Histamine

Catalog No.S3968 Batch:S396802

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Technical Data

Formula

C5H9N3

Molecular Weight 111.15 CAS No. 51-45-6
Solubility (25°C)* In vitro DMSO 22 mg/mL (197.93 mM)
Water 22 mg/mL (197.93 mM)
Ethanol 22 mg/mL (197.93 mM)
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
* Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

Biological Activity

Description Histamine, an organic nitrogenous compound, is involved in local immune responses regulating physiological function in the gut and acting as a neurotransmitter for the brain, spinal cord, and uterus. It is a potent H1 and H2 receptor agonist.
In vitro Histamine stimulates the proliferation of human articular chondrocytes in culture. Histamine is reported to modify the behaviour of many cell types in vitro, including chondrocytes, fibroblasts, macrophages, epithelial cells, endothelial cells, and T cells. Histamine also modulates the production of many cytokines and the expression of their receptors. Histamine regulates cellular processes through the expression of histamine receptors. Histamine stimulates the production of matrix metalloproteinases (MMPs)-13 and -3 (collagenase 3 and stromelysin-1, respectively) by histidine decarboxylase (HAC) in vitro[1].
In vivo Histamine has a recognised role in allergic and inflammatory reactions and is an important modulator of numerous physiological processes, including cell proliferation, angiogenesis, and vasopermeability[1]. Histamine dilates vasculature, increases blood flow, while it induces hyperpermeability in venula. It disrupts endothelial barrier formation of venula indicated by changes in vascular endothelial cadherin (VE-cadherin) localization at endothelial cell junction[3].

Protocol (from reference)

Cell Assay:[1]
  • Cell lines

    human articular chondrocytes

  • Concentrations

    1-100 μmol/l

  • Incubation Time

    6 days

  • Method

    Cells are grown to confluence in 80 cm2 culture flasks in Dulbecco's modified Eagle's medium (DMEM) + 10% fetal calf serum (FCS). At first or second passage, cells are seeded into 96 well culture plates, at densities of approximately 2×103 cells/well. After 24 hours the cells are treated with either DMEM +2% FCS alone (control), or DMEM + 2% FCS plus histamine range 1-100 μmol/l (minimum of eight wells for each treatment). The medium with or without histamine is replenished every 48 hours, and after six days cell growth is estimated.

Animal Study:[2]
  • Animal Models

    New Zealand adult healthy albino rabbits

  • Dosages

    50, 100, 200 μg/kg

  • Administration

    s.c.

Selleck's Histamine has been cited by 2 publications

FUNDC1 alleviates doxorubicin-induced cardiotoxicity by restoring mitochondrial-endoplasmic reticulum contacts and blocked autophagic flux [ Theranostics, 2024, 14(9):3719-3738] PubMed: 38948070
Benidipine, an anti-hypertensive drug, relaxes mouse airway smooth muscle [ Life Sci, 2019, 227:74-81] PubMed: 31002920

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SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.

NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.