IFN-γ producing cells and modulated the protein levels of cytokines and chemokines in the plasma of tumor-bearing mice.
    Animal Model: HBV-transgenic mice[3]
    Dosage: 0-200 mg/kg
    Administration: Vein injection, 5 days
    Result: Reduced serum HBV DNA.
    Clinical Trial
    Molecular Weight

    158.59

    Formula

    C6H7ClN2O

    CAS No.
    SMILES

    O=C(C1=CC=CN=C1)N.[H]Cl

    Structure Classification
    Initial Source
    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    Please store the product under the recommended conditions in the Certificate of Analysis.

    Purity & Documentation
    References
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      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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