1. Induced Disease Models Products GPCR/G Protein MAPK/ERK Pathway NF-κB Neuronal Signaling Metabolic Enzyme/Protease Immunology/Inflammation PI3K/Akt/mTOR Apoptosis
  2. Immunology and Inflammatory Disease Models Digestive System Disease Models Akt p38 MAPK Reactive Oxygen Species (ROS) Histamine Receptor Endogenous Metabolite Apoptosis
  3. Gastrointestinal Inflammation and Ulcer Models Gastrointestinal Disease Models
  4. Gastric Ulcer Models Duodenal Ulcer Models
  5. Histamine

Histamine is the agonist for histamine receptor and a vasodilator. Histamine is an organic nitrogen compound that participates in local immune responses, regulates intestinal physiological functions, and acts as a neurotransmitter. Histamine affects p38 MAPK/Akt signaling pathway, exhibits antitumor, antioxidant and anti-inflammatory activities. Histamine can be used in the research of acute myeloid leukemia, malignant melanoma, and renal cell carcinoma.

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

CAS No. : 51-45-6

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Customer Review

Based on 20 publication(s) in Google Scholar

Other Forms of Histamine:

Top Publications Citing Use of Products

    Histamine purchased from MedChemExpress. Usage Cited in: FASEB J. 2025 Jul 15;39(13):e70778.  [Abstract]

    Changes in HRH1 gene expression in F11 cells after treatment with 10−7 mM histamine for 24 h, as measured by RT–qPCR.

    Histamine purchased from MedChemExpress. Usage Cited in: FASEB J. 2025 Jul 15;39(13):e70778.  [Abstract]

    Changes in HRH1 protein expression in F11 cells after treatment with 10−7 mM histamine for 24 h, as detected by western blotting.

    Histamine purchased from MedChemExpress. Usage Cited in: FASEB J. 2025 Jul 15;39(13):e70778.  [Abstract]

    Increase in the Ca2+ peak (DF/F0) in F11 cells from the control, histamine (10−7 mM for 24 h), and histamine+DLT groups (n = 3 in each group).

    Histamine purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2023 Mar;10(7):e2203869.  [Abstract]

    Confocal microscopy of mitochondrial Ca2+ levels in HepG2 transfected with GCaMP6m. Histamine (100 μM) was applied to stimulate mitochondrial Ca2+ accumulation, and the 475/410 fluorescence ratio was analyzed.

    Histamine purchased from MedChemExpress. Usage Cited in: Front Pharmacol. 2019 Nov 15;10:1380.  [Abstract]

    Effects of histamine (0.1%, 20 µL/site, intradermal injection) on scratching behavior in mice.

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    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Histamine is the agonist for histamine receptor and a vasodilator. Histamine is an organic nitrogen compound that participates in local immune responses, regulates intestinal physiological functions, and acts as a neurotransmitter. Histamine affects p38 MAPK/Akt signaling pathway, exhibits antitumor, antioxidant and anti-inflammatory activities. Histamine can be used in the research of acute myeloid leukemia, malignant melanoma, and renal cell carcinoma[1][2][3][4][5][6][7].

    IC50 & Target

    Human Endogenous Metabolite

     

    Cellular Effect
    Cell Line Type Value Description References
    CHO EC50
    640 nM
    Compound: Histamine
    Agonist activity at human recombinant histamine H3 receptor expressed in CHO cells assessed as [35S]GTPgammaS binding after 1 hr by liquid scintillation counting
    Agonist activity at human recombinant histamine H3 receptor expressed in CHO cells assessed as [35S]GTPgammaS binding after 1 hr by liquid scintillation counting
    [PMID: 20384344]
    HEK293 EC50
    13 nM
    Compound: Histamine
    Agonist activity at human SF-His6-tagged histamine H4 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated response incubated for 5 hrs by luciferase reporter gene assay
    Agonist activity at human SF-His6-tagged histamine H4 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated response incubated for 5 hrs by luciferase reporter gene assay
    [PMID: 27007611]
    HEK293 EC50
    94 nM
    Compound: Histamine
    Agonist activity at mouse SF-His6-tagged histamine H4 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated response incubated for 5 hrs by luciferase reporter gene assay
    Agonist activity at mouse SF-His6-tagged histamine H4 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated response incubated for 5 hrs by luciferase reporter gene assay
    [PMID: 27007611]
    Sf9 EC50
    11 nM
    Compound: Histamine
    Agonist activity at human histamine H4 receptor expressed in sf9 cell membrane co-expressing mammalian Galphai2 and Gbeta1gamma2 incubated for 90 mins by [35S]GTPgammaS binding assay
    Agonist activity at human histamine H4 receptor expressed in sf9 cell membrane co-expressing mammalian Galphai2 and Gbeta1gamma2 incubated for 90 mins by [35S]GTPgammaS binding assay
    [PMID: 27007611]
    Sf9 EC50
    11.6 nM
    Compound: 1
    Activity at human recombinant histamine H4 receptor-RGS4 fusion protein expressed in Sf9 cells coexpressing Galphai2 and G-beta-1-gamma-2 by steady-state GTPase activity assay
    Activity at human recombinant histamine H4 receptor-RGS4 fusion protein expressed in Sf9 cells coexpressing Galphai2 and G-beta-1-gamma-2 by steady-state GTPase activity assay
    [PMID: 18950149]
    Sf9 EC50
    1200 nM
    Compound: 1
    Activity at guinea pig recombinant histamine H2 receptor-Gsalpha fusion protein expressed in Sf9 cells by steady-state GTPase activity assay
    Activity at guinea pig recombinant histamine H2 receptor-Gsalpha fusion protein expressed in Sf9 cells by steady-state GTPase activity assay
    [PMID: 18950149]
    Sf9 EC50
    1200 nM
    Compound: 1
    Activity at human recombinant histamine H2 receptor-Gsalpha fusion protein expressed in Sf9 cells by steady-state GTPase activity assay
    Activity at human recombinant histamine H2 receptor-Gsalpha fusion protein expressed in Sf9 cells by steady-state GTPase activity assay
    [PMID: 18950149]
    Sf9 EC50
    13 nM
    Compound: Histamine
    Agonist activity at human histamine H3 receptor expressed in sf9 cell membrane co-expressing mammalian Galphai2 and Gbeta1gamma2 incubated for 90 mins by [35S]GTPgammaS binding assay
    Agonist activity at human histamine H3 receptor expressed in sf9 cell membrane co-expressing mammalian Galphai2 and Gbeta1gamma2 incubated for 90 mins by [35S]GTPgammaS binding assay
    [PMID: 27007611]
    Sf9 EC50
    190 nM
    Compound: 1
    Activity at human recombinant histamine H1 receptor expressed in Sf9 cells coexpressing RGS4 by steady-state GTPase activity assay
    Activity at human recombinant histamine H1 receptor expressed in Sf9 cells coexpressing RGS4 by steady-state GTPase activity assay
    [PMID: 18950149]
    Sf9 EC50
    190 nM
    Compound: Histamine
    Agonist activity at human histamine H1 receptor expressed in sf9 cell membrane co-expressing RGS4 or RGS9 assessed as increase in 32Pi level incubated for 20 mins by liquid scintillation counting in presence of [gamma32P]GTP
    Agonist activity at human histamine H1 receptor expressed in sf9 cell membrane co-expressing RGS4 or RGS9 assessed as increase in 32Pi level incubated for 20 mins by liquid scintillation counting in presence of [gamma32P]GTP
    [PMID: 27007611]
    Sf9 EC50
    25.1 nM
    Compound: 1
    Activity at human recombinant histamine H3 receptor expressed in Sf9 cells coexpressing Galphai, G-beta-1-gamma-2 and RGS4 by steady-state GTPase activity assay
    Activity at human recombinant histamine H3 receptor expressed in Sf9 cells coexpressing Galphai, G-beta-1-gamma-2 and RGS4 by steady-state GTPase activity assay
    [PMID: 18950149]
    In Vitro

    Histamine (0.01-10 μM, 72 h) exhibits a bidirectional regulatory effect on the proliferation of MDA-MB-231, arrests the cell cycle at G2/M phase, induces the formation of lipid droplet, induces differentiation and apoptosis in MDA-MB-231[4].
    Histamine (10 μM, 24 h) increases the generation of ROS, especially H2O2, reduces the activity of antioxidant enzymes (such as catalase), thereby promoting radiosensitivity in MDA-MB-231[4].
    Histamine (1-100 μM, 12 h) inhibits the migration of microglia and the release of inflammatory mediator IL-1β in LPS (HY-D1056)-stimulated N9 mouse microglial, exhibits anti-inflammatory activity[5].

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

    Cell Proliferation Assay[4]

    Cell Line: MDA-MB-231
    Concentration: 0.01-10 µM
    Incubation Time: 72 h
    Result: Promoted cell proliferation at 10 µM, inhibited cell proliferation at 0.01 µM.

    Apoptosis Analysis[4]

    Cell Line: MDA-MB-231
    Concentration: 10 µM
    Incubation Time: 48 h
    Result: Induced apoptosis.
    In Vivo

    Note:
    Please do not refer to only one article to determine the experimental conditions. It is recommended to determine the optimal experimental conditions (animal strain, age, dosage, frequency and cycle, detection time and indicators, etc.) through preliminary experiments before the formal experiment.

    Histamine (0.05-100 μg/mouse, icv, single dose) exhibits analgesic effect at high doses of histamine (50-100 μg/mouse), causes hyperalgesia at low doses (0.1-1 μg/mouse) in mouse model[3].
    Histamine dihydrochloride (62.5-2000 μg; Intravaginal injection) can exert a similar effect to estrogen in ovariectomized mice, causing a decrease in intravaginal tetrazolium, an increase in epithelial growth, and keratinization[6].
    Histamine can be used in animal modeling to create gastrointestinal ulcer models[1].

    Induction of Gastrointestinal Ulcer[1]
    Background
    Histamine can cause increased gastric acid secretion, decreased mucus production, reflux of pancreatic juice, poor gastric blood flow, and thus gastric ulcers. Stress can cause increased gastrointestinal motility, making the gastric folds more susceptible to damage when exposed to acid.
    Specific Modeling Methods
    Guinea Pig: male • albino • Administration: 5 mg/kg • i.p. • single dose
    Note
    (1) No eating or drinking is allowed 24 hours before the experiment.
    (2) The animals are sacrificed 2 hours after histamine injection, and treated with 1% formalin to check for gastric ulcers.
    Modeling Indicators
    The ulcers were punctate or elongated. After the model was dissected, the ulcer index (the sum of the lengths of the lesions) was measured under a microscope to be 3.4 mm.
    Correlated Product(s): Serotonin (HY-B1473A); Reserpine (HY-N0480)
    Opposite Product(s): Cimetidine (HY-14289)

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

    Animal Model: Mouse model[3]
    Dosage: 0.05-100 μg/mouse
    Administration: icv, single dose
    Result: Prolonged the licking latency at the dose of 50 and 100 μg/mouse.
    Shortened the licking latency at the dose of 0.1-1 μg/mouse.
    Animal Model: Ovariectomized female mice of the SW strain[6]
    Dosage: 62.5-2000 μg
    Administration: Intravaginal injection
    Result: Stimulated a vaginal response similar to that caused by estrogen, resulting in a decrease in intravaginal tetrazolium, increased epithelial growth, and keratinization.
    Clinical Trial
    Molecular Weight

    111.15

    Formula

    C5H9N3

    CAS No.
    Appearance

    Solid

    Color

    White to yellow

    SMILES

    NCCC1=CN=CN1

    Structure Classification
    Initial Source
    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    -20°C, stored under nitrogen, away from moisture

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

    Solvent & Solubility
    In Vitro: 

    H2O : 100 mg/mL (899.69 mM; Need ultrasonic)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 8.9969 mL 44.9843 mL 89.9685 mL
    5 mM 1.7994 mL 8.9969 mL 17.9937 mL
    View the Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (stored under nitrogen, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

    • Molarity Calculator

    • Dilution Calculator

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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    =
    Concentration
    ×
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    Molecular Weight *

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

    C1

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    Volume (start)

    V1

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    C2

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    V2

    In Vivo:

    For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  PBS

      Solubility: 100 mg/mL (899.69 mM); Clear solution; Need ultrasonic

    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

    Dosage

    mg/kg

    Animal weight
    (per animal)

    g

    Dosing volume
    (per animal)

    μL

    Number of animals

    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Calculation results:
    Working solution concentration: mg/mL
    This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
    The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).
    Purity & Documentation

    Purity: 99.99%

    References

    Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (stored under nitrogen, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    H2O 1 mM 8.9969 mL 44.9843 mL 89.9685 mL 224.9213 mL
    5 mM 1.7994 mL 8.9969 mL 17.9937 mL 44.9843 mL
    10 mM 0.8997 mL 4.4984 mL 8.9969 mL 22.4921 mL
    15 mM 0.5998 mL 2.9990 mL 5.9979 mL 14.9948 mL
    20 mM 0.4498 mL 2.2492 mL 4.4984 mL 11.2461 mL
    25 mM 0.3599 mL 1.7994 mL 3.5987 mL 8.9969 mL
    30 mM 0.2999 mL 1.4995 mL 2.9990 mL 7.4974 mL
    40 mM 0.2249 mL 1.1246 mL 2.2492 mL 5.6230 mL
    50 mM 0.1799 mL 0.8997 mL 1.7994 mL 4.4984 mL
    60 mM 0.1499 mL 0.7497 mL 1.4995 mL 3.7487 mL
    80 mM 0.1125 mL 0.5623 mL 1.1246 mL 2.8115 mL
    100 mM 0.0900 mL 0.4498 mL 0.8997 mL 2.2492 mL

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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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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