Histamine [51-45-6]

Katalog-Nummer HY-B1204-100mg

Size : 100mg

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Histamine is an organic nitrogenous compound involved in local immune responses as well as regulating physiological function in the gut and acting as a neurotransmitter.

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Histamine Chemische Struktur

Histamine Chemische Struktur

CAS. Nr. : 51-45-6

This product is a controlled substance and not for sale in your territory.

Based on 8 publication(s) in Google Scholar

Other Forms of Histamine:

  • Histamine phosphate In-stock
  • Histamine dihydrochloride In-stock
  • Histamine-α,α,β,β-d4 dihydrochloride In-stock
Beschreibung

Histamine is an organic nitrogenous compound involved in local immune responses as well as regulating physiological function in the gut and acting as a neurotransmitter.

IC50 & Target

Human Endogenous Metabolite

 

In Vivo

Histamine can be used in animal modeling to construct gastrointestinal ulcer models. After intravenous injection of histamine hydrochloride, the maximum concentration and AUC of histamine in liver and liver tumor tissues were higher than those in subcutaneous tissue[1].
Induction of Gastrointestinal Ulcer[2]
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 Mmodeling 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.

Klinische Studie
Molekulargewicht

111.15

Formel

C5H9N3

CAS. Nr.

51-45-6

Unlabeled Cas

Appearance

Solid

Color

Off-white to yellow

SMILES

NCCC1=CN=CN1

Structure Classification
  • Others
Initial Source
  • Endogenous metabolite
  • Human Gut Microbiota Metabolites
  • Microorganisms
Versand

Room temperature in continental US; may vary elsewhere.

Speicherung

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

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

Lösungsmittel & Löslichkeit
In Vitro: 

H2O : ≥ 34 mg/mL (305.89 mM)

*"≥" means soluble, but saturation unknown.

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.

  • Molaritätsrechner

  • Verdünnungsrechner

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

Mass
=
Concentration
×
Volume
×
Molecular Weight *

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

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

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).
Reinheit & Dokumentation

Purity: 99.99%

Verweise
  • [1]. Rizell M, Naredi P, Lindnér P, Hellstrand K, Sarno M, Jansson PA. Histamine pharmacokinetics in tumor and host tissues after bolus-dose administration in the rat. Life Sci. 2002 Jan 11;70(8):969-76.  [Content Brief]

    [2]. Okabe S, et al. Effects of cimetidine, a histamine H2-receptor antagonist, on various experimental gastric and duodenal ulcers. Am J Dig Dis. 1977 Aug;22(8):677-84.  [Content Brief]

  • [1]. Rizell M, Naredi P, Lindnér P, Hellstrand K, Sarno M, Jansson PA. Histamine pharmacokinetics in tumor and host tissues after bolus-dose administration in the rat. Life Sci. 2002 Jan 11;70(8):969-76.

    [2]. Okabe S, et al. Effects of cimetidine, a histamine H2-receptor antagonist, on various experimental gastric and duodenal ulcers. Am J Dig Dis. 1977 Aug;22(8):677-84.

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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Histamine Related Classifications

  • Induced Disease Models Products
  • Immunology and Inflammatory Disease Models Digestive System Disease Models
  • Gastrointestinal Inflammation and Ulcer Models Gastrointestinal Disease Models
  • Gastric Ulcer Models Duodenal Ulcer Models
  • GPCR/G Protein Neuronal Signaling Immunology/Inflammation Metabolic Enzyme/Protease
  • Histamine Receptor Endogenous Metabolite
Help & FAQs

Keywords:

Histamine51-45-6ErgamineHistamine ReceptorEndogenous MetaboliteInhibitorinhibitorinhibit

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