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histamine

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EntityQ61233· pop 66· linked from 1,846 articles

Also known as 2-(1H-imidazol-5-yl)ethanamine, 2-(1H-imidazol-5-yl)ethylamine, 4-Imidazoleethylamine, 2-(1H-imidazol-4-yl)ethan-1-amine, 4-(2-Aminoethyl)imidazole, 2-Imidazol-4-yl-Ethylamine, Eramin, HSM

Histamine or histamin is an organic nitrogenous compound involved in local immune responses communication, as well as regulating physiological functions in the gut and acting as a neurotransmitter for the brain, spinal cord, and uterus. Discovered in 1910, histamine has been considered a local hormone (autocoid) because it is produced without involvement of the classic endocrine glands; however, in recent years, histamine has been recognized as a central neurotransmitter. Histamine is involved in the inflammatory response and has a central role as a mediator of itching. As part of an immune re

OverviewAI-generated

Histamine is a chemical compound with the formula C₅H₉N₃ and a molecular weight of 111.15. Its IUPAC name is 2-(1H-imidazol-5-yl)ethanamine, and its canonical SMILES representation is C1=C(NC=N1)CCN. The substance has a melting point of 182.3 and a boiling point of 409.1. It possesses a calculated xlogP value of -0.7 and a topological polar surface area of 54.7.

The molecule contains two hydrogen bond donors and two hydrogen bond acceptors, with a net charge of 0. In academic literature, a search for histamine yields 96,190 results. The subject is referenced by 1,846 other encyclopedia articles.

Synthesized by Vinony from 20 facts across 4 sources: Wikidata, PubChem, PubMed, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.

Chemical data

Formula
C5H9N3
Molecular weight
111.15 g/mol
IUPAC name
2-(1H-imidazol-5-yl)ethanamine
SMILES
C1=C(NC=N1)CCN
InChIKey
NTYJJOPFIAHURM-UHFFFAOYSA-N
XLogP
-0.7
Polar surface area
54.7 Ų
H-bond donors
2
H-bond acceptors
2
Formal charge
0

via PubChem

Research

96,190 papers

via PubMed

~23 min read

Encyclopedic overview

20 sections
Contents
  • Properties
  • Synthesis and metabolism
  • Storage and release
  • Degradation
  • Mechanism of action
  • Roles in the body
  • Vasodilation and fall in blood pressure
  • Effects on nasal mucous membrane {{Anchor|Effects on Nasal Mucosa}}
  • Sleep-wake regulation
  • Gastric acid release
  • Protective effects
  • Erection and sexual function
  • Schizophrenia
  • Multiple sclerosis
  • Disorders
  • Measurement
  • History
  • See also
  • References
  • External links

Histamine or histamin is an organic nitrogenous compound involved in local immune responses communication, as well as regulating physiological functions in the gut and acting as a neurotransmitter for the brain, spinal cord, and uterus. Discovered in 1910, histamine has been considered a local hormone (autocoid) because it is produced without involvement of the classic endocrine glands; however, in recent years, histamine has been recognized as a central neurotransmitter. Histamine is involved in the inflammatory response and has a central role as a mediator of itching. As part of an immune response to foreign pathogens, histamine is produced by basophils and by mast cells found in nearby connective tissues. Histamine increases the permeability of the capillaries to white blood cells and some proteins, to allow them to engage pathogens in the infected tissues. It consists of an imidazole ring attached to an ethylamine chain; under physiological conditions, the amino group of the side-chain is protonated.

== Properties == Histamine base, obtained as a mineral oil mull, melts at . Hydrochloride and phosphorus salts form white hygroscopic crystals and are easily dissolved in water or ethanol, but not in ether. In aqueous solution, the imidazole ring of histamine exists in two tautomeric forms, identified by which of the two nitrogen atoms is protonated. The nitrogen farther away from the side chain is the 'tele' nitrogen and is denoted by a lowercase tau sign and the nitrogen closer to the side chain is the 'pros' nitrogen and is denoted by the pi sign. The tele tautomer, Nτ-H-histamine, is preferred in solution as compared to the pros tautomer, Nπ-H-histamine.

Excerpted from Wikipedia’s “histamine” article, available under the CC BY-SA 4.0 licence.

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